Literature DB >> 34083231

A Randomized Controlled Trial Comparing Two Different Schedules for Cisplatin Treatment in Patients with Locoregionally Advanced Nasopharyngeal Cancer.

Wei-Xiong Xia1,2, Xing Lv1,2, Hu Liang1,2, Guo-Ying Liu1,2,3, Rui Sun1,2, Qi Zeng4, Si-Wei Li5, Hao-Yuan Mo1,2, Fei Han1,2, Dong-Hua Luo1,2, Qing Liu6, Meng-Yun Shi3, Yan-Fang Ye3, Jing Yang7, Liang-Ru Ke1,2, Meng-Yun Qiang1,2, Wen-Ze Qiu1,2, Ya-Hui Yu1,2, Kui-Yuan Liu1,2, Xin-Jun Huang1,2, Wang-Zhong Li1,2, Shu-Hui Lv1,2, Zhuo-Chen Cai1,2, Jing-Jing Miao1,2, Ling Guo1,2, Ming-Yuan Chen1,2, Ka-Jia Cao1,2, Lin Wang1,2, Chong Zhao1,2, Pei-Yu Huang1,2, Qiu-Yan Chen1,2, Yi-Jun Hua1,2, Lin-Quan Tang1,2, Chao-Nan Qian1,2, Hai-Qiang Mai8,2, Xiang Guo8,2, Yan-Qun Xiang8,2.   

Abstract

PURPOSE: Previous studies suggest that a cumulative cisplatin dose of 200 mg/m2 might be adequate in the intensity-modulated radiation therapy (IMRT) era for locoregionally advanced nasopharyngeal carcinoma (LANPC). However, two cycles of once-every-3-weeks cisplatin at 100 mg/m2 has never been prospectively compared with standard once-a-week cisplatin regimen. PATIENTS AND METHODS: This trial was conducted at three hospitals from 2011 to 2016. Patients who met the eligibility criteria were recruited (ChiCTR-TRC-12001979) and randomly assigned (1:1) via a computer-generated sequence to receive once-every-3-weeks cisplatin at 100 mg/m2 for two cycles or once-a-week cisplatin at 40 mg/m2 for six cycles concurrently with IMRT. Primary endpoint was failure-free survival and between-group absolute difference of 10% as the noninferiority margin.
RESULTS: A total of 510 patients were enrolled. Median follow-up time was 58.3 months with 85.4% of 3-year failure-free survival in the once-every-3-weeks group and 85.6% in the once-a-week group. An absolute difference of -0.2% (95% confidence interval, -6.3 to 5.9; P noninferiority = 0.0016). Acute toxicities of grade 3 or higher occurred in 55.8% in the once-every-3-weeks group and 66.3% in the once-a-week group (P = 0.015). The most common acute toxicities were hematologic abnormalities, including leukopenia (16% vs. 27%; P = 0.0022) and thrombocytopenia (1% vs. 5%; P = 0.015). The late grade 3-4 auditory loss rate was significantly lower in the once-every-3-weeks group than the once-a-week group (6% vs. 13%; P = 0.0039).
CONCLUSIONS: Once-every-3-weeks cisplatin as concurrent chemoradiotherapy is noninferior to once-a-week cisplatin in the treatment efficacy in the LANPC. Although both regimens are well tolerated, severe acute toxicities and late-onset auditory loss are higher in the once-a-week group. ©2021 The Authors; Published by the American Association for Cancer Research.

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Year:  2021        PMID: 34083231     DOI: 10.1158/1078-0432.CCR-20-4532

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  3 in total

1.  For Head and Neck Cancer, It Is Still Cisplatin, But How Much, How Often, and How Tolerable? New Randomized Phase III Data For the Adjuvant Setting.

Authors:  D Neil Hayes; John Patrick Gleysteen; David Louis Schwartz
Journal:  J Clin Oncol       Date:  2022-04-21       Impact factor: 50.717

2.  Effect of Induction Chemotherapy With Paclitaxel, Cisplatin, and Capecitabine vs Cisplatin and Fluorouracil on Failure-Free Survival for Patients With Stage IVA to IVB Nasopharyngeal Carcinoma: A Multicenter Phase 3 Randomized Clinical Trial.

Authors:  Wang-Zhong Li; Xing Lv; Dan Hu; Shu-Hui Lv; Guo-Ying Liu; Hu Liang; Yan-Fang Ye; Wen Yang; Han-Xiong Zhang; Tai-Ze Yuan; De-Shen Wang; Nian Lu; Liang-Ru Ke; Wu-Bing Tang; Li-Hua Tong; Zhi-Jie Chen; Ting Liu; Ka-Jia Cao; Hao-Yuan Mo; Ling Guo; Chong Zhao; Ming-Yuan Chen; Qiu-Yan Chen; Pei-Yu Huang; Rui Sun; Fang Qiu; Dong-Hua Luo; Lin Wang; Yi-Jun Hua; Lin-Quan Tang; Chao-Nan Qian; Hai-Qiang Mai; Xiang Guo; Yan-Qun Xiang; Wei-Xiong Xia
Journal:  JAMA Oncol       Date:  2022-05-01       Impact factor: 33.006

3.  Weekly Cisplatin Plus Radiation for Postoperative Head and Neck Cancer (JCOG1008): A Multicenter, Noninferiority, Phase II/III Randomized Controlled Trial.

Authors:  Naomi Kiyota; Makoto Tahara; Junki Mizusawa; Takeshi Kodaira; Hirofumi Fujii; Tomoko Yamazaki; Hiroki Mitani; Shigemichi Iwae; Yasushi Fujimoto; Yusuke Onozawa; Nobuhiro Hanai; Takenori Ogawa; Hiroki Hara; Nobuya Monden; Eiji Shimura; Shujiro Minami; Takashi Fujii; Kaoru Tanaka; Akihiro Homma; Seiichi Yoshimoto; Nobuhiko Oridate; Koichi Omori; Tsutomu Ueda; Kenji Okami; Ichiro Ota; Kiyoto Shiga; Masashi Sugasawa; Takahiro Asakage; Yuki Saito; Shigeyuki Murono; Yasumasa Nishimura; Kenichi Nakamura; Ryuichi Hayashi
Journal:  J Clin Oncol       Date:  2022-03-01       Impact factor: 50.717

  3 in total

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