A prognostic model for survival of patients with metastatic upper tract urothelial carcinoma with first-line systemic therapy

被引:0
作者
Li, Siming [1 ]
Wei, Jinchang [1 ]
Xu, Huayan [1 ]
Wu, Xiaowen [1 ]
Li, Juan [1 ]
Zhou, Li [1 ]
Yan, Xieqiao [1 ]
Tang, Bixia [2 ]
Si, Lu [2 ]
Cui, Chuanliang [2 ]
Chi, Zhihong [2 ]
Guo, Jun [1 ]
Sheng, Xinan [1 ]
机构
[1] Peking Univ, Key Lab Carcinogenesis & Translat Res, Dept Genitourinary Oncol, Minist Educ Beijing,Canc Hosp & Inst, 52 Fucheng Rd, Beijing 100142, Peoples R China
[2] Peking Univ, Dept Melanoma & Sarcoma, Key Lab Carcinogenesis & Translat Res, Minist Educ Beijing,Canc Hosp & Inst, Beijing, Peoples R China
关键词
Prognostic model; Survival; First-line therapy; Upper tract urothelial carcinoma; Metastatic disease; TRANSITIONAL-CELL CARCINOMA; PREDICTING SURVIVAL; CHEMOTHERAPY; CANCER; MARKER;
D O I
10.1007/s00345-025-05592-7
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose Upper tract urothelial carcinoma (UTUC) presents distinct clinicopathological, molecular features, and biological behaviors compared to urothelial bladder carcinoma (UBC). Currently, no prognostic model exists for metastatic UTUC (mUTUC). This study aimed to develop a prognostic model for patients with mUTUC receiving first-line systemic therapy. Patients and methods A total of 476 patients with mUTUC who received first-line systemic therapy were included and retrospectively analyzed. Patients were randomly assigned to development and validation cohorts in a 3:1 ratio, with potential prognostic factors recorded prospectively. Univariate analyses identified clinical and laboratory factors significantly associated with median overall survival (mOS) in the development cohort, followed by multivariate analyses to determine independent prognostic factors. These factors were utilized to develop a prognostic model. Internal validation was conducted using the validation cohort. Results The number of metastatic organs, Eastern Cooperative Oncology Group Performance Status (ECOG PS), time to distant metastasis (TTDM), white blood cell (WBC) count and alkaline phosphatase (ALP) were identified as independent prognostic factors for mUTUC. Patients were stratified into three risk categories: favorable (0 risk factors, mOS 65.0 months, 95% confidence interval [CI] 35.5-94.6]), intermediate (1 risk factor, mOS 32.0 months, 95% CI 25.8-38.2), and poor (2 + risk factors, mOS 16.0 months, 95% CI 12.1-19.9) (P < 0.001). The model's concordance statistic (c-statistic) was 0.71. Conclusion We developed and validated a prognostic model to estimate survival of patients with mUTUC receiving first-line systemic therapy. This model is applicable to real-world clinical practice and may inform the design of future clinical trials.
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