Literature DB >> 19372951

Earlier initiation of antiretroviral therapy in treatment-naïve patients: implications of results of treatment interruption trials.

James D Neaton1, Birgit Grund.   

Abstract

PURPOSE OF REVIEW: To discuss the implications of the results of the Strategies for Management of Antiretroviral Therapy Study and other treatment interruption studies on the question of when antiretroviral therapy should be initiated. RECENT
FINDINGS: In the Strategies for Management of Antiretroviral Therapy Study, CD4 count-guided, episodic use of antiretroviral therapy as compared with continuous antiretroviral therapy resulted in an increased risk of all-cause mortality, almost entirely due to causes other than AIDS, and a composite outcome of cardiovascular disease, renal disease and liver disease. Subgroup analyses in the Strategies for Management of Antiretroviral Therapy Study indicated that the increased risk in the episodic antiretroviral therapy group compared with the continuous antiretroviral therapy group was evident in patients taking antiretroviral therapy at entry (antiretroviral therapy stopped after randomization) and in patients not taking antiretroviral therapy at entry (patients remained off antiretroviral therapy until their CD4 count declined to below 250 cells/mm).
SUMMARY: The Strategies for Management of Antiretroviral Therapy Study did not directly address the 'when to start' question. Data from the Strategies for Management of Antiretroviral Therapy Study and other studies strongly suggest, however, that the use of antiretroviral therapy earlier than recommended by current guidelines warrants investigation. Definitive data from randomized studies that are powered to reliably assess risks and benefits are needed to guide when antiretroviral therapy is initiated.

Entities:  

Year:  2008        PMID: 19372951     DOI: 10.1097/COH.0b013e3282f3808b

Source DB:  PubMed          Journal:  Curr Opin HIV AIDS        ISSN: 1746-630X            Impact factor:   4.283


  5 in total

1.  Considerations for Endpoint Selection When Designing HIV Clinical Trials.

Authors:  Katherine Huppler Hullsiek; Birgit Grund
Journal:  Curr Infect Dis Rep       Date:  2012-02       Impact factor: 3.725

2.  Risk of all-cause mortality associated with nonfatal AIDS and serious non-AIDS events among adults infected with HIV.

Authors:  Jacqueline Neuhaus; Brian Angus; Justyna D Kowalska; Alberto La Rosa; Jim Sampson; Deborah Wentworth; Amanda Mocroft
Journal:  AIDS       Date:  2010-03-13       Impact factor: 4.177

3.  Death rates in HIV-positive antiretroviral-naive patients with CD4 count greater than 350 cells per microL in Europe and North America: a pooled cohort observational study.

Authors:  Rebecca K Lodwick; Caroline A Sabin; Kholoud Porter; Bruno Ledergerber; Ard van Sighem; Alessandro Cozzi-Lepri; Pavel Khaykin; Amanda Mocroft; Lisa Jacobson; Stephane De Wit; Niels Obel; Antonella Castagna; Jan-Christian Wasmuth; John Gill; Marina B Klein; Stephen Gange; Melchor Riera; Cristina Mussini; Félix Gutiérrez; Giota Touloumi; Patrizia Carrieri; Jodie L Guest; Norbert H Brockmeyer; Andrew N Phillips
Journal:  Lancet       Date:  2010-07-15       Impact factor: 79.321

Review 4.  The role of HIV in serious diseases other than AIDS.

Authors:  Andrew N Phillips; James Neaton; Jens D Lundgren
Journal:  AIDS       Date:  2008-11-30       Impact factor: 4.177

5.  The 'Antiretrovirals, Sexual Transmission Risk and Attitudes' (ASTRA) study. Design, methods and participant characteristics.

Authors:  Andrew Speakman; Alison Rodger; Andrew N Phillips; Richard Gilson; Margaret Johnson; Martin Fisher; Jane Anderson; Rebecca O'Connell; Monica Lascar; Kazeem Aderogba; Simon Edwards; Jeffrey McDonnell; Nicky Perry; Lorraine Sherr; Simon Collins; Graham Hart; Anne M Johnson; Alec Miners; Jonathan Elford; Anna-Maria Geretti; William J Burman; Fiona C Lampe
Journal:  PLoS One       Date:  2013-10-15       Impact factor: 3.240

  5 in total

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