Clinicopathologic correlation of programmed death ligand-1 expression in non-small cell lung carcinomas: A report from India

Increased expression of Programmed death ligand-1 (PD-L1) on cancer cells and immune cells predict response to PD-1/PDL1 inhibitors. Data regarding frequency and pattern of PD-L1 expression in NSCLC from India is not available. To analyse PD-L1 expression on tumour cells (TC) and immune cells (IC) a...

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Veröffentlicht in:Annals of diagnostic pathology 2017-12, Vol.31, p.56-61
Hauptverfasser: Vallonthaiel, Archana George, Malik, Prabhat Singh, Singh, Varsha, Kumar, Vinay, Kumar, Sunil, Sharma, Mehar Chand, Mathur, Sandeep, Arava, Sudheer, Guleria, Randeep, Jain, Deepali
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Sprache:eng
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Zusammenfassung:Increased expression of Programmed death ligand-1 (PD-L1) on cancer cells and immune cells predict response to PD-1/PDL1 inhibitors. Data regarding frequency and pattern of PD-L1 expression in NSCLC from India is not available. To analyse PD-L1 expression on tumour cells (TC) and immune cells (IC) and to correlate PD-L1 expression with baseline clinico-pathological characteristics, oncogenic drivers and outcome data. PD-L1 expression on tumour cells and immune cells was analysed. Eighty-nine cases of resected NSCLC were included. Squamous cell carcinoma was more common than adenocarcinoma. IC were present in almost all cases. Immunopositivity for PD-L1 in TC and IC was 27% and 18% respectively. PD-L1 immunopositivity in TC or IC did not correlate with age, sex, stage or mutation status however sarcomatoid carcinoma and solid predominant adenocarcinomas showed higher positivity rates. PD-L1 immunopositivity in ICs was found to correlate with better disease free survival. PD-L1 immunopositivity was seen in a quarter of NSCLC patients in India. PDL1 positivity on immune cells may be associated with better prognosis in resected NSCLC. However the prognostic value of PD-L1 and clinical response to check point inhibitors in Indian population need to be validated in larger studies.
ISSN:1092-9134
1532-8198
DOI:10.1016/j.anndiagpath.2017.07.001