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首页> 外文期刊>Lung cancer: Journal of the International Association for the Study of Lung Cancer >Etoposide plus cisplatin followed by concurrent chemo-radiotherapy and irinotecan plus cisplatin for patients with limited-stage small cell lung cancer: A multicenter phase II study
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Etoposide plus cisplatin followed by concurrent chemo-radiotherapy and irinotecan plus cisplatin for patients with limited-stage small cell lung cancer: A multicenter phase II study

机译:依托泊苷加顺铂联合化学放疗,伊立替康加顺铂治疗有限期小细胞肺癌患者:一项多中心II期研究

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Purpose: The combination of irinotecan and cisplatin (IP) has shown at least comparable efficacy to that of etoposide/cisplatin (EP) in patients with extensive-stage small cell lung cancer. We conducted a phase II study to evaluate the efficacy and tolerance of EP regimen followed by thoracic radiotherapy (TRT) and IP consolidation chemotherapy in patients with limited-stage small cell lung cancer.Patients and methods: Thirty-three chemotherapy-naive patients with limited-stage small cell lung cancer (LS-SCLC) were treated with etoposide 100mg/m~2 on days 1-3 and cisplatin 80 mg/m~2 on day 1. Radiotherapy was given 3 weeks after the first treatment cycle concurrently with weekly cisplatin 20 mg/m~2 on day 1 and etoposide 50 mg/m~2 on day 4 within 5-6 weeks, followed by three courses of irinotecan 60 mg/m~2 on days 1,8, and 15 and cisplatin 60 mg/m~2 on day 1 of a 4-week cycle.Results: There were no treatment-related deaths. Toxicities during chemo-radiotherapy were mild including grade 3/4 neutropenia (24%) and grade 2 esophagitis (6%). The major toxicity observed during consolidation chemotherapy was grades 3-4 neutropenia which affected 42% of patients. In an intention-to-treat analysis the overall response rate was 66% (CR: 30% and PR: 36%). After a median follow-up period of 35.7 months (range: 9.6-41.2 months), the median survival time was 19 months (95% CI: 14.5-23.5 months), the median time to tumor progression 8.3 months and the 1- and 2-year survival rates 72% and 27.5%, respectively.Conclusions: Consolidation chemotherapy with IP following concurrent EP plus TRT is a safe and with acceptable toxicity regimen and deserves further phase III testing in patients with LS-SCLC.
机译:目的:伊立替康和顺铂(IP)的组合在广泛期小细胞肺癌患者中显示出至少与依托泊苷/顺铂(EP)相当的疗效。我们进行了II期研究,以评估EP方案,胸腔放疗(TRT)和IP巩固化疗对有限期小细胞肺癌患者的疗效和耐受性。阶段的小细胞肺癌(LS-SCLC)在第1-3天用依托泊苷100mg / m〜2进行治疗,在第1天用顺铂80mg / m〜2进行治疗。第一个治疗周期后第3周开始放疗,每周一次第1天的顺铂20 mg / m〜2,第4天的依托泊苷50 mg / m〜2,在5-6周内,然后在第1,8和15天进行三疗程的伊立替康60 mg / m〜2,顺铂60在4周周期的第1天,mg / m〜2。结果:没有与治疗相关的死亡。化学放疗期间的毒性轻微,包括3/4级中性粒细胞减少症(24%)和2级食管炎(6%)。巩固化疗期间观察到的主要毒性为3-4级中性粒细胞减少,影响42%的患者。在意向性治疗分析中,总缓解率为66%(CR:30%,PR:36%)。在中位随访期为35.7个月(范围:9.6-41.2个月)之后,中位生存时间为19个月(95%CI:14.5-23.5个月),中位肿瘤进展时间为8.3个月,分别为1和结论:两年的生存率分别为72%和27.5%。结论:并发EP加TRT联合IP联合化疗是安全且可接受的毒性方案,值得对LS-SCLC患者进行进一步的III期试验。

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