Fotermustine and dacarbazine plus recombinant interferon alpha2a in the treatment of advanced melanoma

被引:12
|
作者
Comella, P
Daponte, A
Casaretti, R
Ionna, F
Fiore, F
Presutti, F
Frasci, G
Caponigro, F
Gravina, A
Parziale, AP
Mozzillo, N
Comella, G
机构
[1] NATL TUMOR INST,DIV SURG ONCOL B,I-80131 NAPLES,ITALY
[2] NATL TUMOR INST,DEPT RADIOL,I-80131 NAPLES,ITALY
[3] INST RECH INT SERVIER,ROME,ITALY
关键词
melanoma; fotemustine; dacarbazine; rIFN alpha 2a;
D O I
10.1016/S0959-8049(97)00120-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Forty-three consecutive patients with advanced melanoma not previously treated with cytotoxic drugs (22 of them had already received adjuvant recombinant interferon alpha2a (rIFN alpha 2a)) were given a combination of intravenous (i.v.) fotemustine (FM), 100 mg/m(2) on day 1, and dacarbazine (DTIC), 250 mg/m(2) i.v. on days 2-5, every 3 weeks. rIFN alpha 2a was administered at the dosage of 3 MIU subcutaneously 3 times a week until progression. Four complete and 13 partial responses were registered, for an overall response rate of 40% (95% CI, 25-56%). Activity of this regimen was similar in patients with mainly visceral (10/22, 45%) or soft tissue (6/13, 46%) involvement. The median duration of responses was 24 weeks. Median survival time was 40 weeks, with a 13% 2 year survival rate. Neutropenia and thrombocytopenia affected 67% and 51% of patients, but were of WHO grade 4 in only 2% and 5% of them, respectively. Side-effects attributable to rIFN alpha 2a were mild and manageable. In conclusion, the combination of FM + DTIC and rIFN alpha 2a seemed well tolerated and relatively active in patients with advanced melanoma. However, the role of rIFN alpha 2a in affecting the long-term outcome of patients is still questionable. (C) 1997 Published by Elsevier Science Ltd.
引用
收藏
页码:1326 / 1329
页数:4
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