Showing posts with label CMECE. Show all posts
Showing posts with label CMECE. Show all posts

Friday, 21 March 2014

New Guidance Will Up Statin Use by 13 Million (CME/CE)

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Published: Mar 20, 2014 | Updated: Mar 21, 2014

Millions more people are now eligible for statin therapy under the 2013 guidelines from the American College of Cardiology and the American Heart Association.The increase comes mostly from those who would be eligible to take statins for primary prevention, mostly in adults ages 60 to 75, and would be expected to result in many fewer cardiovascular events.

An additional 12.8 million Americans ages 40 to 75 are eligible for statin therapy under the latest prevention guidelines from the American College of Cardiology and American Heart Association, researchers estimated.

That represents an increase from about 43.2 million individuals (37.5% of that age group) eligible for statins under the previous guidelines released about a decade ago to about 56 million (48.6%) under the new guidance, according to Michael Pencina, PhD, of the Duke Clinical Research Institute, and colleagues.

Most of the additional coverage would occur in the primary prevention setting and in individuals 60 and older, they reported online in the New England Journal of Medicine.

"I think this current study emphasizes the fact that if we were to fastidiously apply the new guidelines to the current population of patients we should all in our practices be expanding the indication for statins pretty significantly," commented Sahil Parikh, MD, an interventional cardiologist at University Hospitals Harrington Heart & Vascular Institute in Cleveland.

The authors acknowledged, however, that the estimates assumed that everybody eligible for statin therapy under the guidelines would actually receive a prescription even though "the new guidelines call for an informed risk-benefit discussion between the patient and physician before the initiation of statin therapy."

And that's a key consideration because the discussion should include information on lifestyle and other risk factors, potential adverse effects and drug-drug interactions, and patient preferences, Neil Stone, MD, of Northwestern Memorial Hospital's Bluhm Cardiovascular Institute, in Chicago, told MedPage Today.

"In older adults especially, even if they had a [10-year cardiovascular disease] risk of 7.5% or more, the risk estimator doesn't prescribe a statin, the discussion does," said Stone, who served as chair of the expert panel in charge of the cholesterol guidance. "Some patients whose only risk factor is age may decide with their clinician not to pursue statin therapy. Others who are slightly under the 7.5% but have other important factors mentioned in the report may decide to be on a statin."

"We hope, if careful attention is paid to the guidelines, that we're treating those people more likely to benefit," Stone added.

The ACC/AHA prevention guidelines, which were released in November, include guidance on better assessing the risk of atherosclerotic cardiovascular disease and on managing lifestyle, cholesterol, and weight. But the cholesterol guidance received the most attention because it moved away from treating to LDL cholesterol targets and toward treating the level of risk.

Concerns also were expressed about the increase in the number of individuals who would be deemed eligible for statin therapy in the new guidelines compared with the previous recommendations from the Third Adult Treatment Panel (ATP III) of the National Cholesterol Education Program first released in 2001 and then updated in 2004.

To estimate the actual increase, Pencina and colleagues started with data from 3,773 individuals ages 40 to 75 who participated in the National Health and Nutrition Examination Surveys of 2005 to 2010.

Of those individuals, 42% were receiving or would be eligible for statins based on the ATP III criteria, a figure that increased to 56.6% using the criteria from the new guidelines.

That information was then extrapolated to the population of 115.4 million U.S. adults ages 40 to 75 to identify the increase of 12.8 million who would be eligible for statin therapy under the new guidance. Of the newly eligible people, the median age would be 63.4 and 61.7% would be men. Also, the median LDL cholesterol would be 105.2 mg/dL, which is lower than the median of 120.4 mg/dL for those eligible under the ATP-III criteria.

Most of the increase in those deemed eligible for statin therapy (10.4 million) would occur in adults without cardiovascular disease (primary prevention) and in those in the upper end of the age range (60 to 75).

"Since the prevalence of cardiovascular disease rises markedly with age, the large proportions of older adults who would be eligible for statin therapy may be justifiable," the authors wrote.

They also determined that the increases would occur both in adults who would be expected to have future cardiovascular events and those who would not. Thus, sensitivity rises and specificity drops.

Still, they calculated that about 475,000 cardiovascular events would be prevented using the new guidelines instead of the older ones, assuming full adoption and adherence.

"I think what we'll look forward to seeing is what the economic impact of this is," Parikh said. "In the current era of [the] Affordable Care Act and accountable care organizations I think we're all looking very carefully at resource allocation, and we'll have to see -- is it, in fact, worth the extra money on a population basis to expand the indication for statins when it comes to event reduction?"

Pencina and colleagues noted some limitations of their analysis, including the reliance on NHANES data, the extrapolation of data from a relatively small sample to the larger population, the assumption that the new guidelines would be universally adopted and implemented, and the lack of information on treatment adherence.

The study was supported in part by the Duke Clinical Research Institute's research funds and unrestricted grants from M. Jean de Granpré and Louis and Sylvia Vogel.

Pencina disclosed relevant relationships with McGill University Health Center and AbbVie. One of his co-authors disclosed relevant relationships with Janssen, Eli Lilly, and Boehringer Ingelheim.

From the American Heart Association:

Todd Neale, MedPage Today Staff Writer, got his start in journalism at Audubon Magazine and made a stop in directory publishing before landing at MedPage Today. He received a B.S. in biology from the University of Massachusetts Amherst and an M.A. in journalism from the Science, Health, and Environmental Reporting program at New York University.

BMI Loss Lasting With 3 Bariatric Surgery Options (CME/CE)

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Published: Mar 20, 2014 | Updated: Mar 21, 2014

At 5-year follow-up in a meta-analysis, bariatric surgery appeared to provide sustained effects on weight loss.Sleeve gastrectomy appeared to be more effective in weight loss than adjustable gastric banding and comparable with gastric bypass.

Three commonly performed bariatric surgery procedures led to substantial and durable weight loss with a low mortality risk, concluded the authors of an expansive review and meta-analysis of both randomized clinical trials (RCTs) and observational studies.

Five years after surgery the 161,756 patients included in the analysis maintained 26% to 37% of the loss from baseline body mass index (BMI). Results from 37 randomized clinical trials (RCTs) showed a 30-day mortality of 0.08% and mortality beyond 30 days of 0.31%.

Complications remained fairly common (17% overall), and the reoperation rate was 7%.

Consistent with previous studies, gastric bypass resulted in the greatest weight loss, and adjustable gastric banding was associated with the lowest complication rate. The newer sleeve gastrectomy procedure seemed to offer the best combination of weight loss and safety, as reported online in JAMA Surgery.

"We observed higher mortality in observational studies than in RCTs, which could be attributed to longer follow-up time in observational studies or a higher chance that mortality recorded in observational studies was not associated with surgery," Su-Hsin Chang, PhD, of Washington University in St. Louis, and co-authors reported.

"We also found higher complication, reoperation, and comorbidity remission rates in RCTs. This could be explained by more detailed monitoring and reporting of outcomes in RCTs because of smaller sample sizes and shorter follow-up times. Despite these differences, the direction of the effects is the same in all aspects."

As the database for clinical outcomes in bariatric surgery has grown, several issues have emerged regarding generalizability. Early clinical trials provided data for specific procedures performed in different sets of patients. Some of the better known reviews did not include studies conducted after 2003, the authors noted in their introduction.

Recent meta-analyses focused on RCTs and excluded data from early publications. Moreover, advances in surgical technology and increased experience of surgeons are not adequately represented in previous reviews, the authors continued.

Chang and colleagues performed a systematic review and meta-analysis aimed at quantifying risks and benefits of specific bariatric procedures in adults. They defined risks as perioperative and postoperative mortality, complications, and reoperation rates. Benefits comprised weight loss and remission of obesity-related diseases.

The review encompassed studies reported from Jan. 1, 2003, to March 31, 2012.

The 164 articles included in the final analysis consisted of 62 publications from 2003 to 2007 and 102 from 2008 to 2012. A third of the studies (54) were conducted in North America, 72 in Europe, 13 in Asia, and 25 in other regions. A majority of the studies (92) had follow-up of at least 2 years.

The patients had a mean age of 44.6, preoperative mean BMI of 45.62, and preoperative mean weight of 274 pounds. Almost 80% were women.

Obesity-associated comorbidities included type 2 diabetes in 26%, hypertension in 47%, dyslipidemia in 27%, sleep apnea in 25%, and cardiovascular disease in 7%.

Observational studies reported higher mortality as compared with the RCTs (0.22% at 30 days, 0.35% >30 days). Also in the observational studies, adjustable gastric banding was associated with the lowest perioperative and postoperative mortality (0.07% and 0.21%), followed by sleeve gastrectomy (0.29% and 0.34%), and gastric bypass (0.38% and 0.72%).

Meta-analyses of complications comprised data from 64 studies. Complication rates were 17% in 16 RCTs and 10% in 48 observational studies. Similar rates were associated with each of the three surgical procedures evaluated.

Re-operation rates were similar in RCTs and observational studies (7% and 6%). The re-operation rate was lowest for gastric bypass (3%) in RCTs, whereas sleeve gastrectomy was associated with the lowest re-operation rate in observational studies (3%). Adjustable gastric banding had the highest re-operation rate in RCTs (12%) and observational studies (7%).

Change in BMI at 1 year was reported by 69 studies, and 11 studies had 5-year BMI data. BMI loss within 5 years of surgery ranged from 12 to 17 across observational studies. Two reports from the long-running Swedish Obese Subjects Study showed BMI loss of 6.5 at 10 years and 7.1 at 15 years.

