首页> 美国卫生研究院文献>Journal of Thoracic Disease >18F-FDG PET/CT to predict tumor PD-L1 expression and response to PD-(L)1 blockade in patients with non-small-cell lung cancer
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18F-FDG PET/CT to predict tumor PD-L1 expression and response to PD-(L)1 blockade in patients with non-small-cell lung cancer

机译:18F-FDG PET / CT预测肿瘤PD-L1表达和对非小细胞肺癌患者的PD-(L)1阻断的反应

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摘要

Since the introduction of PD-(L)1 checkpoint inhibitor therapy for the treatment of non-small-cell lung cancer (NSCLC) there is a search for a biomarker that distinguishes responders from non-responders. A reliable biomarker has not been found yet. Tumor PD-L1 expression, assessed by immunohistochemistry (IHC) on a histological tumor sample, is at this point the most widely used and best validated biomarker. Absence of tumor PD-L1 expression predicts for a low overall response rate (ORR) of ~10%, while a tumor PD-L1 expression of ≥50% predicts for an ORR of 30% to 45% ( - ). To acquire enough tumor material in NSCLC for IHC testing and molecular analysis can be challenging. Frailty and comorbidities of patients and limited accessibility of lesions for biopsy on one hand and the increasing number of IHC and genetic tests being requested on the other hand are a constant challenge. Non-invasive techniques for tumor profiling are therefore attractive alternatives.
机译:由于引入PD-(l)1检查点抑制剂治疗非小细胞肺癌(NSCLC),因此寻找生物标志物,使响应者与非响应者区分开来。尚未找到可靠的生物标志物。通过免疫组织化学(IHC)在组织学肿瘤样品上评估的肿瘤PD-L1表达,在组织学肿瘤样品上是最广泛使用和最佳验证的生物标志物。缺乏肿瘤PD-L1表达预测〜10%的低总体反应速率(ORR),而肿瘤PD-L1表达≥50%的表达为30%至45%( - )的ORR预测。为了在NSCLC中获得足够的肿瘤材料进行IHC测试,分子分析可能具有挑战性。一方面的患者的脆弱和患者的可用性有限的活组织检查的病变,另一方面要求越来越多的IHC和遗传测试是一个不变的挑战。因此,肿瘤分析的非侵入性技术是有吸引力的替代方案。

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