# Neoadjuvant Therapies for Prostate Cancer–Current Paradigms and Future Directions

**Authors:** Kieran Sandhu, Abdullah Al-Khanaty, David Hennes, David Chen, Eoin Dinneen, Carlos Delgado, Nathan Lawrentschuk, Renu S. Eapen, Declan G. Murphy, Marlon Perera

PMC · DOI: 10.3390/cancers18010065 · Cancers · 2025-12-24

## TL;DR

This paper reviews current and future neoadjuvant therapies for high-risk prostate cancer, focusing on improving outcomes before definitive treatments like surgery or radiotherapy.

## Contribution

The paper provides a comprehensive review of emerging neoadjuvant therapies and their potential to improve outcomes in aggressive prostate cancer.

## Key findings

- Second-generation androgen receptor pathway inhibitors show survival benefits in metastatic prostate cancer and are being tested pre-surgery.
- Radioligand therapy like [177Lu]Lu-PSMA-617 is being explored as a promising neoadjuvant treatment.
- Future directions include personalized therapies based on genomic and molecular factors to identify immunologically responsive subtypes.

## Abstract

High-risk prostate cancer has a high chance of return despite surgery or radiotherapy. Treatment prior to definitive therapy (neoadjuvant therapy) may help control cancer earlier and reduce spread. Early hormonal therapy improved tumour features but not survival. Second-generation anti-hormonals, radioligand therapy, and immunotherapy are now being explored in the neoadjuvant setting. This review summarises current evidence and ongoing trials exploring how neoadjuvant treatments may improve outcomes for men with aggressive prostate cancer.

High-risk and locally advanced prostate cancer represents 20–25% of new diagnoses of prostate cancer and is associated with high rates of recurrence, morbidity, and mortality. The neoadjuvant window provides a unique opportunity for systemic control prior to definitive therapy with radical prostatectomy or radiotherapy (RT). Early trials with first-generation androgen deprivation therapy (ADT) achieved pathological downstaging but no survival benefit. In the 2000s, the advent of chemohormonal regimes using docetaxel provided excitement but mixed results tempered expectations and is now not recommended prior to surgery. Second-generation androgen receptor pathway inhibitors (ARPIs) combined with ADT have demonstrated significant survival benefit in metastatic prostate cancer and are currently being evaluated in large phase III trials in the neoadjuvant setting. RT remains an alternative curative modality, and recent data highlights similar issues to surgery in eradicating micrometastatic disease despite excellent local control. This has driven parallel efforts to evaluate intensified systemic therapy in the pre-RT/neoadjuvant settings. In addition to the excitement surrounding ARPIs, radioligand therapy, such as [177Lu]Lu-PSMA-617 has shown promise in the neoadjuvant setting and continues to be investigated. Future research aims to incorporate genomic and molecular factors to enable personalised neoadjuvant therapies by identifying damage immunologically responsive subtypes that may derive greater benefit from immune-directed therapies in the peri-operative setting. This narrative review synthesises current evidence for neoadjuvant therapies in high-risk prostate cancer and future directions.

## Linked entities

- **Chemicals:** docetaxel (PubChem CID 148124)
- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Genes:** AR (androgen receptor) [NCBI Gene 367] {aka AIS, AR8, DHTR, HPCX3, HUMARA, HYSP1}
- **Diseases:** Prostate Cancer (MESH:D011471)
- **Chemicals:** docetaxel (MESH:D000077143), [177Lu]Lu-PSMA-617 (-)

## Full text

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## Figures

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## References

90 references — full list in the complete paper: https://tomesphere.com/paper/PMC12784934/full.md

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Source: https://tomesphere.com/paper/PMC12784934