Evaluation of PD-L1 Expression in Colorectal Carcinomas by Comparing Scoring Methods and Their Significance in Relation to Clinicopathologic Parameters

Author:

Frančina Mirela12,Mikuš Mislav3ORCID,Mamić Marin12ORCID,Jovanović Tihomir24,Ćorić Mario3ORCID,Lovrić Božica15,Vukoja Ivan12,Zukanović Goran12,Matković Kristijan1,Rajc Jasmina26,Slišurić Ferdinand1,Jurić-Marelja Mateja1,Augustin Goran7ORCID,Tomaš Ilijan26ORCID

Affiliation:

1. Požega General Hospital, 34000 Požega, Croatia

2. Faculty of Medicine, University of J.J. Strossmayer, 31000 Osijek, Croatia

3. Department of Obstetrics and Gynecology, University Hospital Centre Zagreb, 10000 Zagreb, Croatia

4. General Hospital Pakrac, 34550 Pakrac, Croatia

5. Faculty of Dental Medicine and Health, University of J.J. Strossmayer, 31000 Osijek, Croatia

6. Clinical Hospital Center Osijek, 31000 Osijek, Croatia

7. Department of Surgery, University Hospital Centre Zagreb, 10000 Zagreb, Croatia

Abstract

Background: This study aims to evaluate PD-L1 expression in colorectal carcinomas (CRCs) by using the tumor proportion score (TPS) and the combined positive score (CPS), and to investigate whether there is a correlation with clinicopathologic features. Methods: A cross-sectional study was conducted that included samples from patients with colorectal adenocarcinoma treated with colon resection and rectal resection after neoadjuvant radio- and chemotherapy at the Department of Abdominal Surgery at Požega Hospital in the period from 2017 to 2022. The study included 102 tumor tissue samples from patients after resection and the pathohistological diagnosis of adenocarcinoma. Results: In our study, the PD-L1 positivity rate after the TPS was 42 (41%) samples, and after the CPS, 97 (95%) of them (p < 0.001). The positive expression of PD-L1 in tumor cells using the TPS method showed a statistically significant association with adenocarcinoma (TPS ≥ 10–50% and ≥50%). There were significantly more that were moderately differentiated, with TPS ≥ 50%, and those poorly differentiated had values ≥ 10–50%. There were significantly more patients with a status of more than one positive lymph node with TPS values ≥ 10–50%. Patients without metastases in the lymph nodes are significantly more likely to have CPS values > 50%, compared with other lymph node statuses. Conclusions: These results suggest that the total number of PD-L1-expressing cells, including tumor and immune cells, is a more sensitive biomarker than the number of PD-L1-expressing tumor cells alone in CRC.

Publisher

MDPI AG

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