# Remarkable Response to Etoposide and Cisplatin in Aggressive-Variant Prostate Cancer With Low Prostate-Specific Antigen Levels: A Case Report

**Authors:** Junichi Ikeda, Hisanori Taniguchi, Monta Inoue, Yuki Masuo, Takahiro Nakamoto, Masaaki Yanishi, Katsunori Uchida, Hidefumi Kinoshita

PMC · DOI: 10.7759/cureus.100713 · Cureus · 2026-01-03

## TL;DR

A patient with aggressive prostate cancer and low PSA levels showed significant improvement with etoposide and cisplatin chemotherapy, highlighting the potential of this treatment in similar cases.

## Contribution

Demonstrates the effectiveness of platinum-based chemotherapy in aggressive prostate cancer with low PSA levels.

## Key findings

- The patient showed a partial response to etoposide and cisplatin chemotherapy.
- Radium-223 therapy reduced bone metastases and improved symptoms.
- Low PSA levels did not preclude effective treatment response in this aggressive cancer case.

## Abstract

Prostate-specific antigen (PSA) is a cornerstone of screening for prostate cancer (PC); however, serum PSA levels may remain deceptively low in certain high-grade, aggressive subtypes. Aggressive-variant prostate cancer (AVPC) is a clinical entity characterized by rapid progression, bulky lymphadenopathy, and visceral metastases despite low or non-correlative PSA levels, often requiring treatment approaches beyond conventional therapies. Here, we report the case of a 69-year-old Japanese man with multiple comorbidities, including diabetes, hyperlipidemia, hypertension, angina pectoris, and lower limb occlusive arteriosclerosis, who presented to our center with lower back pain and gait disturbance. Diagnostic imaging demonstrated extensive pelvic bone metastases, seminal vesicle invasion, and pelvic and para-aortic lymphadenopathy. Laboratory evaluation showed a normal PSA level of 2.95 ng/mL and an elevated alkaline phosphatase (ALP) of 669 U/L. A prostate biopsy revealed acinar adenocarcinoma with a Gleason score of 8 (4+4) and intraductal features. Immunohistochemical tests showed positive results for NKX3.1 and androgen receptor but negative results for PSA, synaptophysin, and chromogranin A. Given these findings, the patient was diagnosed with AVPC (cT3bN1M1b) and underwent androgen deprivation therapy combined with etoposide and cisplatin (EP) chemotherapy, achieving a partial response with marked improvements in his symptoms and lymph node lesions. Subsequent radium-223 therapy further reduced bone metastases and normalized ALP levels, leading to substantial functional recovery. This case underscores the necessity of maintaining a high index of suspicion for AVPC when clinical findings contradict low PSA values. Furthermore, the favorable response to EP highlights the potential role of platinum-based chemotherapy in managing low-PSA, high-grade PC. Additional cases are needed to refine the clinical characterization of AVPC and establish evidence-based treatment guidelines.

## Linked entities

- **Proteins:** KLK3 (kallikrein related peptidase 3), NKX3-1 (NK3 homeobox 1)
- **Chemicals:** etoposide (PubChem CID 36462), cisplatin (PubChem CID 5460033), radium-223 (PubChem CID 6335825)
- **Diseases:** prostate cancer (MONDO:0005159), diabetes (MONDO:0005015), hyperlipidemia (MONDO:0021187)

## Full-text entities

- **Genes:** ALPP (alkaline phosphatase, placental) [NCBI Gene 250] {aka ALP, PALP, PLAP, PLAP-1}, 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}, CHGA (chromogranin A) [NCBI Gene 1113] {aka CGA, PHE5, PHES}, NKX3-1 (NK3 homeobox 1) [NCBI Gene 4824] {aka BAPX2, NKX3, NKX3.1, NKX3A}, SYP (synaptophysin) [NCBI Gene 6855] {aka MRX96, MRXSYP, XLID96}
- **Diseases:** angina pectoris (MESH:D000787), lower back pain (MESH:D017116), hyperlipidemia (MESH:D006949), hypertension (MESH:D006973), occlusive arteriosclerosis (MESH:D001161), AVPC (MESH:C565201), lymphadenopathy (MESH:D008206), acinar adenocarcinoma (MESH:D018267), gait disturbance (MESH:D020233), PC (MESH:D011471), diabetes (MESH:D003920), bone metastases (MESH:D009362), lymph node lesions (MESH:D000072717)
- **Chemicals:** EP (-), radium-223 (MESH:C000615150), Etoposide (MESH:D005047), platinum (MESH:D010984), Cisplatin (MESH:D002945)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

12 references — full list in the complete paper: https://tomesphere.com/paper/PMC12863989/full.md

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Source: https://tomesphere.com/paper/PMC12863989