CROI 2013: Complications of HIV disease, viral hepatitis, and antiretroviral therapy
- PMID: 23681961
- PMCID: PMC6148869
CROI 2013: Complications of HIV disease, viral hepatitis, and antiretroviral therapy
Abstract
Studies with direct-acting antivirals (DAAs) for hepatitis C virus (HCV) monoinfection and HIV coinfection were highlighted at the 2013 Conference on Retroviruses and Opportunistic Infections (CROI). In HCV monoinfected patients, several interferon alfa-sparing, all-oral regimens demonstrated cure rates of greater than 90% with 12 weeks of treatment, including for hard-to-treat patients. Cure rates of 75% were attained in HIV/HCV coinfected patients with the addition of the investigational HCV protease inhibitor (PI) simeprevir to peginterferon alfa and ribavirin. Drug-drug interaction data to inform safe coadminstration of antiretroviral therapy with DAA-based HCV treatment were presented. There was continued emphasis on pathogenesis, management, and prevention of the long-term complications of HIV disease and its therapies, including cardiovascular disease, renal disease, alterations in bone metabolism, and vitamin D deficiency, along with a growing focus on biomarkers to predict development of end-organ disease. Understanding the elevated risk for non-AIDS-defining malignancies in the HIV-infected population and optimal management was a focal point of this year's data. Finally, the conference provided important information on tuberculosis coinfection and cryptococcal meningitis.
Conflict of interest statement
Financial Affiliations: Dr Luetkemeyer has received grants and research support awarded to the University of California San Francisco from Bristol-Myers Squibb, Cepheid, Gilead Sciences, Inc, Tobira Therapeutics, Vertex Pharmaceuticals, Inc, and Pfizer, Inc. Dr Havlir has no relevant financial affiliations to disclose. Dr Currier has received research grants awarded to the University of California Los Angeles from Merck & Co, Inc, and has served as a consultant to Gilead Sciences, Inc.
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