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dc.contributor.authorMargalit, Danielle
dc.contributor.authorKasperzyk, Julie
dc.contributor.authorMartin, Neil
dc.contributor.authorSesso, Howard
dc.contributor.authorGaziano, J. Michael
dc.contributor.authorMa, Jing
dc.contributor.authorStampfer, Meir
dc.contributor.authorMucci, Lorelei
dc.date.accessioned2019-09-05T18:09:07Z
dc.date.issued2012
dc.identifier.citationMargalit, Danielle N., Julie L. Kasperzyk, Neil E. Martin, Howard D. Sesso, John Michael Gaziano, Jing Ma, Meir J. Stampfer, and Lorelei A. Mucci. 2012. “Beta-Carotene Antioxidant Use During Radiation Therapy and Prostate Cancer Outcome in the Physicians’ Health Study.” International Journal of Radiation Oncology*Biology*Physics 83 (1): 28–32. https://doi.org/10.1016/j.ijrobp.2011.05.032.
dc.identifier.issn0360-3016
dc.identifier.issn1879-355X
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:41292567*
dc.description.abstractPurpose: The safety of antioxidant supplementation during radiation therapy (RT) for cancer is controversial. Antioxidants could potentially counteract the pro-oxidant effects of RT and compromise therapeutic efficacy. We performed a prospective study nested within the Physicians' Health Study (PHS) randomized trial to determine if supplemental antioxidant use during RT for prostate cancer is associated with an increased risk of prostate cancer death or metastases.Methods and Materials: PHS participants (383) received RT for prostate cancer while randomized to receive beta-carotene (50 mg on alternate days) or placebo. The primary endpoint was time from RT to lethal prostate cancer, defined as prostate cancer death or bone metastases. The Kaplan-Meier method was used to estimate survival probabilities and the log-rank test to compare groups. Cox proportional hazards regression was used to estimate the effect of beta-carotene compared with that of placebo during RT.Results: With a median follow-up of 10.5 years, there was no significant difference between risk of lethal prostate cancer with the use of beta-carotene during RT compared with that of placebo (hazard ratio = 0.72; 95% confidence interval [CI], 0.42-1.24; p = 0.24). After we adjusted for age at RT, prostate-specific antigen serum level, Gleason score, and clinical stage, the difference remained nonsignificant. The 10-year freedom from lethal prostate cancer was 92% (95% CI, 87-95%) in the beta-carotene group and 89% (95% CI, 84-93%) in the placebo group.Conclusion: The use of supplemental antioxidant beta-carotene during RT was not associated with an increased risk of prostate cancer death or metastases. This study suggests a lack of harm from supplemental beta-carotene during RT for prostate cancer.
dc.language.isoen_US
dc.publisherElsevier
dash.licenseLAA
dc.titleBeta-Carotene Antioxidant Use During Radiation Therapy and Prostate Cancer Outcome in the Physicians' Health Study
dc.typeJournal Article
dc.description.versionAccepted Manuscript
dc.relation.journalInternational Journal of Radiation Oncology, Biology, Physics
dash.depositing.authorStampfer, Meir
dc.date.available2019-09-05T18:09:07Z
dash.workflow.comments1Science Serial ID 41376
dc.identifier.doi10.1016/j.ijrobp.2011.05.032
dash.source.volume83;1
dash.source.page28
dash.contributor.affiliatedStampfer, Meir


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