预测根治性前列腺切除术后复发前列腺癌 PSMA-PET 指导的挽救性放疗后生化结果的机器学习方法:回顾性研究

IF 3.3 Q2 ONCOLOGY
JMIR Cancer Pub Date : 2024-09-20 DOI:10.2196/60323
Ali Janbain, Andrea Farolfi, Armelle Guenegou-Arnoux, Louis Romengas, Sophia Scharl, Stefano Fanti, Francesca Serani, Jan C Peeken, Sandrine Katsahian, Iosif Strouthos, Konstantinos Ferentinos, Stefan A Koerber, Marco E Vogel, Stephanie E Combs, Alexis Vrachimis, Alessio Giuseppe Morganti, Simon Kb Spohn, Anca-Ligia Grosu, Francesco Ceci, Christoph Henkenberens, Stephanie Gc Kroeze, Matthias Guckenberger, Claus Belka, Peter Bartenstein, George Hruby, Louise Emmett, Ali Afshar Omerieh, Nina-Sophie Schmidt-Hegemann, Lucas Mose, Daniel M Aebersold, Constantinos Zamboglou, Thomas Wiegel, Mohamed Shelan
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引用次数: 0

摘要

背景:对于根治性前列腺切除术后出现生化复发的患者,挽救性放射治疗(sRT)往往是唯一的根治选择。在前列腺癌根治术后,我们开发并验证了一种预测生化治疗失败的提名图:本研究旨在评估基于前列腺特异性膜抗原-正电子发射断层扫描(PSMA-PET)的前列腺根治术对前列腺切除术后前列腺特异性抗原(PSA)持续或复发的疗效。研究目标包括开发预测生化治疗失败的随机生存森林(RSF)模型,将其与 Cox 模型进行比较,并评估随时间变化的预测准确性。多国队列数据将验证该模型的性能,旨在改善复发性前列腺癌的临床管理:这项多中心回顾性研究收集了来自 5 个国家 13 家医疗机构的数据:方法:这项多中心回顾性研究收集了德国、塞浦路斯、澳大利亚、意大利和瑞士 5 个国家 13 家医疗机构的数据。研究共纳入了 1029 名在 PSMA-PET 评估 PSA 持续或复发后接受 sRT 治疗的患者。患者的治疗时间为 2013 年 7 月至 2020 年 6 月,临床决策以 PSMA-PET 结果和现代标准为指导。主要终点是无生化失败,即治疗后 PSA 连续 2 次上升 >0.2 纳克/毫升。数据分为训练集(708 名患者)、测试集(271 名患者)和外部验证集(50 名患者),用于机器学习算法的开发和验证。使用RSF模型,每个模型有1000棵树,使用哈雷尔一致性指数和布赖尔评分优化预测性能。统计分析使用了 R 统计软件(R 统计计算基金会),并获得了参与机构的伦理批准:结果:分析了1029名接受sRT PSMA-PET评估的患者的基线特征。接受 sRT 时的中位年龄为 70 岁(IQR 64-74 岁)。PSMA-PET扫描显示,43.9%(430/979)的患者有局部复发,27.2%(266/979)的患者有结节复发。35.6%(349/979)的病例接受了剂量递增的盆腔淋巴管 sRT 治疗。外部离群验证集显示出明显的特征,包括较高的淋巴结阳性率(47/50,94% vs 266/979,27.2% in the learning cohort)和较低的 sRT 照射剂量(结论:所开发的 RSF 模型显示出更高的预测准确性,有可能改善患者的预后并协助临床医生做出治疗决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Machine Learning Approach for Predicting Biochemical Outcome After PSMA-PET-Guided Salvage Radiotherapy in Recurrent Prostate Cancer After Radical Prostatectomy: Retrospective Study.

Background: Salvage radiation therapy (sRT) is often the sole curative option in patients with biochemical recurrence after radical prostatectomy. After sRT, we developed and validated a nomogram to predict freedom from biochemical failure.

Objective: This study aims to evaluate prostate-specific membrane antigen-positron emission tomography (PSMA-PET)-based sRT efficacy for postprostatectomy prostate-specific antigen (PSA) persistence or recurrence. Objectives include developing a random survival forest (RSF) model for predicting biochemical failure, comparing it with a Cox model, and assessing predictive accuracy over time. Multinational cohort data will validate the model's performance, aiming to improve clinical management of recurrent prostate cancer.

Methods: This multicenter retrospective study collected data from 13 medical facilities across 5 countries: Germany, Cyprus, Australia, Italy, and Switzerland. A total of 1029 patients who underwent sRT following PSMA-PET-based assessment for PSA persistence or recurrence were included. Patients were treated between July 2013 and June 2020, with clinical decisions guided by PSMA-PET results and contemporary standards. The primary end point was freedom from biochemical failure, defined as 2 consecutive PSA rises >0.2 ng/mL after treatment. Data were divided into training (708 patients), testing (271 patients), and external validation (50 patients) sets for machine learning algorithm development and validation. RSF models were used, with 1000 trees per model, optimizing predictive performance using the Harrell concordance index and Brier score. Statistical analysis used R Statistical Software (R Foundation for Statistical Computing), and ethical approval was obtained from participating institutions.

Results: Baseline characteristics of 1029 patients undergoing sRT PSMA-PET-based assessment were analyzed. The median age at sRT was 70 (IQR 64-74) years. PSMA-PET scans revealed local recurrences in 43.9% (430/979) and nodal recurrences in 27.2% (266/979) of patients. Treatment included dose-escalated sRT to pelvic lymphatics in 35.6% (349/979) of cases. The external outlier validation set showed distinct features, including higher rates of positive lymph nodes (47/50, 94% vs 266/979, 27.2% in the learning cohort) and lower delivered sRT doses (<66 Gy in 57/979, 5.8% vs 46/50, 92% of patients; P<.001). The RSF model, validated internally and externally, demonstrated robust predictive performance (Harrell C-index range: 0.54-0.91) across training and validation datasets, outperforming a previously published nomogram.

Conclusions: The developed RSF model demonstrates enhanced predictive accuracy, potentially improving patient outcomes and assisting clinicians in making treatment decisions.

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来源期刊
JMIR Cancer
JMIR Cancer ONCOLOGY-
CiteScore
4.10
自引率
0.00%
发文量
64
审稿时长
12 weeks
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