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超越 PD-L1 标志物的肺癌免疫治疗。

Beyond PD-L1 Markers for Lung Cancer Immunotherapy.

机构信息

Department of Pneumonology, Oncology and Allergology, Medical University of Lublin, 20-090 Lublin, Poland.

Clinical Oncology Unit, Clinic of Clinical Oncology and Breast Diseases Polish Mother's Memorial Hospital, Research Institute, 93-338 Łódź, Poland.

出版信息

Int J Mol Sci. 2019 Apr 18;20(8):1915. doi: 10.3390/ijms20081915.

Abstract

Immunotherapy using immune checkpoints inhibitors has become the standard treatment for first and second line therapy in patients with non-small cell lung cancer (NSCLC). However, proper predictive factors allowing precise qualification of NSCLC patients for immunotherapy have not been developed so far. Expression of PD-L1 on tumor cells and tumor mutation burden are used in qualification of patients to first line therapy with pembrolizumab and atezolizumab in combination with ipilimumab in prospective clinical trials. Nevertheless, not all patients with these predictive factors benefit from immunotherapy. Major methodological difficulties in testing of these factors and in the interpretation of test results still exist. Therefore, other predictive factors are sought. Intensive research on the recognition of tumor immunophenotype and gut microbiome in NSCLC patients are underway. The first correlations between the effectiveness of immunotherapy and the intensity of inflammatory response in the tumor, microbiome diversity, and the occurrence of certain bacterial species in gut have been described. The purpose of our manuscript is to draw attention to factors affecting the efficacy of immunotherapy with anti-PD-L1 antibodies in NSCLC patients. Additional markers, for example TMB (tumor mutations burden) or microbiome profile, are needed to more accurately determine which patients will benefit from immunotherapy treatment.

摘要

免疫检查点抑制剂的免疫疗法已成为非小细胞肺癌(NSCLC)一线和二线治疗的标准治疗方法。然而,到目前为止,还没有开发出合适的预测因素来准确确定 NSCLC 患者是否适合免疫治疗。在临床试验中,肿瘤细胞 PD-L1 的表达和肿瘤突变负担用于确定患者是否适合使用 pembrolizumab 和 atezolizumab 联合 ipilimumab 进行一线治疗。然而,并非所有具有这些预测因素的患者都能从免疫治疗中获益。在这些因素的检测和测试结果的解释方面仍然存在重大的方法学困难。因此,正在寻找其他预测因素。目前正在对 NSCLC 患者的肿瘤免疫表型和肠道微生物组进行深入研究。已经描述了免疫疗法的有效性与肿瘤炎症反应强度、微生物组多样性以及肠道中某些细菌种类的发生之间的最初相关性。我们的目的是提请注意影响 NSCLC 患者抗 PD-L1 抗体免疫疗法疗效的因素。需要额外的标志物,例如 TMB(肿瘤突变负担)或微生物组特征,以更准确地确定哪些患者将从免疫治疗中受益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c75/6515086/df02b9692ff4/ijms-20-01915-g001.jpg

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