Development and validation of a computed tomography–based immune ecosystem diversity index as an imaging biomarker in non-small cell lung cancer

医学 危险系数 成像生物标志物 生物标志物 肺癌 肿瘤科 内科学 神经组阅片室 队列 比例危险模型 免疫系统 置信区间 放射科 免疫学 生物 磁共振成像 神经学 生物化学 精神科
作者
Lan He,Zhenhui Li,Li‐Xu Yan,Xin Chen,Sebastian Sanduleanu,Wen‐Zhao Zhong,Philippe Lambin,Zhaoxiang Ye,Yingshi Sun,Yulin Liu,Jinrong Qu,Lin Wu,Changling Tu,Madeleine Scrivener,Thierry Pieters,Emmanuel Coche,Qian Yang,Mei Yang,Changhong Liang,Yanqi Huang,Zaiyi Liu
出处
期刊:European Radiology [Springer Science+Business Media]
卷期号:32 (12): 8726-8736 被引量:2
标识
DOI:10.1007/s00330-022-08873-6
摘要

To date, there are no data on the noninvasive surrogate of intratumoural immune status that could be prognostic of survival outcomes in non-small cell lung cancer (NSCLC). We aimed to develop and validate the immune ecosystem diversity index (iEDI), an imaging biomarker, to indicate the intratumoural immune status in NSCLC. We further investigated the clinical relevance of the biomarker for survival prediction.In this retrospective study, two independent NSCLC cohorts (Resec1, n = 149; Resec2, n = 97) were included to develop and validate the iEDI to classify the intratumoural immune status. Paraffin-embedded resected specimens in Resec1 and Resec2 were stained by immunohistochemistry, and the density percentiles of CD3+, CD4+, and CD8+ T cells to all cells were quantified to estimate intratumoural immune status. Then, EDI features were extracted using preoperative computed tomography to develop an imaging biomarker, called iEDI, to determine the immune status. The prognostic value of iEDI was investigated on NSCLC patients receiving surgical resection (Resec1; Resec2; internal cohort Resec3, n = 419; external cohort Resec4, n = 96; and TCIA cohort Resec5, n = 55).iEDI successfully classified immune status in Resec1 (AUC 0.771, 95% confidence interval [CI] 0.759-0.783; and 0.770 through internal validation) and Resec2 (0.669, 0.647-0.691). Patients with higher iEDI-score had longer overall survival (OS) in Resec3 (unadjusted hazard ratio 0.335, 95%CI 0.206-0.546, p < 0.001), Resec4 (0.199, 0.040-1.000, p < 0.001), and TCIA (0.303, 0.098-0.944, p = 0.001).iEDI is a non-invasive surrogate of intratumoural immune status and prognostic of OS for NSCLC patients receiving surgical resection.• Decoding tumour immune microenvironment enables advanced biomarkers identification. • Immune ecosystem diversity index characterises intratumoural immune status noninvasively. • Immune ecosystem diversity index is prognostic for NSCLC patients.
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