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文献详情 >多西紫杉醇和卡铂联合治疗晚期或复发宫颈癌:一项初步研究 收藏

多西紫杉醇和卡铂联合治疗晚期或复发宫颈癌:一项初步研究

Combination chemotherapy of docetaxel and carboplatin in advanced or recurrent cervix cancer.A pilot study

作     者:Nagao S. Fujiwara K. Oda T. 战媛 

作者机构:Dept. of Obstetrics and Gynecology Kawasaki Medical School 577 Matsushima Kurashiki- City 701- 0192 Japan 

出 版 物:《世界核心医学期刊文摘(妇产科学分册)》 (Core Journal in Obstetrics/Gynecology)

年 卷 期:2005年第1卷第7期

页      面:41-42页

学科分类:1002[医学-临床医学] 100214[医学-肿瘤学] 10[医学] 

主  题:联合化疗 新辅助化疗 小细胞癌 腺鳞癌 静脉给药 毒性反应 鳞状细胞癌 肾功能 神经毒性 可测量 

摘      要:Objectives. This is a pilot study for a future trial to assess the efficacy and safety of combination chemotherapy with docetaxel and carboplatin in advanced or recurrent uterine cervix cancer. Methods. The patients eligible for this study had histologically confirmed, advanced (stage IB2- IV) or recurrent uterine cervix cancer. Eligible patients had measurable lesions and must have sufficient bone marrow, renal, and liver functions. Docetaxel was administered intravenously (IV) at 60 mg/m2 followed by IV carboplatin administration based on AUC = 6. Chemotherapy was repeated in 1- 6 courses depending on the purpose of the therapy. The response was evaluated based on RECIST criteria. The toxicity grade was determined by NCI- CTC version 2. Results. During January 2001 and April 2004, 17 patients were entered in this study. The distribution of stage was IB2, 3; IIB, 8; IIIB, 3; IVB, 1; recurrent, 2. There were 9 squamous cell carcinomas, 6 adenocarcinomas, 1 adenosquamous cell carcinoma, and 1 small cell carcinoma. The overall response rate was 76% (2 CR, 11 PR, and 4 SD). No progression of disease was observed. All 5 adenocarcinoma patients in the neoadjuvant chemotherapy group responded including 1 pathological CR. The incidences of grade 3/4 toxicities were 76% for neutrocytopenia, 12% for thrombocytopenia, and 6% for anemia. No grade 3/4 neurotoxicity was observed. Conclusions. The combination of docetaxel and carboplatin is an effective and safe treatment for uterine cervix cancer. Further evaluation particularly targeted on cervical adenocarcinoma is warranted.

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