<p>Here we report long-term outcomes of adjuvant metronomic capecitabine in patients with locoregionally advanced nasopharyngeal carcinoma. In this multicenter, open-label, parallel-group, randomized, controlled, phase 3 trial, 406 patients who had completed definitive chemoradiotherapy were randomly assigned (1:1) to receive either adjuvant metronomic capecitabine (650 mg m<sup>−</sup><sup>2</sup> twice daily for 1 year) or observation. The primary endpoint was failure-free survival; secondary endpoints included overall survival (OS), distant failure-free survival, locoregional failure-free survival, and safety, as reported in this analysis. The trial met its primary endpoint. With a median follow-up of 71.3 months, metronomic capecitabine significantly improved OS (hazard ratio = 0.53, 95% confidence interval, 0.31–0.91, <i>P</i> = 0.019). Grade 3 adverse events occurred in 35 (17%) of 201 patients in the metronomic capecitabine group and 11 (6%) of 200 in the observation group; one (&lt;1%) grade 4 neutropenia was reported. In a post hoc analysis, completion of the 1 year course was associated with improved OS, whereas dose reductions and relative dose intensity showed no association with OS. Patients with a higher post-radiotherapy neutrophil-to-lymphocyte ratio derived greater benefit from metronomic capecitabine. These findings support the long-term therapeutic benefit of adjuvant metronomic capecitabine in locoregionally advanced nasopharyngeal carcinoma. ClinicalTrials.gov identifier: <a href="http://clinicaltrials.gov/ct2/show/NCT02958111">NCT02958111</a>.</p>

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Long-term outcomes of adjuvant metronomic capecitabine in locoregionally advanced nasopharyngeal carcinoma: a randomized, controlled, multicenter, phase 3 study

  • Ya-Lan Tao,
  • Dong-Hong Wu,
  • Qin Zhou,
  • Kun-Yu Yang,
  • Feng Jin,
  • Xiao-Dong Zhu,
  • Mei Shi,
  • Guo-Qing Hu,
  • Yan Sun,
  • Hong-Fen Wu,
  • Hui Wu,
  • Qin Lin,
  • Hui Wang,
  • Ye Tian,
  • Ning Zhang,
  • Xi-Cheng Wang,
  • Liang-Fang Shen,
  • Zheng-Zheng Liu,
  • Jing Huang,
  • Xiu-Ling Luo,
  • Ling Li,
  • Jian Zang,
  • Qi Mei,
  • Bao-Min Zheng,
  • Dan Yue,
  • Jing Xu,
  • San-Gang Wu,
  • Lei Chen,
  • Wen-Fei Li,
  • Guan-Qun Zhou,
  • Rui Sun,
  • Rui Guo,
  • Yuan Zhang,
  • Cheng Xu,
  • Jia-Wei Lv,
  • Ying Guo,
  • Hui-Xia Feng,
  • Ling-Long Tang,
  • Fang-Yun Xie,
  • Xu Liu,
  • Ying Sun,
  • Jun Ma,
  • Yan-Ping Mao,
  • Yu-Pei Chen

摘要

Here we report long-term outcomes of adjuvant metronomic capecitabine in patients with locoregionally advanced nasopharyngeal carcinoma. In this multicenter, open-label, parallel-group, randomized, controlled, phase 3 trial, 406 patients who had completed definitive chemoradiotherapy were randomly assigned (1:1) to receive either adjuvant metronomic capecitabine (650 mg m2 twice daily for 1 year) or observation. The primary endpoint was failure-free survival; secondary endpoints included overall survival (OS), distant failure-free survival, locoregional failure-free survival, and safety, as reported in this analysis. The trial met its primary endpoint. With a median follow-up of 71.3 months, metronomic capecitabine significantly improved OS (hazard ratio = 0.53, 95% confidence interval, 0.31–0.91, P = 0.019). Grade 3 adverse events occurred in 35 (17%) of 201 patients in the metronomic capecitabine group and 11 (6%) of 200 in the observation group; one (<1%) grade 4 neutropenia was reported. In a post hoc analysis, completion of the 1 year course was associated with improved OS, whereas dose reductions and relative dose intensity showed no association with OS. Patients with a higher post-radiotherapy neutrophil-to-lymphocyte ratio derived greater benefit from metronomic capecitabine. These findings support the long-term therapeutic benefit of adjuvant metronomic capecitabine in locoregionally advanced nasopharyngeal carcinoma. ClinicalTrials.gov identifier: NCT02958111.