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Updated: Aug 29, 2025

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Use of Magnetic Resonance Imaging and Biopsy Data to Guide Sampling Procedures for Prostate Cancer Biobanking
Published on: October 10, 2019
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Differential Biopsy Patterns Influence Associations between Multivitamin Use and Prostate Cancer Risk in the Selenium
Jeannette M Schenk1, Cathee Till2, Marian L Neuhouser1
1Public Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, Washington.
Summary
Multivitamin (MVI) use may not increase prostate cancer risk. Initial analysis suggested higher risk, but after accounting for differences in biopsy patterns, the association became insignificant. Further research is needed.
Area of Science:
- Oncology
- Epidemiology
- Preventive Medicine
Background:
- Multivitamin (MVI) use is prevalent, yet its impact on prostate cancer risk remains debated.
- Conflicting evidence exists regarding whether MVI use influences prostate cancer incidence.
Purpose of the Study:
- To evaluate the association between multivitamin (MVI) use and prostate cancer risk using data from the Selenium and Vitamin E Cancer Prevention Trial (SELECT).
- To investigate potential biases in prostate cancer risk assessment due to differential screening and biopsy patterns related to MVI use.
Main Methods:
- Utilized Cox proportional hazards models to assess MVI use associations with total, low-, and high-grade prostate cancer risk.
- Employed longitudinal data to analyze screening and biopsy patterns.
- Developed methods to estimate prostate cancer probability for men with positive screening but no biopsy to account for differential biopsy acceptance.
Main Results:
- Initial analyses of observed biopsy data indicated a 19-21% increased risk of high-grade prostate cancer with current and long-term MVI use.
- Identified that MVI users were more likely to undergo earlier on-study biopsies, suggesting potential detection bias.
- After adjusting for differential biopsy patterns, the association between MVI use and prostate cancer risk was attenuated and no longer statistically significant.
Conclusions:
- Biopsy acceptance patterns in the SELECT trial varied by MVI use.
- Observed associations between MVI use and prostate cancer risk may be biased by differential biopsy ascertainment.
- Analytical adjustments using detailed screening and biopsy data can mitigate bias in risk factor associations.
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