Gemcitabine Plus Platinum versus Docetaxel Plus Platinum as First-Line Therapy for Metastatic Nasopharyngeal Carcinoma: A Randomized Clinical Study

被引:7
作者
Yang, Hui [1 ]
Lu, Ying [1 ]
Xu, Zhuohua [1 ]
Wei, Mingjing [1 ]
Huang, Haixin [1 ]
机构
[1] Guangxi Med Univ, Dept Oncol, Affiliated Hosp 4, Liuzhou 545000, Guangxi, Peoples R China
来源
SAUDI JOURNAL OF MEDICINE & MEDICAL SCIENCES | 2021年 / 9卷 / 02期
关键词
Chemotherapy; docetaxel; gemcitabine; metastatic nasopharyngeal carcinoma; platinum; prognostic factors; survival; INTENSITY-MODULATED RADIOTHERAPY; INDUCTION CHEMOTHERAPY; CONCURRENT CHEMORADIOTHERAPY; CISPLATIN; RECURRENT; 5-FLUOROURACIL; MULTICENTER; SURVIVAL; PATTERNS; CANCER;
D O I
10.4103/sjmms.sjmms_471_20
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: A well-established first-line chemotherapy standard for metastatic nasopharyngeal carcinoma is yet lacking. Objectives: To compare the efficacy and safety of gemcitabine plus platinum versus docetaxel plus platinum regimen as first-line therapies for distal metastatic nasopharyngeal carcinoma. Study Design and Participants: A single center, randomized, open-label, parallel-arm study. The study included 120 patients with metastatic nasopharyngeal carcinoma who met the study requirements. Interventions: Participants were randomized in a 1:1 ratio through a sealed envelope selection. Gemcitabine 1000 mg/m(2)/d intravenously (IV) for >30 min (days 1 and 8) or docetaxel 75 mg/m(2)/d IV for 1 h (day 1) were administered to the respective group participants. Nedaplatin 75 mg/m(2)/d, IV (day 1), cisplatin 75 mg/m(2)/d IV (day 1) or carboplatin (area under the curve set as 5) IV (day 1) were used in both groups. One cycle duration was 21 days, with 4-6 cycles for all participants. Outcomes: The primary assessed outcomes were progression-free survival (PFS) and overall survival (OS), and the secondary outcomes were short-term efficacy [i.e., response rate (RR) and disease control rate (DCR)] and safety. Results: Seven patients withdrew from the study, and efficacy and adverse reactions were obtained for 113 patients (gemcitabine: 56; docetaxel: 57). Compared with the docetaxel plus platinum group, the gemcitabine plus platinum group had significantly higher RR (71.4% vs. 52.6%, P < 0.05); mPFS (9.7 vs. 7.8 months, P < 0.05), and mOS (20.6 vs. 16.8 months, P < 0.01). The significance was not associated with increased adverse reactions, as both groups showed similar Grades 3 and 4 adverse reactions (P > 0.05). DCR was non-significantly higher in the gemcitabine group (85.7% vs. 75.4%, P > 0.05). Multivariable analysis revealed that time to disease progression, number of involved organs, liver metastasis, and grouping were associated with mPFS and mOS (all P < 0.05). Conclusion: The combination of gemcitabine with platinum is likely superior to that of docetaxel with platinum as first-line treatment for metastatic nasopharyngeal carcinoma.
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收藏
页码:125 / 134
页数:10
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