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https://mnclhd.intersearch.com.au/mnclhdjspui/handle/123456789/742| Title: | High-dose vitamin D supplementation and prostate cancer progression: a phase II randomised trial in localised prostate cancer cases with intermediate risk of progression (ProsD) |
| Authors: | Nair-Shalliker, V.;Smith, D. P.;Gebski, V.;Patel, M. I.;Frydenberg, M.;Yaxley, J.;Gardiner, R.;Espinoza, D.;Kimlin, M. G.;Dhillon, V.;Leifert, W.;Gillatt, D.;Woo, H.;Rasiah, K.;Awad, Nader;Symons, J.;Wells, J. K.;Pickett, M.;French, M.;Anderson, P. H.;Armstrong, B. K.;Gurney, H. |
| MNCLHD Author: | Awad, Nader |
| Issue Date: | Mar-2026 |
| Citation: | British Journal of Cancer, Volume 134, Issue 5, pp. 735-745. |
| Abstract: | Background The ProsD trial aimed to determine if oral vitamin D supplementation could prevent prostate cancer ( PC ) progression in men on active surveillance ( AS ). Methods ProsD is a phase-II double-blinded randomized trial of newly diagnosed, low-intermediate risk PC cases, aged between 50 and 80 years and on AS. The intervention was a monthly oral dose of cholecalciferol (50,000IU; Vitamin D) or placebo. Primary and secondary endpoints were active therapy-free ( ATFS ) and progression-free ( PFS ) survival, respectively. Blood samples were analysed for vitamin D metabolites and cytokinesis-block micronucleus cytome (CBMN) markers for lymphocytic genome damage. Results There were 123 randomised participants (81 vitamin D and 42 placebo) included in this analysis. Mean (SD) for age was 66.5 (6.6) years and for 25(OH)D levels were 72.0 (19.9) and 66.4 (18.4) nmol/L at baseline ( p = 0.1), and 91.9 (19.9) and 60.4 (24.4) nmol/L at 24 months, in the vitamin D and placebo arms respectively. There were no appreciable differences in ATFS (p log-rank = 0.44), PFS (p p log-rank = 0.60) and occurrence of adverse events, in each trial arm. There were declines in some of the lymphocytic CBMN markers in the vitamin D arm. Conclusion Vitamin D supplementation did not prevent PC progression, although reduced prevalence of CBMN markers may indicate a benefit of vitamin D supplementation. Trial registration Australia New Zealand Clinical Trials Registry (ACTRN12616001707459). Key points Findings: In this phase 2 randomised trial involving 123 prostate cancer patients with low-intermediate risk of progression, vitamin D supplementation did not prevent patients discontinuing active surveillance in favour of active therapy. However, vitamin D supplementation reduced prevalence of lymphocytic genome damage markers that are predictors of cancer risk. Meaning: Vitamin D supplementation may not prevent progression of well-developed prostate cancers, however reduction in the prevalence of lymphocytic genome damage in the vitamin D arm of the study suggests an anti-cancer effect that may prevent the initiation of new cancers. |
| URI: | https://mnclhd.intersearch.com.au/mnclhdjspui/handle/123456789/742 |
| Keywords: | Prostatic Neoplasms;Dietary Supplements;Vitamin D;Male;Prevalence;Watchful Waiting;Australia;New Zealand |
| Appears in Collections: | Oncology / Cancer |
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