Establishing subdivisions of M1 stage nasopharyngeal carcinoma based on decision tree classification: A multicenter retrospective study

被引:3
作者
Liu, Yang [1 ]
Zuo, Zhi-Chao [2 ]
Zeng, Xiao-Yi [3 ]
Ma, Jie [4 ]
Ma, Cheng-Xian [1 ]
Chen, Rui-Zhong [3 ]
Liang, Zhong-Guo [1 ]
Li, Ling [1 ,5 ]
Qu, Song [1 ,5 ]
Lu, Jie-Yan [4 ]
Zhu, Xiao-Dong [1 ,5 ,6 ]
机构
[1] Guangxi Med Univ, Canc Hosp, Dept Radiat Oncol, 71 He di Rd, Nanning 530021, Peoples R China
[2] Xiangtan Cent Hosp, Dept Radiol, Xiangtan, Peoples R China
[3] Wuzhou Red Cross Hosp, Dept Radiat Oncol, Wuzhou, Peoples R China
[4] Guangxi Med Univ, Med Imaging Dept, Canc Hosp, Nanning, Peoples R China
[5] Guangxi Med Univ, Key Lab High Incidence Tumor Prevent & Treatment, Minist Educ, Nanning, Guangxi, Peoples R China
[6] Guangxi Med Univ, Dept Oncol, Affiliated Wu Ming Hosp, Nanning, Peoples R China
关键词
Distant metastasis; Nasopharyngeal carcinoma; Decision tree; Subdivision; Multimodality treatment; Multicenter study; ANTITUMOR-ACTIVITY; METASTASIS; PROGNOSIS; RECURRENT; CHEMOTHERAPY; SYSTEM;
D O I
10.1016/j.oraloncology.2024.106834
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: To meet the demand for personalized treatment, effective stratification of patients with metastatic nasopharyngeal carcinoma (mNPC) is essential. Hence, our study aimed to establish an M1 subdivision for prognostic prediction and treatment planning in patients with mNPC. Materials and methods: This study included 1239 patients with mNPC from three medical centers divided into the synchronous mNPC cohort (smNPC, n = 556) to establish an M1 stage subdivision and the metachronous mNPC cohort (mmNPC, n = 683) to validate this subdivision. The primary endpoint was overall survival. Univariate and multivariate Cox analyses identified covariates for the decision-tree model, proposing an M1 subdivision. Model performance was evaluated using time-dependent receiver operating characteristic curves, Harrell's concordance index, calibration plots, and decision curve analyses. Results: The proposed M1 subdivisions were M1a (<= 5 metastatic lesions), M1b (>5 metastatic lesions + absent liver metastases), and M1c (>5 metastatic lesions + existing liver metastases) with median OS of 34, 22, and 13 months, respectively (p < 0.001). This M1 subdivision demonstrated superior discrimination (C-index = 0.698; 3-year AUC = 0.707) and clinical utility over those of existing staging systems. Calibration curves exhibited satisfactory agreement between predictions and actual observations. Internal and mmNPC cohort validation confirmed the robustness. Survival benefits from local metastatic treatment were observed in M1a, while immunotherapy improved survival in patients with M1b and M1c disease. Conclusion: This novel M1 staging strategy provides a refined approach for prognostic prediction and treatment planning in patients with mNPC, emphasizing the potential benefits of local and immunotherapeutic interventions based on individualized risk stratification.
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页数:9
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