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随机Ⅱ期临床试验:替加氟/尿嘧啶和顺铂与长春瑞滨和顺铂联合胸部放疗治疗局部晚期不可切除的 III 期非小细胞肺癌: NJLCG 0601。

Randomized phase II trial of uracil/tegafur and cisplatin versus vinorelbine and cisplatin with concurrent thoracic radiotherapy for locally advanced unresectable stage III non-small-cell lung cancer: NJLCG 0601.

机构信息

Department of Pulmonary Medicine, Sendai Kousei Hospital, 4-15 Hirosemachi, Aoba-ku, Sendai 980-0873, Japan.

出版信息

Lung Cancer. 2013 Jul;81(1):91-6. doi: 10.1016/j.lungcan.2013.04.010. Epub 2013 May 1.

Abstract

INTRODUCTION

The optimal chemotherapy with thoracic radiotherapy (TRT) for locally advanced non-small-cell lung cancer (NSCLC) remains to be established. This randomized phase II study of concurrent chemoradiotherapy was conducted to compare uracil/tegafur (UFT) and cisplatin with vinorelbine and cisplatin for stage III NSCLC.

PATIENTS AND METHODS

Patients with unresectable stage III NSCLC were randomized to receive UP (400 mg/m(2) UFT on days 1-14 and 29-42 and 80 mg/m(2) cisplatin on days 8 and 36) or NP (20 mg/m(2) vinorelbine on days 1, 8, 29, and 36 and 80 mg/m(2) cisplatin on days 1 and 29). TRT began on day 1 (total 60 Gy in 30 fractions).

RESULTS

Of 70 enrolled patients, 66 were evaluable for efficacy and safety. The overall response rates were 80% (95% CI: 67-93%) and 71% (95% CI: 55-87%) for the UP arm and the NP arm. With a median follow-up of 20.2 months, the progression-free survival and median survival time were 8.8 and 26.9 months in the UP arm, and 6.8 and 21.7 months in the NP arm. The 2-/3-year survival rates were 51.0/34.3% and 46.9/33.4% for the UP arm and the NP arm, respectively. Grade 3/4 neutropenia occurred in 20% and 58% of patients in the UP and NP arms, respectively.

CONCLUSION

Combined with concurrent TRT, the UP arm achieved better efficacy and safety compared with the NP arm, suggesting it to be a promising candidate as a standard regimen for locally advanced NSCLC. Further evaluation of the UP arm is warranted.

摘要

介绍

局部晚期非小细胞肺癌(NSCLC)的最佳化疗联合胸部放疗(TRT)仍有待确定。本研究为同步放化疗的随机 II 期临床试验,旨在比较 UFT(替加氟)和顺铂与长春瑞滨和顺铂治疗 III 期 NSCLC 的疗效。

患者和方法

不可切除的 III 期 NSCLC 患者被随机分为 UP 组(400 mg/m2 UFT 于第 1-14 天和第 29-42 天,第 8 和 36 天给予 80 mg/m2 顺铂)或 NP 组(20 mg/m2 长春瑞滨,第 1、8、29 和 36 天,第 1 和 29 天给予 80 mg/m2 顺铂)。TRT 于第 1 天开始(总剂量 60 Gy/30 次)。

结果

70 例患者中,66 例可评估疗效和安全性。UP 组和 NP 组的总缓解率分别为 80%(95%CI:67-93%)和 71%(95%CI:55-87%)。中位随访 20.2 个月时,UP 组的无进展生存期和中位生存期分别为 8.8 和 26.9 个月,NP 组分别为 6.8 和 21.7 个月。UP 组和 NP 组的 2 年/3 年生存率分别为 51.0%/34.3%和 46.9%/33.4%。UP 组和 NP 组的 3/4 级中性粒细胞减少症发生率分别为 20%和 58%。

结论

与 NP 组相比,联合同步 TRT 的 UP 组疗效更好,安全性更高,提示其可能成为局部晚期 NSCLC 的标准治疗方案。需要进一步评估 UP 组。

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