Lang, C. and Lantos, A. and Megyesfalvi, Z. and Egger, F. and Hoda, M.A. and Mosleh, B. and Klikovits, T. and Oberndorfer, F. and Timelthaler, G. and Ferencz, B. and Fillinger, J. and Schwendenwein, A. and Querner, A.S. and Boettiger, K. and Renyi-Vamos, F. and Hoetzenecker, K. and Laszlo, V. and Schelch, K. and Dome, B. (2022) Clinical and prognostic implications of CD47 and PD-L1 expression in surgically resected small-cell lung cancer. ESMO OPEN, 7 (6). No.-100631. ISSN 2059-7029
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Abstract
Background: Pharmacological inhibition of the immune-checkpoint molecule CD47 has shown promising results in preclinical small-cell lung cancer (SCLC) models, whereas anti-programmed death-ligand 1 (PD-L1) inhibitors have been recently implemented in the standard of care of advanced-stage SCLC patients. Nevertheless, the expression pattern, clinical relevance and prognostic implication of both CD47 and PD-L1 are rather controversial in surgically treated SCLC patients. Materials and methods: In total, 104 Caucasian SCLC patients from two Central European thoracic centers were included in this study. CD47 and PD-L1 expression as well as the expression of the four major SCLC molecular subtype markers (ASCL1, NEUROD1, YAP1 and POU2F3) were measured by immunohistochemistry. Expression levels were independently evaluated and statistically correlated with clinicopathological data and survival. Results: Positive CD47 and PD-L1 expressions were seen in 84.6% and 9.6% of the samples, respectively. Meanwhile, the tumor-associated stroma was positive for PD-L1 in 59.6% of the cases. Stromal PD-L1 expression correlated with longer overall survival (OS) (versus PD-L1-negative stroma; median OS was 42 versus 14 months, respectively, P = 0.003) and was confirmed as an independent predictor of favorable outcome upon multivariate analysis (hazard ratio 0.530, 95% confidence interval 0.298-0.943, P = 0.031). Notably, neither CD47 nor PD-L1 presence was related to a distinct molecular SCLC subtype. Conclusion: CD47 shows a remarkably high expression while tumoral PD-L1 expression is generally low in surgically treated SCLC. Importantly, stromal PD-L1 expression may indicate a favorable clinical outcome and serve as a novel prognostic factor in these patients. Additional studies are warranted to further investigate the clinical impact of CD47 and PD-L1 expression in SCLC.
Item Type: | Article |
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Uncontrolled Keywords: | small-cell lung cancer, novel therapeutic targets, emerging prognostic factors, immune-checkpoint molecules |
Subjects: | R Medicine / orvostudomány > R1 Medicine (General) / orvostudomány általában |
Depositing User: | Dr. Zsolt Megyesfalvi |
Date Deposited: | 29 Sep 2024 04:37 |
Last Modified: | 29 Sep 2024 04:37 |
URI: | https://real.mtak.hu/id/eprint/206308 |
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