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首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >A phase II randomised trial comparing the cisplatin-etoposide combination chemotherapy with or without carboplatin as second-line therapy for small-cell lung cancer.
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A phase II randomised trial comparing the cisplatin-etoposide combination chemotherapy with or without carboplatin as second-line therapy for small-cell lung cancer.

机译:II期随机试验比较了顺铂-依托泊苷联合化疗联合或不联合卡铂作为小细胞肺癌的二线治疗。

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摘要

BACKGROUND: A phase II randomised trial was performed with patients with SCLC to determine if the addition of carboplatin to cisplatin-etoposide might improve the response rate in second-line therapy. PATIENTS AND METHODS: Sixty-five eligible patients were randomised: 31 for CE (cisplatin 20 mg/m(2) and etoposide 100 mg/m(2) on days 1-3) and 34 for CCE (carboplatin 200 mg/m(2) on day 1, cisplatin 30 mg/m(2) on days 2-3, etoposide 100 mg/m(2) on days 1-3). RESULTS: Eighty-two per cent of these patients had an objective response to first-line therapy and, among responders, 63% had a treatment-free interval of >3 months after previous therapy. The best response rates were 29% [95% confidence interval (CI) 13-45] and 47% (95% CI 30-64) for CE and CCE, respectively, with median survival times of 4.3 and 7.6 months. Dose-intensity analysis revealed a significant improvement in the relative dose-intensity and etoposide absolute dose-intensity for CE. Toxicity was tolerable and comparable between the two study arms. CONCLUSION: CCE appears to be associated with a high objective response rate. The phase II randomised study design suggests that a comparison between the two regimens in a phase III trial would be interesting, but will probably be difficult to perform for reasons of accrual.
机译:背景:一项针对SCLC患者的II期随机试验旨在确定在顺铂-依托泊苷中添加卡铂是否可以提高二线治疗的缓解率。病人和方法:65名符合条件的患者被随机分配:31例CE(顺铂20 mg / m(2)和依托泊苷100 mg / m(2)在第1-3天)和34例CCE(卡铂200 mg / m( 2)在第1天,第2-3天顺铂30 mg / m(2),在第1-3天依托泊苷100 mg / m(2)。结果:这些患者中有82%对一线治疗有客观反应,而在有反应者中,有63%的患者在先前治疗后的3个月内无治疗间隔。 CE和CCE的最佳缓解率分别为29%[95%置信区间(CI)13-45]和47%(95%CI 30-64),中位生存时间为4.3和7.6个月。剂量强度分析显示,CE的相对剂量强度和依托泊苷绝对剂量强度显着改善。两个研究组之间的毒性是可以忍受的,并且具有可比性。结论:CCE似乎与客观应答率高有关。 II期随机研究设计表明,III期试验中两种方案之间的比较会很有趣,但由于应计的原因可能很难执行。

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