Clinical Medicine III. Lectures
Dr. Megyesfalvi, Zsolt
Department of Thoracic Surgery, Semmelweis University and National Institute of Oncology, Budapest
+36204243934
megyesfalvi.zsolt@semmelweis-univ.hu
Elevated PD-L1 Protein Expression Predicts Poor Survival Outcomes in Patients with Malignant Pleural Mesothelioma: An International Multicenter Study
Zsolt Megyesfalvi1,2,3; Thomas Klikovits3; Luka Brcic4; Marko Jakopovic5; Izidor Kern6; Katja Mohorcic6; Swen Seiwerth7; Mirjana Rajer6; Walter Klepetko3; Balázs Hegedüs8; Ferenc Rényi-Vámos1,9; Viktória László2,3; Mir Alireza Hoda3; Martin Filipits10; Balázs Döme1,2,3
1- Department of Thoracic Surgery, Semmelweis University and National Institute of Oncology, Budapest, Hungary
2- Department of Tumor Biology, National Korányi Institute of Pulmonology, Budapest, Hungary
3- Division of Thoracic Surgery, Department of Surgery, Comprehensive Cancer Center, Medical University of Vienna, Austria
4- Institute of Pathology, Medical University of Graz, Graz, Austria
5- University of Zagreb School of Medicine, Department for Respiratory Diseases Jordanovac, University Hospital Center Zagreb, Croatia
6- Department of Pathology, University Clinic Golnik, Golnik, Slovenia
7- Departments of Pharmacology and Pathology, Medical Faculty University of Zagreb, Croatia
8- Translational Laboratory, Department of Thoracic Surgery, Ruhrlandklinik, University Clinic Essen, Essen, Germany
9- Department of Thoracic Surgery, National Korányi Institute of Pulmonology, Budapest, Hungary
10- Institute of Cancer Research and Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria
Clinical Medicine III. Lectures
English
Pathology and Oncology
Clinical Medicine
Introduction: The PD-1/PD-L1 immune-checkpoint blockade is a promising new therapeutic strategy in cancer patients, yet the expression pattern and prognostic significance of both PD-L1 and PD-1 are still partly controversial in human malignant pleural mesothelioma (MPM).
Aims: Our study aimed to investigate the expression of PD-L1/PD-1 in the tumor samples of MPM patients and to analyze potential correlations with clinicopathological parameters.
Method: Diagnostic biopsies of 203 MPM patients were collected from five Central European centers. The formalin-fixed paraffin-embedded samples were evaluated for PD-L1 and PD-1 expression on tumor cells and tumor-infiltrating lymphocytes by immunohistochemistry, and their prognostic significance was examined. To assess the PD-L1 and PD-1 expression pattern threshold value of 10% was used regardless of intensity.
Results: High (>10%) tumor cell PD-L1 expression was found in 8% of samples and high (>10%) tumor-infiltrating lymphocyte PD-1 expression in 24%. No significant associations were found between PD-L1/PD-1 expression and clinicopathological variables (patients’ age, gender, histological subtype, stage and treatment modality). As for their prognostic relevance, the median overall survival time of patients with high (>10%) PD-L1 expression on tumor cells was significantly shorter compared to those with lower PD-L1 expression (6.2 vs. 15.1 months, respectively; p<0.001). Notably, high PD-L1 expression (>10%) proved to be an independent prognostic factor in the multivariate Cox regression analysis as well regardless of histology (hazard ratio HR] 2.711; 95% confidence interval [CI] 1.201 to 6.118; p=0.016). No significant difference was found in overall survival regarding PD-1 expression (p=0.481).
Conclusion: The results of this multicenter study demonstrate that high (>10%) PD-L1 expression on tumor cells is an independent prognostic factor for worse survival outcomes in MPM. Furthermore, this is the first report comprehensively evaluating the expression and prognostic value of PD-1 on tumor-infiltrating lymphocytes.
Supervisor: Balázs Döme;
E-mail address: balazs.dome@meduniwien.ac.at.
Szóbeli
Szabad
elfogadva
szóbeli
nem rendelkezett róla
4071
11:40
11:55
Zsolt Megyesfalvi1,2,3; Thomas Klikovits3; Luka Brcic4; Marko Jakopovic5; Izidor Kern6; Katja Mohorcic6; Swen Seiwerth7; Mirjana Rajer6; Walter Klepetko3; Balázs Hegedüs8; Ferenc Rényi-Vámos1,9; Viktória László2,3; Mir Alireza Hoda3; Martin Filipits10; Balázs Döme1,2,3
1- Department of Thoracic Surgery, Semmelweis University and National Institute of Oncology, Budapest, Hungary
2- Department of Tumor Biology, National Korányi Institute of Pulmonology, Budapest, Hungary
3- Division of Thoracic Surgery, Department of Surgery, Comprehensive Cancer Center, Medical University of Vienna, Austria
4- Institute of Pathology, Medical University of Graz, Graz, Austria
5- University of Zagreb School of Medicine, Department for Respiratory Diseases Jordanovac, University Hospital Center Zagreb, Croatia
6- Department of Pathology, University Clinic Golnik, Golnik, Slovenia
7- Departments of Pharmacology and Pathology, Medical Faculty University of Zagreb, Croatia
8- Translational Laboratory, Department of Thoracic Surgery, Ruhrlandklinik, University Clinic Essen, Essen, Germany
9- Department of Thoracic Surgery, National Korányi Institute of Pulmonology, Budapest, Hungary
10- Institute of Cancer Research and Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria