Evidence map›Paper›PMID 42634178›Full record

ArticleCancer medicine2026

Prognostic Impact of PD-L1 Expression in Ovarian Cancer: Analysis of a Real-World Cohort Treated With Primary Platinum-Based Chemotherapy.

Jitka Hausnerova, Petra Ovesna, Lucie Ehrlichova, Michal Felsinger, Monika Nalezinska, Kvetoslava Matulova, Lubos Minar, Leos Kren, Ondrej Slaby, Vit Weinberger and 1 more

Abstract read
In one paragraph

Article in Cancer medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Jitka HausnerovaDepartment of Pathology, University Hospital Brno and Faculty of Medicine, Masaryk University Brno, Brno, Czech Republic.
Petra OvesnaInstitute of Biostatistics and Analyses, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Lucie EhrlichovaDepartment of Internal Medicine, Hematology and Oncology, University Hospital Brno and Faculty of Medicine, Masaryk University Brno, Brno, Czech Republic.
Michal FelsingerDepartment of Obstetrics and Gynecology, University Hospital Brno and Faculty of Medicine, Masaryk University Brno, Brno, Czech Republic.
Monika NalezinskaDepartment of Gynecologic Oncology, Department of Surgical Oncology, Masaryk Memorial Cancer Institute and Medical Faculty of Masaryk University, Brno, Czech Republic.
Kvetoslava MatulovaDepartment of Pathology, University Hospital Brno and Faculty of Medicine, Masaryk University Brno, Brno, Czech Republic.
Lubos MinarDepartment of Obstetrics and Gynecology, University Hospital Brno and Faculty of Medicine, Masaryk University Brno, Brno, Czech Republic.
Leos KrenDepartment of Pathology, University Hospital Brno and Faculty of Medicine, Masaryk University Brno, Brno, Czech Republic.
Ondrej SlabyDepartment of Biology, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Vit WeinbergerDepartment of Obstetrics and Gynecology, University Hospital Brno and Faculty of Medicine, Masaryk University Brno, Brno, Czech Republic.
Marketa BednarikovaDepartment of Internal Medicine, Hematology and Oncology, University Hospital Brno and Faculty of Medicine, Masaryk University Brno, Brno, Czech Republic.ORCID https://orcid.org/0000-0003-3189-7028

Funding

Ministry of Health of the Czech Republic NU21-03-00306
6 · The paper itself

Abstract

backgroundProgrammed death-ligand 1 (PD-L1) has emerged as a potential biomarker for prognosis and treatment response in various solid tumors. However, its clinical relevance in ovarian carcinoma (OC) remains unclear, with published studies reporting inconsistent associations with platinum sensitivity and survival. These discrepancies are likely related to the biological heterogeneity of OC and methodological variability in PD-L1 evaluation. In the absence of a standardized, OC-specific assessment methodology, the Combined Positive Score (CPS) with cutoffs of ≥ 1 and ≥ 10, applied in other tumor types, represents a pragmatic approach.

methodsWe retrospectively analyzed a real-world cohort of 146 patients with ovarian carcinoma treated with primary platinum-based chemotherapy at University Hospital Brno between 2010 and 2020. PD-L1 expression was assessed using the 22C3 antibody and CPS methodology on archival, treatment-naive tumor samples obtained from primary tumors or metastatic lesions. Associations between PD-L1 status, platinum treatment-free interval (TFIp), and disease-specific survival (DSS) were evaluated, including subgroup analyses by histological subtypes.

resultsAmong the 144 evaluable cases, 65 patients (45%) demonstrated positive PD-L1 expression (CPS ≥ 1), while 35 patients (24%) exhibited strong positive expression (CPS ≥ 10). In the high-grade serous carcinoma (HGSC) subgroup, CPS ≥ 1 and CPS ≥ 10 were detected in 58/121 (48%) and 30/121 (25%) cases, respectively. PD-L1 positivity did not differ significantly between HGSC and non-HGSC subtypes or between primary and metastatic lesions. PD-L1 positivity defined as CPS ≥ 10 was significantly associated with platinum sensitivity (TFIp ≥ 6 months; p = 0.035 overall; p = 0.028 in HGSC) and longer DSS (p = 0.029). No associations were observed when PD-L1 positivity was defined using a CPS ≥ 1 cutoff.

conclusionsPD-L1 expression assessed by CPS, particularly at a cutoff of ≥ 10, may have prognostic relevance in ovarian cancer and could help identify patients more likely to benefit from platinum-based chemotherapy. Prospective validation is warranted.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsB7-H1 AntigenBiomarkers, TumorOvarian NeoplasmsAdultAgedAged, 80 and overFemaleHumansMiddle AgedPrognosisRetrospective StudiesB7-H1 AntigenBiomarkers, TumorCD274 protein, humancombined positive score (CPS)high‐grade serous carcinomaovarian cancerPD‐L1platinum‐based chemotherapyprognostic biomarkerreal‐world data

Identifiers

PMID42634178
PMCPMC13500898

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