Randomized Trial of Radiotherapy Plus Concurrent-Adjuvant Chemotherapy vs Radiotherapy Alone for Regionally Advanced Nasopharyngeal Carcinoma

被引:272
|
作者
Lee, Anne W. M. [1 ]
Tung, Stewart Y. [2 ]
Chua, Daniel T. T. [3 ]
Ngan, Roger K. C. [3 ]
Chappell, Rick [7 ]
Tung, Raymond [4 ]
Siu, Lillian [8 ]
Ng, W. T. [1 ]
Sze, W. K. [2 ]
Au, Gordon K. H. [3 ]
Law, Stephen C. K. [3 ]
O'Sullivan, Brian [8 ]
Yau, T. K. [1 ]
Leung, T. W. [2 ]
Au, Joseph S. K. [3 ]
Sze, W. M. [1 ]
Choi, C. W. [5 ]
Fung, K. K. [5 ]
Lau, Joseph T. [6 ]
Lau, W. H. [3 ]
机构
[1] Pamela Youde Nethersole Eastern Hosp, Dept Clin Oncol, Chaiwan, Hong Kong, Peoples R China
[2] Tuen Mun Hosp, Dept Clin Oncol, Hong Kong, Hong Kong, Peoples R China
[3] Queen Mary Hosp, Dept Clin Oncol, Hong Kong, Hong Kong, Peoples R China
[4] Hong Kong Canc Fund, Hong Kong, Hong Kong, Peoples R China
[5] Hong Kong Anticanc Soc, Hong Kong, Hong Kong, Peoples R China
[6] Chinese Univ Hong Kong, Ctr Epidemiol & Biostat, Hong Kong, Hong Kong, Peoples R China
[7] Wisconsin Med Sch, Dept Biostat, Madison, WI USA
[8] Princess Margaret Hosp, Ontario Canc Inst, Toronto, ON M4X 1K9, Canada
关键词
PHASE-III; INDUCTION CHEMOTHERAPY; CISPLATIN-RADIOTHERAPY; THERAPEUTIC GAIN; CANCER; CHEMORADIOTHERAPY; SURVIVAL; BOOST; INTERGROUP; RADIATION;
D O I
10.1093/jnci/djq258
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Current practice of adding concurrent-adjuvant chemotherapy to radiotherapy (CRT) for treating advanced nasopharyngeal carcinoma is based on the Intergroup-0099 Study published in 1998. However, the outcome for the radiotherapy-alone (RT) group in that trial was substantially poorer than those in other trials, and there were no data on late toxicities. Verification of the long-term therapeutic index of this regimen is needed. Methods Patients with nonkeratinizing nasopharyngeal carcinoma staged T1-4N2-3M0 were randomly assigned to RT (176 patients) or to CRT (172 patients) using cisplatin (100 mg/m(2)) every 3 weeks for three cycles in concurrence with radiotherapy, followed by cisplatin (80 mg/m2) plus fluorouracil (1000 mg per m(2) per day for 4 days) every 4 weeks for three cycles. Primary endpoints included overall failure-free rate (FFR) (the time to first failure at any site) and progression-free survival. Secondary endpoints included overall survival, locoregional FFR, distant FFR, and acute and late toxicity rates. All statistical tests were two-sided. Results The two treatment groups were well balanced in all patient characteristics, tumor factors, and radiotherapy parameters. Adding chemotherapy statistically significantly improved the 5-year FFR (CRT vs RT: 67% vs 55%; P = .014) and 5-year progression-free survival (CRT vs RT: 62% vs 53%; P = .035). Cumulative incidence of acute toxicity increased with chemotherapy by 30% (CRT vs RT: 83% vs 53%; P < .001), but the 5-year late toxicity rate did not increase statistically significantly (CRT vs RT: 30% vs 24%; P = .30). Deaths because of disease progression were reduced statistically significantly by 14% (CRT vs RT: 38% vs 24%; P = .008), but 5-year overall survival was similar (CRT vs RT: 68% vs 64%; P = .22; hazard ratio of CRT = 0.81, 95% confidence interval = 0.58 to 1.13) because deaths due to toxicity or incidental causes increased by 7% (CRT vs RT: 1.7% vs 0, and 8.1% vs 3.4%, respectively; P = .015). Conclusions Adding concurrent-adjuvant chemotherapy statistically significantly reduced failure and cancer-specific deaths when compared with radiotherapy alone. Although there was no statistically significant increase in major late toxicity, increase in noncancer deaths narrowed the resultant gain in overall survival. J Natl Cancer Inst 2010; 102: 1188-1198
引用
收藏
页码:1188 / 1198
页数:11
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