Comparison of programmed death-ligand 1 protein expression between primary and metastatic lesions in patients with lung cancer
Autor: | Myrto Moutafi, James Haberberger, Brian M. Alexander, Wei Wei, Weiwei Tao, David L. Rimm, Konstantinos N. Syrigos, Richard S.P. Huang, Ioannis A. Vathiotis, Jeffrey S. Ross, Lajos Pusztai, Shakti H. Ramkissoon |
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Rok vydání: | 2021 |
Předmět: |
Adult
Male Cancer Research medicine.medical_specialty tumor Lung Neoplasms medicine.medical_treatment Immunology Context (language use) Gastroenterology B7-H1 Antigen programmed cell death 1 receptor Young Adult Internal medicine Carcinoma Non-Small-Cell Lung Immunotherapy Biomarkers medicine Biomarkers Tumor Immunology and Allergy Humans Lung cancer RC254-282 Aged Retrospective Studies Pharmacology Aged 80 and over business.industry Neoplasms. Tumors. Oncology. Including cancer and carcinogens Soft tissue biomarkers Retrospective cohort study Histology Immunotherapy Middle Aged medicine.disease Immunohistochemistry Oncology Molecular Medicine Female Lymph immunotherapy business |
Zdroj: | Journal for Immunotherapy of Cancer Journal for ImmunoTherapy of Cancer, Vol 9, Iss 4 (2021) |
ISSN: | 2051-1426 |
Popis: | Assessment of programmed cell death-ligand 1 (PD-L1) expression by immunohistochemistry (IHC) is the definite diagnostic test to guide treatment for patients with advanced-stage non-small cell lung cancer. Intratumoral heterogeneity and discrepancy of PD-L1 expression between primary and metastatic lesions may increase the risk of tumor misclassification. We performed a retrospective study of the Foundation Medicine, Inc clinical database on lung cancer cases that were evaluated for PD-L1 expression by IHC in the context of routine care. All cases were assessed with the Food and Drug Administration-approved 22C3 pharmDx assay and scoring system. 15,028 lung cancer cases, including 8285 primary tumors and 6743 unmatched metastatic lesions were analyzed. Metastatic lesions (mets) were more frequently high positive (tumor proportion score (TPS) ≥50%) for PD-L1 expression than primary lesions (33.8% vs 28.4%; OR, 1.28; 95% CI, 1.19 to 1.37; p |
Databáze: | OpenAIRE |
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