The analysis of comorbidity outcomes comprised data from 53 studies. Remission of type 2 diabetes occurred in 92% of patients in RCTs and 86% of patients in observational studies. Hypertension remission rates were 75% in RCTs and 74% in observational studies.

The analysis of dyslipidemia remission included five RCTs, 20 observational studies, and almost 1,800 patients. Remission rates were 76% in the RCTs and 68% in the observational studies.

Sleep apnea remission was reported in five RCTs and 27 observational studies involving a total of 9,900 patients. The apnea remission rate was 96% for the RCTs and 90% for the observational studies. Of 27 patients with cardiovascular disease 58% met criteria for remission.

The study represents an important update of outcomes with different bariatric surgery procedures, said Vivek Prachand, MD, of the University of Chicago. The analysis relied on information published since 2003, whereas previous publications involved older studies.

The use of data from both RCTs and observational studies also distinguishes the analysis from prior reviews, most of which relied on RCTs.

The analysis shows that "bariatric surgery, overall, appears to be a very effective treatment for severe obesity, and it is a safe treatment in terms of mortality rate and complication rate," Prachand told MedPage Today.

"The fact of the matter is, there are several different operations that are being performed and there are differences in outcomes, differences in complications that need to be taken into account when recommending any particular procedure for any individual patient.

One caveat, he added: Chang and colleagues included data from the Swedish trial, which evaluated outcomes with bariatric procedures that are no longer used.

The study was supported by the National Cancer Institute, Foundation for Barnes-Jewish Hospital, and the American Cancer Society.

The authors disclosed no relevant relationships.

Working from Houston, home to one of the world's largest medical complexes, Charles Bankhead has more than 20 years of experience as a medical writer and editor. His career began as a science and medical writer at an academic medical center. He later spent almost a decade as a writer and editor for Medical World News, one of the leading medical trade magazines of its era. His byline has appeared in medical publications that have included Cardio, Cosmetic Surgery Times, Dermatology Times, Diagnostic Imaging, Family Practice, Journal of the National Cancer Institute, Medscape, Oncology News International, Oncology Times, Ophthalmology Times, Patient Care, Renal and Urology News, The Medical Post, Urology Times, and the International Medical News Group newspapers. He has a BA in journalism and MA in mass communications, both from Texas Tech University.

HIV and MS: Could a Link Lead to New MS Treatment? (CME/CE)

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Published: Mar 20, 2014 | Updated: Mar 21, 2014

By John Gever, Deputy Managing Editor, MedPage TodayReviewed by Robert Jasmer, MD; Associate Clinical Professor of Medicine, University of California, San Francisco and Dorothy Caputo, MA, BSN, RN, Nurse PlannerTwo clinical trials now underway offer the first tests of an intriguing but still not widely accepted theory of multiple sclerosis -- that its trigger lies in human endogenous retroviruses," or HERVs.Note that this theory has prompted one trial of the HIV drug raltegravir (Isentress) in MS patients, and another of a monoclonal antibody called GNbAC1 targeting a specific HERV element.

Two clinical trials are now underway that offer the first tests of an intriguing but still not widely accepted theory of multiple sclerosis -- that its trigger lies within a part of the human genome that medical research has largely ignored.

Some researchers in Great Britain and Europe now believe that MS results from activation of "human endogenous retroviruses," or HERVs -- remnants of retroviruses that infected humans eons ago and became incorporated into the germline, such as that it is now part of the human genome.

This theory has prompted a group in the U.K. to begin a trial of the HIV drug raltegravir (Isentress) in about 25 MS patients, to see if the drug affects brain lesions seen in MRI scans. The trial is expected to conclude this August, with results potentially reported before the year is out.

Separately, a Swedish company called GeNeuro Innovation, founded by Swiss researcher Herve Perron, PhD, has developed a monoclonal antibody called GNbAC1 targeting a specific HERV element; safety results from a phase II trial are slated for presentation next month at the American Academy of Neurology's annual meeting.

Background

When the first full sequences of the human genome were released, one of the biggest surprises was how much of the genome appeared to encode retroviral elements such as integrase and helicase enzymes. By one estimate, 8% of the entire genome was made up of such sequences.

At first, these were assumed to be nonfunctional. But subsequent research established that, under some circumstances, they can become activated to express proteins.

It has yet to be proven conclusively that these are pathogenic, as even the proponents of HERV theories of disease will admit. One of the leaders of the U.K. raltegravir trial, Julian Gold, MBBS, MD, of the Albion Street Centre in Sydney, Australia, told attendees at an MS conference last fall that current laboratory methods aren't currently able to provide such proof, at least not for MS.

But there is circumstantial evidence -- several laboratories have isolated HERV proteins from MS lesion samples, and Epstein-Barr virus (EBV), which has itself been a suspected environmental cause of MS, has been found to activate HERV expression in lab studies.

Gavin Giovannoni, MBBCh, of Barts and the London School of Medicine and Dentistry in London, who also helps lead the raltegravir trial with Gold, told MedPage Today that all herpes viruses, of which EBV is one, can trigger HERV expression. But, he said, "EBV is particularly effective in activating HERVs."

Also, according to Gold, HERV expression has been linked to activation of both the innate and adaptive immune systems, providing a connection to the well-documented immunological and inflammatory features of MS.

Although the HERV theory doesn't explain everything about MS, such as the gender imbalance, Giovannoni said the conventional autoimmune paradigm has "lots of holes" too.

"It doesn't explain everything about MS, and as part of a causation theory it should explain everything. It doesn't explain the epidemiology very well, it doesn't explain the sex ratio, it doesn't explain some of the responses to certain therapies," he said.

"That's a clue that we don't know the whole story."

The HIV Connection

Perhaps the most significant piece of evidence for the HERV theory of MS is even more indirect: People with HIV appear to be at vastly reduced risk for MS.

What does HIV status have to do with HERVs or MS? Because nowadays, essentially everyone with HIV in developed countries where broad-based epidemiological research can be conducted is treated with antiretroviral drugs.

Gold is an HIV specialist -- the Albion Street Centre, which he directs, is Australia's largest HIV outpatient clinic. His "aha" moment came when an HIV-positive patient who also had MS came under his care. This patient was first diagnosed with HIV infection in 1985 but managed to avoid developing AIDS before the advent of highly active antiretroviral therapy (HAART) in 1996.

In a 2011 letter published in the European Journal of Neurology, Gold and colleagues described what happened after HAART was begun in 1996:

"Within months of commencing HAART, all MS symptoms gradually improved. Within 2 years, his urinary incontinence was controlled to the extent that he stopped wearing pads and fecal incontinence resolved. He has had no MS relapses."

The disease was not completely eliminated, the researchers indicated, because gadolinium-enhanced MRI scans made in 2002 continued to show lesions consistent with MS, even though clinical symptoms had largely disappeared.

Large-scale epidemiological studies have supported the notion that anti-HIV therapy may suppress MS pathology. A Danish national registry study published in letter form last year in Epidemiology, comparing 5,018 HIV-positive patients with some 50,000 age- and sex-matched individuals from the general population, found that the rate of MS incidence was markedly lower in the HIV patients (3.1 versus 10.4 per 100,000). However, it was not statistically significant because only one HIV patient developed MS during the study period.

Gold and colleagues conducted a similar (but as yet unpublished) study using the much larger U.K. general practice database, which covers some 55 million Britons. At the European MS meeting where he spoke last fall, he reported on results from some 21,000 HIV-positive individuals and 6.7 million controls, followed for a mean of 7 years.

In addition to matching controls to HIV patients by age and sex, they were also matched by region within the country and by the week in which they first came into contact with the national health system.

The relative risk for MS in the HIV patients versus controls was 0.38 (95% CI 0.15-0.79, P=0.011), he reported. The relative risk was even lower, 0.22, when only MS diagnoses occurring more than 1 year after HIV diagnosis were counted (at which point HAART is presumably well established in British HIV patients).

The Clinical Trials

There is no animal model for HERVs in MS, and the ability to study HERVs even in cell culture is limited, Gold said. He argued that "their exact role will only be obtained following appropriate clinical trials. If we wait for the laboratory to give us the answer, we will all have been retired."

Raltegravir was chosen for the U.K. trial for several reasons. One is that it is an HIV integrase inhibitor. "The integrases across HERVs and HIV are quite conserved," Giovannoni said, so that it is likely to be more effective in suppressing HERV elements than other types of antiretroviral drugs. He said it was also unique among antiretrovirals in also showing some potency against members of the herpesvirus family (though only in vitro -- this effect hasn't been studied clinically).

And, its manufacturer was willing to support the small, short-term trial. Gold pointed out that no company that markets MS medications is active in HIV drug development, or vice versa. He and Giovannoni were able to persuade raltegravir's maker, Merck's European subsidiary, to fund the 25-patient study which includes just 3 months of drug treatment after a 3-month baseline observation period. Gold said a longer and larger study would have been preferable but it could not be arranged.

The GNbAC1 monoclonal antibody's sponsor GeNeuro appears to have more resources, with France's Institut Merieux as a major investor. It has already completed a phase I safety study with the agent in healthy volunteers; the results to be presented at the AAN meeting next month are from 10 MS patients.

According to the abstract, no safety problems were seen, and a larger efficacy study is warranted. However, GeNeuro has not said whether or when such a trial would be undertaken.

Caution Reigns

MS specialists in the U.S. contacted by MedPage Today were unanimous in urging caution about HERV theory, although some were warmer to it than others.

