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Expert Analysis

Timing and Choice of First-Line Antiretroviral Therapy

Source: CCO Official Conference Coverage of the 2008 International AIDS Conference

Timing and Choice of First-Line Antiretroviral Therapy


Faculty:

Joel E. Gallant, MD, MPHJosé Gatell, MDW. David Hardy, MD
  • Joel E. Gallant, MD, MPH
  • José Gatell, MD
  • W. David Hardy, MD

CREDIT INFORMATION

Release Date: October 08, 2008

Expiration Date: October 07, 2009


Physicians: maximum of 1.5 AMA PRA Category 1 Credits

Registered Nurses: 1.5 Nursing contact hours

Pharmacists: 1.5 contact hours (0.15 CEUs)

Status: The activity is not currently available for credit.


Begin the Expert Analysis

Learning Objectives

Upon completion of this activity, participants should be able to:

  • Explain new findings from prospective and retrospective studies comparing different NRTI backbones in first-line antiretroviral therapy
  • Discuss new data on the relative efficacy of various antiretroviral agents in first-line therapy
  • Describe the role of immunologic response to HAART in patient outcomes and the implications for the benefit of early first-line treatment
  • Cite new results on the safety and efficacy of different boosted PI regimens among racial subgroups

Topics covered include:

  • ACTG 5202: Abacavir/Lamivudine vs Tenofovir/Emtricitabine in Treatment-Naive Patients With HIV-1 RNA ≥ 100,000 copies/mL
  • Reanalysis of Abacavir Studies Using ACTG 5202 Endpoints
  • HEAT Study: Abacavir/Lamivudine vs Tenofovir/Emtricitabine, Both With Lopinavir/Ritonavir, at 96 Weeks
  • Efavirenz vs Lopinavir/Ritonavir in Treatment-Naive Patients With Very Low CD4+ Cell Counts
  • Protocol 004: Efavirenz vs Raltegravir in Treatment-Naive Patients at 96 Weeks
  • Rilpivirine, a Second-Generation NNRTI vs Efavirenz in Treatment-Naive Patients at 96 Weeks
  • First-line Didanosine-EC, Emtricitabine, Atazanavir in Resource-Limited Settings
  • 100-mg Film-Coated Tablet Formulation of Ritonavir Is Bioequivalent to the Soft-Gel Capsule in Single-Dose, Open-Label Crossover Study
  • MONARK: Lopinavir/Ritonavir Monotherapy at 96 Weeks
  • GS 903E: 7-Year Data, in a Small Cohort of Patients, on the Safety and Efficacy of Tenofovir/Emtricitabine Plus Efavirenz
  • Substitution of Abacavir/Lamivudine for Thymidine Analogue NRTIs Maintains Virologic Efficacy and Offers Some Immunologic Advantages
  • Analyses of Response to Antiretrovirals by Race
  • Treatment of Acute HIV Infection With an NNRTI-Based Regimen Rather Than a Boosted PI-Based Regimen Effective in a Small Cohort
  • IDX899 and RDEA06, 2 Novel NNRTIs, Show Considerable Promise in Phase IIa Trials
  • Data From the MACS Cohort Indicate That Higher CD4+ Cell Counts Are Independently Associated With Lower Risk of AIDS and Death
  • ATHENA Cohort: The Importance of Early Diagnosis


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CCO Resources

Timing and Choice of First-Line Antiretroviral Therapy