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March 4, 2026Journal of Clinical Oncology0 citations

Adiposity and response to ADT ± AR pathway inhibitors (ARPI) in men with metastatic hormone-sensitive prostate cancer (mHSPC).

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MBMitchell BoshkosThe University of Texas MD Anderson Cancer CenterMSMaria Julia Moura Nascimento SantosThe University of Texas MD Anderson Cancer CenterRTRebecca Slack TidwellThe University of Texas MD Anderson Cancer Center

Key Points

  • This study aims to understand how intrinsic and acquired adiposity affect the response to androgen receptor pathway inhibitors in men with metastatic hormone-sensitive prostate cancer.
  • Included men with metastatic hormone-sensitive prostate cancer from three trials with baseline CT imaging.
  • Used AI segmentation to measure body composition before and after six months of treatment.
  • Evaluated treatment response through six-month PSA levels and progression-free survival.
  • Intrinsic subcutaneous adiposity was linked to improved six-month PSA response.
  • Greater acquired adiposity after treatment was associated with a worse PSA response.
  • No significant association was found between adiposity and progression-free survival.

Abstract

233 Background: Adiposity has a complex influence on prostate cancer outcomes that may be stage- and/or treatment-dependent. While linked to worse outcomes in localized disease, increased adiposity has been associated with an improved response to ARPI in metastatic castration-resistant prostate cancer (mCRPC). However, how pre-treatment (intrinsic) versus on-treatment (acquired) adiposity affects outcomes in men with mHSPC receiving ADT ± ARPI is unknown. We hypothesized that elevated intrinsic and greater acquired adiposity would improve the efficacy of ARPI in mHSPC. Methods: Men with mHSPC from a pooled cohort of three single-center, investigator-initiated trials with baseline L3 vertebra CT imaging prior to initiating ADT ± ARPI were included. An AI segmentation tool, Voronoi DAFS, measured body composition (normalized for height m²) on CTs obtained before and after six months of ADT ± ARPI. Response to ARPI was evaluated using 6-month PSA response, defined as PSA 4 ng/mL, and mCRPC progression-free survival (PFS), defined as time from ADT start to development of CRPC or death. Chi-square tests, the Kaplan-Meier method, and proportional hazards regression were used for analysis. Results: In 152 men with mHSPC, median age was 66.0 years, and median PSA was 15.9 ng/mL. Antihypertensive medication use was prevalent (61.8%), 21.1% had type 2 diabetes mellitus (T2DM), and 14.5% had coronary artery disease (CAD). Intrinsic subcutaneous adiposity (SATi) was associated with 6-month PSA response (p = 0.004), with the middle tertile of intrinsic adiposity showing the most favorable response. In contrast, greater acquired SATi after six months of ADT ± ARPI was associated with an inferior 6-month PSA response (p 4 p-value <43.833 37 22 (59.5%) 11 (29.7%) 4 (10.8%) 0.004 43.833 to <86.884 71 60 (84.5%) 11 (15.5%) 0 (0.0%) ≥86.884 38 24 (63.2%) 10 (26.3%) 4 (10.5%) Multivariable acquired SATi Change 0.002 Change < 15.9 79 57 (72.2%) 21 (26.6%) 1 (1.3%) Change ≥ 15.9 24 11 (45.8%) 7 (29.2%) 6 (25.0%)

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Cite This Study

Boshkos et al. (2026) studied this question.

synapsesocial.com/papers/69a7cd3dd48f933b5eed963fhttps://doi.org/10.1200/jco.2026.44.7_suppl.233
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