Department of Pulmonary Medicine, Sendai Kousei Hospital, 4-15 Hirosemachi, Aoba-ku, Sendai 980-0873, Japan.
Lung Cancer. 2013 Jul;81(1):91-6. doi: 10.1016/j.lungcan.2013.04.010. Epub 2013 May 1.
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 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).
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.
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.
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。
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)。
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%。
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。