A Frassoldati, M Federico, F Barbieri, M Brausi, C Pollastri, G Berri, G Castagnetti, P P Palladini, V Silingardi
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引用次数: 7
摘要
M-VEC(甲氨蝶呤、长春花碱、epidoxorubicin和顺铂)是一种新的联合用药方案,以epidoxorubicin取代阿霉素,以降低原来的M-VAC化疗的毒性,已在23例局部晚期移行细胞膀胱癌(T2-T4 No Mo)患者中进行了试验。经过2 ~ 4个疗程后,19例患者客观缓解,13例临床完全缓解。7例患者化疗后行膀胱切除术:1例患者膀胱标本未见肿瘤残留,5例患者手术根除,1例患者仅部分切除。8例膀胱癌复发,其中3例发生在手术治疗的患者中,5例发生在未行膀胱切除术的患者中,中位复发时间为9.7个月。24个月无进展生存率为52.3%。M-VEC方案似乎对局部晚期TCBC有效,毒性可接受。
Methotrexate, vinblastine, epidoxorubicin and cisplatin (M-VEC) in patients with locally advanced transitional bladder cancer.
M-VEC (methotrexate, vinblastine, epidoxorubicin and cisplatin), a new combined drug regimen in which epidoxorubicin has been substituted to adriamycin to reduce the toxicity of the original M-VAC chemotherapy, has been tested in 23 patients with locally advanced transitional cell bladder cancer (TCBC) (stage T2-T4 No Mo). After two to four courses, an objective response was observed in 19 patients, with 13 clinical complete responses. Seven patients underwent cystectomy after chemotherapy: one patient had no residual tumor on bladder specimens, five patients had a surgical eradication of the disease, while one patient had only a partial resection. Eight relapses of bladder carcinoma were observed, three among the surgically treated patients and five among patients who did not undergo cystectomy, with a median time-to-relapse of 9.7 months. Progression-free survival at 24 months was 52.3%. M-VEC regimen appears to be effective in locally advanced TCBC, with acceptable toxicity.