Development and prospective validation of a risk score model in guiding individualized concurrent chemoradiotherapy in stage II nasopharyngeal carcinoma in intensity-modulated radiotherapy era

被引:3
|
作者
Yang, Shan-Shan [1 ]
Pang, Ya-Jun [2 ]
Wang, Zhi-Qiang [3 ]
Zhang, Bao-Yu [1 ]
Liu, Zhi-Qiao [1 ]
Chen, En-Ni [1 ]
Ouyang, Pu-Yun [1 ]
Xie, Fang-Yun [1 ]
机构
[1] Sun Yat Sen Univ, Collaborat Innovat Ctr Canc Med, State Key Lab Oncol South China,Canc Ctr, Dept Radiat Oncol,Guangdong Key Lab Nasopharyngea, 651 Dongleng East Rd, Guangzhou 510060, Peoples R China
[2] Guangdong Med Univ, Canc Ctr, Affiliated Hosp, Zhanjiang, Guangdong, Peoples R China
[3] Southern Med Univ, Dongguan Peoples Hosp, Dept Radiotherapy, Affiliated Dongguan Peoples Hosp, Dongguan, Guangdong, Peoples R China
来源
CANCER MEDICINE | 2022年 / 11卷 / 04期
关键词
concurrent chemoradiotherapy; intensity-modulated radiotherapy; nasopharyngeal carcinoma; tumor burden; RADIATION-THERAPY; CHEMOTHERAPY; SURVIVAL; OUTCOMES; VOLUME;
D O I
10.1002/cam4.4520
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose We aimed to develop and prospectively validate a risk score model to guide individualized concurrent chemoradiotherapy (CCRT) for patients with stage II nasopharyngeal carcinoma (NPC) in intensity-modulated radiotherapy (IMRT) era. Materials and Methods In total, 1220 patients who received CCRT or IMRT alone were enrolled in this study, including a training cohort (n = 719), a validation cohort (n = 307), and a prospective test cohort (n = 194). Patients were stratified into different risk groups by a risk score model based on independent prognostic factors, which were developed in the training cohort. Survival rates were compared by the log-rank test. The validation and prospective test cohorts were used for validation. Results Total tumor volume, Epstein-Barr virus DNA, and lactate dehydrogenase were independent risk factors for failure-free survival (FFS, all p < 0.05). A risk score model based on these three risk factors was developed to classify patients into low-risk group (no risk factor, n = 337) and high-risk group (one or more factors, n = 382) in the training cohort. In the high-risk group, CCRT had better survival rates than IMRT alone (5-year FFS: 82.6% vs. 74.0%, p = 0.028). However, there was no survival difference between CCRT and IMRT alone either in the whole training cohort (p = 0.15) or in the low-risk group (p = 0.15). The results were verified in the validation and prospective test cohorts. Conclusion A risk score model was developed and prospectively validated to precisely select high-risk stage II NPC patients who can benefit from CCRT, and thus guided individualized treatment in IMRT era.
引用
收藏
页码:1109 / 1118
页数:10
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