首页> 外文期刊>Lung cancer: Journal of the International Association for the Study of Lung Cancer >Randomized phase II study of concurrent cisplatin/etoposide or paclitaxel/carboplatin and thoracic radiotherapy in patients with stage III non-small cell lung cancer
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Randomized phase II study of concurrent cisplatin/etoposide or paclitaxel/carboplatin and thoracic radiotherapy in patients with stage III non-small cell lung cancer

机译:Ⅲ期非小细胞肺癌患者同时进行顺铂/依托泊苷或紫杉醇/卡铂联合胸腔放疗的II期随机研究

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摘要

Objective: To evaluate the activity and safety of concurrent thoracic radiotherapy (TRT) plus weekly paclitaxel/carboplatin (PC) regimen compared with widely used cisplatin/etoposide (PE) regimen in patients with unresectable stage III non-small cell lung cancer (NSCLC). Patients and methods: Patients were randomly assigned to receive the following treatments: PE arm, cisplatin (50mg/m 2) on days 1, 8, 29, and 36 and etoposide (50mg/m 2) on days 1-5 and 29-33 plus 60Gy of TRT; PC arm, weekly concurrent carboplatin (AUC=2) and paclitaxel (45mg/m 2) plus 60Gy of TRT. Results: A total of 65 patients were randomized (PE arm, n= 33; PC arm, n= 32). The 3-year overall survival (OS) was significantly better in the PE arm than in the PC arm (33.1% vs. 13%, P= .04). The incidence of Grade 3/4 neutropenia was 78.1% in the PE arm and 51.5% in the PC arm (P= .05). The rate of Grade 2 or greater radiation pneumonitis was 25% in the PE arm and 48.5% in the PC arm (P= .09). Conclusions: Compared to PE regimen, weekly PC regimen cannot be recommended since it failed to achieve an improvement in either OS or PFS.
机译:目的:比较广泛应用的顺铂/依托泊苷(PE)方案治疗不可切除的III期非小细胞肺癌(NSCLC)患者的同期胸腔放疗(TRT)加每周紫杉醇/卡铂(PC)方案的活性和安全性。患者和方法:患者被随机分配接受以下治疗:第1、8、29和36天使用PE臂,顺铂(50mg / m 2),第1-5和29天使用依托泊苷(50mg / m 2)- 33加60 Gy的TRT; PC臂,每周并发卡铂(AUC = 2)和紫杉醇(45mg / m 2)加60Gy TRT。结果:总共65例患者被随机分组​​(PE组,n = 33; PC组,n = 32)。 PE组的3年总生存期(OS)明显优于PC组(33.1%vs. 13%,P = .04)。 PE组的3/4级中性粒细胞减少症的发生率为78.1%,PC组的为51.5%(P = .05)。 PE组为2级或更高级别的放射性肺炎的发生率为25%,PC组为48.5%(P = .09)。结论:与PE方案相比,不建议每周PC方案,因为它不能改善OS或PFS。

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