# Achieving Complete Response in Metastatic Prostate Cancer With Triplet Therapy and Local Radiation: A Case Report

**Authors:** Katsuki Muramoto, Fumihiko Urabe, Keigo Sakanaka, Hajime Onuma, Soshi Kadena, Yuma Goto, Mana Nakata, Tatsuya Shimomura, Takahiro Kimura

PMC · DOI: 10.7759/cureus.84310 · Cureus · 2025-05-17

## TL;DR

A 68-year-old man with advanced prostate cancer achieved a complete response through a combination of therapies and local radiation.

## Contribution

This case report demonstrates the potential for complete response in metastatic prostate cancer using triplet therapy and local radiation.

## Key findings

- Triplet therapy led to a rapid decline in PSA to undetectable levels within four months.
- Complete response was achieved on imaging 17 months after treatment initiation.
- Local radiation was effective in addressing residual tumor cells after initial therapy.

## Abstract

Triplet therapy, consisting of androgen deprivation therapy, docetaxel, and androgen receptor signaling inhibitors, has been approved for the treatment of metastatic castration-sensitive prostate cancer (mCSPC) and is primarily recommended for high-volume disease. A 68-year-old man presented with suspected prostate cancer following the detection of lumbar spine metastases. Prostate-specific antigen (PSA) was as high as 69.76 ng/mL at the first visit. Imaging revealed widespread metastases in the bones and lungs, and a biopsy confirmed prostate cancer with a Gleason score of 4+5=9 (cT3b, N1, M1c). Triplet therapy (surgical castration, docetaxel, and darolutamide) was initiated, resulting in a rapid decline in PSA to <0.01 ng/mL within four months. Metastatic lesions progressively regressed, and a complete response was achieved on imaging 17 months after treatment initiation. However, repeat prostate biopsy revealed residual viable tumor cells (Gleason score of 4+5=9), prompting local radiation therapy to the prostate. Two months after radiation, the patient remained on darolutamide monotherapy, with PSA persistently <0.01 ng/mL.

This case highlights the potential for achieving a complete response in mCSPC with triplet therapy. Even in metastatic disease, first-line treatment may lead to a complete response, underscoring the need for further studies to identify patients who may benefit most from this approach.

## Linked entities

- **Chemicals:** docetaxel (PubChem CID 148124), darolutamide (PubChem CID 67171867)
- **Diseases:** prostate cancer (MONDO:0005159), metastatic prostate cancer (MONDO:0004956)

## Full-text entities

- **Genes:** KLK3 (kallikrein related peptidase 3) [NCBI Gene 354] {aka APS, KLK2A1, PSA, hK3}, AR (androgen receptor) [NCBI Gene 367] {aka AIS, AR8, DHTR, HPCX3, HUMARA, HYSP1}
- **Diseases:** tumor (MESH:D009369), androgen (MESH:D014770), Prostate Cancer (MESH:D011471), metastases (MESH:D009362)
- **Chemicals:** darolutamide (MESH:C000607739), docetaxel (MESH:D000077143)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12171650/full.md

## References

12 references — full list in the complete paper: https://tomesphere.com/paper/PMC12171650/full.md

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Source: https://tomesphere.com/paper/PMC12171650