Brandi Mario, Vici Patrizia, Lopez Massimo, Valerio Maria Rosaria, Giotta F, Gebbia Nicola, Schittulli Francesco, Colucci Giuseppe
Medical and Experimental Oncology Department, Oncology Institute, Bari, Italy.
Semin Oncol. 2004 Apr;31(2 Suppl 5):13-9. doi: 10.1053/j.seminoncol.2004.03.022.
The goals of this study were to evaluate the efficacy and toxicity of the gemcitabine/docetaxel combination in metastatic breast cancer previously treated with anthracyclines. Fifty-three patients with metastatic breast cancer who had failed or relapsed after anthracycline-based chemotherapy entered the study and were evaluable. Patients received gemcitabine (1,000 mg/m(2) days 1 and 8) and docetaxel (80 mg/m(2) day 8), every 3 weeks. The regimen was generally well tolerated with good feasibility. A complete response occurred in six patients (9.4%) and partial response in 23 (43.4%) for an overall response rate of 53% (95% confidence interval, 38.9% to 66.7%). Median survival rate was 70%; and the duration of response, time to progression, and overall survival were 6, 7.5, and 16.5 months, respectively. We conclude that the gemcitabine/docetaxel combination constitutes a manageable and tolerable combination as salvage chemotherapy in metastatic breast cancer and may represent a valid treatment option in patients previously treated with anthracyclines.
本研究的目的是评估吉西他滨/多西他赛联合方案用于先前接受过蒽环类药物治疗的转移性乳腺癌的疗效和毒性。53例在基于蒽环类药物的化疗后出现失败或复发的转移性乳腺癌患者进入本研究并可进行评估。患者接受吉西他滨(第1天和第8天,1000mg/m²)和多西他赛(第8天,80mg/m²)治疗,每3周重复一次。该方案总体耐受性良好,可行性佳。6例患者(9.4%)出现完全缓解,23例(43.4%)出现部分缓解,总缓解率为53%(95%置信区间,38.9%至66.7%)。中位生存率为70%;缓解持续时间、疾病进展时间和总生存期分别为6个月、7.5个月和16.5个月。我们得出结论,吉西他滨/多西他赛联合方案作为转移性乳腺癌的挽救化疗是一种可管理且耐受性良好的联合方案,对于先前接受过蒽环类药物治疗的患者可能是一种有效的治疗选择。