AKR1C3-negative high-risk metastatic castration-sensitive prostate cancer has long-term response to first-line

Tsuyoshi Yoshizawa1, Yoko Nakanishi2, Daisuke Obinata1

  • 1Department of Urology, Nihon University School of Medicine, Japan.

Urology Case Reports
|April 15, 2024
PubMed

Insights

High-risk metastatic castration-sensitive prostate cancer (mCSPC) patients with negative AKR1C3 expression showed sustained long-term response to abiraterone. This suggests a potential biomarker for predicting treatment efficacy in mCSPC.

Area of Science:

  • Oncology
  • Urology
  • Medical Biochemistry

Background:

  • Metastatic castration-sensitive prostate cancer (mCSPC) requires effective first-line treatments.
  • Abiraterone acetate is a standard treatment for advanced prostate cancer.
  • Prognostic markers for treatment response in mCSPC are crucial.

Observation:

  • Four cases of high-risk mCSPC were treated with first-line abiraterone.
  • Tumor tissue analysis revealed negative expression of aldo-keto reductase family 1 member C3 (AKR1C3).
  • All patients demonstrated sustained responses exceeding 5 years.

Findings:

  • Negative AKR1C3 expression in high-risk mCSPC correlates with long-term response to abiraterone.
  • AKR1C3 is typically associated with poor prognosis in metastatic castration-resistant prostate cancer (mCRPC).
  • This study is the first to report the association between high-risk mCSPC, negative AKR1C3, and abiraterone response.

Implications:

  • Negative AKR1C3 may serve as a predictive biomarker for abiraterone efficacy in high-risk mCSPC.
  • This finding could guide personalized treatment strategies for prostate cancer patients.
  • Further research is warranted to validate AKR1C3 as a biomarker in larger mCSPC cohorts.