Evidence map›Paper›PMID 40784918›Full record

ArticleJournal of cancer research and clinical oncology2025

Targeted therapies in primary vaginal cancer.

Laura Tascón Padrón, Carolin Schröder, Milka Marinova, Thore Thiesler, Luzia A Otten, Glen Kristiansen, Alexander Mustea, Eva K Egger

Abstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2025. 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

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Laura Tascón PadrónDepartment of Gynecology and Gynecologic Oncology, University Hospital of Bonn, Bonn, Germany.
Carolin SchröderDepartment of Gynecology and Gynecologic Oncology, University Hospital of Bonn, Bonn, Germany.
Milka MarinovaDepartment of Nuclear Medicine, University Hospital Bonn, Bonn, Germany.
Thore ThieslerDepartment of pathology, University Hospital Bonn, Bonn, Germany.
Luzia A OttenDepartment of Gynecology and Gynecologic Oncology, University Hospital of Bonn, Bonn, Germany.
Glen KristiansenDepartment of pathology, University Hospital Bonn, Bonn, Germany.
Alexander MusteaDepartment of Gynecology and Gynecologic Oncology, University Hospital of Bonn, Bonn, Germany.
Eva K EggerDepartment of Gynecology and Gynecologic Oncology, University Hospital of Bonn, Bonn, Germany. eva-katharina.egger@ukbonn.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivePrimary vaginal cancer (PVC) accounts for 1–2% of all gynecological malignancies. Therefore, clinical trials lack and there is a paucity of approved medications beyond radiation or chemoradiation as main first line therapy. The GOG 240 and the Keynote 826 have shown significant improvements in survival in cervical cancer patients. Both concepts are approved medications for the treatment of advanced, recurrent or metastastic cervical cancer. However, the efficacy of Bevacizumab and Pembrolizumab and other Immunotherapies in PVC is mainly unknown. This study evaluates the efficacy and potential of targeted therapies and immunotherapies in patients with metastatic primary vaginal cancer, based on therapeutic strategies established for cervical cancer.

methodsIn this retrospective study, 6 patients with metastatic PVC were treated with Carboplatin/Paclitaxel/Bevacizumab with or without Pembrolizumab. Due to Her2neu expression one patient was treated with Her2neu targeted therapy and one patient is on Nivolumab at present.

results4 patients received Bevacizumab (Bev) in addition to Carboplatin (C) and Paclitaxel (Pac). Duration of response was 6 and 13 month and one patient is still on Bev. One patient progressed after 5 cycles of C/P/Bev. 2 Patients were treated with Pembrolizumab (P) mono after C/Pac/Bev. One out of 2 patients showed a duration of response of 36 month despite late stage metastatic disease. Local progress was controlled by adjunct local radiation therapy. The other patient progressed and died. Two patients were treated with C/Pac/Bev/P. One patient is still on therapy and one patient has died due to progressive disease. One patient is on Nivolumab with good response.

conclusionThese data provide a proof of concept to adopt therapeutic modalities from cervical cancer patients in PVC patients. In addition, our findings underscore the importance of collecting real-world data to guide clinical decision-making in metastatic primary vaginal cancer.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsMolecular Targeted TherapyVaginal NeoplasmsAgedAntibodies, Monoclonal, HumanizedBevacizumabCarboplatinFemaleHumansMiddle AgedPaclitaxelRetrospective StudiesAntibodies, Monoclonal, HumanizedBevacizumabCarboplatinPaclitaxelpembrolizumabBevacizumabHPVPembrolizumabPrimary vaginal cancer

Identifiers

PMID40784918
PMCPMC12336100

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