# Historical Perspective of HER2 Testing and Treatment in Prostate Cancer

**Authors:** Natalia Zamalloa, Jacqueline Rose, Coen J. Lap, Rithika Rajendran, Fayez Estephan, Karan Jatwani, Aarati Poudel, Ramesh Subrahmanyam, Paula J. Hurley, Victor E. Nava, Maneesh Jain

PMC · DOI: 10.3390/curroncol33020091 · Current Oncology · 2026-02-02

## TL;DR

This paper discusses the history and future of HER2 testing in prostate cancer, emphasizing the need for a prostate-specific scoring system to better identify patients who may benefit from HER2-targeted therapies like T-DXd.

## Contribution

The paper proposes a prostate-specific HER2 IHC scoring system and highlights clinical responses to T-DXd in prostate cancer patients.

## Key findings

- A prostate-specific HER2 IHC scoring system was developed to better reflect HER2 expression in prostate cancer.
- Two patients with metastatic prostate cancer showed clinical responses to T-DXd using the proposed scoring system.
- Previous HER2-targeted therapies in prostate cancer had limited success due to inadequate testing methods.

## Abstract

A commentary examining the historical significance of human epidermal growth factor receptor 2 (HER2) immunohistochemistry (IHC) in prostate cancer, summarizing the early clinical trials related to HER2-positive prostate cancer, showcasing new trials using HER2 antibody-drug conjugate (ADC) transtuzumab deruxtecan (T-DXd), underscoring the need for a prostate-specific HER2 IHC scoring system, proposing a scoring system in comparison with the current Breast and Gastroesophageal Junction HER-2 scoring system and possible future targeted therapy in HER2-positive prostate cancer. We aim to highlight the need for a Prostate Cancer specific HER2 scoring system.

Human epidermal growth factor receptor 2 (HER2) is a molecular target of interest in prostate cancer due to its association with poor prognosis and its potential role in androgen receptor signaling. However, earlier clinical trials investigating HER2-targeted therapies, including antibodies and small molecules, have shown limited efficacy. More recent studies using the HER2 antibody-drug conjugate (ADC) trastuzumab deruxtecan (T-DXd) suggest potential therapeutic benefit in prostate cancer. However, its effective utilization requires a HER2 IHC scoring system that accurately represents HER2 expression patterns unique to prostate cancer, which is currently not established. We have developed a modified HER2 IHC scoring system that, unlike the breast and gastrointestinal tumor HER2 IHC grading scales, considers the distinct spatiotemporal expression of HER2 in prostate tumors. In this commentary, we discussed two patients with metastatic prostate cancer who were classified as HER2 IHC 3+ using our prostate cancer-specific scoring system and who demonstrated meaningful clinical responses and responded to treatment with T-DXd. We further review the historical evolution of HER2 testing in prostate cancer, as well as factors that may have contributed to the failure of previous clinical trials targeting HER2 in prostate tumors. Our aim is to highlight the need for developing a standardized HER2 IHC grading model in prostate cancer, which could improve the predictive value of HER2 IHC expression, enabling a more accurate identification of patients likely to benefit from HER2-targeted ADCs.

## Linked entities

- **Genes:** ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064]
- **Diseases:** prostate cancer (MONDO:0005159), metastatic prostate cancer (MONDO:0004956)

## Full-text entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, TXK (TXK tyrosine kinase) [NCBI Gene 7294] {aka BTKL, PSCTK5, PTK4, RLK, TKL}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, AR (androgen receptor) [NCBI Gene 367] {aka AIS, AR8, DHTR, HPCX3, HUMARA, HYSP1}
- **Diseases:** breast cancer (MESH:D001943), gastrointestinal tumor (MESH:D005770), GEJC (MESH:D004938), prostate tumors (MESH:D011472), liver metastasis (MESH:D009362), breast (MESH:D061325), brain (MESH:D001927), breast, gastric, and gastro-esophageal junction cancer (MESH:D013274), injury to (MESH:D014947), Prostate Cancer (MESH:D011471), Gastroesophageal Junction Cancer (MESH:D009369), prostate adenocarcinoma (MESH:D000230), bladder, cervical, endometrial, ovarian and pancreatic tumors (MESH:D010195)
- **Chemicals:** trastuzumab deruxtecan (MESH:C000614160), docetaxel (MESH:D000077143), T-DXd (-), carboplatin (MESH:D016190), pertuzumab (MESH:C485206), lapatinib (MESH:D000077341), Herceptin (MESH:D000068878), abiraterone (MESH:C089740), cabazitaxel (MESH:C552428)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12939083/full.md

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Source: https://tomesphere.com/paper/PMC12939083