Deep Learning-Based Body Composition Analysis for Outcome Prediction in Relapsed/Refractory Diffuse Large B-Cell Lymphoma: Insights From the LOTIS-2 Trial.

IF 2.8 Q2 ONCOLOGY
JCO Clinical Cancer Informatics Pub Date : 2025-07-01 Epub Date: 2025-07-16 DOI:10.1200/CCI-25-00051
Russ A Kuker, Juan P Alderuccio, Sunwoo Han, Mark K Polar, Tracy E Crane, Craig H Moskowitz, Fei Yang
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Abstract

Purpose: The present study aimed to investigate the role of body composition as an independent image-derived biomarker for clinical outcome prediction in a clinical trial cohort of patients with relapsed or refractory (rel/ref) diffuse large B-cell lymphoma (DLBCL) treated with loncastuximab tesirine.

Materials and methods: The imaging cohort consisted of positron emission tomography/computed tomography scans of 140 patients with rel/ref DLBCL treated with loncastuximab tesirine in the LOTIS-2 (ClinicalTrials.gov identifier: NCT03589469) trial. Body composition analysis was conducted using both manual and deep learning-based segmentation of three primary tissue compartments-skeletal muscle (SM), subcutaneous fat (SF), and visceral fat (VF)-at the L3 level from baseline CT scans. From these segmented compartments, body composition ratio indices, including SM*/VF*, SF*/VF*, and SM*/(VF*+SF*), were derived. Pearson's correlation analysis was used to examine the agreement between manual and automated segmentation. Logistic regression analyses were used to assess the association between the derived indices and treatment response. Cox regression analyses were used to determine the effect of body composition indices on time-to-event outcomes. Body composition indices were considered as continuous and binary variables defined by cut points. The Kaplan-Meier method was used to estimate progression-free survival (PFS) and overall survival (OS).

Results: The manual and automated SM*/VF* indices, as dichotomized, were significant predictors in univariable and multivariable logistic models for failure to achieve complete metabolic response. The manual SM*/VF* index as dichotomized was significantly associated with PFS, but not OS, in univariable and multivariable Cox models.

Conclusion: The pretreatment SM*/VF* body composition index shows promise as a biomarker for patients with rel/ref DLBCL undergoing treatment with loncastuximab tesirine. The proposed deep learning-based approach for body composition analysis demonstrated comparable performance to the manual process, presenting a more cost-effective alternative to conventional methods.

基于深度学习的体成分分析用于复发/难治性弥漫性大b细胞淋巴瘤的预后预测:来自LOTIS-2试验的见解
目的:本研究旨在探讨身体成分作为一种独立的图像衍生生物标志物,在一组接受loncastuximab tesirine治疗的复发或难治性(rel/ref)弥漫性大b细胞淋巴瘤(DLBCL)患者的临床试验中预测临床结局的作用。材料和方法:在LOTIS-2 (ClinicalTrials.gov识别码:NCT03589469)试验中,成像队列包括140例使用loncastuximab tesirine治疗的rel/ref DLBCL患者的正电子发射断层扫描/计算机断层扫描。在基线CT扫描的L3水平,使用手动和基于深度学习的三个主要组织区室-骨骼肌(SM),皮下脂肪(SF)和内脏脂肪(VF)进行身体成分分析。从这些分割的隔室中,导出了SM*/VF*、SF*/VF*和SM*/(VF*+SF*)等体成分比指标。使用Pearson相关分析来检验人工和自动分割之间的一致性。采用Logistic回归分析来评估衍生指标与治疗反应之间的相关性。采用Cox回归分析确定身体成分指数对事件发生时间结局的影响。身体成分指数被认为是连续的二元变量,由切点定义。Kaplan-Meier法用于估计无进展生存期(PFS)和总生存期(OS)。结果:在单变量和多变量logistic模型中,手动和自动SM*/VF*指标作为二分类,是未能实现完全代谢反应的显著预测因子。在单变量和多变量Cox模型中,手工SM*/VF*指数与PFS显著相关,但与OS无关。结论:预处理SM*/VF*体成分指数有望作为rel/ref DLBCL患者接受loncastuximab tesirine治疗的生物标志物。所提出的基于深度学习的身体成分分析方法显示出与手动过程相当的性能,提供了一种比传统方法更具成本效益的替代方法。
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来源期刊
CiteScore
6.20
自引率
4.80%
发文量
190
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