Sequential vs Concurrent Chemoradiation for Stage III Non-Small Cell Lung Cancer: Randomized Phase III Trial RTOG 9410

被引:1059
作者
Curran, Walter J., Jr. [1 ,2 ]
Paulus, Rebecca [3 ]
Langer, Corey J. [4 ]
Komaki, Ritsuko [5 ]
Lee, Jin S. [6 ]
Hauser, Stephen [7 ,8 ]
Movsas, Benjamin [9 ,10 ]
Wasserman, Todd [11 ]
Rosenthal, Seth A. [12 ]
Gore, Elizabeth [13 ]
Machtay, Mitchell [14 ]
Sause, William [15 ]
Cox, James D. [5 ]
机构
[1] Emory Univ, Dept Radiat Oncol, Atlanta, GA 30322 USA
[2] Emory Univ, Winship Canc Inst, Atlanta, GA 30322 USA
[3] Radiat Therapy Oncol Grp Stat Ctr, Philadelphia, PA USA
[4] Univ Penn, Med Ctr, Abramson Canc Ctr, Philadelphia, PA 19104 USA
[5] Univ Texas MD Anderson Canc Ctr, Div Radiat Oncol, Houston, TX 77030 USA
[6] Natl Canc Ctr, Lung Canc Branch, Kyonggi Do, South Korea
[7] Univ Calif San Francisco, San Francisco, CA 94143 USA
[8] Hartford Hosp, Gray Canc Ctr, Dept Radiat Oncol, Hartford, CT 06115 USA
[9] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[10] Henry Ford Hosp, Dept Radiat Oncol, Detroit, MI 48202 USA
[11] Washington Univ, Dept Radiat Oncol, St Louis, MO USA
[12] Radiol Associates Sacramento, Sacramento, CA USA
[13] Med Coll Wisconsin, Dept Radiat Oncol, Milwaukee, WI 53226 USA
[14] Case Western Reserve Univ, Sch Med, Dept Radiat Oncol, Cleveland, OH USA
[15] Intermt Med Ctr, Dept Radiat Oncol, Murray, UT USA
关键词
THERAPY-ONCOLOGY-GROUP; RADIATION-THERAPY; RADIOTHERAPY; CISPLATIN; CHEMORADIOTHERAPY; CHEMOTHERAPY; CARBOPLATIN; VINORELBINE; IRRADIATION; PACLITAXEL;
D O I
10.1093/jnci/djr325
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background The combination of chemotherapy with thoracic radiotherapy (TRT) compared with TRT alone has been shown to confer a survival advantage for good performance status patients with stage III non-small cell lung cancer. However, it is not known whether sequential or concurrent delivery of these therapies is the optimal combination strategy. Methods A total of 610 patients were randomly assigned to two concurrent regimens and one sequential chemotherapy and TRT regimen in a three-arm phase III trial. The sequential arm included cisplatin at 100 mg/m(2) on days 1 and 29 and vinblastine at 5 mg/m(2) per week for 5 weeks with 60 Gy TRT beginning on day 50. Arm 2 used the same chemotherapy regimen as arm 1 with 60 Gy TRT once daily beginning on day 1. Arm 3 used cisplatin at 50 mg/m(2) on days 1, 8, 29, and 36 with oral etoposide at 50 mg twice daily for 10 weeks on days 1, 2, 5, and 6 with 69.6 Gy delivered as 1.2 Gy twice-daily fractions beginning on day 1. The primary endpoint was overall survival, and secondary endpoints included tumor response and time to tumor progression. Kaplan-Meier analyses were used to assess survival, and toxic effects were examined using the Wilcoxon rank sum test. All statistical tests were two-sided. Results Median survival times were 14.6, 17.0, and 15.6 months for arms 1-3, respectively. Five-year survival was statistically significantly higher for patients treated with the concurrent regimen with once-daily TRT compared with the sequential treatment (5-year survival: sequential, arm 1, 10% [20 patients], 95% confidence interval [CI] = 7% to 15%; concurrent, arm 2, 16% [31 patients], 95% CI = 11% to 22%, P = .046; concurrent, arm 3, 13% [22 patients], 95% CI = 9% to 18%). With a median follow-up time of 11 years, the rates of acute grade 3-5 nonhematologic toxic effects were higher with concurrent than sequential therapy, but late toxic effects were similar. Conclusion Concurrent delivery of cisplatin-based chemotherapy with TRT confers a long-term survival benefit compared with the sequential delivery of these therapies.
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收藏
页码:1452 / 1460
页数:9
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