Observational studyThe Prostate2026
Corticosteroid Use and Risk of Adverse Events in Metastatic Hormone-Sensitive Prostate Cancer.
Observational study in The Prostate, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
9 authors.
Funding
Abstract
backgroundAmong the approved therapies for metastatic hormone-sensitive prostate cancer (mHSPC), abiraterone and docetaxel are administered concomitantly with corticosteroids. This study evaluated the association between corticosteroid use and risk of adverse events among patients with mHSPC.
methodsWe conducted an observational cohort study among patients ≥ 65 years of age who were enrolled in Medicare parts A, B, or D, and initiated treatment for mHSPC. The primary exposure was corticosteroids between June 1, 2017-December 31, 2023. Primary outcomes were nine composite adverse event outcomes. Exploratory outcomes were all-cause death, all-cause hospitalization, and adverse event-related hospitalization. Conventional Cox models were used to model corticosteroid exposure as a binary time-varying covariate, and weighted cumulative exposure models were used to account for varying doses, durations, and timing of corticosteroid exposure.
resultsOf 24,857 patients, 12,839 (52%) received at least one dose of corticosteroids during the follow-up period. Compared with patients who were not exposed to at least one ≥ 5 mg prednisone-equivalent dose of corticosteroids, patients exposed to corticosteroids during follow-up were at significantly higher risk of all adverse event types, except ophthalmic events, and had a 34% higher risk of all-cause death (adjusted hazard ratio: 1.34; 95% confidence interval: 1.27-1.42). Risks increased with prolonged corticosteroid exposure and with higher daily doses.
conclusionsOur findings suggest that patients exposed to corticosteroids are at increased risk of adverse events, hospitalization, and death. As not all mHSPC treatments require concomitant use of corticosteroids, these findings may help to inform treatment decision-making.
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