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作 者:薛妍[1] 斯晓明[1] 杨静悦[1] 陈衍[1] 尤向辉[1] 刘文超[1]
机构地区:[1]第四军医大学西京医院肿瘤科,陕西西安710032
出 处:《现代肿瘤医学》2010年第5期920-923,共4页Journal of Modern Oncology
摘 要:目的:观察埃坡霉素类似物(BMS-247550)联合卡培他滨治疗晚期乳腺癌的疗效与安全性。方法:2005年12月至2007年6月,以埃坡霉素类似物联合卡培他滨治疗晚期乳腺癌12例。埃坡霉素类似物40mg/m2,静滴,持续3h以上,第1天;卡培他滨1000mg/m2,口服,2次/日,连用14天,21天为1周期。本组中位化疗周期数为6个(2-10周期)。结果:12例均可评价疗效及不良反应。完全缓解(CR)0例(0%),部分缓解(PR)8例(66.7%),稳定(SD)4例(33.3%),进展(PD)0例(0%),总有效率(CR+PR)66.7%。中位肿瘤进展时间(TTP)6.5个月,1年生存率75.0%。主要毒性为骨髓抑制、黏膜炎、腹泻、恶心、呕吐、便秘、手足综合征、神经毒性。结论:埃坡霉素类似物和卡培他滨联合方案治疗晚期乳腺癌的疗效较好,使用方便,毒性反应可以耐受,是晚期乳腺癌的有效解救治疗方案。Obiective:To evaluate the efficacy and safety of combination chemotherapy of Epothilone B Analogue ( BMS - 247550) combined with capecitabine for advanced breast cancer (ABC). Methods: From December 2005 to June 2007,12 patients with advanced breast cancer (ABC) were treated with combination chemotherapy of Epothilone B Analogue and eapecitabine. Epothilone B Analogue dOmg/m2 was used for more than 3 hours on day 1 every three weeks ,and capecitabine 1000mg/m2 was used twice per day on day 1 - 14 every three weeks. The median number of cycles was 6 (range:2- 10 cycles). Results: Response rates and side effects could be evaluated in all 12 patients. The overall response rate was 66.7% with a median time to progression of 6.5 months. One - year survival rate was 75.0%. The main side effects were hematologic and gastrointestinal toxieities, including grade 3 to 4 leukopenia in 10 patients (83.4%) ,neutropenia in 10 patients (83.4%) ,platelets reduction in 2 patients (16.7%), and grade 3 to 4 mucositis in 2 patients (16.7%) ,diarrhea in 1 patient (8.3%) ,nausea and vomiting in 1 patient (8.3%) ,con- stipation in 1 patient (8.3%) ,as well as grade 3 to 4 hand and foot symdrome in 1 patient (8.3%) ,neurotoxicity in 1 patient (8.3%). Condusion:Epothilone B Analogue and capecitabine combination is active in the treatment of advanced breast cancer patient with an acceptable toxicity, and may be a therapeutic alternative for advanced breast cancer.
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