TY - JOUR
T1 - Biases in recommendations for and acceptance of prostate biopsy significantly affect assessment of prostate cancer risk factors
T2 - Results from two large randomized clinical trials
AU - Tangen, Catherine M.
AU - Goodman, Phyllis J.
AU - Till, Cathee
AU - Schenk, Jeannette M.
AU - Lucia, M. Scott
AU - Thompson, Ian M.
N1 - Funding Information:
Supported by National Institutes of Health, National Cancer Institute Grants UM1 CA182883, P30 CA065174, U01 CA086402, U10 CA37429.
Publisher Copyright:
© 2016 by American Society of Clinical Oncology.
PY - 2016/12/20
Y1 - 2016/12/20
N2 - Purpose To identify factors related to who undergoes a prostate biopsy in a screened population and to estimate the impact of biopsy verification on risk factor-prostate cancer associations. Patients and Methods Men who were screened regularly from the placebo arms of two large prostate cancer prevention trials (Prostate Cancer Prevention Trial [PCPT] and Selenium and Vitamin E Cancer Prevention Trial [SELECT]) were examined to define incident prostate cancer cohorts. Because PCPT had an end-ofstudy biopsy, prostate cancer cases were categorized by a preceding prostate-specific antigen/digital rectal examination prompt (yes/no) and noncases by biopsy-proven negative status (yes v no). We estimated the association of risk factors (age, ethnicity, family history, body mass index, medication use) with prostate cancer and quantified differences in risk associations across cohorts. Results Men 60 to 69 years of age, those with benign prostatic hyperplasia, and those with a family history of prostate cancer were more likely, and those with a higher body mass index ($ 25), diabetes, or a smoking history were less likely, to undergo biopsy, adjusting for age and longitudinal prostatespecific antigen and digital rectal examination. Medication use, education, and marital status also influenced who underwent biopsy. Some risk factor estimates for prostate cancer varied substantially across cohorts. Black (v other ethnicities) had odds ratios (ORs) that varied from 1.20 for SELECT (community screening standards, epidemiologic-like cohort) to 1.83 for PCPT (end-of-study biopsy supplementedwith imputed end points). Statin use in SELECT provided anOR of 0.65 and statin use in in PCPT provided an OR of 0.99, a relative difference of 34%. Conclusion Among screenedmen enrolled in prostate cancer prevention trials, differences in risk factor estimates for prostate cancer likely underestimate the magnitude of bias found in other cohorts with varying screening and biopsy recommendations and acceptance. Risk factors for prostate cancer derived from epidemiologic studies not only may be erroneous but may lead to misdirected research efforts.
AB - Purpose To identify factors related to who undergoes a prostate biopsy in a screened population and to estimate the impact of biopsy verification on risk factor-prostate cancer associations. Patients and Methods Men who were screened regularly from the placebo arms of two large prostate cancer prevention trials (Prostate Cancer Prevention Trial [PCPT] and Selenium and Vitamin E Cancer Prevention Trial [SELECT]) were examined to define incident prostate cancer cohorts. Because PCPT had an end-ofstudy biopsy, prostate cancer cases were categorized by a preceding prostate-specific antigen/digital rectal examination prompt (yes/no) and noncases by biopsy-proven negative status (yes v no). We estimated the association of risk factors (age, ethnicity, family history, body mass index, medication use) with prostate cancer and quantified differences in risk associations across cohorts. Results Men 60 to 69 years of age, those with benign prostatic hyperplasia, and those with a family history of prostate cancer were more likely, and those with a higher body mass index ($ 25), diabetes, or a smoking history were less likely, to undergo biopsy, adjusting for age and longitudinal prostatespecific antigen and digital rectal examination. Medication use, education, and marital status also influenced who underwent biopsy. Some risk factor estimates for prostate cancer varied substantially across cohorts. Black (v other ethnicities) had odds ratios (ORs) that varied from 1.20 for SELECT (community screening standards, epidemiologic-like cohort) to 1.83 for PCPT (end-of-study biopsy supplementedwith imputed end points). Statin use in SELECT provided anOR of 0.65 and statin use in in PCPT provided an OR of 0.99, a relative difference of 34%. Conclusion Among screenedmen enrolled in prostate cancer prevention trials, differences in risk factor estimates for prostate cancer likely underestimate the magnitude of bias found in other cohorts with varying screening and biopsy recommendations and acceptance. Risk factors for prostate cancer derived from epidemiologic studies not only may be erroneous but may lead to misdirected research efforts.
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U2 - 10.1200/JCO.2016.68.1965
DO - 10.1200/JCO.2016.68.1965
M3 - Article
C2 - 27998216
AN - SCOPUS:85009799771
SN - 0732-183X
VL - 34
SP - 4338
EP - 4344
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 36
ER -