Endpoints are a continuing source of controversy in clinical trials of
antiretroviral (specifically, anti-HIV) treatments. The most visible
disagreement is about the respective roles of morbidity and mortality
as endpoints, and laboratory measurements as endpoints. Laboratory mea
surements have been intensely examined as possible surrogates for clin
ical outcomes, but the definition of the usual clinical outcome - firs
t occurrence or recurrence of an AIDS-defining condition or death - ha
s received little critical scrutiny. First disease progression has ser
ious weakness as an endpoint, and one should consider alternatives. In
this paper, we suggest using rule-based schemes to rank patients' pos
t-randomization histories and then using the ranks as an outcome measu
re, an extension of the work by Follmann et al. on heart disease. We e
valuated six rule-based ranking schemes for antiretroviral trials by a
pplying them to 60 participants in CPCRA 002 and comparing the results
to subjective rankings given by five experts. The expert's rankings w
ere in good agreement with each other, and the six rule-based schemes
were clearly differentiated by their degree of agreement with the expe
rt's rankings. The ranking scheme most in accord with the experts rank
ed patients first by seriousness of their most serious AIDS-defining d
isease, second by the timing of that disease, and the third by the tot
al number of AIDS-defining diseases they experienced. Finally, we used
this rule-based rankings to re-analyse CPCRA 002. (C) 1997 by John Wi
ley & Sons, Ltd.