Important note: Information in this article was accurate in 1992. The state of the art may have changed since the publication date.
PHASE II TRIAL OF PROLONGED, LOW-DOSE, ORAL VP-16 IN AIDS-RELATED KAPOSI'S SARCOMA (KS) (MEETING ABSTRACT)
Proc Annu Meet Am Soc Clin Oncol; 11:A13 1992. Unique Identifier : AIDSLINE ICDB/92680744 Bufill JA; Grace WR; Astrow AB; Oncology Section, Dept. of Medicine, St. Vincent's Hosp., New; York, NY 10011
Abstract:
Fourteen homosexual men with KS were given 50 mg/day VP-16 po for 21 consecutive days q 28-35 days. Eight patients (pts) had received prior treatment with either interferon (6) or chemotherapy (2), and most pts had experienced an opportunistic infection prior to entry. Their mean absolute CD4 count was 39 cells/mm3 (range 10-119 cells/mm3). All pts completed at least 1 cycle; 8 pts completed 3 or more cycles. No growth factors were administered during or after VP-16 therapy. There were no complete responses. Partial responses occurred in 3 pts (21%). Among pts classified as nonresponders, minor responses were seen in 5 (36%), suggesting some biological effect of the therapy. Predominant toxicities included leukopenia, anemia, infections, alopecia (9 pts), diarrhea (5) and nausea (3). Treatment-related infections included thrush (4 pts), herpes virus infections (4), PCP (2), sepsis (2) and bacterial pneumonia (1). These results, observed in pts with advanced AIDS, suggest that further study of oral VP-16 schedules is warranted, and that routine prophylaxis for thrush and herpes may be indicated.
Keywords: Acquired Immunodeficiency Syndrome/*COMPLICATIONS/IMMUNOLOGY Administration, Oral Antigens, CD4/ANALYSIS Biological Markers Drug Administration Schedule Drug Evaluation Etoposide/ADMINISTRATION & DOSAGE/*TOXICITY/*THERAPEUTIC USE Human Sarcoma, Kaposi's/*DRUG THERAPY/*ETIOLOGY/IMMUNOLOGY CLINICAL TRIAL ABSTRACT
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