首页> 外文期刊>Lung cancer: Journal of the International Association for the Study of Lung Cancer >A phase II study of amrubicin and topotecan combination therapy in patients with relapsed or extensive-disease small-cell lung cancer: Okayama Lung Cancer Study Group Trial 0401.
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A phase II study of amrubicin and topotecan combination therapy in patients with relapsed or extensive-disease small-cell lung cancer: Okayama Lung Cancer Study Group Trial 0401.

机译:氨柔比星和拓扑替康联合疗法在复发或广泛疾病小细胞肺癌患者中的II期研究:冈山肺癌研究小组试验0401。

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BACKGROUNDS: Chemotherapy is a mainstay in the treatment of extensive-disease small-cell lung cancer (ED-SCLC), although the survival benefit remains modest. We conducted a phase II trial of amrubicin (a topoisomerase II inhibitor) and topotecan (a topoisomerase I inhibitor) in chemotherapy-naive and relapsed SCLC patients. METHODS: Amrubicin (35 mg/m(2)) and topotecan (0.75 mg/m(2)) were administered on days 3-5 and 1-5, respectively. The objective response rate (ORR) was set as the primary endpoint, which was assessed separately in chemotherapy-naive and relapsed cases. RESULTS: Fifty-nine patients were enrolled (chemotherapy-naive 31, relapsed 28). The ORRs were 74% and 43% in the chemotherapy-naive and relapsed cases, respectively. Survival data were also promising, with a median progression-free survival time and median survival time of 5.3 and 14.9 months and 4.7 and 10.2 months in the chemotherapy-naive and relapsed cases, respectively. Even refractory-relapsed cases responded to the treatment favorably (27% ORR). The primary toxicity was myelosuppression with grades 3 or 4 neutropenia in 97% of the patients, which led to grades 3 or 4 febrile neutropenia in 41% of the patients and two toxic deaths. CONCLUSION: This phase II study showed the favorable efficacy and moderate safety profiles of a topotecan and amrubicin two-drug combination especially in relapsed patients with ED-SCLC.
机译:背景:化学疗法是治疗广泛疾病小细胞肺癌(ED-SCLC)的主要手段,尽管其生存获益仍然不高。我们对未经化疗和复发的SCLC患者进行了氨柔比星(一种拓扑异构酶II抑制剂)和拓扑替康(一种拓扑异构酶I抑制剂)的II期试验。方法:分别在第3-5天和第1-5天施用氨柔比星(35 mg / m(2))和托泊替康(0.75 mg / m(2))。客观缓解率(ORR)设置为主要终点,在未接受化疗和复发的病例中分别进行评估。结果:59例患者入组(未接受化学疗法的患者31例,复发28例)。单纯化疗和复发病例的ORR分别为74%和43%。生存数据也令人鼓舞,在未经化疗的患者和复发的患者中,无进展生存时间的中位数为5.3和14.9个月,中位生存时间为4.7和10.2个月。即使是难治性复发病例也对治疗反应良好(27%ORR)。主要的毒性反应是97%的患者出现3级或4级中性粒细胞减少的骨髓抑制,导致41%的患者出现3级或4级发热性中性粒细胞减少和2例中毒死亡。结论:该II期研究显示了拓扑替康和氨柔比星两种药物组合的良好疗效和中等安全性,特别是对于ED-SCLC复发患者。

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