Tumor residue in patients with stage II-IVA nasopharyngeal carcinoma who received intensity-modulated radiation therapy: development and validation of a prediction nomogram integrating postradiotherapy plasma Epstein-Barr virus deoxyribonucleic acid, clinical stage, and radiotherapy dose

被引:2
作者
Huang, Ying-Ying [1 ,2 ]
Zhou, Jia-Yu [1 ,2 ]
Zhan, Ze-Jiang [1 ,2 ]
Ke, Liang-Ru [1 ,3 ]
Xia, Wei-Xiong [1 ,2 ]
Cao, Xun [1 ,4 ]
Cai, Zhuo-Chen [1 ,2 ]
Deng, Ying [1 ,2 ]
Chen, Xi [1 ,2 ]
Zhang, Lu-Lu [1 ,2 ]
Huang, Hao-Yang [1 ,2 ]
Guo, Xiang [1 ,2 ]
Lv, Xing [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Collaborat Innovat Ctr Canc Med, State Key Lab Oncol South China, Guangdong Key Lab Nasopharyngeal Carcinoma Diag &, 651 Dongfeng East Rd, Guangzhou 510060, Peoples R China
[2] Sun Yat Sen Univ, Dept Nasopharyngeal Carcinoma, Canc Ctr, 651 Dongfeng East Rd, Guangzhou 510060, Peoples R China
[3] Sun Yat Sen Univ, Dept Med Imaging, Canc Ctr, 651 Dongfeng East Rd, Guangzhou 510060, Peoples R China
[4] Sun Yat Sen Univ, Dept Crit Care Med, Canc Ctr, 651 Dongfeng East Rd, Guangzhou 510060, Peoples R China
基金
中国国家自然科学基金;
关键词
Nasopharyngeal carcinoma; Intensity-modulated radiotherapy; Tumor residue; Epstein-Barr virus deoxyribonucleic acid; Prognostic value; Prediction nomogram; 8TH EDITION; DNA; CANCER; DISEASE; NODE; MRI;
D O I
10.1186/s12885-023-10827-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundTo develop and validate a predictive nomogram for tumor residue 3-6 months after treatment based on postradiotherapy plasma Epstein-Barr virus (EBV) deoxyribonucleic acid (DNA), clinical stage, and radiotherapy (RT) dose in patients with stage II-IVA nasopharyngeal carcinoma (NPC) treated with intensity-modulated radiation therapy (IMRT).MethodsIn this retrospective study, 1050 eligible patients with stage II-IVA NPC, who completed curative IMRT and underwent pretreatment and postradiotherapy (-7 to +28 days after IMRT) EBV DNA testing, were enrolled from 2012 to 2017. The prognostic value of the residue was explored using Cox regression analysis in patients (n=1050). A nomogram for predicting tumor residues after 3-6 months was developed using logistic regression analyses in the development cohort (n=736) and validated in an internal cohort (n=314).ResultsTumor residue was an independent inferior prognostic factor for 5-year overall survival, progression-free survival, locoregional recurrence-free survival and distant metastasis-free survival (all P<0.001). A prediction nomogram based on postradiotherapy plasma EBV DNA level (0 vs. 1-499 vs. >= 500 copies/ml), clinical stage (II vs. III vs. IVA), and RT dose (68.00-69.96 vs. 70.00-74.00 Gy) estimated the probability of residue development. The nomogram showed better discrimination (area under the curve (AUC): 0.752) than either the clinical stage (0.659) or postradiotherapy EBV DNA level (0.627) alone in the development and validation cohorts (AUC: 0.728).ConclusionsWe developed and validated a nomogram model integrating clinical characteristics at the end of IMRT for predicting whether tumor will residue or not after 3-6 months. Thus, high-risk NPC patients who might benefit from immediate additional intervention could be identified by the model, and the probability of residue can be reduced in the future.
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页数:13
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