# Case Report: Deep and durable PSA response to same-agent enzalutamide rechallenge in metastatic castration-resistant prostate cancer without chemotherapy

**Authors:** Huan Chen, Yan Wang, Min Qu, Xu Gao

PMC · DOI: 10.3389/fonc.2026.1759642 · Frontiers in Oncology · 2026-02-10

## TL;DR

A patient with prostate cancer had a strong and lasting response to a drug he had previously taken, suggesting that reusing the same drug could be effective in some cases.

## Contribution

This case report demonstrates a durable PSA response to enzalutamide rechallenge in a chemotherapy-naïve patient with mCRPC.

## Key findings

- PSA levels decreased by ~85% after enzalutamide rechallenge and remained low for ≥5 months.
- The response occurred without new adverse events or increased pain medication use.
- The case suggests ARSI resistance may be reversible in some patients.

## Abstract

Contemporary guidelines recommend docetaxel as first-line chemotherapy for chemotherapy-naïve men with metastatic castration-resistant prostate cancer (mCRPC) who progress on an androgen receptor signaling inhibitor (ARSI). Cabazitaxel is preferred after prior docetaxel and one ARSI. However, real-world constraints—such as patient preference, access, or comorbidity—often preclude chemotherapy, and cross-resistance among ARSIs is common, making robust responses to same-agent rechallenge uncommon. We report a 74-year-old man diagnosed in 2015 with de novo metastatic hormone-sensitive prostate cancer (Gleason 4 + 4; cT4N1M1b). Under continuous medical castration, he received sequential first- and next-generation ARSIs but consistently declined chemotherapy and radiotherapy. Following biochemical progression on enzalutamide in early 2025, which was accompanied by imaging findings suggestive of a new T12 lesion, and after a brief bicalutamide interval, enzalutamide was rechallenged under a time-limited, PCWG3-aligned protocol with predefined stop rules. Over five months, prostate-specific antigen (PSA) levels declined from 17.73 ng/mL to 2.62 ng/mL (~85% reduction); this PSA response was maintained for ≥5 months through the last follow-up while the patient remained on enzalutamide, without new adverse events or increased analgesic use. This case suggests that in a preference-constrained, chemotherapy-naïve patient, same-agent enzalutamide rechallenge can yield a clinically meaningful PSA response. The observation raises the hypothesis that ARSI resistance may be reversible in a subset of patients, warranting prospective evaluation of biomarker-guided rechallenge strategies to optimize patient selection and minimize opportunity cost.

## Linked entities

- **Chemicals:** enzalutamide (PubChem CID 15951529), bicalutamide (PubChem CID 2375), docetaxel (PubChem CID 148124), cabazitaxel (PubChem CID 9854073)
- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Genes:** FOLH1 (folate hydrolase 1) [NCBI Gene 2346] {aka FGCP, FOLH, GCP2, GCPII, NAALAD1, PSM}, NR3C1 (nuclear receptor subfamily 3 group C member 1) [NCBI Gene 2908] {aka GCCR, GCR, GCRST, GR, GRL}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, AR (androgen receptor) [NCBI Gene 367] {aka AIS, AR8, DHTR, HPCX3, HUMARA, HYSP1}, KLK3 (kallikrein related peptidase 3) [NCBI Gene 354] {aka APS, KLK2A1, PSA, hK3}, CYP3A4 (cytochrome P450 family 3 subfamily A member 4) [NCBI Gene 1576] {aka CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, ARSI (arylsulfatase family member I) [NCBI Gene 340075] {aka ASI, SPG66}
- **Diseases:** fatigue (MESH:D005221), T12 lesion (MESH:D009059), castration resistance (MESH:D064129), falls (MESH:C537863), visceral crisis (MESH:D007418), pain (MESH:D010146), Prostate Cancer (MESH:D011471), urinary obstruction (MESH:D001748), cancer (MESH:D009369), prostate adenocarcinoma (MESH:D000230), lymph node metastases (MESH:D008207), prostatitis (MESH:D011472), hypertension (MESH:D006973), Symptom (MESH:D012816), bone metastases (MESH:D009362), AR dependence (MESH:D013734), cytotoxic (MESH:D064420)
- **Chemicals:** Testosterone (MESH:D013739), flutamide (MESH:D005485), bicalutamide (MESH:C053541), Cabazitaxel (MESH:C552428), Abiraterone (MESH:C089740), prednisone (MESH:D011241), Enzalutamide (MESH:C540278), docetaxel (MESH:D000077143), Denosumab (MESH:D000069448), ADT (-), Apalutamide (MESH:C572045)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** F877L, T878A

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## Figures

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## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12929114/full.md

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Source: https://tomesphere.com/paper/PMC12929114