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作 者:李倩[1] 周宇红[1] 王妍[1] 李泓[1] 申峰[1] 刘天舒[1] 金文[1] 庄荣源[1]
机构地区:[1]复旦大学附属中山医院肿瘤内科,上海200032
出 处:《肿瘤》2015年第1期65-71,共7页Tumor
摘 要:目的:观察GT(吉西他滨联合多西他赛)方案一线治疗复发/转移性腹膜后平滑肌肉瘤(retroperitoneal leiomyosarcoma,RLMS)患者的疗效和不良反应。方法:采用GT方案治疗12例复发/转移性RLMS患者:吉西他滨900mg/m^2静脉滴注第1天和第8天,多西他赛75 mg/m^2静脉滴注第8天;每21 d为1个化疗周期。观察疗效和不良反应。结果:12例可评估患者共完成49个化疗周期,中位化疗周期数为3个(范围:1~8个)。2例(16.7%)患者为部分缓解,4例(33.3%)为疾病稳定,6例(50.0%)为疾病进展,疾病控制率达50.0%。中位无进展生存期为4.0个月(95%可信区间:2.9~5.1个月),中位生存期为18.0个月(95%可信区间:5.4~30.6个月)。最常见的不良反应为骨髓抑制,其中3/4级不良反应主要为白细胞/中性粒细胞减少4例(33.3%)、血小板减少1例(8.3%)、贫血1例(8.3%)。无因不良反应导致退组或致死病例。结论:GT方案一线治疗复发/转移性原发RLMS的疗效肯定且耐受性良好。Objective:To evaluate the efficacy and toxicity of CT regimen(gemcitabine and docetaxel) in patients with current/metastatic retroperitoneal leiomyosarcoma(RLMS) as first line therapy.Methods:Twelve eligible patients were treated with CT regimen(gemcitabine 900 mg/m^2 d 1 and d 8,combined with docetaxel 75 mg/m^2 d 8;repeated every 21 days).Response and toxicity were evaluated.Results:Twelve patients were enrolled and completed at least 1 cycle and received a total of 49 cycles[median:3 cycles(range:l-8)]of CT regimen.All patients were evaluable for efficacy:no complete response,2 patients(16.7%)attained partial response,4 patients(33.3%) were stable disease,6 patients(50.0%) were of progressive disease.The disease control rate was 50.0%.The median progression-free survival and the median survival time were 4.0 months(95%confidence internal:2.9-5.1) and 1 8.0months(95%confidence internal:5.4-30.6),respectively.The most common toxicity was marrow suppression.The 3/4 grade toxicities included leukopenia/neutropenia in 4(33.3%)patients,thrombopenia in 1(8.3%),and anemina in 1(8.3%).No patients died or withdrew due to toxicity.Conclusion:GT regime as a first line treatment for current/metastatic RLMS is highly active and well tolerated.
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