Abstract

Small cell lung carcinoma (SCLC) is characterized by rapid growth and an aggressive clinical course. Standard therapy regimes have limited effects on disease course; therefore theprognosis ofSCLC is poor. In thecurrent study, thefrequency ofprogrammed death ligand 1 (PD-L1) expression in SCLC and its correlation with clinico-pathological features were evaluated. Thestudy included 100 cases ofSCLC wherein testing for PD-L1 was done with theSP263 clone on theVentana benchmark XT system. Cases with > 1% PD-L1 expression in tumour cells or immune cells were categorized as positive. PD-L1 expression was identified in 14% ofcases using thecut-off of≥ 1%. Thetumour proportion score was 10% and theimmune proportion score was 9.78% using acut-off of≥ 1%. PD-L1 positive expression was more frequent in themale population with age > 40 years. All thepatients with positive PD-L1 expression were smokers. In thePD-L1 positive group, presence ofnecrosis was identified in 71.4% ofcases and when compared with thePD-L1 negative subgroup this finding was statistically significant (p = 0.010). Personalized targeted therapy for cases ofSCLC is still under evaluation. Theuse ofimmunotherapeutic targets, such as PD-L1, may help to define anew treatment strategy for SCLC. Development ofnew treatment strategies may improve prognosis and survival.

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