首页> 美国卫生研究院文献>Scientific Reports >Assessment of Concurrent Chemoradiotherapy plus Induction Chemotherapy in Advanced Nasopharyngeal Carcinoma: Cisplatin Fluorouracil and Docetaxel versus Gemcitabine and Cisplatin
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Assessment of Concurrent Chemoradiotherapy plus Induction Chemotherapy in Advanced Nasopharyngeal Carcinoma: Cisplatin Fluorouracil and Docetaxel versus Gemcitabine and Cisplatin

机译:晚期鼻咽癌同时放化疗联合诱导化疗的评估:顺铂氟尿嘧啶和多西他赛与吉西他滨和顺铂

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摘要

Induction chemotherapy treatment for nasopharyngeal carcinoma (NPC) is controversial. The aim of this study was to evaluate the treatment outcomes and toxicities between two induction chemotherapy regimens, with both followed by concurrent chemoradiotherapy. The first strategy used docetaxel, cisplatin and fluorouracil for induction chemotherapy (TPF), and the second utilised gemcitabine and cisplatin (GP). A retrospective analysis was performed on eligible NPC patients attending our hospital between May 2009 and Dec 2014. A total of 113 patients were enrolled with 58 patients receiving TPF and 55 receiving GP induction chemotherapy. Ninety-four patients (83.2%) were alive after 36-months follow-up. The median overall survival (OS) and progression-free survival (PFS) time were 48.3 and 39.7 months, respectively. The 3-year OS for the TPF regimen was 87.9% and 87.4% with GP chemotherapy (P = 0.928). The 3-year PFS of the TPF treatment was 84.5%, while it was 83.5% for the GP group (P = 0.551). Univariate analysis showed that lymph node metastasis was a significant PFS prognostic factor, while N3 stage was an independent predictor of PFS and distant failure-free survival (DMFS) in multivariate analysis. There were no significant differences in adverse toxicities or treatment efficacy between the chemotherapy regimens in the treatment of locoregionally advanced NPC.
机译:诱导化学疗法治疗鼻咽癌(NPC)是有争议的。这项研究的目的是评估两种诱导化疗方案之间的治疗结果和毒性,并同时进行同步放化疗。第一种策略使用多西他赛,顺铂和氟尿嘧啶进行诱导化疗(TPF),第二种策略使用吉西他滨和顺铂(GP)。对2009年5月至2014年12月在我院就诊的合格NPC患者进行回顾性分析。共入组113例患者,其中58例接受TPF,55例接受GP诱导化疗。随访36个月后,有94例患者(占83.2%)还活着。中位总生存时间(OS)和无进展生存时间(PFS)分别为48.3和39.7个月。 TPF方案的3年OS为87.9%,GP化疗为87.4%(P = 0.928)。 TPF治疗的3年PFS为84.5%,而GP组为33.5%(P = 0.551)。单因素分析表明,在多因素分析中,淋巴结转移是PFS的重要预后因素,而N3期是PFS和远距离无衰竭生存率(DMFS)的独立预测因子。在局部晚期NPC的治疗中,化疗方案之间的不良毒性或治疗效果无显着差异。

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