# Combined BRAF/MEK inhibition for BRAF-mutant melanoma brain metastases in pregnancy: A case report

**Authors:** Jaroslav Melus, Michaela Jezberova, Silvia Mikulajova, Katarina Komaromy Gerincova, Martin Karlik, Igor Straka, Marek Krivosik, Peter Valkovic, Gabriela Timarova

PMC · DOI: 10.3892/ol.2025.15361 · Oncology Letters · 2025-10-24

## TL;DR

A pregnant woman with BRAF-mutant melanoma brain metastases received combined targeted therapy, showing the possibility of managing advanced cancer during pregnancy.

## Contribution

This case report presents a rare instance of BRAF-mutant melanoma brain metastases managed with targeted therapy during pregnancy.

## Key findings

- Combined BRAF/MEK inhibition with dabrafenib and trametinib was initiated in the third trimester for disease progression.
- The neonate was delivered at 33 weeks and showed normal growth and development at follow-up.
- The mother achieved partial remission and remains alive 16 months after diagnosis.

## Abstract

Melanoma is a highly aggressive malignancy with the potential to metastasize to the placenta and fetus. Pregnancy-associated melanoma (PAM) complicated by brain metastases (MTS) is exceedingly rare, and its management requires balancing maternal survival with fetal safety. A 35-year-old pregnant woman with a history of superficial spreading melanoma presented at 24 weeks of gestation with multiple brain MTS. Following multidisciplinary consultation and after obtaining informed consent, two symptomatic brain MTS were surgically resected during pregnancy. Histopathology and immunohistochemistry confirmed metastatic melanoma, and molecular testing identified a B-Raf proto-oncogene serine/threonine kinase V600E mutation. Due to disease progression, targeted therapy with dabrafenib and trametinib was initiated in the third trimester. At 33 weeks of gestation, an acute cesarean section was performed following a focal impaired consciousness seizure. A premature male neonate was delivered, requiring respiratory support and intensive care. Following stabilization, the growth and psychomotor development of the neonate remained normal at follow-up. Postpartum, the mother transitioned to immune checkpoint inhibitor therapy and remains alive with partial remission 16 months after the diagnosis of brain MTS. The present case demonstrates the feasibility of combined neurosurgical and targeted therapeutic approaches for PAM with brain MTS. The case provides valuable clinical and ethical insights into individualized decision-making when managing advanced melanoma during pregnancy, a scenario that remains rare and poorly documented.

## Linked entities

- **Chemicals:** dabrafenib (PubChem CID 44462760), trametinib (PubChem CID 11707110)
- **Diseases:** melanoma (MONDO:0005105)

## Full-text entities

- **Genes:** MAP2K7 (mitogen-activated protein kinase kinase 7) [NCBI Gene 5609] {aka JNKK2, MAPKK7, MEK, MEK 7, MKK7, PRKMK7}, BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}
- **Diseases:** malignancy (MESH:D009369), MTS (MESH:D009362), Melanoma (MESH:D008545), brain metastases (MESH:D001932), PAM (MESH:D020150), impaired consciousness seizure (MESH:D003244)
- **Chemicals:** dabrafenib (MESH:C561627), trametinib (MESH:C560077)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** serine/threonine, V600E

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12592975/full.md

## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12592975/full.md

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Source: https://tomesphere.com/paper/PMC12592975