Intensity-modulated radiotherapy alone compared with intensity-modulated radiotherapy plus concurrent chemotherapy in intermediate-risk nasopharyngeal carcinoma

被引:0
作者
Liao, Shufang [1 ]
Zhang, Bin [2 ]
Su, Yixin [3 ]
Pan, Yufei [4 ]
Zhang, Jian [5 ]
Ye, Zhenkai [6 ]
Zhang, Rongjun [1 ]
Kong, Xiangyun [1 ]
Qin, Guanjie [1 ]
Mo, Yunyan [7 ]
Ruan, Xiaolan [4 ]
Liu, Jian [1 ]
Gan, Chunqiao [1 ]
Dai, Jinxuan [1 ]
Zhang, Ruyun [1 ]
Luo, Guanhong [1 ]
Liao, Xiaofei [1 ]
Jiang, Wei [1 ,7 ]
机构
[1] Guilin Med Univ, Affiliated Hosp, Dept Radiat Oncol,Key Lab Oncol, Educ Dept Guangxi Zhuang Autonomous Reg, 15 Lequn Rd, Guilin 541001, Peoples R China
[2] Wuzhou Red Cross Hosp, Dept Radiat Oncol, Wuzhou 543002, Peoples R China
[3] Lingshan Peoples Hosp, Dept Radiat Oncol, Zhongxiu Rd, Lingshan 535400, Peoples R China
[4] Nan Xishan Hosp, Dept Oncol, 46 Chongxin Rd, Guilin 541001, Peoples R China
[5] Peoples Hosp Laibin, Dept Oncol, Laibin 546100, Peoples R China
[6] Peoples Hosp Guangxi Zhuang Autonomous Reg, Dept Radiat Oncol, Nanning 530021, Peoples R China
[7] Guilin Med Univ, Dept Gastroenterol, Affiliated Hosp, 15 Lequn Rd, Guilin 541001, Peoples R China
基金
中国国家自然科学基金;
关键词
Chemoradiotherapy; IMRT; Nasopharyngeal; Tumor; Toxicities; UICC/AJCC STAGING SYSTEM; RADIATION-THERAPY; CHEMORADIOTHERAPY; CANCER; METAANALYSIS; SURVIVAL; OUTCOMES; TOXICITY; PATTERNS; CRITERIA;
D O I
10.1007/s00066-024-02201-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background This study aimed to investigate the clinical benefit of adding concurrent chemotherapy to intensity-modulated radiotherapy (IMRT) for nasopharyngeal carcinoma (NPC) patients with an intermediate risk (stage II and T3N0M0). Methods A multicenter phase II randomized trial was conducted in intermediate-risk NPC patients. Enrolled patients were previously untreated and aged ranged from 18 to 70 years without severe coexisting diseases. Patients were randomly assigned to receive IMRT alone or IMRT+concurrent chemotherapy (CC; three cycles of 80 mg/m2 cisplatin every 3 weeks). Primary endpoint was defined as 3-year progression-free survival (PFS). The secondary endpoints were distant metastasis-free survival (DMFS), locoregional relapse-free survival (LRRFS), overall survival (OS), and treatment-associated toxicity. We registered this study with Chinese Clinical Trial Registry (CliCTR1800017132; registered July 13, 2018, study start July 13, 2018). Results From November 2015 to July 2019, 42 patients with stage II and T3N0M0 NPC were enrolled; 20 patients received IMRT alone while 22 patients received IMRT+CC. After a median of 58 months of follow-up, we estimated the 3-year PFS rates as 90% (IMRT group) and 86.4% (IMRT+CC group; hazard ratio 1.387, 95% confidence interval 0.240-8.014; P = 0.719). The 3-year PFS, OS, and cumulative DMFS and LRRFS showed no significant differences between the two groups (P > 0.05). However, the IMRT group displayed a lower incidence of nausea/vomiting, leucopenia, and dry mouth than the IMRT+CC group. Conclusion Adding CC to IMRT provided no survival benefit but increased treatment-associated toxicities in patients with intermediate-risk NPC.
引用
收藏
页码:867 / 875
页数:9
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