摘要
目的观察吉西他滨/顺铂21天方案(GP方案),二、三线治疗转移性三阴乳腺癌(advanced triplenegative breastcancer,ATNBC)患者的疗效和不良反应。方法34例三阴乳腺癌患者,吉西他滨1.0g/In。第1、8天静脉滴注;顺铂25mg/m2。第1—3天静脉滴注,21天为一疗程,直到疾病进展或无法耐受或最多接受6周期化疗。结果34例患者共完成141个周期化疗,中位化疗周期3.5周期。均可评价疗效和不良反应。其中完全缓解0例(0%),部分缓解11例(32.35%),稳定9例(26.44%),进展14例(41.18%)。有效率(CR+PR)32.4%(95%可信区间24.15%-40.55%),疾病控制率(CR+PR+SD)58.8%,中位疾病进展时间(TTP)3.9月,中位生存期(OS)10.0月。治疗后主要不良反应为血液学毒性,血小板减少发生率为61.8%。结论三阴性乳腺癌预后差,GP方案治疗ATNBC患者安全有效,不良反应可以耐受。
Objective To evaluate the clinical efficacy and tolerability of a 3-week regimen of cisplatin(DDP) with gemcitabine (GEM) as second- or third-line for patients with advanced triple-negative breast cancer. Methods Thirty-four patients with advanced triple-negative breast cancer were enrolled in this study. All the patients were given gemicitabine 1.0 g,/m2 on days 1,8 ,combined with cisplatin 25 mg/m2 daily on days 1 -3. The combined chemotherapy was repeated every 21 days as one cycle. The maximum of 6 cycles were given. Results All of the 34 patients completed 141 cycles of chemotherapy with a median number of 3.5 cycles per patient. Toxicity and clinical efficacy were evaluated on all the 34 patients. No patents (0%) achieved a complete response, 1l patients (32.4%) had a partial response, stable disease was documented in 9 patients (26.4%), while progressive disease occurred in 14 patients (41.2%). The overall response rate ( CR + PR) was 32.4% (95% CI:24.15% -40.55% ) and disease control rate ( CR + PR+ SD) was 58.8%. The median time to progress (TI'P) was 3.9 months,and median overall survival time (OS) was 10.0 months. The major adverse event of drugs was hematologic toxicity, The incidence of I ~ II grade thrombocytopenia was 61.8%. Conclusions Metastatic triple-negative breast cancer contributes to the poor prognosis. Cisplatin combined with gemeitabine is an effective and safe chemotherapeutic regimen for ATNBC patients and the adverse effects are well-tolerated.
出处
《实用肿瘤杂志》
CAS
北大核心
2011年第3期278-281,共4页
Journal of Practical Oncology