Eligibility criteria for HIV clinical trials and generalizability of results: the gap between published reports and study protocols

被引:82
作者
Gandhi, M
Ameli, N
Bacchetti, P
Sharp, GB
French, AL
Young, M
Gange, SJ
Anastos, K
Holman, S
Levine, A
Greenblatt, RM
机构
[1] Univ Calif San Francisco, Div Infect Dis, Dept Med, San Francisco, CA 94122 USA
[2] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94122 USA
[3] NIAID, Div Aids, NIH, Bethesda, MD 20892 USA
[4] Rush Med Coll, Cook Cty Hosp, CORE Ctr, Chicago, IL 60612 USA
[5] Georgetown Univ, Dept Med, Washington, DC 20007 USA
[6] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA
[7] Lincoln Med & Mental Hlth Ctr, Bronx, NY 10451 USA
[8] SUNY Brooklyn, Dept Prevent Med & Community Hlth, Brooklyn, NY USA
[9] Univ So Calif, Dept Med, Los Angeles, CA USA
关键词
HIV; clinical trials; eligibility criteria; protocols; publications; generalizability;
D O I
10.1097/01.aids.0000189866.67182.f7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: Applicability of randomized controlled clinical trial (RCT) results to 'real world' situations is dependent on the comparability of trial participants to general patient populations. A full disclosure of criteria employed for trial enrollment is necessary for clinicians to assess generalizability. We sought to assess both the impact on generalizability and the disclosure rate of enrollment criteria for 32 major HIV RCTs in the AIDS Clinical Trial Group (ACTG) and Community Programs for Clinical Research on AIDS (CPCRA) trial networks. Design and methods: Eligibility criteria were compared in complete protocols to criteria listed in publications from these 32 NIH-funded HIV RCTs. We then applied these criteria to the Women's Interagency HIV Study (WIHS), the largest cohort study of HIV-infected women in the US. Results: When applied to WIHS, eligibility criteria from protocols excluded 0-67.6% (median 42%) of WIHS participants (50.6% excluded from ACTG trials). Eligibility criteria in publications excluded 0-62% (median 19.6%) of WIHS (21.2% excluded from ACTC, trials). The number of women in WIHS seemingly ineligible for trial participation per enrollment criteria listed in publications averaged only 60% of those actually excluded based on the protocols. Conclusions: We found that HIV RCT eligibility criteria excluded a large proportion of a representative cohort of HIV-infected women from trial participation. Furthermore, trial publications are not fully reflective of protocols in terms of disclosing eligibility criteria. Standardization and full disclosure of trial methodology will allow clinicians and researchers to more fully assess the generalizability of findings to their patient populations. (c) 2005 Lippincott Williams & Wilkins.
引用
收藏
页码:1885 / 1896
页数:12
相关论文
共 70 条
[1]   A COMPARATIVE TRIAL OF DIDANOSINE OR ZALCITABINE AFTER TREATMENT WITH ZIDOVUDINE IN PATIENTS WITH HUMAN-IMMUNODEFICIENCY-VIRUS INFECTION [J].
ABRAMS, DI ;
GOLDMAN, AI ;
LAUNER, C ;
KORVICK, JA ;
NEATON, JD ;
CRANE, LR ;
GRODESKY, M ;
WAKEFIELD, S ;
MUTH, K ;
KORNEGAY, S ;
COHN, DL ;
HARRIS, A ;
LUSKINHAWK, R ;
MARKOWITZ, N ;
SAMPSON, JH ;
THOMPSON, M ;
DEYTON, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (10) :657-662
[2]   Nelfinavir, efavirenz, or both after the failure of nucleoside treatment of HIV infection. [J].
Albrecht, MA ;
Bosch, RJ ;
Hammer, SM ;
Liou, SH ;
Kessler, H ;
Para, MF ;
Eron, J ;
Valdez, H ;
Dehlinger, M ;
Katzenstein, DA .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (06) :398-407
[3]   Adherence to protease inhibitors, HIV-1 viral load, and development of drug resistance in an indigent population [J].
Bangsberg, DR ;
Hecht, FM ;
Charlebois, ED ;
Zolopa, AR ;
Holodniy, M ;
Sheiner, L ;
Bamberger, JD ;
Chesney, MA ;
Moss, A .
AIDS, 2000, 14 (04) :357-366
[4]  
Bangsberg DR, 2001, J ACQ IMMUN DEF SYND, V26, P435, DOI 10.1097/00126334-200104150-00005
[5]   The Women's Interagency HIV Study [J].
Barkan, SE ;
Melnick, SL ;
Preston-Martin, S ;
Weber, K ;
Kalish, LA ;
Miotti, P ;
Young, M ;
Greenblatt, R ;
Sacks, H ;
Feldman, J .
EPIDEMIOLOGY, 1998, 9 (02) :117-125
[6]   A randomized study of antiretroviral management based on plasma genotypic antiretroviral resistance testing in patients failing therapy [J].
Baxter, JD ;
Mayers, DL ;
Wentworth, DN ;
Neaton, JD ;
Hoover, ML ;
Winters, MA ;
Mannheimer, SB ;
Thompson, MA ;
Abrams, DI ;
Brizz, BJ ;
Ioannidis, JPA ;
Merigan, TC .
AIDS, 2000, 14 (09) :F83-F93
[7]   Improving the quality of reporting of randomized controlled trials - The CONSORT statement [J].
Begg, C ;
Cho, M ;
Eastwood, S ;
Horton, R ;
Moher, D ;
Olkin, I ;
Pitkin, R ;
Rennie, D ;
Schulz, KF ;
Simel, D ;
Stroup, DF .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 276 (08) :637-639
[8]   Clarithromycin or rifabutin alone or in combination for primary prophylaxis of Mycobacterium avium complex disease in patients with AIDS:: A randomized, double-blind, placebo-controlled trial [J].
Benson, CA ;
Williams, PL ;
Cohn, DL ;
Becker, S ;
Hojczyk, P ;
Nevin, T ;
Korvick, JA ;
Heifets, L ;
Child, CC ;
Lederman, MM ;
Reichman, RC ;
Powderly, WG ;
Notario, GF ;
Wynne, BA ;
Hafner, R .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (04) :1289-1297
[9]   A prospective, randomized trial examining the efficacy and safety of clarithromycin in combination with ethambutol, rifabutin, or both for the treatment of disseminated Mycobacterium avium complex disease in persons with acquired immunodeficiency syndrome [J].
Benson, CA ;
Williams, PL ;
Currier, JS ;
Holland, F ;
Mahon, LF ;
MacGregor, RR ;
Inderlied, CB ;
Flexner, C ;
Neidig, J ;
Chaisson, R ;
Notario, GF ;
Hafner, R .
CLINICAL INFECTIOUS DISEASES, 2003, 37 (09) :1234-1243
[10]  
Britton A, 1999, J Health Serv Res Policy, V4, P112