LIPOSOMAL-ENTRAPPED DOXORUBICIN - AN ACTIVE AGENT IN AIDS-RELATED KAPOSIS-SARCOMA

被引:134
作者
HARRISON, M
TOMLINSON, D
STEWART, S
机构
[1] ST MARYS HOSP,DEPT ONCOL,LONDON W2 1NY,ENGLAND
[2] ST MARYS HOSP,DEPT GENITOURINARY MED,LONDON W2 1NY,ENGLAND
关键词
D O I
10.1200/JCO.1995.13.4.914
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: A phase II study was performed of single-agent liposomally entrapped doxorubicin ([LED] Doxil; Liposome Technology Inc, Menlo Pork, CA) against locally advanced cutaneous/systemic AIDS-related Kaposi's sarcoma (KS). Patients and Methods: Thirty-four patients with AIDS-related advanced cutaneous/systemic KS were treated with 20 mg/m(2) of LED every 3 weeks on an outpatient basis, The median age was 39 years and the median Karnofsky score was 70. All patients had poor prognostic disease os judged by AIDS Clinical Trials Group (ACTG) criteria. Nineteen of 34 patients had received prior chemotherapy for KS, although no patient had received prior anthracyclines. Results: An overall response rate of 73.5% (25 of 34) was observed, Partial responses (PRs) occurred in 67.7% (23 of 34) and complete responses (CRs) in 5.8% (two of 34). In patients who had received previous chemotherapy, the response rate was 68.4% (13 of 19), and all responses were PRs. The median time to response was 6 weeks. The median duration of response was 9 weeks. Toxicity according to World Health Organization (WHO) criteria was as follows: neutropenia (grade greater than or equal to 3), 34%; alopecia (grade 1 only), 9%; and nausea and vomiting (grade 1), 18%. One patient died of heart failure, which was not considered to be anthracycline-induced. Conclusion: LED appears to be highly active against AIDS-related KS. The major toxicity is neutropenia, which seems to be progressive in patients who receive several cycles of therapy. Comparative studies of LED versus con ventional chemotherapy are needed. J Clin Oncol 13:914-920. (C) 1995 by American Society of Clinical Oncology.
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页码:914 / 920
页数:7
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