Statistical Issues in the Design of HIV Vaccine Trials

Author:

Schaper Carl1,Fleming Thomas R.1,Self Steven G.2,Rida Wasima N.3

Affiliation:

1. Department of Biostatistics, University of Washington, Seattle, Washington 98195

2. Program in Biostatistics, Fred Hutchison Cancer Research Center, Seattle, Washington, 98104

3. Division of AIDS, NIAID, Bethesda, Maryland 20892

Abstract

HIV vaccine trials present significant challenges related to trial endpoints, vaccine efficacy measurement, and the role of nonvaccine interventions. Infection is a valid endpoint for detecting sterilizing immunity. But if the vaccine prevents AIDS without preventing infection, infection may be a misleading surrogate. Appropriate endpoints must be defined for other mechanisms of vaccine action. Direct, indirect, behavioral, and biological effects all determine vaccine efficacy. False security among HIV-vaccine recipients may make negative behavioral effects an important component of vaccine performance. Both biological potency and a more comprehensive program effectiveness should be measured. These goals may require unblinded designs or community randomization. Nonvaccine interventions are currently the only HIV-prevention strategy. Support for larger scale implementation requires more rigorous evaluation that is less dependent on self-reported behavioral changes. The vaccine trial cohorts provide a unique opportunity to cost-effectively evaluate behavioral interventions.

Publisher

Annual Reviews

Subject

Public Health, Environmental and Occupational Health,General Medicine

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