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An update on companion and complementary diagnostic assays for PD-1/PD-L1 checkpoint inhibitors in NSCLC
被引:5
|作者:
Jorgensen, Jan Trost
[1
]
机构:
[1] Dx Rx Inst, Med Sci, Fredensborg, Denmark
关键词:
Atezolizumab;
durvalumab;
nivolumab;
pembrolizumab;
ventana PD-L1 (SP142);
ventana PD-L1 (SP263);
PD-L1;
IHC;
28-8;
pharmDx;
22c3;
companion diagnostics;
complementary diagnostic;
CELL LUNG-CANCER;
OPEN-LABEL;
IHC ASSAY;
IMMUNOHISTOCHEMISTRY;
PEMBROLIZUMAB;
DOCETAXEL;
NIVOLUMAB;
PERSPECTIVE;
ATEZOLIZUMAB;
MULTICENTER;
D O I:
10.1080/14737159.2021.1920396
中图分类号:
R36 [病理学];
学科分类号:
100104 ;
摘要:
Introduction: Development within molecular medicine has given us an increased understanding of the pathophysiology of malignant diseases. This understanding has been the key to a development of a number of new effective target-specific drugs, including the PD-1/PD-L1 checkpoint inhibitors. Areas covered: This review will focus on the clinical validation and utility of the commercially available IHC PD-L1 expression assays linked to the different PD-1/PD-L1 checkpoint inhibitors indicated for treatment of NSCLC. For the discussion of this subject, mainly data from studies where the PD-1/PD-L1 checkpoint inhibitors have been given as monotherapy will be reported. Expert opinion: Although PD-L1 expression is not the perfect biomarker; the different IHC PD-L1 expression assays have had major impact on the clinical development of PD-1/PD-L1 checkpoint inhibitors for treatment of NSCLC. A number of clinical studies in NSCLC have shown that the efficacy of the PD-1/PD-L1 checkpoint inhibitors are positively correlated to the level of PD-L1 expression. Based on studies presented in this review, the recommendation is that monotherapy should mainly be used for treatment of NSCLC patients with a high PD-L1 expression, as defined by the cutoff values for the individual assays linked to the specific PD-1/PD-L1 checkpoint inhibitor.
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页码:445 / 454
页数:10
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