Alessandro Serra, MD, of University Hospitals Case Medical Center in Cleveland, told MedPage Today that "many studies" had supported the association between HERV-expressed proteins and MS.

However, these proteins also appear "in patients with other neurological conditions, and even in a proportion of healthy individuals," Serra said.

He said the debate in the community was over "whether HERVs are just bystanders within the normal immune response of MS patients, perhaps unable to handle these viruses, or whether they actually represent a key component of the pathogenic process of MS and even have a causative role."

Jerry Wolinsky, MD, of the University of Texas Health Science Center in Houston, pointed out that the search for MS triggers has been going on for decades and wound up in many blind alleys. Viruses have long been a popular suspect, but "thus far not fruitful."

With regard to retroviruses lurking within the human genome, "to my knowledge there has been no consistently recovered retrovirus sequence associated with brain or other tissues from patients with multiple sclerosis," Wolinsky said.

"That does not mean that one might not be afoot, but the technology is well enough developed that it would be unusual to expect that one will be found in the future, given the failure to do so even with application of modern tools."

Wolinsky added that the 2011 case report from Gold and colleagues, of the HIV/MS patient whose neurological symptoms resolved with HAART, did not persuade him. "The course of MS is very unpredictable," he said, and the disappearance of symptoms may simply have been "serendipitous."

Other experts were also supportive of research while agnostic or skeptical about the HERV theory. For example, Robert Bermel, MD, head of the Cleveland Clinic's Mellen Center for Multiple Sclerosis, told MedPage Today that "It becomes difficult ... to separate the specific effect of antiretroviral therapy from the effect of altered immune status related to HIV, or from the natural tendency of MS disease activity to decline over time."

On the other hand, Anthony Reder, MD, of the University of Chicago, called the HERV theory "important" as well as plausible.

HERVs, he said, result from "hundreds of millions of years of battles with retroviruses. The residual DNA fragments do not produce complete viruses but DNA fragments and retrovirus proteins do leak out and are seen by the immune system."

Serra said he hoped that the two clinical trials wouldn't be taken as make-or-break for the HERV theory. "We need more rigorous models, especially animal models that have been lacking so far. I know there are groups that are looking into it."

In the meantime, everyone who spoke to MedPage Today emphasized that it would be premature for physicians or patients to try antiretroviral drugs on their own as MS therapies. Giovannoni said that some patients have told him that they had succeeded in obtaining raltegravir.

"That's a little premature and we wouldn't recommend it," he said.

The raltegravir trial is supported by Merck. The monoclonal antibody study is funded by GeNeuro.

Giovannoni has had relationships with Bayer Schering Healthcare, Biogen Idec, GW Pharma, Merck Serono, Merz, Novartis, Teva, Sanofi, Eisai, Elan, Five Prime Therapeutics, Genzyme, Genentech, GSK, Ironwood Pharma, Merck Pfizer, Roche, Synthon BV, Teva, UCB Pharma, and Vertex Pharmaceuticals. Other sources reported no potential conflicts of interest.

John Gever, Senior Editor, has covered biomedicine and medical technology for 30 years. He holds a B.S. from the University of Michigan and an M.S. from Boston University. Now based in Pittsburgh, he is the daily assignment editor for MedPage Today as well as general factotum on the reporting side. Go Pirates/Penguins/Steelers!

HIV and MS: Could a Link Lead to New MS Treatment? (CME/CE)

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Published: Mar 20, 2014 | Updated: Mar 21, 2014

By John Gever, Deputy Managing Editor, MedPage TodayReviewed by Robert Jasmer, MD; Associate Clinical Professor of Medicine, University of California, San Francisco and Dorothy Caputo, MA, BSN, RN, Nurse PlannerTwo clinical trials now underway offer the first tests of an intriguing but still not widely accepted theory of multiple sclerosis -- that its trigger lies in human endogenous retroviruses," or HERVs.Note that this theory has prompted one trial of the HIV drug raltegravir (Isentress) in MS patients, and another of a monoclonal antibody called GNbAC1 targeting a specific HERV element.

Two clinical trials are now underway that offer the first tests of an intriguing but still not widely accepted theory of multiple sclerosis -- that its trigger lies within a part of the human genome that medical research has largely ignored.

Some researchers in Great Britain and Europe now believe that MS results from activation of "human endogenous retroviruses," or HERVs -- remnants of retroviruses that infected humans eons ago and became incorporated into the germline, such as that it is now part of the human genome.

This theory has prompted a group in the U.K. to begin a trial of the HIV drug raltegravir (Isentress) in about 25 MS patients, to see if the drug affects brain lesions seen in MRI scans. The trial is expected to conclude this August, with results potentially reported before the year is out.

Separately, a Swedish company called GeNeuro Innovation, founded by Swiss researcher Herve Perron, PhD, has developed a monoclonal antibody called GNbAC1 targeting a specific HERV element; safety results from a phase II trial are slated for presentation next month at the American Academy of Neurology's annual meeting.

Background

When the first full sequences of the human genome were released, one of the biggest surprises was how much of the genome appeared to encode retroviral elements such as integrase and helicase enzymes. By one estimate, 8% of the entire genome was made up of such sequences.

At first, these were assumed to be nonfunctional. But subsequent research established that, under some circumstances, they can become activated to express proteins.

It has yet to be proven conclusively that these are pathogenic, as even the proponents of HERV theories of disease will admit. One of the leaders of the U.K. raltegravir trial, Julian Gold, MBBS, MD, of the Albion Street Centre in Sydney, Australia, told attendees at an MS conference last fall that current laboratory methods aren't currently able to provide such proof, at least not for MS.

But there is circumstantial evidence -- several laboratories have isolated HERV proteins from MS lesion samples, and Epstein-Barr virus (EBV), which has itself been a suspected environmental cause of MS, has been found to activate HERV expression in lab studies.

Gavin Giovannoni, MBBCh, of Barts and the London School of Medicine and Dentistry in London, who also helps lead the raltegravir trial with Gold, told MedPage Today that all herpes viruses, of which EBV is one, can trigger HERV expression. But, he said, "EBV is particularly effective in activating HERVs."

Also, according to Gold, HERV expression has been linked to activation of both the innate and adaptive immune systems, providing a connection to the well-documented immunological and inflammatory features of MS.

Although the HERV theory doesn't explain everything about MS, such as the gender imbalance, Giovannoni said the conventional autoimmune paradigm has "lots of holes" too.

"It doesn't explain everything about MS, and as part of a causation theory it should explain everything. It doesn't explain the epidemiology very well, it doesn't explain the sex ratio, it doesn't explain some of the responses to certain therapies," he said.

"That's a clue that we don't know the whole story."

The HIV Connection

Perhaps the most significant piece of evidence for the HERV theory of MS is even more indirect: People with HIV appear to be at vastly reduced risk for MS.

What does HIV status have to do with HERVs or MS? Because nowadays, essentially everyone with HIV in developed countries where broad-based epidemiological research can be conducted is treated with antiretroviral drugs.

Gold is an HIV specialist -- the Albion Street Centre, which he directs, is Australia's largest HIV outpatient clinic. His "aha" moment came when an HIV-positive patient who also had MS came under his care. This patient was first diagnosed with HIV infection in 1985 but managed to avoid developing AIDS before the advent of highly active antiretroviral therapy (HAART) in 1996.

In a 2011 letter published in the European Journal of Neurology, Gold and colleagues described what happened after HAART was begun in 1996:

"Within months of commencing HAART, all MS symptoms gradually improved. Within 2 years, his urinary incontinence was controlled to the extent that he stopped wearing pads and fecal incontinence resolved. He has had no MS relapses."

The disease was not completely eliminated, the researchers indicated, because gadolinium-enhanced MRI scans made in 2002 continued to show lesions consistent with MS, even though clinical symptoms had largely disappeared.

Large-scale epidemiological studies have supported the notion that anti-HIV therapy may suppress MS pathology. A Danish national registry study published in letter form last year in Epidemiology, comparing 5,018 HIV-positive patients with some 50,000 age- and sex-matched individuals from the general population, found that the rate of MS incidence was markedly lower in the HIV patients (3.1 versus 10.4 per 100,000). However, it was not statistically significant because only one HIV patient developed MS during the study period.

Gold and colleagues conducted a similar (but as yet unpublished) study using the much larger U.K. general practice database, which covers some 55 million Britons. At the European MS meeting where he spoke last fall, he reported on results from some 21,000 HIV-positive individuals and 6.7 million controls, followed for a mean of 7 years.

In addition to matching controls to HIV patients by age and sex, they were also matched by region within the country and by the week in which they first came into contact with the national health system.

The relative risk for MS in the HIV patients versus controls was 0.38 (95% CI 0.15-0.79, P=0.011), he reported. The relative risk was even lower, 0.22, when only MS diagnoses occurring more than 1 year after HIV diagnosis were counted (at which point HAART is presumably well established in British HIV patients).

The Clinical Trials

There is no animal model for HERVs in MS, and the ability to study HERVs even in cell culture is limited, Gold said. He argued that "their exact role will only be obtained following appropriate clinical trials. If we wait for the laboratory to give us the answer, we will all have been retired."

Raltegravir was chosen for the U.K. trial for several reasons. One is that it is an HIV integrase inhibitor. "The integrases across HERVs and HIV are quite conserved," Giovannoni said, so that it is likely to be more effective in suppressing HERV elements than other types of antiretroviral drugs. He said it was also unique among antiretrovirals in also showing some potency against members of the herpesvirus family (though only in vitro -- this effect hasn't been studied clinically).

