Comparing Paclitaxel Plus Fluorouracil Versus Cisplatin Plus Fluorouracil in Chemoradiotherapy for Locally Advanced Esophageal Squamous Cell Cancer: A Randomized, Multicenter, Phase III Clinical Trial

Author:

Chen Yun1,Ye Jinjun2,Zhu Zhengfei1,Zhao Weixin1,Zhou Jialiang3,Wu Chaoyang4,Tang Huarong4,Fan Min1,Li Ling1,Lin Qin5,Xia Yi6,Li Yunhai6,Li Jiancheng7,Jia Huixun18,Lu Saiquan1,Zhang Zhen1,Zhao Kuaile1

Affiliation:

1. Fudan University Shanghai Cancer Center, Shanghai, China

2. Jiangsu Cancer Hospital, Nanjing, China

3. Affiliated Hospital of Jiangnan University, Wuxi, China

4. Zhenjiang First People’s Hospital, Zhenjiang, China

5. The First Affiliated Hospital of Xiamen University, Xiamen, China

6. Fudan University Shanghai Cancer Center Minhang Branch Hospital, Shanghai, China

7. Fujian Provincial Cancer Hospital, Fuzhou, China

8. Shanghai General Hospital, Shanghai, China

Abstract

PURPOSE This trial aimed to assess the efficacy and safety of the paclitaxel plus fluorouracil regimen versus the cisplatin plus fluorouracil regimen in definitive concurrent chemoradiotherapy (dCRT) in patients with locally advanced esophageal squamous cell carcinoma (ESCC). PATIENTS AND METHODS Patients with locally advanced ESCC were enrolled and randomly assigned to either the paclitaxel plus fluorouracil group or the cisplatin plus fluorouracil group. The patients in the paclitaxel plus fluorouracil group were treated with paclitaxel and fluorouracil one cycle per week in dCRT for five cycles followed by paclitaxel and fluorouracil one cycle per month in consolidation chemotherapy for two cycles. The patients in the cisplatin/5-fluorouracil group were treated with cisplatin and fluorouracil one cycle per month in dCRT for two cycles followed by two cycles in consolidation chemotherapy. The radiotherapy dose was 61.2 Gy delivered in 34 fractions. The primary end point was 3-year overall survival (OS). RESULTS Four hundred thirty-six patients with ESCC in six centers were recruited at a 1:1 ratio between April 2012 and July 2015. The median follow-up of the surviving patients was 48.7 months (interquartile range, 42.6-60.9). The 3-year OS was 55.4% in the paclitaxel plus fluorouracil group and 51.8% in the cisplatin plus fluorouracil group (hazard ratio, 0.905 [95% CI, 0.698 to 1.172]; P = .448). The 3-year progression-free survival was also not significantly different between the paclitaxel plus fluorouracil group and the cisplatin plus fluorouracil group (43.7% v 45.5%, respectively; hazard ratio, 0.973 [95% CI, 0.762 to 1.243]; P = .828). Compared with the cisplatin plus fluorouracil group, the paclitaxel plus fluorouracil group had significantly lower incidences of acute grade 3 or higher anemia, thrombocytopenia, anorexia, nausea, vomiting, and fatigue ( P < .05), but higher incidences of acute grade 3 or higher leukopenia, radiation dermatitis, and radiation pneumonitis ( P < .05). CONCLUSION The paclitaxel plus fluorouracil regimen did not significantly prolong the OS compared with the standard cisplatin plus fluorouracil regimen in dCRT in patients with locally advanced ESCC.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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