# Pembrolizumab for high TMB castration-resistant prostate cancer: A precision medicine case report

**Authors:** Vincenzo Terrano, Erica Perri, Chiara Cioffo, Giusi Mastroianni, Maria Antonina Palumbo, Fortunato Ciardiello, Teresa Troiani, Stefania Napolitano

PMC · DOI: 10.1007/s13691-025-00833-3 · International Cancer Conference Journal · 2026-01-12

## TL;DR

A 68-year-old man with two cancers showed a strong response to pembrolizumab after a liquid biopsy revealed high tumor mutational burden.

## Contribution

Demonstrates successful off-label use of pembrolizumab in high TMB mCRPC guided by precision medicine and liquid biopsy.

## Key findings

- Patient with high TMB and multiple mutations responded well to pembrolizumab.
- Target lung metastases disappeared and durable remission was maintained.
- Only mild side effects were observed during treatment.

## Abstract

This case report describes the clinical management of a 68-year-old man with concurrent invasive melanoma and metastatic castration-resistant prostate cancer (mCRPC). Initially diagnosed with BRAF V600E-mutated melanoma, he received Dabrafenib and Trametinib. Later, prostate cancer was diagnosed with bilateral pulmonary metastases. Despite initial treatment with Triptorelin, Docetaxel, and Abiraterone, disease progression occurred. A liquid biopsy revealed an extremely high Tumor Mutational Burden (TMB) and mutations including POLE, BRCA2, ATM, and TP53. Due to the high TMB, off-label Pembrolizumab was initiated. Radiological evaluations at 3 and 6 months showed a marked response, with disappearance of target lung metastases and durable remission maintained through February 2025. Only grade 1 asthenia was reported, without significant treatment interruptions. This case illustrates the value of precision medicine and the role of liquid biopsy in guiding immunotherapy decisions for complex oncological cases. It supports the relevance of molecular profiling in selecting effective treatments beyond standard indications.

## Linked entities

- **Genes:** BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673], POLE (DNA polymerase epsilon, catalytic subunit) [NCBI Gene 5426], BRCA2 (BRCA2 DNA repair associated) [NCBI Gene 675], ATM (ATM serine/threonine kinase) [NCBI Gene 472], TP53 (tumor protein p53) [NCBI Gene 7157]
- **Chemicals:** Dabrafenib (PubChem CID 44462760), Trametinib (PubChem CID 11707110), Triptorelin (PubChem CID 25074470), Docetaxel (PubChem CID 148124), Abiraterone (PubChem CID 132971)

## Full-text entities

- **Genes:** ATM (ATM serine/threonine kinase) [NCBI Gene 472] {aka AT1, ATA, ATC, ATD, ATDC, ATE}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, BRCA2 (BRCA2 DNA repair associated) [NCBI Gene 675] {aka BRCC2, BROVCA2, FACD, FAD, FAD1, FANCD}, BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}
- **Diseases:** asthenia (MESH:D001247), melanoma (MESH:D008545), Tumor (MESH:D009369), castration-resistant prostate cancer (MESH:D064129), lung (MESH:D008171), prostate cancer (MESH:D011471), metastases (MESH:D009362)
- **Chemicals:** Abiraterone (MESH:C089740), Pembrolizumab (MESH:C582435), Dabrafenib (MESH:C561627), Trametinib (MESH:C560077), Docetaxel (MESH:D000077143)
- **Mutations:** V600E

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13038841/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC13038841/full.md

---
Source: https://tomesphere.com/paper/PMC13038841