Concurrent chemoradiotherapy plus adjuvant chemotherapy versus concurrent chemoradiotherapy alone in patients with locoregionally advanced nasopharyngeal carcinoma: a phase 3 multicentre randomised controlled trial

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• 作者：Lei Chen ; MD^&dagger ; ; ^a ; Prof Chao-Su Hu ; MD^d ; ^&dagger ; ; Prof Xiao-Zhong Chen ; MD^e ; ^&dagger ; ; Prof Guo-Qing Hu ; MD^f ; Prof Zhi-Bin Cheng ; MD^g ; Prof Yan Sun ; MD^h ; Prof Wei-Xiong Li ; MDⁱ ; Yuan-Yuan Chen ; MD^a ; Fang-Yun Xie ; MD^a ; Shao-Bo Liang ; MD^a ; Yong Chen ; MD^a ; Ting-Ting Xu ; MD^d ; Bin Li ; MD^e ; Guo-Xian Long ; MD^f ; Si-Yang Wang ; MD^g ; Bao-Min Zheng ; MD^h ; Ying Guo ; PhD^b ; Ying Sun ; MD^a ; Yan-Ping Mao ; MD^a ; Ling-Long Tang ; MD^a ; Prof Yu-Ming Chen ; PhD^c ; Prof Meng-Zhong Liu ; MD^a ; Prof Jun Ma ; MD^a ; ^{majun2@mail.sysu.edu.cn}
• 刊名：Lancet Oncology
• 出版年：2012
• 出版时间：February 2012
• 年：2012
• 卷：13
• 期：2
• 页码：163-171
• 全文大小：210 K

文摘

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Summary

Background

The effect of the addition of adjuvant chemotherapy to concurrent chemoradiotherapy in locoregionally advanced nasopharyngeal carcinoma is unclear. We aimed to assess the contribution of adjuvant chemotherapy to concurrent chemoradiotherapy versus concurrent chemoradiotherapy alone.

Methods

We did an open-label phase 3 multicentre randomised controlled trial at seven institutions in China. Randomisation was by a computer-generated random number code. Patients were stratified by treatment centre and randomly assigned in blocks of four. Treatment allocation was not masked. We randomly assigned patients with non-metastatic stage III or IV (except T3-4N0) nasopharyngeal carcinoma to receive concurrent chemoradiotherapy plus adjuvant chemotherapy or concurrent chemoradiotherapy alone. Patients in both groups received 40 mg/m² cisplatin weekly up to 7 weeks, concurrently with radiotherapy. Radiotherapy was given as 2¡¤0-2¡¤27 Gy per fraction with five daily fractions per week for 6-7 weeks to a total dose of 66 Gy or greater to the primary tumour and 60-66 Gy to the involved neck area. The concurrent chemoradiotherapy plus adjuvant chemotherapy group subsequently received 80 mg/m² adjuvant cisplatin and 800 mg/m² per day fluorouracil for 120 h every 4 weeks for three cycles. Our primary endpoint was failure-free survival. We did efficacy analyses in our intention-to-treat population. Our trial is ongoing; in this report we present the 2 year survival results and acute toxic effects. This trial is registered with , number .

Findings

251 patients were assigned to the concurrent chemoradiotherapy plus adjuvant chemotherapy group and 257 to the concurrent chemoradiotherapy alone group. After a median follow-up of 37¡¤8 months (range 1¡¤3-61¡¤0), the estimated 2 year failure-free survival rate was 86 % (95 % CI 81-90) in the concurrent chemoradiotherapy plus adjuvant chemotherapy group and 84 % (78-88) in concurrent chemoradiotherapy only group (hazard ratio 0¡¤74, 95 % CI 0¡¤49-1¡¤10; p=0¡¤13). Stomatitis was the most commonly reported grade 3 or 4 adverse event during both radiotherapy (76 of 249 patients in the concurrent chemoradiotherapy plus adjuvant chemotherapy group and 82 of 254 in the concurrent chemoradiotherapy alone group) and adjuvant chemotherapy (43 [21 % ] of 205 patients treated with adjuvant chemotherapy).

Interpretation

Adjuvant cisplatin and fluorouracil chemotherapy did not significantly improve failure-free survival after concurrent chemoradiotherapy in locoregionally advanced nasopharyngeal carcinoma. Longer follow-up is needed to fully assess survival and late toxic effects, but such regimens should not, at present, be used outside well-designed clinical trials.

Funding

Sun Yat-sen University Clinical Research 5010 Programme (No 2007037), Science Foundation of Key Hospital Clinical Programme of Ministry of Health PR China (No 2010-178), and Guangdong Province Universities and Colleges Pearl River Scholar Funded Scheme (2010).