PD‐L1 expression in resected lung adenocarcinoma: prevalence and prognostic significance in relation to the IASLC grading system

Author:

Hwang Soohyun1ORCID,Hong Tae Hee23ORCID,Kim Hong Kwan345,Cho Juhee456,Lee Genehee45,Choi Sangjoon1,Park Sehhoon7,Lee Se‐Hoon7,Lee Yoonseo3,Jeon Yeong Jeong3,Lee Junghee3,Park Seong Yong3,Cho Jong Ho3,Choi Yong Soo3,Kim Jhingook3,Zo Jae Il3,Shim Young Mog3,Choi Yoon‐La1

Affiliation:

1. Department of Pathology and Translational Genomics Sungkyunkwan University School of Medicine, Samsung Medical Center Seoul Korea

2. Department of Digital Health, SAIHST Sungkyunkwan University Seoul Korea

3. Department of Thoracic and Cardiovascular Surgery Sungkyunkwan University School of Medicine, Samsung Medical Center Seoul Korea

4. Samsung Medical Center Patient‐Centered Outcomes Research Institute Seoul Korea

5. Department of Clinical Research Design and Evaluation, SAIHST Sungkyunkwan University Seoul Korea

6. Center for Clinical Epidemiology, Samsung Medical Center Future Medicine Institute Seoul Korea

7. Division of Hematology‐Oncology, Department of Medicine, Samsung Medical Center Sungkyunkwan University School of Medicine Seoul Korea

Abstract

AimsProgrammed death‐ligand 1 (PD‐L1) expression is a predictive biomarker for adjuvant immunotherapy and has been linked to poor differentiation in lung adenocarcinoma. However, its prevalence and prognostic role in the context of the novel histologic grade has not been evaluated.MethodsWe analysed a cohort of 1233 patients with resected lung adenocarcinoma where PD‐L1 immunohistochemistry (22C3 assay) was reflexively tested. Tumour PD‐L1 expression was correlated with the new standardized International Association for the Study of Lung Cancer (IASLC) histologic grading system (G1, G2, and G3). Clinicopathologic features including patient outcome were analysed.ResultsPD‐L1 was positive (≥1%) in 7.0%, 23.5%, and 63.0% of G1, G2, and G3 tumours, respectively. PD‐L1 positivity was significantly associated with male sex, smoking, and less sublobar resection among patients with G2 tumours, but this association was less pronounced in those with G3 tumours. PD‐L1 was an independent risk factor for recurrence (adjusted hazard ratio [HR] = 3.25, 95% confidence intervals [CI] = 1.93–5.48, P < 0.001) and death (adjusted HR = 2.69, 95% CI = 1.13–6.40, P = 0.026) in the G2 group, but not in the G3 group (adjusted HR for recurrence = 0.94, 95% CI = 0.64–1.40, P = 0.778).ConclusionPD‐L1 expression differs substantially across IASLC grades and identifies aggressive tumours within the G2 subgroup. This knowledge may be used for both prognostication and designing future studies on adjuvant immunotherapy.

Publisher

Wiley

Subject

General Medicine,Histology,Pathology and Forensic Medicine

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