Methotrexate, vinblastine, doxorubicin and cisplatin combination regimen as salvage chemotherapy for patients with advanced or metastatic transitional cell carcinoma after failure of gemcitabine and cisplatin chemotherapy

被引:40
作者
Han, K. S. [1 ]
Joung, J. Y. [1 ]
Kim, T. S. [1 ]
Jeong, I. G. [1 ]
Seo, H. K. [1 ]
Chung, J. [1 ]
Lee, K. H. [1 ]
机构
[1] Natl Canc Ctr, Ctr Specif Organs Canc, Urol Oncol Clin, Goyang, South Korea
关键词
transitional cell carcinoma; chemotherapy; cisplatin; metastasis;
D O I
10.1038/sj.bjc.6604113
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We investigated the safety and efficacy of a methotrexate, vinblastine, doxorubicin and cisplatin ( M-VAC) combination regimen as second-line chemotherapy for patients with advanced or metastatic transitional cell carcinoma who failed first-line gemcitabine and cisplatin ( GC) chemotherapy. Thirty patients who had progressed or relapsed after GC chemotherapy as first-line treatment were enrolled in this study. The major toxicities were neutropaenia and thrombocytopaenia. A grade 3 or 4 neutropaenia occurred in 19 ( 63.3%) and a grade 3 or 4 thrombocytopaenia developed in nine patients ( 30.0%). There were no life-threatening complications during the study. The overall response was 30%. A complete response was achieved in two patients ( 6.7%) and a partial response in seven ( 23.3%). The overall disease control rate was 50%. Seven out of 16 patients who had responded previously to GC responded to M-VAC, while 2 out of 14 who had not responded to GC responded to M-VAC. The median response duration was 3.9 months and the median progression-free survival was 5.3 months. The median overall survival was 10.9 months. M-VAC showed encouraging efficacy and reversible toxicities in patients who had progressed after GC chemotherapy and, especially, M-VAC appears to be a reasonable option as a sequential treatment regimen in patients who responded previously to GC chemotherapy.
引用
收藏
页码:86 / 90
页数:5
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