Department of Medical Oncology, National Center for Tumor Diseases (NCT) Heidelberg, Heidelberg University Hospital, Im Neuenheimer Feld 460, 69120, Heidelberg, Germany.
Liquid Biobank, National Center for Tumor Diseases (NCT) Heidelberg, Heidelberg University Hospital, Heidelberg, Germany.
Cancer Immunol Immunother. 2019 Dec;68(12):2005-2014. doi: 10.1007/s00262-019-02428-3. Epub 2019 Nov 7.
Checkpoint inhibitors (CPI) have significantly changed the therapeutic landscape of oncology. We adopted a non-invasive metabolomic approach to understand immunotherapy response and failure in 28 urological cancer patients. In total, 134 metabolites were quantified in patient sera before the first, second, and third CPI doses. Modeling the association between metabolites and CPI response and patient characteristics revealed that one predictive metabolite class (n = 9/10) were very long-chain fatty acid-containing lipids (VLCFA-containing lipids). The best predictive performance was achieved through a multivariate model, including age and a centroid of VLCFA-containing lipids prior to first immunotherapy (sensitivity: 0.850, specificity: 0.825, ROC: 0.935). We hypothesize that the association of VLCFA-containing lipids with CPI response is based on enhanced peroxisome signaling in T cells, which results in a switch to fatty acid catabolism. Beyond use as a novel predictive non-invasive biomarker, we envision that nutritional supplementation with VLCFA-containing lipids might serve as an immuno sensitizer.
检查点抑制剂 (CPI) 显著改变了肿瘤学的治疗格局。我们采用非侵入性代谢组学方法来理解 28 例泌尿生殖系统癌症患者的免疫治疗反应和失败。总共在患者血清中定量了 134 种代谢物,这些患者在接受第一、第二和第三次 CPI 剂量之前接受了检测。通过对代谢物与 CPI 反应和患者特征之间的关联进行建模,发现一个具有预测性的代谢物类别(n = 9/10)是含有非常长链脂肪酸的脂质(含 VLCFA 的脂质)。通过包括年龄和免疫治疗前 VLCFA 脂质质心在内的多元模型,可以实现最佳的预测性能(敏感性:0.850,特异性:0.825,ROC:0.935)。我们假设,含 VLCFA 的脂质与 CPI 反应的关联是基于 T 细胞中过氧化物酶体信号的增强,这导致脂肪酸分解代谢的转变。除了用作新型预测性非侵入性生物标志物之外,我们设想含有 VLCFA 的脂质的营养补充可能作为一种免疫敏化剂。