Open AccessFeasibility and reliability of evaluate PD‐L1 expression determination using small biopsy specimens in non‐small cell lung cancer
Author(s) -
Chen Minjiang,
Xu Yan,
Zhao Jing,
Li Ji,
Liu Xiangning,
Zhong Wei,
Wang Mengzhao
Publication year - 2021
Publication title -
thoracic cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.823
H-Index - 28
eISSN - 1759-7714
pISSN - 1759-7706
DOI - 10.1111/1759-7714.14075
Subject(s) - medicine , biopsy , lung cancer , immunotherapy , immunohistochemistry , stage (stratigraphy) , cancer , biomarker , oncology , radiology , pathology , paleontology , biochemistry , chemistry , biology
Abstract Background Programmed cell death ligand‐1 (PD‐L1) is a useful biomarker in non‐small cell lung cancer (NSCLC) patients who would probably benefit from immunotherapy. In most patients with advanced stage NSCLC, only small biopsy specimens were available for the evaluation of PD‐L1 expression. In this study, we evaluated the feasibility and reliability of PD‐L1 testing on small biopsy samples. Methods Small specimens of advanced NSCLC patients obtained via endobronchial ultrasound‐guided transbronchial needle aspiration (EBUS‐TBNA), endobronchial biopsy (EBB), or computed tomography (CT)‐guided core‐needle biopsy were collected. Tumor cell count and tissue sufficiency for PD‐L1 immunohistochemistry (IHC) were evaluated and compared. The clinical course of patients who received immunotherapy in the study population was also examined. Results Tissue acquisitions for PD‐L1 testing in three groups were all above 90%, with no statistically significant differences. The PD‐L1 expressions levels were concordant in most patients with more than one sample (8/11). In the EBB group, PD‐L1‐positive patients had higher objective response rate (ORR) (53.2% vs. 26.9%, p = 0.048) and longer progression‐free survival (PFS) (312 vs. 179 days, p = 0.035) than PD‐L1 negative patients. In the core needle biopsy group, patients with positive PD‐L1 expression also trended to have higher ORR and longer PFS. However, in the EBUS‐TBNA group, both ORR and PFS were similar between patients with positive or negative PD‐L1 expression. Conclusions This study showed that EBUS‐TBNA, EBB, and core needle biopsy provides adequate samples for PD‐L1 testing. The predictive value of PD‐L1 expression on different small samples still warrants further studies.