@article{3a21319585f64127bf5070426fd342f6,
title = "Precision Medicine in Active Surveillance for Prostate Cancer: Development of the Canary-Early Detection Research Network Active Surveillance Biopsy Risk Calculator",
abstract = "Background Men on active surveillance (AS) face repeated biopsies. Most biopsy specimens will not show disease progression or change management. Such biopsies do not contribute to patient management and are potentially morbid and costly. Objective To use a contemporary AS prospective trial to develop a tool to predict AS biopsy outcomes. Design, setting, and participants Biopsy samples (median: 2; range: 2-9 per patient) from 859 men participating in the Canary Prostate Active Surveillance Study and with Gleason 6 prostate cancer (median follow-up: 35.8 mo; range: 3.0-148.7 mo) were analyzed. Outcome measurements and statistical analysis Logistic regression was used to predict progression, defined as an increase in Gleason score from ≤6 to ≤7 or increase in percentage of cores positive for cancer from <34% to ≤34%. Fivefold internal cross-validation was performed to evaluate the area under the receiver operating characteristic curve (AUC). Results and limitations Statistically significant risk factors for progression on biopsy were prostate-specific antigen (odds ratio [OR]: 1.045; 95% confidence interval [CI], 1.028-1.063), percentage of cores positive for cancer on most recent biopsy (OR: 1.401; 95% CI, 1.301-1.508), and history of at least one prior negative biopsy (OR: 0.524; 95% CI, 0.417-0.659). A multivariable predictive model incorporating these factors plus age and number of months since last biopsy achieved an AUC of 72.4%. Conclusions A combination of readily available clinical measures can stratify patients considering AS prostate biopsy. Risk of progression or upgrade can be estimated and incorporated into clinical practice. Patient summary The Canary-Early Detection Research Network Active Surveillance Biopsy Risk Calculator, an online tool, can be used to guide patient decision making regarding follow-up prostate biopsy.",
keywords = "Active surveillance, Biopsy, Progression, Prostate-specific antigen",
author = "Ankerst, {Donna P.} and Jing Xia and Thompson, {Ian M.} and Josef Hoefler and Newcomb, {Lisa F.} and Brooks, {James D.} and Carroll, {Peter R.} and Ellis, {William J.} and Gleave, {Martin E.} and Lance, {Raymond S.} and Nelson, {Peter S.} and Wagner, {Andrew A.} and Wei, {John T.} and Ruth Etzioni and Lin, {Daniel W.}",
note = "Funding Information: Donna P. Ankerst certifies that all conflicts ofinterest, including specific financial interests and relationships andaffiliations relevant to the subject matter or materials discussed in themanuscript (eg, employment/affiliation, grants or funding, consultancies,honoraria, stock ownership or options, expert testimony, royalties,or patents filed, received, or pending), are the following: Peter Carroll hasreceived honoraria from Takeda and GHI, has received research supportfrom Myriad Genetics and Genomic Health International, and is anadvisor to Medivation/Astellas. Ian M. Thompson is a consultant forExosome Diagnostics. Martin Gleave is a consultant for and an investor inOncogenex. John Wei is a study trial investigator for NCI, Histosonics,and Exosome.Funding/Support and role of the sponsor: The Canary Foundation and theUS National Institutes of Health sponsored the study and reviewed themanuscript. Funding Information: Our AS calculator has the potential to reduce the burdens of AS—morbidity, cost, anxiety—while maintaining the very high rate of cancer-specific survival expected from a low-risk cohort. It brings us closer to developing an individualized protocol for determining surveillance biopsy frequency and establishes a baseline against which other predictive models, potentially incorporating novel markers or diagnostic tests, can be compared. With this tool, physicians can now have a conversation with patients about AS regarding the potential outcomes of their surveillance biopsy and, ideally, tailoring the intensity of AS (including biopsy frequency) to the patient's risk of disease progression. Author contributions: Donna P. Ankerst had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. Study concept and design: Ankerst, Thompson. Acquisition of data: Thompson, Brooks, Carroll, Ellis, Gleave, Lance, Nelson, Wagner, Wei, Lin. Analysis and interpretation of data: Ankerst, Xia, Newcomb, Etzioni. Drafting of the manuscript: Ankerst, Thompson. Critical revision of the manuscript for important intellectual content: Ankerst, Thompson, Etzioni, Lin. Statistical analysis: Xia, Hoefler. Obtaining funding: Thompson, Newcomb, Etzioni, Lin. Administrative, technical, or material support: Hoefler, Newcomb. Supervision: Ankerst, Etzioni. Other (specify): None. Financial disclosures: Donna P. Ankerst certifies that all conflicts of interest, including specific financial interests and relationships and affiliations relevant to the subject matter or materials discussed in the manuscript (eg, employment/affiliation, grants or funding, consultancies, honoraria, stock ownership or options, expert testimony, royalties, or patents filed, received, or pending), are the following: Peter Carroll has received honoraria from Takeda and GHI, has received research support from Myriad Genetics and Genomic Health International, and is an advisor to Medivation/Astellas. Ian M. Thompson is a consultant for Exosome Diagnostics. Martin Gleave is a consultant for and an investor in Oncogenex. John Wei is a study trial investigator for NCI, Histosonics, and Exosome. Funding/Support and role of the sponsor: The Canary Foundation and the US National Institutes of Health sponsored the study and reviewed the manuscript. Appendix A Publisher Copyright: {\textcopyright} 2015 European Association of Urology.",
year = "2015",
doi = "10.1016/j.eururo.2015.03.023",
language = "English (US)",
volume = "68",
pages = "1083--1088",
journal = "European Urology",
issn = "0302-2838",
publisher = "Elsevier",
number = "6",
}