Kuker Russ A, Alderuccio Juan P, Han Sunwoo, Polar Mark K, Crane Tracy E, Moskowitz Craig H, Yang Fei
Division of Nuclear Medicine, Department of Radiology, Sylvester Comprehensive Cancer Center, University of Miami School of Medicine, Miami, FL.
Division of Hematology, Department of Medicine, Sylvester Comprehensive Cancer Center, University of Miami School of Medicine, Miami, FL.
JCO Clin Cancer Inform. 2025 Jul;9:e2500051. doi: 10.1200/CCI-25-00051. Epub 2025 Jul 16.
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.
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).
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.
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.
本研究旨在探讨在接受loncastuximab tesirine治疗的复发或难治性(rel/ref)弥漫性大B细胞淋巴瘤(DLBCL)患者的临床试验队列中,身体成分作为一种独立的影像衍生生物标志物对临床结局预测的作用。
影像队列包括在LOTIS-2(ClinicalTrials.gov标识符:NCT03589469)试验中接受loncastuximab tesirine治疗的140例rel/ref DLBCL患者的正电子发射断层扫描/计算机断层扫描。使用基于手动和深度学习的分割方法,对基线CT扫描L3水平的三个主要组织成分——骨骼肌(SM)、皮下脂肪(SF)和内脏脂肪(VF)进行身体成分分析。从这些分割的成分中,得出身体成分比率指数,包括SM*/VF*、SF*/VF和SM/(VF*+SF*)。采用Pearson相关分析来检验手动分割和自动分割之间的一致性。使用逻辑回归分析来评估得出的指数与治疗反应之间的关联。使用Cox回归分析来确定身体成分指数对事件发生时间结局的影响。身体成分指数被视为由切点定义的连续变量和二元变量。采用Kaplan-Meier方法来估计无进展生存期(PFS)和总生存期(OS)。
作为二分变量的手动和自动SM*/VF指数,在单变量和多变量逻辑模型中是未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,作为二分变量的手动SM/VF*指数与PFS显著相关,但与OS无关。
治疗前SM*/VF*身体成分指数有望成为接受loncastuximab tesirine治疗的rel/ref DLBCL患者的生物标志物。所提出的基于深度学习的身体成分分析方法表现出与手动方法相当的性能,为传统方法提供了一种更具成本效益的替代方案。