And, its manufacturer was willing to support the small, short-term trial. Gold pointed out that no company that markets MS medications is active in HIV drug development, or vice versa. He and Giovannoni were able to persuade raltegravir's maker, Merck's European subsidiary, to fund the 25-patient study which includes just 3 months of drug treatment after a 3-month baseline observation period. Gold said a longer and larger study would have been preferable but it could not be arranged.

The GNbAC1 monoclonal antibody's sponsor GeNeuro appears to have more resources, with France's Institut Merieux as a major investor. It has already completed a phase I safety study with the agent in healthy volunteers; the results to be presented at the AAN meeting next month are from 10 MS patients.

According to the abstract, no safety problems were seen, and a larger efficacy study is warranted. However, GeNeuro has not said whether or when such a trial would be undertaken.

Caution Reigns

MS specialists in the U.S. contacted by MedPage Today were unanimous in urging caution about HERV theory, although some were warmer to it than others.

Alessandro Serra, MD, of University Hospitals Case Medical Center in Cleveland, told MedPage Today that "many studies" had supported the association between HERV-expressed proteins and MS.

However, these proteins also appear "in patients with other neurological conditions, and even in a proportion of healthy individuals," Serra said.

He said the debate in the community was over "whether HERVs are just bystanders within the normal immune response of MS patients, perhaps unable to handle these viruses, or whether they actually represent a key component of the pathogenic process of MS and even have a causative role."

Jerry Wolinsky, MD, of the University of Texas Health Science Center in Houston, pointed out that the search for MS triggers has been going on for decades and wound up in many blind alleys. Viruses have long been a popular suspect, but "thus far not fruitful."

With regard to retroviruses lurking within the human genome, "to my knowledge there has been no consistently recovered retrovirus sequence associated with brain or other tissues from patients with multiple sclerosis," Wolinsky said.

"That does not mean that one might not be afoot, but the technology is well enough developed that it would be unusual to expect that one will be found in the future, given the failure to do so even with application of modern tools."

Wolinsky added that the 2011 case report from Gold and colleagues, of the HIV/MS patient whose neurological symptoms resolved with HAART, did not persuade him. "The course of MS is very unpredictable," he said, and the disappearance of symptoms may simply have been "serendipitous."

Other experts were also supportive of research while agnostic or skeptical about the HERV theory. For example, Robert Bermel, MD, head of the Cleveland Clinic's Mellen Center for Multiple Sclerosis, told MedPage Today that "It becomes difficult ... to separate the specific effect of antiretroviral therapy from the effect of altered immune status related to HIV, or from the natural tendency of MS disease activity to decline over time."

On the other hand, Anthony Reder, MD, of the University of Chicago, called the HERV theory "important" as well as plausible.

HERVs, he said, result from "hundreds of millions of years of battles with retroviruses. The residual DNA fragments do not produce complete viruses but DNA fragments and retrovirus proteins do leak out and are seen by the immune system."

Serra said he hoped that the two clinical trials wouldn't be taken as make-or-break for the HERV theory. "We need more rigorous models, especially animal models that have been lacking so far. I know there are groups that are looking into it."

In the meantime, everyone who spoke to MedPage Today emphasized that it would be premature for physicians or patients to try antiretroviral drugs on their own as MS therapies. Giovannoni said that some patients have told him that they had succeeded in obtaining raltegravir.

"That's a little premature and we wouldn't recommend it," he said.

The raltegravir trial is supported by Merck. The monoclonal antibody study is funded by GeNeuro.

Giovannoni has had relationships with Bayer Schering Healthcare, Biogen Idec, GW Pharma, Merck Serono, Merz, Novartis, Teva, Sanofi, Eisai, Elan, Five Prime Therapeutics, Genzyme, Genentech, GSK, Ironwood Pharma, Merck Pfizer, Roche, Synthon BV, Teva, UCB Pharma, and Vertex Pharmaceuticals. Other sources reported no potential conflicts of interest.

John Gever, Senior Editor, has covered biomedicine and medical technology for 30 years. He holds a B.S. from the University of Michigan and an M.S. from Boston University. Now based in Pittsburgh, he is the daily assignment editor for MedPage Today as well as general factotum on the reporting side. Go Pirates/Penguins/Steelers!

Friday, 5 July 2013

Nevirapine Toxicity May Be Linked to Race (CME/CE)

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Published: Jul 2, 2013

By Ed Susman, Contributing Writer, MedPage TodayReviewed by Zalman S. Agus, MD; Emeritus Professor, Perelman School of Medicine at the University of Pennsylvania and Dorothy Caputo, MA, BSN, RN, Nurse PlannerNote that this study was published as an abstract and presented at a conference. These data and conclusions should be considered to be preliminary until published in a peer-reviewed journal.In this retrospective analysis of patients started on nevirapine-based antiretroviral therapy, almost one-third discontinued therapy due to toxicities, and Malays had the highest incidence of toxicity compared with the other races.

KUALA LUMPUR -- A higher percentage of Malay people experienced treatment-limiting toxicity with the non-nucleoside reverse transcriptase anti-HIV drug nevirapine compared with other groups, and genetic differences may be the reason, researchers reported here.

"Malays had the highest incidence of treatment-limiting nevirapine toxicity amongst the different racial groups," said Joyce Yeap, MS, a clinical pharmacist at Sungai Buloh Hospital in Selangor, Malaysia. Malays had an incidence of treatment-limiting toxicity of 38.4%, compared with Indians, who had the lowest incidence of treatment-limiting nevirapine toxicities at 23.6% (P=0.016), she told MedPage Today.

It is difficult to understand why there should be a racial difference even after performing adjustments for age, sex, HIV transmission category, nadir CD4-positive cell counts, hepatitis B or C virus co-infection and other concomitant medication, Yeap said in her poster presentation at the International AIDS Society Conference on HIV Pathogenesis, Treatment and Prevention.

However, outcomes at 12 months were not different between the patients who developed toxicities and were switched to other regimens and those who did not have dose-limiting adverse events (P=0.456), Yeap said.

"Malays are 1.7 times more likely than Chinese or Indians or other ethnicities to develop treatment-limiting nevirapine toxicities," she noted. The researchers performed various logistic regression analyses and determined that toxicities to nevirapine were more frequent in the Malay population of Malaysia which has a polyglot of different races, including several indigenous peoples.

"We did not have resources to perform genome studies," she said, "but it could be due to some type of gene sub-types that makes the Malays more sensitive to nevirapine toxicity."

Yeap said that when treating Malays, physicians need to factor in sex and CD4 counts as well. "We might be more cautious in giving nevirapine to these individuals," she suggested.

While other treatment regimens are possible for HIV-infected individuals, Yeap noted that for a developing country with limited resources, nevirapine is one of the most cost-effective therapies available.

The average age of the 662 HIV-infected patients in her study was 37.4 years, and 75.8% of the patients were men. Their average nadir CD4 cell counts were 134.8 cells/mm3. The researchers identified 34.6% of the patients as Malay; 42.1% were Chinese; 10.9% were Indian; and 9.2% were foreigners.

Rash was the nevirapine treatment-limiting adverse event among 156 patients; flu-like illnesses were observed in 130 patients; hepatotoxicity was seen in 44 patients. She said 102 patients presented with rash, flu-like illness and liver toxicity.

A possible explanation for the treatment-limiting toxicity might have to do more with clinical observation rather than genetics, suggested Graeme Moyle, MBBS, director of research at Chelsea and Westminster Hospital, London.

"There are studies here that look at the genetic linkage between adverse events and specific drugs," Moyle told MedPage Today as he reviewed the poster presentation. "There appear to be certain alleles that are associated with nevirapine toxicity, especially the cutaneous toxicities. It may be due to allele variations across certain ethnic populations."

He said that another possibility that is often discussed is that among black patients nevirapine-associated rash appeared more severe. He said that may be caused by the fact that the rash may be more difficult to observe among darker-skinned individuals. Since the rash is non-itchy, the skin color may mask the rash until it reaches a more severe level, Moyle suggested.

"When you have darker skin you don't recognize early rash that can lead to discontinuation when the rash is mild," he said. "People continue to take therapy and the rash continues to a more severe event."

Yeap had no disclosures.

Moyle has reported commercial interests with Gilead, Ardea Biosciences, Abbott Laboratories, Bristol-Myers Squibb, GlaxoSmithKline, Merck, Tobira Therapeutics, Panacos Pharmaceuticals, Pfizer and Tibotec.

Primary source: International AIDS Society
Source reference:
Yeap J, et al "Incidence and risk factors for treatment-limiting toxicities in patients starting nevirapine-containing antiretroviral therapy" IAS 2013; Abstract MOPE092.

Teens with HIV Need Transition to Adult Care (CME/CE)

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Published: Jun 24, 2013

Reviewed by Zalman S. Agus, MD; Emeritus Professor, Perelman School of Medicine at the University of Pennsylvania and Dorothy Caputo, MA, BSN, RN, Nurse PlannerWith current antiretroviral therapy, most HIV-infected children now survive into adulthood. Successful transition requires several factors according to a policy statement of the American Academy of Pediatrics.The care transition should include a written policy for the transfer of HIV-infected youth to adult care and the plan should be introduced to the youth in early adolescence and modified as the youth approaches transition.

HIV-positive adolescents, who face isolation, ostracization, and confusion as they transition to adulthood, need sensitive and directed guidance to an adult healthcare provider, according to the American Academy of Pediatrics.

Clinicians should follow four steps to guide HIV-positive teens to successfully maintain their healthcare: create a formal, written transition care plan, start communications about HIV status and transition around age 12, make the transition between 18 to 25 years of age, and document and evaluate the transition upon completion, the AAP outlined in a policy statement published online in Pediatrics.

