Investigation of PD-L1 Biomarker Testing Methods for PD-1 Axis Inhibition in Non-squamous Non-small Cell Lung Cancer

被引:27
|
作者
Sheffield, Brandon S. [1 ,7 ]
Fulton, Regan [2 ]
Kalloger, Steve E. [1 ]
Milne, Katy [3 ]
Geller, Georgia [4 ]
Jones, Martin [5 ]
Jacquemont, Celine [2 ]
Zachara, Susanna [1 ]
Zhao, Eric [5 ]
Pleasance, Erin [5 ]
Laskin, Janessa [4 ]
Jones, Steven J. M. [5 ]
Marra, Marco A. [5 ]
Yip, Stephen [1 ]
Nelson, Brad H. [3 ]
Gown, Allen M. [2 ]
Ho, Cheryl [4 ]
Ionescu, Diana N. [6 ]
机构
[1] Univ British Columbia, Dept Pathol & Lab Med, 910 W 10th Ave, Vancouver, BC V5Z 1M9, Canada
[2] PhenoPath Labs, Seattle, WA USA
[3] BC Canc Agcy, Trev & Joyce Deeley Res Ctr, Vancouver, BC, Canada
[4] BC Canc Agcy, Div Med Oncol, Vancouver, BC, Canada
[5] BC Canc Agcy, Canadas Michael Smith Genome Sci Ctr, Vancouver, BC, Canada
[6] BC Canc Agcy, Dept Lab Med & Pathol, Vancouver, BC, Canada
[7] Abbotsford Reg Hosp & Canc Ctr, Dept Pathol, Abbotsford, BC, Canada
关键词
biomarker; immunotherapy; lung cancer; non-small cell lung carcinoma; NSCLC; PD-1; PD-L1; LONG-TERM SAFETY; MUTATIONAL PROCESSES; EXPRESSION; NIVOLUMAB; IMMUNOHISTOCHEMISTRY; SIGNATURES; DOCETAXEL; SURVIVAL; BLOCKADE; ANTIBODY;
D O I
10.1369/0022155416665338
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Inhibitors of the programmed cell death 1 (PD-1) signaling axis have recently demonstrated efficacy and are rapidly being incorporated into the treatment of non-small cell lung cancers (NSCLCs). Despite clear benefits to certain patients, the association of these responses with a predictive biomarker remains uncertain. Several different biomarkers have been proposed, with differing results and conclusions. This study compares multiple methods of biomarker testing for treatment of NSCLCs with PD1-axis inhibitors. Tissue microarrays of matched primary and metastatic NSCLCs were used to compare four different PD-1 ligand (PD-L1) IHC techniques, as well as RNA ISH. Additional cases with whole genome and transcriptome data were assessed for molecular correlates of PD-L1 overexpression. Eighty cases were included in the IHC study. Multiple IHC methodologies showed a high rate of agreement (Kappa = 0.67). When calibrated to RNA expression, agreement improved significantly (Kappa = 0.90, p=0.0049). PD-L1 status of primary and metastatic tumors was discordant in 17 (22%) cases. This study suggests that different IHC methodologies for PD-L1 assessment provide slightly different results. There is significant discordance between the PD-L1 status of primary tumors and lymph node metastases. RNA ISH may be a useful adjunct to complement PD-L1 IHC testing.
引用
收藏
页码:587 / 600
页数:14
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