# Case Report: Personalized peptide-based immunization in an advanced-stage prostate cancer patient with bone metastasis

**Authors:** Nils Heinrich Thoennissen, Mari Carmen Martos-Contreras, Mehdi Manoochehri, Mauro Nogueira, Franziska Bremm, Jan Dörrie, Jan Christoph, Meik Kunz, Wolfgang Schönharting

PMC · DOI: 10.3389/fonc.2025.1596315 · Frontiers in Oncology · 2025-07-22

## TL;DR

A prostate cancer patient with bone metastasis showed tumor regression after personalized peptide immunization, with minimal side effects.

## Contribution

A novel personalized immunization method (BITAP) is shown to induce tumor regression in a prostate cancer case as a monotherapy.

## Key findings

- The patient experienced significant regression of both primary and metastatic tumor lesions.
- Low levels of prostate-specific antigen (PSA) were observed following immunization.
- BITAP immunization was well-tolerated with only mild and temporary side effects.

## Abstract

Neoantigens, which are recognized as non-self and trigger an immune response, are novel antigens generated by tumor cells. Here, we report a de novo metastatic hormone-sensitive prostate cancer (mHSPC) case, which benefited from our personalized peptide immunization named BioInformatic Tumor Address Peptides (BITAP) in a monotherapeutic setting. Our in-house bioinformatics pipeline involved identifying somatic variations, analyzing their expression, and computationally predicting novel epitopes from both metastatic and primary tumors, separately. As stand-alone therapy, the patient has been administered multiple injections of two peptide pools (BITAP-1 and BITAP-2). Several months following immunizations, a significant regression of both metastatic and primary tumor lesions was recorded along with low-level of prostate-specific antigen (PSA). Besides mild and short-lasting local and systemic reactions, no serious treatment-related adverse effects were reported by the patient. In conclusion, this case suggests that BITAP immunization is feasible and safe, and may present an immunotherapeutic approach inducing sustainable tumor regressions in mHSPC patients.

## Linked entities

- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Genes:** FOLH1 (folate hydrolase 1) [NCBI Gene 2346] {aka FGCP, FOLH, GCP2, GCPII, NAALAD1, PSM}, NKX3-1 (NK3 homeobox 1) [NCBI Gene 4824] {aka BAPX2, NKX3, NKX3.1, NKX3A}, KLK3 (kallikrein related peptidase 3) [NCBI Gene 354] {aka APS, KLK2A1, PSA, hK3}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}
- **Diseases:** melanoma (MESH:D008545), death (MESH:D003643), nocturia (MESH:D053158), urinary urgency (MESH:D014548), bone metastases (MESH:D009362), lymph node metastases (MESH:D008207), primary tumor (MESH:D001932), Tumor (MESH:D009369), prostatic adenocarcinoma (MESH:D000230), PrCa (MESH:D011471), erectile dysfunction (MESH:D007172), renal cell carcinoma (MESH:D002292), prostate enlargement (MESH:D011472), castration-resistant disease (MESH:D064129), lung cancer (MESH:D008175), bone (MESH:D001847)
- **Chemicals:** Tamsulosin (MESH:D000077409), alcohol (MESH:D000438), abiraterone (MESH:C089740), BITAP (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** P504S

## Full text

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## Figures

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## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC12321524/full.md

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Source: https://tomesphere.com/paper/PMC12321524