"Pediatricians and adolescent and family medicine providers have a pivotal role in facilitating seamless and effective transition at a very vulnerable and anxious time of life for both HIV-infected youth and their families," wrote Russell B. Van Dyke, MD, FAAP, and Rana Chakraborty, MD, for the AAP's Committee on Pediatric AIDS. "These essential transitional activities can improve health outcomes for HIV-infected adolescents."

HIV infection is the seventh-leading cause of death among youth and adolescents and 12,200 (25.7%) of all new HIV infections in 2010 were in youths. Nearly six out of 10 (59.5%) were unaware of their infection, a higher percentage than in any other age group, the authors wrote.

The written care plan should include supporting documents that assist the new team, according to the policy statement, including goals and a timeline. An important piece of the plan, the authors noted, is a system, such as a registry, to track youth as they make their way through the transition process so as to minimize loss to care that might accompany a move out of the family home.

Introducing the concept of transition is important, the policy stated, because children who are unaware of their status should be fully informed at age 10 to 12, depending on maturity and neurocognitive abilities. Readiness assessment tools may help identify strengths and weaknesses that can focus patient attention.

The teenager's or young adult's educational, vocational, and social service needs should be addressed, as well.

"The plan should emphasize education of all involved parties and empowerment of the HIV-infected youth to assume responsibility for his or her own healthcare," the authors wrote." It is important to encourage independence through personal ownership and management of healthcare. Particular attention should be paid to identifying and addressing behavioral, emotional, and mental health problems."

Helping the patient successfully make the actual transition depends greatly on the team handing off care, the policy stated. Creating and maintaining a portable medical summary and an emergency care plan is essential.

Transition should include direct contact between providers and a letter of transition, the portable medical summary, and electronic health records before the patient transfers to the new provider.

"Ideally, the youth would be introduced to the adult healthcare provider personally by the pediatric, adolescent, or family medicine provider, either in the referring or adult clinic," the AAP authors wrote.

"This support could consist of periodic contact by a member of the referring healthcare team, such as a nurse or social worker. A peer support group may assist youth with dealing with anxiety resulting from the transition process."

However, once adult care is established, the pediatric, adolescent, or family medicine provider should bow out to prevent confusion and reinforce the adult healthcare provider.

"Adolescence is a developmental stage characterized by immature concrete reasoning often manifested by denial of illness, a sense of invulnerability reflected by risk taking, and behaviors that are strongly influenced by peer norms," the authors wrote. "These characteristics all have a direct negative effect on the ability to adhere to complex medical regimens."

Dramatic improvements in HIV care combined with psychosocial stressors including loss of a parent, foster care, poverty, homelessness, unemployment, discrimination, and abuse have made for a generation of HIV-infected youth whose future -- and others -- depends on managing their chronic condition on their own, the policy stated.

Furthermore, among HIV-infected youth 18 and older who transitioned from National Institutes of Health clinical research protocols to adult care, 15% reported not having health insurance.

No conflict of interest statements were published with the policy statement.

Kathleen Struck joined MedPage Today after serving as Managing Editor for EverydayHealth.com, Stars and Stripes and MediaNews Group. She lived and traveled internationally for more than 15 years and has written and edited for publications including, Washington Post, Baltimore Sun, Newsday and Regulatory Affairs Professional Society. At MedPage Today, she reports and edits on general news and information.

New Guidelines Advocate Earlier HIV Treatment (CME/CE)

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Published: Jul 1, 2013

By Ed Susman, Contributing Writer, MedPage TodayReviewed by F. Perry Wilson, MD, MSCE; Instructor of Medicine, Perelman School of Medicine at the University of Pennsylvania and Dorothy Caputo, MA, BSN, RN, Nurse PlannerNote that these new World Health Organization guidelines recommend treatment for HIV when CD4 counts fall below 500 cells/mm3.In addition, the guidelines recommend treatment of all those who are coinfected with HIV and either hepatitis B or tuberculosis.

KUALA LUMPUR -- New international guidelines suggest that people diagnosed with human immunodeficiency virus (HIV) be treated earlier in the course of the disease -- effectively making another 9.2 million people eligible for antiretroviral therapy, researchers said here.

Currently in the underdeveloped world, where HIV has devastated many nations, 9.7 million people out of an estimated 16.7 million who should be treated receive effective antiretroviral therapy, said Gundo Weiler, MD, PhD, medical and health policy adviser of the National German AIDS Organization in Berlin. But the impact of the new World Health Organization (WHO) guidelines will increase the number of patients who need to be treated to 25.9 million.

The major increase comes from earlier treatment -- commencing highly active antiretroviral therapy (HAART) when infected persons' CD4-positive cell counts drop below 500 cells/mm3, Weiler, who helped write the recommendations, said at the International AIDS Society Conference on HIV Pathogenesis, Treatment and Prevention. The previous guidelines suggested treating patients once those immune system markers fell below 350 cells/mm3.

Weiler said the 2013 WHO guidelines would result in 3 million deaths due to HIV being avoided between 2013 and 2025 when compared with 2010 guidelines. The implementation of the guidelines also would reduce new HIV infections by 36% by 2025 compared with projections using the 2010 guidelines.

The change in definition of when to commence treatment adds 3.9 million persons to the "should be in treatment" statistics. The new guidelines also expand the use of antiretroviral therapy in children. Under the old guidelines, 1.2 million children needed to be in treatment; the new guidelines expand that to 2.6 million children.

The new guidelines suggests that all HIV-positive pregnant women, regardless of CD4 count, be placed on antiretroviral therapy -- adding 700,000 people to those needing treatment.

The new guidelines also advocate immediate treatment with HAART therapy for those 3.2 million people now coinfected with tuberculosis or hepatitis B infection.

All told, the new guidelines increase the numbers of patients needing HAART by 9.2 million.

Weiler said that by increasing contributions from governments and other agencies by 10% a year, it will be possible to have those patients under treatment by 2025. But because treatment reduces infections, after 2025, the number of patients living with HIV and the number of people on treatment will begin to merge.

"Generally, in the U.S. and Canada we are already using these guidelines to treat our patients," Julio Montaner, MD, professor of medicine at the University of British Columbia, Vancouver, told MedPage Today.

"What these guidelines will do, however, is to convince doctors who are on the fence about where to begin treatment to start treating their patients earlier," Montaner said.

He also said that in Europe -- especially in countries that are experiencing economic crises -- the guidelines will help convince those health providers to initiate HAART therapy earlier. Montaner did not participate in the WHO guideline-writing process.

The new guidelines recommend: Treating adults, adolescents, and older children earlier -- starting antiretroviral therapy in all individuals with a CD4 cell count of 500 cells/mm3 or less and giving priority to individuals with severe or advanced HIV disease and those with a CD4 cell count of 350 cells/mm3 of less.Starting antiretroviral therapy at any CD4 cell count for certain populations with HIV, including people with active tuberculosis disease, people with hepatitis B coinfection with severe chronic liver disease, HIV-positive partners in serodiscordant couples, pregnant and breastfeeding women, and children younger than 5 years of age.A new preferred first-line antiretroviral regimen harmonized for adults, pregnant and breastfeeding women and children ages 3 or older. That first-line therapy should be a fixed-dose combination of tenofovir plus lamivudine or emtricitabine plus efavirenz.Support to actively accelerate the phasing out of stavudine (d4T) in first-line regimens for adults and adolescents.

The guidelines also include new recommendations for testing for HIV.

Montaner reported commercial relationships with Abbott, Gilead Sciences, GlaxoSmithKline, and Merck.

Weiler reported no disclosures.

Primary source: International Aids Society
Source reference:
World Health Organization "Consolidated guidelines on the use of antiretroviral drugs for treating and preventing HIV Infection" IAS 2013.

5-Drug HIV Tx Given Early Cuts Viral Reservoir (CME/CE)

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Published: Jul 2, 2013 | Updated: Jul 2, 2013

Reviewed by Zalman S. Agus, MD; Emeritus Professor, Perelman School of Medicine at the University of Pennsylvania and Dorothy Caputo, MA, BSN, RN, Nurse PlannerNote that this study was published as an abstract and presented at a conference. These data and conclusions should be considered to be preliminary until published in a peer-reviewed journal.Patients with primary HIV infection receiving early treatment with five-drug highly active antiretroviral therapy (HAART) achieved lower cell-associated HIV-DNA levels and a better immune reconstitution than chronically infected patients on intensified long-term suppressive HAART.

KUALA LUMPUR -- For patients in the early stages of HIV infection, initial treatment with five antiretroviral drugs, rather than three, may be a first step toward remission, a researcher said here.


In 2-year results from a 7-year prospective trial, such intense therapy resulted in a sharp decline in HIV DNA that is integrated into cells, according to Eva Wolf, PhD, of MUC Research in Munich, Germany.


But in patients with chronic HIV infection who were also given an intensified regimen, there was no change over time in the so-called cell-associated or proviral DNA, Wolf reported at the 7th International AIDS Society Meeting on HIV Pathogenesis, Treatment, and Prevention.


The drop in proviral DNA was accompanied by a reconstitution of the immune system, Wolf told MedPage Today, and may be the first step toward remission or a "functional cure" -- the ability to control HIV replication without drug therapy.


In a French cohort of patients treated early in the course of HIV infection -- the so-called Visconti cohort -- the level of cell-associated DNA appears to be an important predictor of such a functional cure, she said.


