Grant: Project Grant
University of British Columbia
$906,525.00
Prostate cancer risk stratification for active surveillance using computer-aided analysis of histopathology and transcriptomics
EF 2020-21
Résumé
Prostate cancer remains the 2nd most common cause of cancer-related death in North American men. There are different risk categories; many that are diagnosed at an early stage will either become more dangerous over time, or will never impact on a man's longevity or general health. These latter cases can be managed with active surveillance, which avoids overtreatment and associated negative effects on quality of life. Current risk stratification tools, however, do not allow us to distinguish reliably which patients are best-suited for active surveillance and which are likely to develop higher-risk cancer over time.
The artificial intelligence (AI) field is advancing at a staggering rate, accelerated by modern hardware and software. Across the board, healthcare is characterized by a tremendous proliferation of data, including huge amounts generated by digitizing pathology slides. A fundamental question is whether the computer can identify features in a biopsy that cannot be recognized by the human brain? We will deploy AI-based techniques to analyze digitized tumour tissue images and genetic markers in patients undergoing active surveillance. Our goal is to discover new pathologic and genetic markers that can more accurately stratify risk of progression in newly diagnosed prostate cancer so that a greater number can be monitored safely with active surveillance, including a subset that would be considered intermediate risk by current criteria, while higher risk cases can be selected for definitive treatment. Novel biomarkers will be extremely valuable to patients, caregivers and physicians in deciding on best treatment. This could dramatically decrease the risks of undesirable and unexpected cancer progression, and anxieties related to being on a cancer surveillance program. Further, the intensity of invasive and costly sequential prostate biopsies can be reduced in low-risk patients, leading to a better quality of life and decreased health care utilization.
Programme
Project Grant
Bénéficiaire
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
433061
Name
Bashashati Ali
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Medical Physics & Imaging
Projecttitle
Prostate cancer risk stratification for active surveillance using computer-aided analysis of histopathology and transcriptomics
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$906,525
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Computational Pathology; Digital Pathology; Image Analysis; Machine Learning; Prostate Cancer; Transcriptomics
Abstract
Prostate cancer remains the 2nd most common cause of cancer-related death in North American men. There are different risk categories; many that are diagnosed at an early stage will either become more dangerous over time, or will never impact on a man's longevity or general health. These latter cases can be managed with active surveillance, which avoids overtreatment and associated negative effects on quality of life. Current risk stratification tools, however, do not allow us to distinguish reliably which patients are best-suited for active surveillance and which are likely to develop higher-risk cancer over time.
The artificial intelligence (AI) field is advancing at a staggering rate, accelerated by modern hardware and software. Across the board, healthcare is characterized by a tremendous proliferation of data, including huge amounts generated by digitizing pathology slides. A fundamental question is whether the computer can identify features in a biopsy that cannot be recognized by the human brain? We will deploy AI-based techniques to analyze digitized tumour tissue images and genetic markers in patients undergoing active surveillance. Our goal is to discover new pathologic and genetic markers that can more accurately stratify risk of progression in newly diagnosed prostate cancer so that a greater number can be monitored safely with active surveillance, including a subset that would be considered intermediate risk by current criteria, while higher risk cases can be selected for definitive treatment. Novel biomarkers will be extremely valuable to patients, caregivers and physicians in deciding on best treatment. This could dramatically decrease the risks of undesirable and unexpected cancer progression, and anxieties related to being on a cancer surveillance program. Further, the intensity of invasive and costly sequential prostate biopsies can be reduced in low-risk patients, leading to a better quality of life and decreased health care utilization.
Competitiondate
202010
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Bashashati, Ali; Black, Peter C; Goldenberg, Larry; Salcudean, Septimiu E
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $906,525~ $0~