# Case Report: Could genetic factors influence the outcomes of first-line enfortumab vedotin plus pembrolizumab therapy in patients with metastatic urothelial carcinoma? Two cases of patients harbouring a BRCA mutation

**Authors:** Giuseppe Salfi, Chiara Maria Agrippina Clerici, Giovanna Pecoraro, Martino Pedrani, Marialuisa Puglisi, Luigi Tortola, Ricardo Pereira Mestre, Ursula Vogl, Ilaria Colombo, Jessica Barizzi, Milo Frattini, Rossella Graffeo, Stefania Rizzo, Andrea Gallina, Fabio Monni, Nicola Fossati, Silke Gillessen, Fabio Turco

PMC · DOI: 10.3389/fonc.2025.1648230 · Frontiers in Oncology · 2025-10-03

## TL;DR

Two patients with BRCA mutations had poor outcomes with enfortumab vedotin plus pembrolizumab but better results with platinum-based chemotherapy for metastatic urothelial carcinoma.

## Contribution

First report of BRCA-mutant patients with metastatic UC showing poor response to EV-P and better response to platinum-based chemotherapy.

## Key findings

- Patients with BRCA mutations had short progression-free survival with first-line EV-P therapy.
- Second-line platinum-based chemotherapy provided more durable responses in these patients.
- BRCA mutations may predict better outcomes with platinum-based chemotherapy over EV-P in UC.

## Abstract

The introduction of enfortumab vedotin combined with pembrolizumab (EV-P) as a first-line treatment for advanced urothelial carcinoma (UC) has transformed the therapeutic landscape and holds great promise for improving patient outcomes. However, predictive and prognostic biomarkers for this novel regimen remain limited, and no specific subgroup has yet been identified for whom frontline EV-P could be withheld in favor of platinum-based chemotherapy. We report the first two cases of patients with BRCA-mutant metastatic UC who experienced markedly short progression-free survival with first-line EV-P but achieved more durable responses with second-line platinum-based chemotherapy. These observations raise important questions about the potential predictive role of BRCA - and more broadly, DNA damage repair - mutations in the evolving treatment paradigm of UC. Given the known sensitivity of BRCA-mutated tumors to platinum agents, frontline platinum-based chemotherapy may warrant consideration in this molecularly defined subgroup. Larger studies are needed to validate these preliminary findings and inform treatment selection.

## Linked entities

- **Genes:** Brca2 (BRCA2, DNA repair associated) [NCBI Gene 37916]
- **Diseases:** urothelial carcinoma (MONDO:0040679)

## Full-text entities

- **Genes:** BRCA1 (BRCA1 DNA repair associated) [NCBI Gene 672] {aka BRCAI, BRCC1, BROVCA1, FANCS, IRIS, PNCA4}
- **Diseases:** tumors (MESH:D009369), UC (MESH:D014523)
- **Chemicals:** pembrolizumab (MESH:C582435), enfortumab vedotin (MESH:C000632577), EV-P (-), platinum (MESH:D010984)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12531046/full.md

## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12531046/full.md

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Source: https://tomesphere.com/paper/PMC12531046