# Successful application of chemosaturation with percutaneous hepatic perfusion in metastatic uveal melanoma patient progressing after systemic treatment options: a case report

**Authors:** Damla Gunenc, Ahmet Anil Ozluk, Utku Mahir Yıldırım, Paolo A. Ascierto, Burcak Karaca

PMC · DOI: 10.3389/fonc.2024.1355971 · Frontiers in Oncology · 2024-04-10

## TL;DR

A patient with advanced uveal melanoma showed a strong response to a local liver treatment after failing other therapies, suggesting new treatment strategies could improve outcomes.

## Contribution

This case report highlights the potential of sequential therapeutic strategies in metastatic uveal melanoma.

## Key findings

- A patient with metastatic uveal melanoma showed a remarkable response to percutaneous hepatic perfusion after progressing on systemic treatments.
- Local treatment targeting liver metastasis may offer improved outcomes in advanced uveal melanoma.
- Sequential therapeutic approaches could enhance treatment efficacy and patient prognosis in metastatic uveal melanoma.

## Abstract

Uveal melanoma (UM) is a rare subtype of melanoma, accounting for less than 5% of all melanoma cases. Metastatic UM differs notably from cutaneous melanoma, exhibiting variations in etiology, prognosis, driver mutations, metastatic patterns, and poor responses to immune checkpoint inhibitors (ICI). Beyond local treatment options, such as resection, radiation therapy, and enucleation, and systemic treatments, such as ICIs, the approval of tebentafusp, a bispecific gp100 peptide-HLA-directed CD3 T-cell engager, marks a breakthrough in treating HLA-A*02:01 metastatic UM. Despite the advancements in treatment options, the long-term survival rates remain inadequate. We report a patient with metastatic UM who previously received ICI and progressed on tebentafusp treatment but subsequently exhibited a remarkable response to local treatment targeting liver metastasis. Such observations highlight the significance of exploring sequential therapeutic strategies for advanced UM, offering potential avenues to enhance treatment efficacy and patient prognosis.

## Linked entities

- **Proteins:** PMEL (premelanosome protein)
- **Diseases:** uveal melanoma (MONDO:0006486)

## Full-text entities

- **Genes:** PMEL (premelanosome protein) [NCBI Gene 6490] {aka D12S53E, HMB-45, HMB45, ME20, ME20-M, ME20M}, HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}
- **Diseases:** cutaneous melanoma (MESH:C562393), UM (MESH:C536494), liver metastasis (MESH:D009362), melanoma (MESH:D008545)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC11040682/full.md

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Source: https://tomesphere.com/paper/PMC11040682