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

被引:19
作者
Sugawara, Shunichi [1 ]
Maemondo, Makoto [2 ]
Tachihara, Motoko [3 ]
Inoue, Akira [4 ]
Ishimoto, Osamu [1 ]
Sakakibara, Tomohiro [4 ]
Usui, Kazuhiro [5 ]
Watanabe, Hiroshi [1 ]
Matsubara, Nobumichi [2 ]
Watanabe, Kana [2 ]
Kanazawa, Kenya [3 ]
Ishida, Takashi [3 ]
Saijo, Yasuo [6 ]
Nukiwa, Toshihiro [4 ]
机构
[1] Sendai Kousei Hosp, Dept Pulm Med, Aoba Ku, Sendai, Miyagi 9800873, Japan
[2] Miyagi Canc Ctr, Dept Resp Med, Natori, Miyagi 9811293, Japan
[3] Fukushima Med Univ, Dept Pulm Med, Fukushima 9601295, Japan
[4] Tohoku Univ, Dept Resp Med, Aoba Ku, Sendai, Miyagi 9808574, Japan
[5] NIT Med Ctr Tokyo, Div Respirol, Shinagawa Ku, Tokyo 1410022, Japan
[6] Hirosaki Univ, Grad Sch Med, Dept Med Oncol, Hirosaki, Aomori 0368562, Japan
关键词
UFT; Vinorelbine; Cisplatin; Chemoradiotherapy; Locally advanced; Non-small-cell lung cancer; Randomized phase II trial; PLUS CISPLATIN; COMBINATION CHEMOTHERAPY; RADIATION-THERAPY; ONCOLOGY-GROUP; REGIMENS; S-1; CHEMORADIOTHERAPY; CARBOPLATIN; VINDESINE; DOCETAXEL;
D O I
10.1016/j.lungcan.2013.04.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:91 / 96
页数:6
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