Literature DB >> 31150573

Gemcitabine and Cisplatin Induction Chemotherapy in Nasopharyngeal Carcinoma.

Yuan Zhang1, Lei Chen1, Guo-Qing Hu1, Ning Zhang1, Xiao-Dong Zhu1, Kun-Yu Yang1, Feng Jin1, Mei Shi1, Yu-Pei Chen1, Wei-Han Hu1, Zhi-Bin Cheng1, Si-Yang Wang1, Ye Tian1, Xi-Cheng Wang1, Yan Sun1, Jin-Gao Li1, Wen-Fei Li1, Yu-Hong Li1, Ling-Long Tang1, Yan-Ping Mao1, Guan-Qun Zhou1, Rui Sun1, Xu Liu1, Rui Guo1, Guo-Xian Long1, Shao-Qiang Liang1, Ling Li1, Jing Huang1, Jin-Hua Long1, Jian Zang1, Qiao-Dan Liu1, Li Zou1, Qiong-Fei Su1, Bao-Min Zheng1, Yun Xiao1, Ying Guo1, Fei Han1, Hao-Yuan Mo1, Jia-Wei Lv1, Xiao-Jing Du1, Cheng Xu1, Na Liu1, Ying-Qin Li1, Melvin L K Chua1, Fang-Yun Xie1, Ying Sun1, Jun Ma1.   

Abstract

BACKGROUND: Platinum-based concurrent chemoradiotherapy is the standard of care for patients with locoregionally advanced nasopharyngeal carcinoma. Additional gemcitabine and cisplatin induction chemotherapy has shown promising efficacy in phase 2 trials.
METHODS: In a parallel-group, multicenter, randomized, controlled, phase 3 trial, we compared gemcitabine and cisplatin as induction chemotherapy plus concurrent chemoradiotherapy with concurrent chemoradiotherapy alone. Patients with locoregionally advanced nasopharyngeal carcinoma were randomly assigned in a 1:1 ratio to receive gemcitabine (at a dose of 1 g per square meter of body-surface area on days 1 and 8) plus cisplatin (80 mg per square meter on day 1), administered every 3 weeks for three cycles, plus chemoradiotherapy (concurrent cisplatin at a dose of 100 mg per square meter every 3 weeks for three cycles plus intensity-modulated radiotherapy) or chemoradiotherapy alone. The primary end point was recurrence-free survival (i.e., freedom from disease recurrence [distant metastasis or locoregional recurrence] or death from any cause) in the intention-to-treat population. Secondary end points included overall survival, treatment adherence, and safety.
RESULTS: A total of 480 patients were included in the trial (242 patients in the induction chemotherapy group and 238 in the standard-therapy group). At a median follow-up of 42.7 months, the 3-year recurrence-free survival was 85.3% in the induction chemotherapy group and 76.5% in the standard-therapy group (stratified hazard ratio for recurrence or death, 0.51; 95% confidence interval [CI], 0.34 to 0.77; P = 0.001). Overall survival at 3 years was 94.6% and 90.3%, respectively (stratified hazard ratio for death, 0.43; 95% CI, 0.24 to 0.77). A total of 96.7% of the patients completed three cycles of induction chemotherapy. The incidence of acute adverse events of grade 3 or 4 was 75.7% in the induction chemotherapy group and 55.7% in the standard-therapy group, with a higher incidence of neutropenia, thrombocytopenia, anemia, nausea, and vomiting in the induction chemotherapy group. The incidence of grade 3 or 4 late toxic effects was 9.2% in the induction chemotherapy group and 11.4% in the standard-therapy group.
CONCLUSIONS: Induction chemotherapy added to chemoradiotherapy significantly improved recurrence-free survival and overall survival, as compared with chemoradiotherapy alone, among patients with locoregionally advanced nasopharyngeal carcinoma. (Funded by the Innovation Team Development Plan of the Ministry of Education and others; ClinicalTrials.gov number, NCT01872962.).
Copyright © 2019 Massachusetts Medical Society.

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Year:  2019        PMID: 31150573     DOI: 10.1056/NEJMoa1905287

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   91.245


  175 in total

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8.  Administration of nimotuzumab combined with cisplatin plus 5-fluorouracil as induction therapy improves treatment response and tolerance in patients with locally advanced nasopharyngeal carcinoma receiving concurrent radiochemotherapy: a multicenter randomized controlled study.

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9.  Survival benefit of induction chemotherapy for locally advanced nasopharyngeal carcinoma: prognosis based on a new risk estimation model.

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10.  Genetic Polymorphisms of Long Non-coding RNA Linc00312 Are Associated With Susceptibility and Predict Poor Survival of Nasopharyngeal Carcinoma.

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