Factors contributing to the efficacy of concurrent-adjuvant chemotherapy for locoregionally advanced nasopharyngeal carcinoma: Combined analyses of NPC-9901 and NPC-9902 Trials

被引:178
作者
Lee, Anne W. M. [1 ]
Tung, Stewart Y. [2 ]
Ngan, Roger K. C. [3 ]
Chappell, Rick [4 ]
Chua, Daniel T. T. [5 ]
Lu, T. X. [6 ]
Siu, Lillian [7 ]
Tan, Terence [8 ]
Chan, L. K. [1 ]
Ng, W. T. [1 ]
Leung, T. W. [2 ]
Fu, Y. T. [3 ]
Au, Gordon K. H. [5 ]
Zhao, C. [6 ]
O'Sullivan, Brian [7 ]
Tan, E. H. [8 ]
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 Elizabeth Hosp, Dept Clin Oncol, Hong Kong, Hong Kong, Peoples R China
[4] Univ Wisconsin, Dept Biostat, Sch Med, Madison, WI USA
[5] Queen Mary Hosp, Dept Clin Oncol, Hong Kong, Hong Kong, Peoples R China
[6] Sun Yat Sen Univ, Ctr Canc, Guangzhou 510275, Guangdong, Peoples R China
[7] Princess Margaret Hosp, Ontario Canc Inst, Toronto, ON M4X 1K9, Canada
[8] Natl Canc Ctr, Dept Clin Oncol, Singapore, Singapore
关键词
Nasopharyngeal carcinoma; Concurrent-adjuvant chemotherapy; PROGRESSION-FREE SURVIVAL; PHASE-III; RANDOMIZED-TRIAL; ACCELERATED FRACTIONATION; THERAPEUTIC GAIN; RADIOTHERAPY; CHEMORADIOTHERAPY; CANCER; INTERGROUP; PATIENT;
D O I
10.1016/j.ejca.2010.10.026
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The current standard treatment for locoregionally advanced nasopharyngeal carcinoma (NPC) was conventional-fractionation radiotherapy plus concurrent-adjuvant chemotherapy as recommended by the Intergroup-0099 Study. This combined analysis of the NPC-9901 and the NPC-9902 Trials aims to provide more comprehensive data to evaluate the efficacy of the Intergroup-0099 regimen and the contributing factors. Methods: Eligible patients with stage III-IVB non-keratinizing NPC were randomly assigned to radiotherapy-alone (RTi group: 218 patients) or chemoradiotherapy (CRTi group: 223 patients) using cisplatin (100 mg/m(2)) for three cycles in concurrence with radiotherapy, followed by cisplatin (80 mg/m(2)) plus fluorouracil (1000 mg/m(2)/day for 4 days) for three cycles. The median follow-up was 6.1 years. Findings: Comparison by intention-to-treat showed that the CRTi group achieved significant improvement in overall failure-free rate (FFR), locoregional-FFR and cancer-specific survival (p <= 0.019); but the improvements for distant-FFR and overall survival (OS) were statistically insignificant (p >= 0.14). Further exploratory studies based on actual treatment showed that an additional improvement achieved was a significant gain in OS (CRTa versus RTa group: 72% versus 63% at 5-year, p = 0.037). Multivariate analyses showed that the dose of cisplatin during the concurrent phase had significant impact on locoregional-FFR and OS, while that of fluorouracil during the adjuvant phase was significant for distant-FFR. The 5-year locoregional-FFR for patients who received 0-1, 2 and 3 concurrent cycles were 79%, 88% and 88%, respectively; the corresponding distant-FFR by adjuvant cycles were 68%, 78% and 77%, respectively. Interpretation: Our results support the current practice of adding concurrent cisplatin plus adjuvant cisplatin-fluorouracil to radiotherapy for treating patients with locoregionally advanced NPC. The concurrent phase is important for locoregional control and survival, cisplatin 200 mg/m(2) in two concurrent cycles might be adequate. Additional chemotherapy using fluorouracil-containing combination contributed to improving distant control. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:656 / 666
页数:11
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