Reanalysis of the NCCN PD-L1 companion diagnostic assay study for lung cancer in the context of PD-L1 expression findings in triple-negative breast cancer

被引:24
|
作者
Rimm, David L. [1 ,10 ]
Han, Gang [2 ]
Taube, Janis M. [3 ]
Yi, Eunhee S. [4 ]
Bridge, Julia A. [5 ]
Flieder, Douglas B. [6 ]
Homer, Robert [1 ,7 ]
Roden, Anja C. [4 ]
Hirsch, Fred R. [8 ]
Wistuba, Ignacio I. [9 ]
Pusztai, Lajos [1 ]
机构
[1] Yale Univ, Sch Med, New Haven, CT 06520 USA
[2] Texas A&M, College Stn, TX USA
[3] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[4] Mayo Clin, Rochester, MN USA
[5] Univ Nebraska Med Ctr, Omaha, NE USA
[6] Fox Chase Canc Ctr, 7701 Burholme Ave, Philadelphia, PA 19111 USA
[7] VA Connecticut HealthCare Syst, West Haven, CT USA
[8] Univ Colorado, Anschutz Med Campus, Aurora, CO USA
[9] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[10] Yale Univ, Sch Med, Yale Pathol Tissue Serv, Dept Pathol, 310 Cedar St BML 116,POB 208023, New Haven, CT 06520 USA
关键词
Non-small cell lung cancer; PD-L1; Immunohistochemistry; Triple-negative breast cancer; Atezolizumab;
D O I
10.1186/s13058-019-1156-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The companion diagnostic test for checkpoint inhibitor immune therapy is an immunohistochemical test for PD-L1. The test has been shown to be reproducible for expression in tumor cells, but not in immune cells. Immune cells were used in the IMpassion130 trial which showed PD-L1 expression was associated with a better outcome. Two large studies have been done assessing immune cell PD-L1 expression in lung cancer. Here, we reanalyze one of those studies, to show that, even with an easier scoring method, there is still only poor agreement between assays and pathologist for immune cell PD-L1 expression.
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页数:3
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