The proviral DNA is thought to be an important part of the HIV reservoir, which forms the basis for the ability of the virus to rebound when antiretroviral therapy is stopped.


The Visconti cohort includes 14 people who were treated in the first weeks of their infection with standard antiretroviral therapy. When they later stopped therapy for various reasons, they did not have a viral rebound, although HIV was still present.


Wolf and colleagues hypothesized that intensified therapy might have a similar effect, and to test the idea, they enrolled 20 patients with primary infection as well as 20 with chronic infection, who had been on successful antiretroviral therapy for at least 3 years.


The early patients were given five drugs -- two nucleoside reverse transcriptase inhibitors, a protease inhibitor, the entry inhibitor maraviroc (Selzentry) and the integrase inhibitor raltegravir (Isentress).


The chronically infected patients remained on their stable regimen, Wolf said, with the addition of maraviroc and raltegravir.


The primary outcome measures were successful interruption of HIV replication and depletion of the proviral DNA, measured as copies per million peripheral blood mononuclear cells.


After 2 years of the study, she reported, the chronic patients had a slight but nonsignificant increase in proviral DNA. On the other hand, those with primary infection had a median decline of 1.4 log10 copies per million cells (P<0.001).


Whether that is sufficient to lead to a functional cure is an open question. Wolf said, and she and colleagues are considering "pulsed treatment" to see if there is viral rebound in the absence of antiretroviral drugs.


Outside experts, though, cautioned that intensified treatment has been tried before without a clear benefit.


First , "you can't compare the groups" because it's already known that people with chronic disease don't see a marked reduction in proviral DNA with additional therapy, commented Sharon Lewin, MD, of Monash University in Melbourne, Australia, a leader in research aimed at curing HIV.


"They've taken people with an established reservoir, added in extra drugs (and found) no change in DNA because you're already at steady state," Lewin told MedPage Today.


Meanwhile, those with primary infection already are known to have a better response even with three-drug therapy, she noted, based on a study in 2012 in Thailand.


"If you really want to say the extra drugs made a difference, you'd compare three drugs and five drugs," she said.


In fact, there is so far no evidence that so-called mega-HAART makes a difference in the size of the proviral DNA reservoir in early infection, commented John Frater, MD, PhD, of Oxford University. Frater was one of the leaders of the so-called Spartac trial that invesigated the effects of therapy in the early stages of HIV infection using three standard drugs.


That trial showed a benefit of early treatment in terms of improving immune function, and delaying the time that patients would need to go back on therapy after stopping. But it's not clear that adding drugs would have had an additional benefit, he told MedPage Today.


He and colleagues are currently planning a trial in which raltegravir will be added to standard therapy in early infection -- but not because the investigators think it will markedly affect the reservoir compared with three drugs. Instead, Frater said, they hope the rapid decline in viral replication associated with raltegravir might "tip the balance" and help limit the establishment of the reservoir.


He added it's still not known how small the reservoir of proviral DNA has to be to allow patients to go off therapy and it is still not possible to measure the size of the reservoir accurately. "The errors in our assays are enormous," he said.


The study was supported by AbbVie; Merck, Sharp & Dohme; and Pfizer/ViiV Healthcare.


Wolf made no disclosures.


Lewin has reported grant support from Gilead and Merck.


Frater has not reported recent financial links with industry.


Primary source: International AIDS Society
Source reference:
Wolf E, et al "5-drug HAART during primary HIV infection leads to a reduction of proviral DNA levels in comparison to levels achievable during chronic infection" IAS 2013; Abstract MOPE097.

North American Correspondent for MedPage Today, is a three-time winner of the Science and Society Journalism Award of the Canadian Science Writers' Association. After working for newspapers in several parts of Canada, he was the science writer for the Toronto Star before becoming a freelancer in 1994. His byline has appeared in New Scientist, Science, the Globe and Mail, United Press International, Toronto Life, Canadian Business, the Toronto Star, Marketing Computers, and many others. He is based in Toronto, and when not transforming dense science into compelling prose he can usually be found sailing.

Low-Dose Drug Combo Safe in Kids with HIV (CME/CE)

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Published: Jul 5, 2013

By Ed Susman, Contributing Writer, MedPage TodayReviewed by Robert Jasmer, MD; Associate Clinical Professor of Medicine, University of California, San FranciscoThis study was published as an abstract and presented at a conference. These data and conclusions should be considered to be preliminary until published in a peer-reviewed journal.A low-dose treatment regimen with lopinavir/ritonavir antiretroviral therapy appears to have similar efficacy with fewer adverse events than standard dosing in HIV-infected children.Note that children treated with the lower dose of the protease inhibitor had significantly lower cholesterol and triglyceride levels.

KUALA LUMPUR -- A low-dose treatment regimen with lopinavir/ritonavir antiretroviral therapy appears to have similar efficacy with fewer adverse events than standard dosing in HIV-infected children, researchers said here.

In the intention-to-treat analysis, 89 of 101 children (88.1%) on the low-dose regimen achieved undetectable viral loads using the 50 copies/ml assay (P=0.38) compared with 90 of 98 children treated with the standard dose of lopinavir/ritonavir (Kaletra), said Thanyawee Puthanakit, MD, from Chulalongkorn University in Bangkok, and colleagues.

"This study demonstrated non-inferiority in virologic efficacy of low dose compared to standard dose lopinavir/ritonavir tablets as maintenance therapy," she reported at the International AIDS Society Conference on HIV Pathogenesis, Treatment and Prevention.

In terms of adverse effects, the study showed that children treated with the lower dose of the protease inhibitor had significantly lower cholesterol levels. She said that 34.4% of children on the standard dose had cholesterol levels greater than 200 mg/dl at the end of the 48 week trial compared with 20.6% of children treated with the low-dose regimen (P=0.03).

In addition, triglyceride levels greater than 150 mg/dl were observed among 60.4% of the children on the standard dosing regimen and in 44.3% of those on the low dose of lopinavir/ritonavir (P=0.03), Puthanakit reported.

"This dosing regimen conferred adequate lopinavir blood level with reduced drug cost, and reduced potential long-term complications such as dyslipidemia," she said.

"Lopinavir/ritonavir is the most commonly used HIV regimen used in children," Puthanakit pointed out.

In the trial, which was conducted from December to June 2011, the children assigned to the standard, weight-based dose received an average of 284 mg/m2 twice daily. The children in the low-dose group received an average of 210 mg/m2. The lower dose represents about 70% of the recommended treatment dose in the U.S., Puthanakit said.

Of the 199 patients in the study, seven children in both arms were lost to follow-up.

The average age of the children was 13.2 years and their CD4-positive cell counts was 786 cells/mm3. All were on protease inhibitor regimens. The background nucleoside reverse transcriptase inhibitors included zidovudine and lamivudine; zidovudine and didanosine; lamivudine and tenofovir; lamivudine alone; and lamivudine and didanosine.

The study was devised as a way to deliver maintenance therapy for children whose HIV was well controlled, with all of the children at baseline having undetectable HIV plasma viral loads using the 50 copies/mm3.

Puthanakit noted that the study results could only be generalized to children with controlled, undetectable viral loads and should not, at this time, be expanded to include children with high viral loads who may just be beginning antiretroviral therapy.

Diana Gibb, MD, from the Medical Research Council Clinical Trials Unit in London also cautioned that the results "would not apply to the use of liquid lopinavir/ritonavir therapy since this study was done with tablets that have a higher bioavailability."

Puthanakit concurred, noting that her study did not include infants and young children who are treated with liquid formulations of the antiretroviral regimen.

The study was part of the long-standing HIV Netherlands Australia Thailand Research Collaboration (HIV-NAT).

The study was funded by Thai governmental agencies.

Puthanakit and Gibb reported no conflicts of interest.

Primary source: International AIDS Society
Source reference:
Puthanakit T, et al "A randomized study comparing low dose versus standard dose lopinavir/ritonavir among HIV-infected children with virological suppression" IAS 2013; Abstract MOAB0101.

BMD Correlates with Number of HIV Regimens (CME/CE)

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Published: Jul 3, 2013 | Updated: Jul 3, 2013

By Ed Susman, Contributing Writer, MedPage TodayReviewed by Robert Jasmer, MD; Associate Clinical Professor of Medicine, University of California, San Francisco and Dorothy Caputo, MA, BSN, RN, Nurse PlannerNote that this study was published as an abstract and presented at a conference. These data and conclusions should be considered to be preliminary until published in a peer-reviewed journal.The number of HIV treatment regimens a patient undergoes appears to correlate with loss of bone mineral density.Note that the study did not find that current use of or cumulative exposure to antiretrovirals, antiretroviral class, or specific antiretroviral agents independently predicted lower bone mineral density.

KUALA LUMPUR -- The number of HIV treatment regimens a patient undergoes appears to correlate with loss of bone mineral density (BMD), researchers reported here at the International Aids Society Conference on HIV Pathogenesis, Treatment, and Prevention.

In the multivariate analysis involving 210 patients with HIV infection, the parameter estimate for BMD loss at the femoral neck was -0.011 g/cm2 for each regimen a patient had taken (95% CI minus 0.022-minus 0.0003, P=0.05), reported Aoife Cotter, MD, a fellow in infectious diseases at University College Dublin.

"Unexpectedly, we did not find that current use of or cumulative exposure to antiretrovirals, antiretroviral class, or specific antiretroviral agents independently predicted lower bone mineral density," Cotter told MedPage Today at her poster presentation.

