A feasibility study using polychemotherapy (cisplatin plus vindesine plus dacarbazine) plus interferon-alpha or monochemotherapy with dacarbazine plus interferon-alpha in metastatic melanoma

被引:8
作者
Bajetta, E
Del Vecchio, M
Vitali, M
Martinetti, A
Ferrari, L
Queirolo, P
Sertoli, MR
Cainelli, T
Cellerino, R
Cascinelli, N
机构
[1] Ist Nazl Studio & Cura Tumori, Unit Nucl Med, I-20133 Milan, Italy
[2] Ist Nazl Ric Canc, Div Med Oncol, I-16132 Genoa, Italy
[3] Osped Riuniti Bergamo, Dermatol Clin, Bergamo, Italy
[4] Osped Reg USL 12, Div Clin Oncol, Ancona, Italy
[5] Ist Nazl Tumori Studio & Cura Tumori, Unit Med Oncol B, I-20133 Milan, Italy
关键词
chemotherapy; immunotherapy; melanoma;
D O I
10.1177/030089160108700402
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aims and background: This trial evaluated the feasibility and tolerability of an immunochemotherapeutic approach that uses cisplatin, vindesine, and dacarbazine (DTIC), or only DTIC, in combination with Interferon alpha-2a (IFN-alpha), in patients with metastatic melanoma, considering the significant toxicity of several different regimens used up to now. Methods: Between May 1995 and September 1997, 51 melanoma patients (50 of whom were assessable) entered a multicentric trial and were randomized to receive cisplatin (30 mg/m(2) daily for 3 days) + vindesine (2.5 mg/m(2) only day 1) + DTIC (250 mg/m(2) daily for 3 consecutive days) + IFN-alpha (3 MIU im 3x/wk continuously) (CVD arm) versus DTIC (800 mg/m(2) day 1) + IFN-alpha (3 MIU im 3x/wk continuously) (DTIC arm). The chemotherapy was recycled every 21 days. Patient reevaluation was performed every two cycles, and the treatment was continued in case of objective response or stabilization of disease. Results: We observed 3 complete responses, 2 partial responses and 5 stable diseases in the CVD arm, and 2 partial responses and 4 stabilizations of disease in the DTIC arm. Conclusions: We conclude that these chemotherapeutic regimens are well tolerated regimens with modest toxicity. Future trials will be conducted associating the CVD regimen with biological response modifiers (IFN, IL-2) in order to improve the results.
引用
收藏
页码:219 / 222
页数:4
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