Zheng Hui, Pan Qin, Zhu Wenchao, Li Hongsen, Niu Zhongfeng, Fang Yong, Li Da, Lou Haizhou, Hu Hong, Shou Jiawei, Pan Hongming
Department of Medical Oncology, Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
Department of Radiology, Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
Front Oncol. 2021 Mar 8;11:628693. doi: 10.3389/fonc.2021.628693. eCollection 2021.
Previous studies have indicated that the changes in body composition during treatment are prognostic in lung cancer. The question which follows is it may be too late to identify vulnerable patients after treatment and to improve outcomes for these patients. In our study, we sought to explore the alterations of body composition and weight before the outset of the antiangiogenic treatment and its role in predicting clinical response and outcomes.
In this retrospective study, 122 patients with advanced lung cancer treated with anlotinib or apatinib were analyzed. The changes in weight and body composition including skeletal muscle index (SMI), subcutaneous adipose tissue (SAT), and visceral adipose tissue (VAT) for 3 months before the outset of antiangiogenic treatment and other clinical characteristics were evaluated with LASSO Cox regression and multivariate Cox regression analysis, which were applied to construct nomograms. The performance of the nomograms was validated internally by using bootstrap method with 1,000 resamples models and was assessed by the concordance index (C-index), calibration plots, decision curve analysis (DCA).
The median progression-free survival (PFS) and overall survival (OS) were 128 (95% CI 103.2-152.8) days and 292 (95% CI 270.9-313.1) days. Eastern Cooperative Oncology Group performance status (ECOG PS), brain metastases, the Glasgow Prognostic Score (GPS), clinical response, therapeutic regimen, and ΔL1SMI per 90 days were significantly associated with PFS, while ECOG PS, GPS, clinical response, therapeutic regimen, ΔL1SMI per 90 days were identified for OS. The C-index for the nomograms of PFS and OS were 0.763 and 0.748, respectively. The calibration curves indicated excellent agreement between the predicted and actual survival outcomes of 3- and 4-month PFS and 7- and 8-month OS. DCA showed the considerable value of the model.
Nomograms were developed from clinical features and nutritional indicators to predict the probability of achieving 3-month and 4-month PFS and 7-month and 8-month OS with antiangiogenic therapy for advanced lung cancer. Dynamic changes in body composition before the initiation of treatment contributed to early detection of poor outcome.
既往研究表明,治疗期间身体成分的变化对肺癌具有预后意义。随之而来的问题是,在治疗后识别易损患者并改善这些患者的预后可能为时已晚。在我们的研究中,我们试图探讨抗血管生成治疗开始前身体成分和体重的变化及其在预测临床反应和预后中的作用。
在这项回顾性研究中,分析了122例接受安罗替尼或阿帕替尼治疗的晚期肺癌患者。采用LASSO Cox回归和多因素Cox回归分析评估抗血管生成治疗开始前3个月的体重和身体成分变化,包括骨骼肌指数(SMI)、皮下脂肪组织(SAT)和内脏脂肪组织(VAT)以及其他临床特征,并应用这些分析构建列线图。通过使用1000次重采样模型的自助法对列线图的性能进行内部验证,并通过一致性指数(C指数)、校准图、决策曲线分析(DCA)进行评估。
中位无进展生存期(PFS)和总生存期(OS)分别为128天(95%CI 103.2 - 152.8)和292天(95%CI 270.9 - 313.1)。东部肿瘤协作组体能状态(ECOG PS)、脑转移、格拉斯哥预后评分(GPS)、临床反应、治疗方案以及每90天的ΔL1SMI与PFS显著相关,而ECOG PS、GPS、临床反应、治疗方案以及每90天的ΔL1SMI与OS相关。PFS和OS列线图的C指数分别为0.763和0.748。校准曲线表明3个月和4个月PFS以及7个月和8个月OS的预测生存结果与实际生存结果之间具有良好的一致性。DCA显示该模型具有相当大的价值。
根据临床特征和营养指标开发了列线图,以预测晚期肺癌抗血管生成治疗实现3个月和4个月PFS以及7个月和8个月OS的概率。治疗开始前身体成分的动态变化有助于早期发现不良预后。