In addition to the multivariate analysis finding of lower BMD at the femoral neck, Cotter and colleagues also noted that the lumbar spine BMD loss was also associated with the number of HIV regimens. At the lumbar spine there was a loss of 0.015 g/cm2 (P=0.03), she reported.

Cotter reviewed data in the prospective HIV UPBEAT (Understanding the Pathology of Bone Disease in HIV-infected Subjects) which enrolled HIV-positive and HIV-negative participants from similar demographic backgrounds. The median age of the HIV-infected patients was 39, mean BMI was 26 kg/m2, 58.6% were men, 60.5% were Caucasians, 39.5% were of African ethnicity, 34.8% were current smokers.

Cotter said the researchers considered that the number of HIV regimens might be a surrogate measure for time with HIV infection, but in performing the multivariate analysis they did not find a correlation that was statistically significant.

"We suggest that these findings are consistent with data demonstrating greater reductions in bone mineral density associated with antiretroviral-induced HIV suppression occurring with multiple antiretroviral regimens," she said.

In the multivariate analysis, the researchers did not see a significant difference in bone mineral density loss when comparing injecting drug users with non-injecting drug users with HIV infection (P=0.54); with baseline CD4-positive T-cell counts- (P=0.21); with nadir CD4 cell counts (P=0.09); duration since HIV diagnosis (P=0.86); cumulative antiretroviral exposure (P=0.40); cumulative nucleoside reverse transcriptase inhibitor exposure (P=0.41); cumulative tenofovir exposure (P=0.34); cumulative non-nucleoside reverse transcriptase inhibitor exposure (P=0.63), or cumulative protease inhibitor exposure (P=0.11).

In commenting on the study, Ian Woolley, MBBS, professor of medicine at Monash University in Melbourne, Australia, told MedPage Today, "The number of HIV regimens may be a surrogate for lack of adherence by these patients."

He added, "There are usually two reasons why patients change regimens. It is because of resistance or because of toxicity. It is also possible there is a phenotype that is more likely to develop toxicity."

He noted that resistance often arises when patients are not adherent in taking their antiretroviral medications.

Cotter and Woolley had no disclosures.

Primary source: International AIDS Society
Source reference:
Cotter A, et al "Number of different antiretroviral regimens rather than cumulative exposure to antiretrovirals associated with lower bone mineral density in HIV-positive subjects" IAS 2013; Abstract MOPE078.

Investigational HIV Treatment Promising (CME/CE)

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Published: Jul 3, 2013 | Updated: Jul 3, 2013

Reviewed by Zalman S. Agus, MD; Emeritus Professor, Perelman School of Medicine at the University of Pennsylvania and Dorothy Caputo, MA, BSN, RN, Nurse PlannerNote that this study was published as an abstract and presented at a conference. These data and conclusions should be considered to be preliminary until published in a peer-reviewed journal.In this double-blind, phase III study in HIV-1 infected, treatment-experienced but integrase-naive adults, dolutegravir, an investigational integrase inhibitor given once daily, was superior to twice-daily raltegravir.

KUALA LUMPUR -- The investigational anti-HIV drug dolutegravir outperformed raltegravir (Isentress) in a randomized trial among patients needing salvage therapy, a researcher said here.

After 48 weeks of therapy, HIV patients who had failed earlier regimens were significantly more likely to control their virus if they were taking dolutegravir, according to Pedro Cahn, MD, of Fundación Huesped in Buenos Aires.

At the same time, there were no major differences in the rate of adverse events in the so-called SAILING trial, Cahn reported at the 7th International Aids Society Conference on HIV Pathogenesis, Treatment, and Prevention.

Both drugs are members of a relatively new class of anti-HIV drugs, the integrase inhibitors. Raltegravir was the first approved integrase inhibitor, and a second drug in the class, elvitegravir, is so far only approved as part of a fixed-dose combination.

Dolutegravir is regarded as an attractive alternative because it is given once daily, at 50 milligrams, compared with 400 milligrams twice a day for raltegravir.

To test the comparative efficacy of the two drugs, Cahn and colleagues enrolled 715 treatment-experienced patients who had not yet been given an integrase inhibitor for a randomized, double-blinded, double-dummy trial.

The primary endpoint was the proportion of patients who reached an undetectable level of plasma RNA, defined as fewer than 50 copies per milliliter.

Along with the integrase inhibitor, patients were given an optimized two-drug background in which at least one drug had to be fully active, Cahn told reporters.

After 48 weeks of treatment, he said, 64% of patients taking raltegravir had reached the primary endpoint, compared with 71% of those taking dolutegravir (P=0.03).

The treatment difference was significant, Cahn said, allowing the investigators to conclude that "superiority can be claimed for dolutegravir on a statistical basis."

Interestingly, among patients whose background regimen included the protease inhibitor darunavir (Prezista) -- and who had no resistance to the drug -- there was no difference in efficacy between raltegravir and dolutegravir, Cahn told MedPage Today.

That's probably because darunavir itself is very potent in salvage therapy, Cahn said, so that its benefit swamps any difference between the integrase inhibitors.

Both integrase inhibitors are "extremely safe," he said, with very few patients stopping therapy because of adverse events -- 3% in the dolutegravir arm and 4% in the raltegravir arm.

The most commonly reported adverse events were diarrhea and upper respiratory tract infection, which occurred at similar rates in the two treatment arms, Cahn reported.

The study adds to the "very promising data" on dolutegravir, commented Jintanat Ananworanich, MD, PhD, of the Thai Red Cross AIDS Research Center in Bangkok, who was not part of the study but who moderated a press conference at which some details were presented.

The drug has shown very rapid reductions in viral load at low doses, Ananworanich told MedPage Today, which might allow it to be used at lower cost than other members of the class.

As a pediatrician, she added, she's following it closely because it also appears to very effective in children.

The study was supported by GlaxoSmithKline. Cahn has previously disclosed financial relationships with Abbott, Avexa, Boehringer Ingelheim, Bristol-Myers Squibb, GlaxoSmithKline, Merck, Pfizer, Pharmasset, Schering-Plough, and Tibotec.

Ananworanich made no disclosures.

Primary source: International AIDS Society
Source reference:
Cahn P, et al "Dolutegravir (DTG) is superior to raltegravir (RAL) in ART-experienced, integrase naive subjects: week 48 results from SAILING" IAS 2013; Abstract WELBB03.

North American Correspondent for MedPage Today, is a three-time winner of the Science and Society Journalism Award of the Canadian Science Writers' Association. After working for newspapers in several parts of Canada, he was the science writer for the Toronto Star before becoming a freelancer in 1994. His byline has appeared in New Scientist, Science, the Globe and Mail, United Press International, Toronto Life, Canadian Business, the Toronto Star, Marketing Computers, and many others. He is based in Toronto, and when not transforming dense science into compelling prose he can usually be found sailing.

HIV Drugs Getting Better (CME/CE)

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Published: Jul 5, 2013

Note that this study was published as an abstract and presented at a conference. These data and conclusions should be considered to be preliminary until published in a peer-reviewed journal.
Note that this large meta-analysis demonstrated that preferred HIV regimens are indeed superior to alternative regimens in terms of suppressing viral replication.There is a suggestion that the newer integrase inhibitors are more efficacious than other classes when added to the standard backbone of HIV therapy.

KUALA LUMPUR -- The efficacy of HIV drugs in clinical trials has increased markedly over time, according to a meta-analysis of 144 studies with more than 40,000 participants.

Efficacy -- defined as the proportion of patients able to suppress HIV to undetectable levels -- was about 47% in trials conducted before 2000, according to Frederick Lee, MD, of the St. Vincent's Centre for Applied Medical Research, Sydney, in Australia.

In studies after 2008, efficacy was about 82%, Lee reported at the 7th International AIDS Society Conference on HIV Pathogenesis, Treatment, and Prevention.

Interestingly, the so-called "preferred" regimens of the U.S. Department of Health and Human Services (DHHS) guidelines panel outperformed the "alternative" regimens, which in turn did better than other combinations, Lee reported.

Lee noted that guidelines are based on serial assessments of individual trials, so a meta-analysis of all available trials should increase the ability to evaluate outcomes in subpopulations of patients and identify predictors of treatment success.

He and colleagues looked at all reported prospective drug trials in treatment-naive HIV patients with at least 48 weeks of follow-up and an intent-to-treat efficacy analysis.

All told, they found 144 phase II, III, and IV studies with 216 treatment groups, starting with 10 trials from the pre-1996 era through to 17 in 2009 and 2010.

On average, follow-up was 82 weeks and efficacy on treatment was 60%, Lee reported. About 25% of participants stopped treatment during their trial, usually because of adverse events and less commonly because the drugs weren't working to suppress the virus.

The nucleoside reverse transcriptase inhibitor backbone of tenofovir and emtricitabine was significantly more efficacious than most other backbones, with the exception of emtricitabine and didanosine, which was equally good, Lee and colleagues found.

The third drug in triple-drug therapy until recently has usually been either a non-nucleoside reverse transcriptase inhibitor or a protease inhibitor, and analysis suggested they were equally efficacious at 61% and 67%, respectively.

Considered as a group the new integrase inhibitors yield efficacy of about 81%, Lee and colleagues found, which was significantly better (at P=0.002) than either of the other two classes.

Finally, an analysis of preferred DHHS regimens over time showed efficacy of 75%, compared with 65% for alternative regimens, and 55% for other treatment options.

The difference between the preferred and alternative regimens was significant (P<0.001), Lee reported.

The study finding delivers good news in one sense, commented Dan Kuritzkes, MD, of Brigham and Women's Hospital in Boston -- it shows that guidelines committees are doing a good job.

