Machine Learning Models Combining [68Ga]Ga-PSMA-11 PET Radiomics and Clinical Features to Predict Overall Survival for Metastatic Castration-resistant Prostate Cancer Treated with [177Lu]Lu-PSMA Radioligand Therapy.

IF 8.5 1区 医学 Q1 ONCOLOGY
Lucas Edouard, Léa Papillon, Loïc Ferrer, Yann Godbert, Marie Meyer, Vincent Prega-Renaud, Céline Subreville, Nadège Anizan, Nicolas Benziane-Ouaritini, Olivier Gallinato, Mathilde Cabart, Diego Teyssonneau, Guilhem Roubaud, Thierry Colin, Paul Schwartz
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引用次数: 0

Abstract

Purpose: Metastatic castration-resistant prostate cancer (mCRPC) remains incurable despite recent therapeutic advances. [177Lu]Lu-PSMA RLT (lutetium-177 labelled prostate-specific membrane antigen radioligand therapy) provides meaningful clinical benefit in selected patients. However, ∼30% of the patients do not respond to [177Lu]Lu-PSMA RLT. Although several baseline prognostic factors are well known, reliable pretherapeutic predictive biomarkers are still lacking. We developed and compared several predictive machine learning (ML) models integrating clinical, biochemical, and imaging data, including [68Ga]Ga-PSMA-11 PET (gallium-68 labelled prostate-specific membrane antigen ligand positron emission tomography) radiomic features, to estimate overall survival (OS) in patients with mCRPC treated with [177Lu]Lu-PSMA RLT.

Methods: This retrospective monocentric study included 102 patients with mCRPC treated with [177Lu]Lu-PSMA between January 2022 and March 2024. Five lesions per patient were segmented on their pretherapeutic [68Ga]Ga-PSMA-11 PET/computed tomography (CT) scans. Radiomic features were extracted following Image Biomarker Standardization Initiative guidelines. Multimodal ML models integrating clinical, genomic, biochemical, and imaging features (including radiomics) were developed to predict OS.

Results: Median OS of the total cohort was 11.2 mo. Intralesional homogeneity, characterized by the second-order radiomic feature normalized inverse difference moment, was associated with shorter OS (p = 0.025). The best-performing ML model achieved a 12-mo area under the curve (AUC) of 0.778 by combining 22 clinical, biochemical, genomic, and radiomic features. The model leveraging PET data alone achieved strong performance, with an AUC comparable to the clinical model (0.715 vs 0.766).

Conclusions: ML models based on [68Ga]Ga-PSMA-11 PET/CT, including radiomic features, offer a noninvasive, standardized, and widely accessible approach to predict OS in patients with mCRPC treated with [177Lu]Lu-PSMA RLT. This study highlights the strong predictive potential of PSMA PET imaging for patient stratification in a real-world setting.

结合[68Ga]Ga-PSMA-11 PET放射组学和临床特征的机器学习模型预测转移性去势抵抗性前列腺癌接受[177Lu]Lu-PSMA放射配体治疗的总生存率。
目的:转移性去势抵抗性前列腺癌(mCRPC)仍然无法治愈,尽管最近的治疗进展。[177Lu]Lu-PSMA RLT (luteium -177标记前列腺特异性膜抗原放射配体治疗)在选定的患者中提供了有意义的临床益处。然而,约30%的患者对[177Lu]Lu-PSMA RLT没有反应。虽然一些基线预后因素是众所周知的,但可靠的治疗前预测性生物标志物仍然缺乏。我们开发并比较了几种整合临床、生化和成像数据的预测机器学习(ML)模型,包括[68Ga]Ga-PSMA-11 PET(镓-68标记的前列腺特异性膜抗原配体正电子发射断层扫描)放射学特征,以估计接受[177Lu]Lu-PSMA RLT治疗的mCRPC患者的总生存率(OS)。方法:这项回顾性单中心研究纳入了2022年1月至2024年3月期间接受[177Lu]Lu-PSMA治疗的102例mCRPC患者。在治疗前[68Ga]Ga-PSMA-11 PET/计算机断层扫描(CT)上对每位患者的5个病变进行了分割。根据图像生物标志物标准化倡议指南提取放射学特征。多模态ML模型整合了临床、基因组、生化和影像学特征(包括放射组学),用于预测OS。结果:整个队列的中位生存期为11.2个月。病灶内均匀性,以二阶放射特征归一化逆差矩为特征,与较短的生存期相关(p = 0.025)。结合22个临床、生化、基因组和放射学特征,表现最好的ML模型达到了0.778的12个月曲线下面积(AUC)。仅利用PET数据的模型获得了强大的性能,AUC与临床模型相当(0.715 vs 0.766)。结论:基于[68Ga]Ga-PSMA-11 PET/CT的ML模型,包括放射学特征,为预测接受[177Lu]Lu-PSMA RLT治疗的mCRPC患者的OS提供了一种无创、标准化且可广泛获取的方法。这项研究强调了PSMA PET成像在现实世界中对患者分层的强大预测潜力。
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来源期刊
CiteScore
15.50
自引率
2.40%
发文量
128
审稿时长
20 days
期刊介绍: Journal Name: European Urology Oncology Affiliation: Official Journal of the European Association of Urology Focus: First official publication of the EAU fully devoted to the study of genitourinary malignancies Aims to deliver high-quality research Content: Includes original articles, opinion piece editorials, and invited reviews Covers clinical, basic, and translational research Publication Frequency: Six times a year in electronic format
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