膀胱切除术
膀胱癌
医学
置信区间
内科学
临床试验
生存分析
肿瘤科
泌尿科
癌症
总体生存率
外科
化疗
随机对照试验
区间(图论)
放射治疗
膀胱
梅德林
存活率
作者
Adnan Fazili,Seyed Behzad Jazayeri,Kyle Rose,Christopher Guske,Lexiaochuan Wen,Adri Durant,Megan Prunty,Laura Bukavina,Mark D. Tyson,G. Daniel Grass,Hongzhi Xu,Philippe E. Spiess,Scott M. Gilbert,Wade J. Sexton,Logan Zemp,Rodrigo Rodrigues Pessoa,Michael Poch,Seth P. Lerner,Roger Li
出处
期刊:BJUI
[Wiley]
日期:2025-09-11
卷期号:137 (1): 181-188
摘要
Objectives To compare survival and oncological outcomes of cisplatin‐ineligible patients (Cis‐I) and cisplatin‐eligible (Cis‐E) patients with muscle‐invasive bladder cancer (MIBC) undergoing immediate radical cystectomy (IRC), as IRC is currently considered the standard‐of‐care for Cis‐I patients with MIBC. Patients and Methods Data from patients with clinical (c)T2–4cN0–1M0 MIBC undergoing IRC, between 2006 and 2021, were retrospectively analysed from four tertiary care centres in the United States. Overall, recurrence‐free and event‐free survival were described using the Kaplan–Meier method and tested using the log‐rank test. For context, we compared survival outcomes against those in Cis‐E patients with MIBC undergoing IRC from the Southwest Oncology Group (SWOG)‐8710 trial. Results Overall, 379 Cis‐I and 125 Cis‐E patients with cT2–4cN0–1M0 MIBC who underwent IRC were included. Cis‐I patients included 44.8% cT3/4 vs 60% cT3/4 in the Cis‐E group. Overall, 83.3% of Cis‐I and 79.2% of Cis‐E patients died during follow‐up. The median event‐free and overall survival were 12.1 and 14.5 months for the Cis‐I group and 28.8 and 60.1 months for the Cis‐E group ( P < 0.001). [Correction added on 10 October 2025, after first online publication: The preceding sentence has been revised in this version.] Limitations include retrospective comparison of contemporary multi‐institutional data with that of a randomised control trial. Conclusions The Cis‐I patients with MIBC undergoing IRC fared poorly, with a median overall survival of 14.5 (95% confidence interval 11.1–17.9) months, mostly due to non‐cancer‐related deaths. These results provide a benchmark for clinical trials exploring novel agents or alternative chemotherapy regimens in Cis‐I patients with MIBC.
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