As a member of the DHHS guidelines panel, Kuritzkes said he was gratified to find that "it turns out that a bunch of experts sitting around and looking at data actually get it right."

The study "is confirmatory that we are having better drugs, more friendly drugs, and easier (drugs) to use," commented Pedro Cahn, MD, of Fundación Huesped in Buenos Aires and a former president of the IAS.

Those improvements are "the reason we are seeing increasing efficacy over time," he told MedPage Today.

The study was supported by the National Health and Medical Reserach Council of Australia. Lee made no disclosures.

Cahn has reported financial links with Abbott, Pfizer, GlaxoSmithKline, Pharmacia, and Roche.

Primary source: International AIDS Society
Source reference:
Lee FJ, et al "Efficacy of initial antiretroviral therapy: a meta-analysis of 40,124 adults with up to 144 weeks' follow-up" IAS 2013; Abstract WEAB0104.

North American Correspondent for MedPage Today, is a three-time winner of the Science and Society Journalism Award of the Canadian Science Writers' Association. After working for newspapers in several parts of Canada, he was the science writer for the Toronto Star before becoming a freelancer in 1994. His byline has appeared in New Scientist, Science, the Globe and Mail, United Press International, Toronto Life, Canadian Business, the Toronto Star, Marketing Computers, and many others. He is based in Toronto, and when not transforming dense science into compelling prose he can usually be found sailing.

Low-Dose Drug Combo Safe in Kids with HIV (CME/CE)

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Published: Jul 5, 2013

By Ed Susman, Contributing Writer, MedPage TodayReviewed by Robert Jasmer, MD; Associate Clinical Professor of Medicine, University of California, San FranciscoThis study was published as an abstract and presented at a conference. These data and conclusions should be considered to be preliminary until published in a peer-reviewed journal.A low-dose treatment regimen with lopinavir/ritonavir antiretroviral therapy appears to have similar efficacy with fewer adverse events than standard dosing in HIV-infected children.Note that children treated with the lower dose of the protease inhibitor had significantly lower cholesterol and triglyceride levels.

KUALA LUMPUR -- A low-dose treatment regimen with lopinavir/ritonavir antiretroviral therapy appears to have similar efficacy with fewer adverse events than standard dosing in HIV-infected children, researchers said here.

In the intention-to-treat analysis, 89 of 101 children (88.1%) on the low-dose regimen achieved undetectable viral loads using the 50 copies/ml assay (P=0.38) compared with 90 of 98 children treated with the standard dose of lopinavir/ritonavir (Kaletra), said Thanyawee Puthanakit, MD, from Chulalongkorn University in Bangkok, and colleagues.

"This study demonstrated non-inferiority in virologic efficacy of low dose compared to standard dose lopinavir/ritonavir tablets as maintenance therapy," she reported at the International AIDS Society Conference on HIV Pathogenesis, Treatment and Prevention.

In terms of adverse effects, the study showed that children treated with the lower dose of the protease inhibitor had significantly lower cholesterol levels. She said that 34.4% of children on the standard dose had cholesterol levels greater than 200 mg/dl at the end of the 48 week trial compared with 20.6% of children treated with the low-dose regimen (P=0.03).

In addition, triglyceride levels greater than 150 mg/dl were observed among 60.4% of the children on the standard dosing regimen and in 44.3% of those on the low dose of lopinavir/ritonavir (P=0.03), Puthanakit reported.

"This dosing regimen conferred adequate lopinavir blood level with reduced drug cost, and reduced potential long-term complications such as dyslipidemia," she said.

"Lopinavir/ritonavir is the most commonly used HIV regimen used in children," Puthanakit pointed out.

In the trial, which was conducted from December to June 2011, the children assigned to the standard, weight-based dose received an average of 284 mg/m2 twice daily. The children in the low-dose group received an average of 210 mg/m2. The lower dose represents about 70% of the recommended treatment dose in the U.S., Puthanakit said.

Of the 199 patients in the study, seven children in both arms were lost to follow-up.

The average age of the children was 13.2 years and their CD4-positive cell counts was 786 cells/mm3. All were on protease inhibitor regimens. The background nucleoside reverse transcriptase inhibitors included zidovudine and lamivudine; zidovudine and didanosine; lamivudine and tenofovir; lamivudine alone; and lamivudine and didanosine.

The study was devised as a way to deliver maintenance therapy for children whose HIV was well controlled, with all of the children at baseline having undetectable HIV plasma viral loads using the 50 copies/mm3.

Puthanakit noted that the study results could only be generalized to children with controlled, undetectable viral loads and should not, at this time, be expanded to include children with high viral loads who may just be beginning antiretroviral therapy.

Diana Gibb, MD, from the Medical Research Council Clinical Trials Unit in London also cautioned that the results "would not apply to the use of liquid lopinavir/ritonavir therapy since this study was done with tablets that have a higher bioavailability."

Puthanakit concurred, noting that her study did not include infants and young children who are treated with liquid formulations of the antiretroviral regimen.

The study was part of the long-standing HIV Netherlands Australia Thailand Research Collaboration (HIV-NAT).

The study was funded by Thai governmental agencies.

Puthanakit and Gibb reported no conflicts of interest.

Primary source: International AIDS Society
Source reference:
Puthanakit T, et al "A randomized study comparing low dose versus standard dose lopinavir/ritonavir among HIV-infected children with virological suppression" IAS 2013; Abstract MOAB0101.

Single HIV Pill Not Always Best (CME/CE)

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Published: Jul 5, 2013

This study was published as an abstract and presented at a conference. These data and conclusions should be considered to be preliminary until published in a peer-reviewed journal.This retrospective study demonstrated similar rates of medication discontinuation whether HIV-positive patients were taking a single-pill or multipill regimen.Note that all patients in the single-pill regimen group were taking Atripla, limiting the ability to determine whether the discontinuation rate was due to side-effects unique to this drug.

KUALA LUMPUR -- HIV patients taking single pills containing three drugs are thought to be less likely to stop taking their medications than those on more complicated regimens, but that may not be completely accurate, researchers said here.

In a retrospective, observational study, people taking the most widely used single pill were just as likely to switch therapies as were those on multipill regimens, according to Benoit Trottier, MD, of Clinique Medicale L'Actuel in Montreal, and colleagues at the AIDS Society Conference on HIV Pathogenesis, Treatment, and Prevention.

On the other hand, it was true that taking the single pill containing efavirenz, tenofovir, and emtricitabine (Atripla) was more likely to result in sustained control of HIV than multipill regimens, he reported.

But even there, one multipill regimen did just as well, Trottier reported.

There are currently three such single-pill regimens on the market: Atripla (Complera): A combination of efavirenz, tenofovir, and emtricitabineStribild: A combination of elvitegravir, cobicistat, tenofovir, and emtricitabine

Trottier and colleagues used their clinic records to see what happened to new HIV patients who started on Atripla, or one of three other recommended first-line regimens that have a higher number of pills.

The primary endpoint of the study was the time to stopping the first regimen, while a secondary endpoint was the loss of virological control.

Of the 575 patients who started therapy at the clinic from 2007 through March 2012, 32% stopped their initial regimen -- 35% of the 187 who started on Atripla and 31% of the 388 who started on another regimen.

That difference wasn't significant, but when the researchers compared Atripla with individual multipill regimens, they found that one -- based on the integrase inhibitor raltegravir (Isentress) -- was actually significantly less likely to lead to switching treatment.

The main reasons for switching treatment were side effects and toxicities, Trottier noted.

The single-pill regimen was significantly better in maintaining viral control as patients on multipill regimens were overall 85% more likely to have a virological failure.

But again, the raltegravir-based regimen did as well as Atripla, he reported, while the other multipill regimens were significantly worse.

The main problem with the study is that it doesn't distinguish between the effects of a single tablet regimen as such and the effects of the component drugs, commented Joel Gallant, MD, of Johns Hopkins University School of Medicine, who was not part of the study but who moderated the session at which it was presented.

"You couldn't necessarily extrapolate these findings to other (single tablet regimens)," he told MedPage Today, noting that efavirenz is known to have distressing central nervous system adverse effects not shared by most other HIV drugs.

But he added that the analyses that have suggested such regimens have more durable and effective results may suffer themselves from selection biases -- physicians tend to put highly motivated patients on Atripla knowing they are unlikely to miss doses.

If adherence is likely to be an issue, he added, doctors might choose regimens that are more forgiving.

Trottier agreed that the lack of data on other single-pill combinations is "a limit of our study."

But, he told MedPage Today, that's because other single tablet regimens have only recently reached the market so he and colleagues have limited numbers of patients on which to base an analysis.

Trottier said the study and the researchers had no external support from industry.

Gallant has disclosed commercial relationships with Bristol-Myers Squibb, Gilead Sciences, Janssen Therapeutics, Merck, RAPID Pharmaceuticals, and Sangamo Biosciences.

Primary source: International AIDS Society
Source reference:
Trottier B, et al "Single tablet regimens do not necessarily translate into more durable HIV treatments" IAS 2013; Abstract TUPDB0106.

North American Correspondent for MedPage Today, is a three-time winner of the Science and Society Journalism Award of the Canadian Science Writers' Association. After working for newspapers in several parts of Canada, he was the science writer for the Toronto Star before becoming a freelancer in 1994. His byline has appeared in New Scientist, Science, the Globe and Mail, United Press International, Toronto Life, Canadian Business, the Toronto Star, Marketing Computers, and many others. He is based in Toronto, and when not transforming dense science into compelling prose he can usually be found sailing.