Division of Hematology-Oncology, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital, 123, Ta-Pei Rd, Niao-Sung Hsiang, Kaohsiung Hsien, Taiwan.
Jpn J Clin Oncol. 2011 Apr;41(4):455-61. doi: 10.1093/jjco/hyq232. Epub 2010 Dec 30.
Patients with metastatic breast cancer usually accept several lines of chemotherapy. This retrospective study is to analyze the therapeutic effect and tolerance of weekly paclitaxel/gemcitabine combination on patients with metastatic breast cancer.
Paclitaxel 80 mg/m(2) and gemcitabine 800 mg/m(2) were administered sequentially on days 1, 8 and 15 every 28 days. Patients with measurable metastatic breast cancer or locally advanced breast cancer were included.
From March 2005 to December 2006, 50 patients received this treatment at Chang Gung Memorial Hospital, Kaohsiung Medical Center. Thirteen (26%) patients accepted this regimen as their first-line treatment for metastatic breast cancer and 25 (50%) patients accepted this regimen after at least three lines of therapies for metastatic breast cancer. The overall response rate was 56% (95% confidence interval: 42.2-69.8%), 2 patients achieved complete response and 26 patients (52, 95% confidence interval: 38.2-65.9%) achieved partial response. The median progression free survival was 7.4 months (95% confidence interval: 5.5-9.3 months), and the median overall survival was 19.0 months (95% confidence interval: 9.7-28.3 months). Except alopecia, the most common Grade 3/4 toxicities were anemia and leucopenia; the incidences of both were fewer than 10%.
The combination of weekly gemcitabine and paclitaxel in patients with advanced breast cancer showed acceptable outcome and excellent toxic profiles. This therapeutic benefit could be achieved in any linage of patients with good performance status; earlier usage of this regimen can provide better result.
转移性乳腺癌患者通常接受多线化疗。本回顾性研究旨在分析每周紫杉醇/吉西他滨联合方案治疗转移性乳腺癌的疗效和耐受性。
紫杉醇 80mg/m2 与吉西他滨 800mg/m2 序贯给药,第 1、8 和 15 天,每 28 天为一个周期。纳入可测量的转移性乳腺癌或局部晚期乳腺癌患者。
2005 年 3 月至 2006 年 12 月,长庚纪念医院高雄医学中心共有 50 例患者接受该方案治疗。13 例(26%)患者将该方案作为转移性乳腺癌的一线治疗,25 例(50%)患者在转移性乳腺癌至少接受三线治疗后接受该方案治疗。总缓解率为 56%(95%置信区间:42.2-69.8%),2 例患者完全缓解,26 例患者(52 例,95%置信区间:38.2-65.9%)部分缓解。中位无进展生存期为 7.4 个月(95%置信区间:5.5-9.3 个月),中位总生存期为 19.0 个月(95%置信区间:9.7-28.3 个月)。除脱发外,最常见的 3/4 级毒性为贫血和白细胞减少症;两者的发生率均低于 10%。
每周吉西他滨联合紫杉醇治疗晚期乳腺癌的疗效可接受,毒性谱良好。该治疗方案在任何体力状态良好的患者中均能取得疗效;更早使用该方案可获得更好的效果。