Some important issues in the planning of phase III HIV vaccine efficacy trials

被引:22
作者
Boily, MC [1 ]
Mâsse, BR
Desai, K
Alary, M
Anderson, RM
机构
[1] CHA Hop St Sacrement, Grp Rech Epidemiol, 1050 Chemin Ste Foy, Quebec City, PQ G1S 4L8, Canada
[2] Univ Laval, Dept Social & Prevent Med, Quebec City, PQ, Canada
[3] Univ Oxford, Wellcome Ctr epidemiol Infect Dis, Oxford, England
基金
英国惠康基金;
关键词
HIV; AIDS; vaccine; clinical trials; efficacy measures; sample size; mathematical models; trial simulations;
D O I
10.1016/S0264-410X(98)00316-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Given that interesting HIV vaccine candidates, including live preparations and DNA plasmids, exist and that the first phase III vaccine (AIDSVAX) testing is due to begin this summer, 1998, in the U.S., adequately addressing trial preparedness is a pressing issue. Despite double-blind randomized controlled clinical trial design, there may be difficulties with interpretation and use of the usual measures of vaccinal efficacy and calculation of sample size. Difficulties arise from vaccine characteristics (e.g. mode of action, time-lag, waning) and population heterogeneities (e.g. differences in susceptibility, sexual behaviour, mixing preferences) causing frailty effects that can exacerbate bias and time-dependent effects already known to exist in simple cases. Since vaccine properties, particularly mode of action, are unlikely to be known before the onset of clinical trials, choosing an efficacy measure and the associated analyses and sample size calculations will be problematic. Interim analyses designed to decide whether a study will be prolonged may be tenuous if based on a time-dependent measure and will influence sample size determination. Despite shortcomings, general recommendations can be made to minimise pernicious effects. The objectives of this paper are principally to review the current state of knowledge of the different stages in the preparation of large phase III HIV vaccine efficacy trials, the methodological difficulties related to their design, and the analysis of data collected from them. Mathematical models and trial simulations are used to demonstrate that further research is necessary to study the behaviour of vaccine efficacy measures under heterogeneous conditions of population, vaccine action, and trial design and identify a time-independent efficacy measure. Alternative methods to validate sample size calculations have to be developed in order to reduce the chances of unnecessary economic and human cost in phase III HIV vaccine trials. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:989 / 1004
页数:16
相关论文
共 110 条
[1]   HIV - TO VACCINATE OR NOT TO VACCINATE [J].
ADA, G ;
BLANDEN, B ;
MULLBACHER, A .
NATURE, 1992, 359 (6396) :572-572
[2]  
*AIDS VACC ADV COA, 1998, MOV EFF STUD
[3]   RANDOMIZED TRIAL OF EFFICACY OF SPF66 VACCINE AGAINST PLASMODIUM-FALCIPARUM MALARIA IN CHILDREN IN SOUTHERN TANZANIA [J].
ALONSO, PL ;
SMITH, T ;
SCHELLENBERG, JRMA ;
MASANJA, H ;
MWANKUSYE, S ;
URASSA, H ;
DEAZEVEDO, IB ;
CHONGELA, J ;
KOBERO, S ;
MENENDEZ, C ;
HURT, N ;
THOMAS, MC ;
LYIMO, E ;
WEISS, NA ;
HAYES, R ;
KITUA, AY ;
LOPEZ, MC ;
KILAMA, WL ;
TEUSCHER, T ;
TANNER, M .
LANCET, 1994, 344 (8931) :1175-1181
[4]  
ANDERSON R M, 1991
[5]  
ANDERSON RM, 1990, J ACQ IMMUN DEF SYND, V3, P417
[6]   IMMUNIZATION AND HERD-IMMUNITY [J].
ANDERSON, RM ;
MAY, RM .
LANCET, 1990, 335 (8690) :641-645
[7]   Low-efficacy HIV vaccines: Potential for community-based intervention programmes [J].
Anderson, RM ;
Garnett, GP .
LANCET, 1996, 348 (9033) :1010-1013
[8]   QUANTITATIVE INVESTIGATIONS OF DIFFERENT VACCINATION POLICIES FOR THE CONTROL OF CONGENITAL-RUBELLA SYNDROME (CRS) IN THE UNITED-KINGDOM [J].
ANDERSON, RM ;
GRENFELL, BT .
JOURNAL OF HYGIENE, 1986, 96 (02) :305-333
[9]   THE EPIDEMIOLOGY OF MUMPS IN THE UK - A PRELIMINARY-STUDY OF VIRUS TRANSMISSION, HERD-IMMUNITY AND THE POTENTIAL IMPACT OF IMMUNIZATION [J].
ANDERSON, RM ;
CROMBIE, JA ;
GRENFELL, BT .
EPIDEMIOLOGY AND INFECTION, 1987, 99 (01) :65-84
[10]   The role of behavioral research in HIV/AIDS prevention [J].
Auerbach, JD .
CURRENT OPINION IN INFECTIOUS DISEASES, 1998, 11 (01) :3-7