Safety and efficacy of lobaplatin combined with 5-fluorouracil as first-line induction chemotherapy followed by lobaplatinradiotherapy in locally advanced nasopharyngeal carcinoma: preliminary results of a prospective phase II trial

被引:24
作者
Ke, Liang-Ru [1 ,2 ]
Xia, Wei-Xiong [1 ,2 ]
Qiu, Wen-Ze [1 ,2 ]
Huang, Xin-Jun [1 ,2 ]
Yang, Jing [1 ,2 ]
Yu, Ya-Hui [1 ,2 ]
Liang, Hu [1 ,2 ]
Liu, Guo-Ying [1 ,2 ]
Ye, Yan-Fang [1 ,2 ]
Xiang, Yan-Qun [1 ,2 ]
Guo, Xiang [1 ,2 ]
Lv, Xing [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Dept Nasopharyngeal Carcinoma, Ctr Canc, 651 Dongfeng Rd East, Guangzhou 510060, Guangdong, Peoples R China
[2] Collaborat Innovat Ctr Canc Med, State Key Lab Oncol Southern China, Guangzhou 510060, Guangdong, Peoples R China
来源
BMC CANCER | 2017年 / 17卷
关键词
Lobaplatin; Nasopharyngeal carcinoma; Locally advanced; First-line; Chemotherapy; COMPARING NEOADJUVANT CHEMOTHERAPY; MODULATED RADIATION-THERAPY; RANDOMIZED CONTROLLED-TRIAL; LONG-TERM SURVIVAL; CONCURRENT CHEMORADIOTHERAPY; ADJUVANT CHEMOTHERAPY; SINGLE-ARM; RADIOTHERAPY; CISPLATIN; MULTICENTER;
D O I
10.1186/s12885-017-3080-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Due to improvements in imaging and radiological techniques as well as the use of chemotherapy, distant metastasis has become the predominant mode of treatment failure in patients with locally advanced nasopharyngeal carcinoma (LA-NPC). Platinum-based systemic chemotherapy has shown survival benefits and is now the standard strategy for systemic therapy in patients with LA-NPC. Notably, the third-generation platinum reagent lobaplatin has shown anti-tumor effects in several solid tumors with lower incidences of gastrointestinal, hepatic and renal toxicity relative to other platinum drugs. However, the safety and efficacy of lobaplatin as a first-line regimen in patients with LA-NPC are undetermined. Methods: Patients with stage III-IVa-b NPC received lobaplatin at a dose of 30 mg/m2 on days 1 and 22 combined with a continuous 120-h intravenous injection of 5-fluorouracil at a dose of 4 g/m2 followed by lobaplatin at a dose of 50 mg/m2 on days 43 and 64 concomitant with intensity-modulated radiation therapy. Objective response rates and acute toxicity were assessed based on RECIST (1.1) and CTCAE v.3.0, respectively. Kaplan-Meier analysis was used to calculate survival rates. Results: Fifty-nine patients were enrolled, and 44 patients (74.6%) received allocated cycles of chemotherapy. The objective response rates were 88.1% (95% confidence interval [CI], 0.77 to 0.95) and 100% after induction chemotherapy (ICT) and concurrent chemoradiotherapy (CRT), respectively. With a median follow-up period of 44 months, the 3-year estimated progression-free survival and overall survival were 86.4% (95% CI, 69.8 to 98.8) and 94.9% (95% CI, 89.5 to 100), respectively. The most common grade 3-4 toxicities were neutropenia (8.5%) and thrombocytopenia (40.7%) after ICT and CRT, respectively.
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收藏
页数:9
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