局部进展期鼻咽癌诱导同步放化疗与诱导化疗和放疗的比较。

Pei-Yu Huang, Hai-Qiang Mai, Dong-Hua Luo, Fang Qiu, Ning-Wei Li, Yan-Qun Xiang, Qiu-Yan Chen, Li Zhang, Rui Sun, Ka-Jia Cao, Ling Guo, Man-Quan Deng, Hao-Yuan Mo, Xiang Guo, Feng Zhang, Su-Mei Cao, Min-Yuan Chen, Ying Guo, Yu-Ying Fan, Wen Hu, Yi-Jun Hua, Guo-Feng Xie, Ming-Huang Hong
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引用次数: 14

摘要

背景与目的:诱导化疗和放疗或同步放化疗是局部进展期鼻咽癌(NPC)患者最有效的两种治疗方法。本研究旨在比较诱导同步放化疗与诱导化疗和放疗对局部区域晚期鼻咽癌患者的疗效。方法:2002年8月~ 2005年4月,将408例患者随机分为诱导同步放化疗(IC/CCRT)组和诱导化疗放疗(IC/RT)组。两组患者均接受相同的诱导化疗,包括两个周期氟尿定(FuDR)加卡铂(FuDR750 mg/m2, d1-5;卡铂AUC = 6)。所有患者在诱导化疗结束一周后接受放疗。IC/CCRT组患者在放疗的第7、28、49天也接受卡铂治疗(AUC=6)。8例患者不符合纳入标准,被排除在外。对其余400例进行分析。结果:IC/CCRT组出现III/IV级毒性的患者比例为28.4%,IC/RT组为13.1% (P < 0.001)。中位随访时间为3.9年,IC/CCRT组和IC/RT组的3年总生存率分别为75.9%和83.4% (P = 0.12)。两组患者的无故障生存率、局部区域控制率、远端控制率均无显著差异。结论:与IC/RT方案相比,IC/CCRT方案不能提高局部区域晚期鼻咽癌患者的总生存率。
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Induction-concurrent chemoradiotherapy versus induction chemotherapy and radiotherapy for locoregionally advanced nasopharyngeal carcinoma.

Background and objective: Induction chemotherapy and radiotherapy or concurrent chemoradiotherapy are the most two effective treatments for patients with locoregionally advanced nasopharyngeal carcinoma (NPC). This study was to compare the efficacy of induction-concurrent chemoradiotherapy versus induction chemotherapy and radiotherapy for patients with locoregionally advanced NPC.

Methods: From August 2002 to April 2005, 408 patients were randomly divided into the induction-concurrent chemoradiotherapy (IC/CCRT) group and the induction chemotherapy and radiotherapy (IC/RT) group. Patients in both groups received the same induction chemotherapy, including two cycles of floxuridine (FuDR) plus carboplatin (FuDR750 mg/m2, d1-5; carboplatin AUC=6). All the patients underwent radiotherapy one week after completing the induction chemotherapy. The patients in the IC/CCRT group also received carboplatin (AUC=6) on day 7, 28, and 49 during radiotherapy. Eight patients did not meet the inclusion criteria and were excluded. The remaining 400 cases were analyzed.

Results: Grade III/IV toxicity was found in 28.4% of the patients in the IC/CCRT group and 13.1% in the IC/RT group (P < 0.001). After a median follow up time of 3.9 years, the three-year overall survival was 75.9% and 83.4% (P = 0.12) in the IC/CCRT and IC/RT groups, respectively. No significant differences in the failure-free survival rate, the locoregional control rate, and the distant control rate were found between the two groups.

Conclusion: The IC/CCRT program does not improve the overall survival rate in patients with locoregionally advanced NPC compared with the IC/RT program.

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