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紫杉醇联合蒽环类药物治疗晚期乳腺癌的临床观察 被引量:6

Combination of paclitaxel and anthracycline for treatment of patients with advanced breast cancer
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摘要 目的观察紫杉醇联合吡柔比星(THP)/表阿霉素(E-ADM)治疗晚期乳腺癌患者的临床疗效和不良反应。方法95例患者均为晚期乳腺癌,化疗方案为THP50mg/m^2或E—ADM70mg/m^2,快速静滴15min,d1;国产紫杉醇135~175mg/m^2,静滴3h,d2。21d为一个周期,连用2个周期以上评价疗效。结果全组95例均可评价疗效,总有效率为40.0%。完全缓解率为15.8%,部分缓解率为24.2%。无治疗相关死亡,丰要不良反成为骨髓抑制和脱发。THP组脱发发生率较E-ADM组少,差异有显著性。结论紫杉醇联合THP/E-ADM化疗晚期乳腺癌缓解率较高,不良夏应可耐受,是治疗晚期乳腺癌安全有效的化疗方案。 Objective To investigate efficacy of combination of paclitaxel and anthraeycline in treatment of advanced breast cancer, and its toxicity. Methods Ninety-five patients with advanced breast cancer received this regimen (50 mg/m^2 of THP or 70 mg/m^2 of E-ADM intravenous infusion for 15 min, day 1 ; 135-175 mg/m^2 of paclitaxel, intravenous infusion for 3 hr, day 2) , every 21 days was a cycle. Efficacy and toxicity were evaluated after 2 eycles. Results Total response rate was 40. 0% , with 15 eases of complete remission( CR 15.8% ) and 23 cases of partial remission( PR 24.2% ). No treatment-related death occurred. Myelosuppression and alopecia were main toxicity. Group of THP was better than group of E-ADM in alopecia, with significant difference. Conclusion The combination of paclitaxel and THP/E-ADM may achieve a high response rate with toxicity tolerable by patients with advanced hreast cancer.
作者 郭凯平 何燕
出处 《中国肿瘤临床与康复》 2006年第1期66-68,共3页 Chinese Journal of Clinical Oncology and Rehabilitation
关键词 乳腺肿瘤/化学疗法 紫杉醇 吡柔比星 表阿霉素 Breast neoplasms/chemotherapy Paclitaxel Pirarubicin Epirubiein
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  • 1Hutchins L,Green S, Ravdin P,et al. CMF versus CAF with and without tamoxifen in high risk node negative breast cancer patients and a natural history follow-up study in low risk node negative patients: first results of Intergroup trial in 0102 [J]. Proc Am Soc Clin Oncol, 1998,17 : Abst 2.
  • 2Henderson IC, Berry D, Demetri GD, et al. Improved outcomes from adding sequential paclitaxel but not from eslating doxorubicin dose in an adjuvant chemotherapy regimen for patients with node-positive primary breast cancer [J]. J Clin Oncol, 2003,21(6):976-983.
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