Evidence map›Paper›PMID 41428174›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2026

Folate receptor alpha in platinum-resistant ovarian cancer: prevalence in a multicenter Polish cohort and review of the evidence.

Jędrzej Borowczak, Justyna Durślewicz, Monika Durzyńska, Jakub Cheliński, Maria Filipek, Marek Zdrenka, Łukasz Szylberg

Abstract readMulticenter Study
In one paragraph

Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Jędrzej BorowczakFaculty of Medicine, Bydgoszcz University of Science and Technology, Aleje Prof. S. Kaliskiego 7, 85-796, Bydgoszcz, Poland. jedrzej.borowczak@pbs.edu.pl.ORCID http://orcid.org/0000-0001-9873-3285
Justyna DurślewiczFaculty of Medicine, Bydgoszcz University of Science and Technology, Aleje Prof. S. Kaliskiego 7, 85-796, Bydgoszcz, Poland.
Monika DurzyńskaDepartment of Pathology, Maria Sklodowska-Curie National Research Institute of Oncology, 02-781, Warsaw, Poland.
Jakub ChelińskiFaculty of Medicine, Bydgoszcz University of Science and Technology, Aleje Prof. S. Kaliskiego 7, 85-796, Bydgoszcz, Poland.
Maria FilipekFaculty of Medicine, Bydgoszcz University of Science and Technology, Aleje Prof. S. Kaliskiego 7, 85-796, Bydgoszcz, Poland.
Marek ZdrenkaDepartment of Tumor Pathology and Pathomorphology, Oncology Centre - Prof. Franciszek Łukaszczyk Memorial Hospital, 85-796, Bydgoszcz, Poland.
Łukasz SzylbergDepartment of Tumor Pathology and Pathomorphology, Oncology Centre - Prof. Franciszek Łukaszczyk Memorial Hospital, 85-796, Bydgoszcz, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFolate receptor alpha (FRα, FOLR1) is the required biomarker for mirvetuximab soravtansine, a treatment option for patients with platinum-resistant ovarian cancer. Since its approval, the drug has been introduced into national drug programs, but prevalence data from the Polish population are lacking. This study provides the first multicenter assessment of FOLR1 expression in Polish ovarian cancer in the context of treatment eligibility.

methodsWe retrospectively analyzed two institutional cohorts comprising 229 epithelial ovarian cancer cases from the Oncology Center in Bydgoszcz and the National Institute of Oncology in Warsaw. Immunohistochemistry was performed on formalin-fixed, paraffin-embedded tissue using the VENTANA FOLR1 (FOLR1-2.1) RxDx Assay on the BenchMark ULTRA platform. Membranous staining of moderate or strong intensity in ≥ 75% of viable tumor cells was considered positive, in accordance with criteria for FOLR1-targeted therapy.

resultsPositive FOLR1 expression was observed in 116 of 229 (50.7%, 95% CI 44.2-57.2) analyzed tumors, with 40% showing high expression. In most of these cases, staining intensity was moderate to strong, meeting the established threshold for therapeutic eligibility. In ~ 18% of tumors, FOLR1 expression fell into the borderline range (65-85%).

conclusionApproximately half of the ovarian cancer patients in this multicenter Polish cohort demonstrated FOLR1 positivity. Although this prevalence is lower than that reported in high-grade serous carcinoma cohorts, it likely reflects histological heterogeneity and methodological differences between studies. These findings provide the first population-based evidence from Poland and support the implementation of FOLR1 testing to guide access to mirvetuximab soravtansine. Further research integrating clinical and molecular data is warranted to validate these results and assess implications for cost-effectiveness and patient outcomes.

Indexed as

Biomarkers, TumorCarcinoma, Ovarian EpithelialDrug Resistance, NeoplasmFolate Receptor 1Ovarian NeoplasmsAdultAgedAged, 80 and overAntibodies, Monoclonal, HumanizedCohort StudiesFemaleHumansImmunoconjugatesMaytansineMiddle AgedPolandAntibodies, Monoclonal, HumanizedBiomarkers, TumorFolate Receptor 1FOLR1 protein, humanImmunoconjugatesMaytansinemirvetuximab soravtansineEpidemiologyFOLR1FRαMirvetuximabOvarian cancerPlatin-resistant

Identifiers

PMID41428174
PMCPMC13186900

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.