Document 2843 DOCN M94A2843 TI Impact of AZT monotherapy versus sequential or combination antiretroviral therapy on survival. DT 9412 AU Thompson M; Creagh T; Rimland D; Thompson S; Toomey K; AIDS Research Consortium of Atlanta, Inc., Georgia. SO Int Conf AIDS. 1994 Aug 7-12;10(1):212 (abstract no. PB0279). Unique Identifier : AIDSLINE ICA10/94369732 AB OBJECTIVE: To examine the impact of AZT mono- vs sequential or combination antiretroviral therapy on survival. METHODS: Data from the Georgia cohort of the CDC-sponsored Adult Spectrum of Disease Study were analyzed. The cohort includes HIV-infected adults enrolled since 2/1/90 from the offices of 32 private practices and 3 public clinics. Data are collected by chart abstraction at 6-month intervals. 5,300 patients have been followed for a median of 36 months. Antiretroviral (AR) therapy was categorized as: AZT monotherapy (received only AZT in > or = 3 consecutive 6-month intervals), sequential (received ddC or ddI following AZT, but not in the same interval after initiation), or combination (received ddC or ddI with AZT in > or = 3 consecutive intervals). RESULTS: 2019 patients met the above AR criteria. Proportional hazards analyses revealed no independent effect of gender, race, or transmission mode when stratified by CD4 count at initiation of AZT therapy. Product limit survival analyses were compared by logrank test. There was no significant difference in survival between sequential AZT/ddC and AZT/ddI or between combination AZT/ddC and AZT/ddI in any CD4 category. Survival times at 36 months for different strategies vs AZT monotherapy were as follows: TABULAR DATA, SEE ABSTRACT VOLUME. Many fewer patients were maintained for three intervals on combo AZT/dddI than combo AZT/ddC, and this may have biased the analysis of the combo AZT/ddI strategy. DISCUSSION AND CONCLUSIONS: Sequential and combination AR therapy with AZT/ddC or AZT/ddI conferred a survival benefit compared with AZT monotherapy in some CD4 categories. Analyses comparing sequential with combination therapy are not presented because of the possibility of confounding by different levels of AZT intolerance between the groups. DE Adult Cohort Studies Comparative Study Didanosine/ADMINISTRATION & DOSAGE/THERAPEUTIC USE Drug Therapy, Combination Georgia/EPIDEMIOLOGY Human HIV Infections/*DRUG THERAPY/MORTALITY Proportional Hazards Models Survival Analysis Treatment Outcome Zalcitabine/ADMINISTRATION & DOSAGE/THERAPEUTIC USE Zidovudine/ADMINISTRATION & DOSAGE/*THERAPEUTIC USE MEETING ABSTRACT MULTICENTER STUDY SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).