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首页> 外文期刊>Journal of thoracic oncology: official publication of the International Association for the Study of Lung Cancer >Randomized phase II study of maintenance irinotecan therapy versus observation following induction chemotherapy with irinotecan and cisplatin in extensive disease small cell lung cancer.
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Randomized phase II study of maintenance irinotecan therapy versus observation following induction chemotherapy with irinotecan and cisplatin in extensive disease small cell lung cancer.

机译:在广泛疾病的小细胞肺癌中,维持伊立替康维持治疗与伊立替康和顺铂诱导化疗后的观察的随机II期研究。

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INTRODUCTION: To determine whether irinotecan maintenance therapy in extensive disease-small cell lung cancer can improve survival of patients who responded to irinotecan plus cisplatin (IP) induction therapy. METHODS: A total of 120 chemo-naive patients with adequate organ functions and Eastern Cooperative Oncology Group performance status of 0 to 2 were enrolled from March 2003 through April 2006. After IP induction therapy, with either schedule A (I: 60 mg/m intravenously (IV) on days 1, 8, and 15; P: 30 mg/m IV on days 1 and 8, every 4 weeks for six cycles) or schedule B (I: 60 mg/m and P: 30 mg/m IV on days 1, and 8, every 3 weeks for eight cycles), responding patients were randomized to either maintenance with irinotecan 100 mg/m IV on days 1, 8, and 15, every 4 weeks up to six cycles, or observation. RESULTS: Overall, 100 (83%) of 120 patients achieved objective tumor responses (12 complete responses, 88 partial responses) after IP induction therapy. Of those patients who remained in remission upon completion of planned cycles of induction therapy, 45 were randomized to maintenance (n = 21) or observation (n = 24). Median progression-free survival (PFS) and overall survival (OS) for all patients were 7.2 and 14.0 months, respectively. For the maintenance arm, median PFS and OS were 12.0 and 17.6 months, respectively. For the observation arm, median PFS and OS were 9.9 and 20.5 months, respectively, which was not significantly different from the maintenance arm. CONCLUSIONS: IP chemotherapy is very useful for the treatment of small cell lung cancer. However, maintenance irinotecan therapy did not seem to further affect the clinical outcome of patients who had responded to IP induction therapy.
机译:简介:为了确定在广泛疾病-小细胞肺癌中的伊立替康维持疗法是否可以改善对伊立替康加顺铂(IP)诱导疗法有反应的患者的生存率。方法:从2003年3月至2006年4月,共纳入120例具有适当器官功能且东部合作肿瘤小组工作状态为0到2的未接受过化学治疗的患者。IP诱导治疗后,采用两种方案A(I:60 mg / m在第1、8和15天静脉注射(IV); P:第1天和第8天静脉注射30 mg / m,每4周一次,共六个周期)或时间表B(I:60 mg / m和P:30 mg / m在第1天和第8天进行静脉输注,每3周进行8个周期),将有反应的患者随机分组,在第1天,第8天和第15天进行静脉输注伊立替康100 mg / m,每4周进行一次,直至六个周期,或进行观察。结果:总体上,在120例患者中,有100例(83%)在IP诱导治疗后达到了客观的肿瘤缓解(12例完全缓解,88例部分缓解)。在计划的诱导治疗周期完成后仍处于缓解状态的患者中,有45名被随机分配到维持治疗(n = 21)或观察(n = 24)。所有患者的中位无进展生存期(PFS)和总体生存期(OS)分别为7.2和14.0个月。对于维护部门,中位PFS和OS分别为12.0和17.6个月。对于观察组,中位PFS和OS分别为9.9和20.5个月,与维持组无显着差异。结论:IP化疗对于治疗小细胞肺癌非常有用。然而,维持伊立替康治疗似乎并未进一步影响对IP诱导疗法有反应的患者的临床结局。

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