Etoposide and cisplatin versus paclitaxel and carboplatin with concurrent thoracic radiotherapy in unresectable stage III non-small cell lung cancer: a multicenter randomized phase III trial

医学 卡铂 养生 依托泊苷 放射治疗 肺癌 临床终点 化疗 内科学 顺铂 外科 随机对照试验 泌尿科
作者
Jun Liang,Nan Bi,Shixiu Wu,M. Chen,Chao Lv,Lujun Zhao,A. SHI,Wei Jiang,Yuanji Xu,Zongmei Zhou,W. Wang,D. Chen,Zhouguang Hui,Jingwei Lv,H. Zhang,Qinfu Feng,Zefen Xiao,Xianze Wang,Lihui Liu,Tianyu Zhang
出处
期刊:Annals of Oncology [Elsevier BV]
卷期号:28 (4): 777-783 被引量:177
标识
DOI:10.1093/annonc/mdx009
摘要

BackgroundThe optimal chemotherapy regimen administered currently with radiation in patients with stage III non-small cell lung cancer (NSCLC) remains unclear. A multicenter phase III trial was conducted to compare the efficacy of concurrent thoracic radiation therapy with either etoposide/cisplatin (EP) or carboplatin/paclitaxel (PC) in patients with stage III NSCLC.Patients and methodsPatients were randomly received 60–66 Gy of thoracic radiation therapy concurrent with either etoposide 50 mg/m2 on days 1–5 and cisplatin 50 mg/m2 on days 1 and 8 every 4 weeks for two cycles (EP arm), or paclitaxel 45 mg/m2 and carboplatin (AUC 2) on day 1 weekly (PC arm). The primary end point was overall survival (OS). The study was designed with 80% power to detect a 17% superiority in 3-year OS with a type I error rate of 0.05.ResultsA total of 200 patients were randomized and 191 patients were treated (95 in the EP arm and 96 in the PC arm). With a median follow-up time of 73 months, the 3-year OS was significantly higher in the EP arm than that of the PC arm. The estimated difference was 15.0% (95% CI 2.0%–28.0%) andP value of 0.024. Median survival times were 23.3 months in the EP arm and 20.7 months in the PC arm (log-rank testP = 0.095, HR 0.76, 95%CI 0.55–1.05). The incidence of Grade ≥2 radiation pneumonitis was higher in the PC arm (33.3% versus 18.9%,P = 0.036), while the incidence of Grade ≥3 esophagitis was higher in the EP arm (20.0% versus 6.3%,P = 0.009).ConclusionEP might be superior to weekly PC in terms of OS in the setting of concurrent chemoradiation for unresectable stage III NSCLC.Trial registration IDNCT01494558.

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