Wang Wen, Xu Xintian, Liu Hongming, Cui Yongxia, Han Qian, Yang Tingting, Tian Mengxing, Qian Yu, Jin Xin, Lei Lei
Department of Nutrition, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, Henan, China.
Department of Pharmacy, Hubei Cancer Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Oncologist. 2025 Jun 4;30(6). doi: 10.1093/oncolo/oyaf114.
Sarcopenic obesity (SO) is a prognostic factor and its impact on response to immunotherapy is still unknown in lung cancer. We aimed to explore the role of SO and body composition in predicting overall survival (OS) in patients with lung cancer receiving immune checkpoint inhibitors (ICIs).
We conducted a retrospective study involving 119 patients with lung cancer who underwent immunotherapy. The subcutaneous fat area (SFA), visceral fat area (VFA) and skeletal muscle index (SMI) were determined by the cross-sectional computed tomography at the L3 lumbar vertebral level. Sarcopenia and SO were defined by SMI and body mass index. Kaplan-Meier and Cox proportional hazard analyses were used to evaluate the impact of body composition on survival. The propensity score matching (PSM) analysis was used to reduce bias and a nomogram was created to predict the OS.
The Kaplan-Meier survival showed that patients with sarcopenia and SO had poor survival time in the total and PSM cohort. The Cox analyses revealed that sarcopenia (Hazard ratio (HR): 2.04, 95% Confidence Interval (CI): 1.04-4.01, P = 0.039) and SO (HR: 3.17, 95%CI: 1.49-6.75, P = 0.003) were independent OS predictors. SFA and VFA were not associated with OS. The SMI, age, stage, albumin level and SFA were used to develop a nomogram. Patients with high nomogram scores had worse OS (P < 0.0001).
Sarcopenia and SO are prognostic factors in patients with lung cancer receiving ICIs. A nomogram that integrates body composition is sufficiently accurate for predicting OS in patients with lung cancer receiving immunotherapy.
肌少症性肥胖(SO)是一种预后因素,其对肺癌免疫治疗反应的影响尚不清楚。我们旨在探讨SO和身体成分在预测接受免疫检查点抑制剂(ICI)治疗的肺癌患者总生存期(OS)中的作用。
我们进行了一项回顾性研究,纳入了119例接受免疫治疗的肺癌患者。通过L3腰椎水平的横断面计算机断层扫描确定皮下脂肪面积(SFA)、内脏脂肪面积(VFA)和骨骼肌指数(SMI)。根据SMI和体重指数定义肌少症和SO。采用Kaplan-Meier法和Cox比例风险分析评估身体成分对生存的影响。使用倾向评分匹配(PSM)分析减少偏差,并创建列线图来预测OS。
Kaplan-Meier生存分析显示,肌少症和SO患者在总队列和PSM队列中的生存时间较差。Cox分析显示,肌少症(风险比(HR):2.04,95%置信区间(CI):1.04-4.01,P = 0.039)和SO(HR:3.17,95%CI:1.49-6.75,P = 0.003)是独立的OS预测因素。SFA和VFA与OS无关。使用SMI、年龄、分期、白蛋白水平和SFA构建列线图。列线图评分高的患者OS较差(P < 0.0001)。
肌少症和SO是接受ICI治疗的肺癌患者的预后因素。整合身体成分的列线图在预测接受免疫治疗的肺癌患者OS方面具有足够的准确性。