Document 2993 DOCN M94A2993 TI Chemotherapy and didanosine (DDI) in AIDS-lymphoma. DT 9412 AU Harrington WJ; Ucar A; Cabral L; Lai S; Byrnes JJ; Univ. of Miami, FL. SO Int Conf AIDS. 1994 Aug 7-12;10(1):178 (abstract no. PB0138). Unique Identifier : AIDSLINE ICA10/94369582 AB OBJECTIVE: To explore the hypothesis that combined antiretroviral and antitumor chemotherapy is feasible and more effective. METHOD: A randomized clinical trial was undertaken of stage II-IV intermediate or high grade lymphoma. 16 pts were randomized to the DDI (+) arm and 14 to the DDI (-) arm. Chemotherapy was delivered over 12 weeks: mitoxantrone (8 mg/m2) and VP-16 (100 mg/m2) on odd weeks; cyclophosphamide 350 mg/m2 on wks 1, 5, and 9; bleomycin (10 u/m2) and vincristine 2 mg on even weeks; and methylprednisolone (1g/m2) weekly. In addition, patients received prophylaxis with Bactrim, difluconazole and acyclovir. RESULTS: The response rate in the DDI(+) arm was 85% (61% CR and 25% PR) versus 71% (43% CR and 28% PR) in the DDI (-) arm. The median duration of CR has been 50+ weeks. Logistic regression analyses show that a higher CD4 count, a higher CD8 count, a higher serum albumin, a lower serum lactic dehydrogenase, and DDI usage were associated with complete remission and longer survival. DDI toxicities included: pancreatitis, paresthesias, and diarrhea. There was less febrile neutropenia in the DDI (+) arm. CONCLUSIONS: Concurrent chemotherapy and DDI is feasible and well tolerated. This treatment program is delivered over a short period of time (12) weeks, with acceptable toxicity and a high response rate. DE Acquired Immunodeficiency Syndrome/*DRUG THERAPY/MORTALITY/ PATHOLOGY Antineoplastic Agents, Combined/*THERAPEUTIC USE Combined Modality Therapy Comparative Study Didanosine/*THERAPEUTIC USE Dose-Response Relationship, Drug Drug Administration Schedule Follow-Up Studies Human Lymphoma, AIDS-Related/*DRUG THERAPY/MORTALITY/PATHOLOGY Neoplasm Staging Remission Induction Survival Rate CLINICAL TRIAL MEETING ABSTRACT RANDOMIZED CONTROLLED TRIAL SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).