A major challenge to the adoption of personalized medicine approaches to diagnosis and treatment, usinggenomic information, is that the data required to address critical questions relevant to clinical applications,economics, policy, and regulatory issues are widely dispersed. An immediate concern is to identify thepersonalized medicine approaches that are now being used in clinical practice or are in advanced stages ofdevelopment, and then to evaluate how those approaches came to be adopted, their apparent value to date,and what their impact has been.We have been developing and piloting a framework for the collection and synthesis of data related topersonalized medicine with the goal of establishing an evidence base on technologies and research fortranslating research findings into clinical practice and policy. The Evidence Project will build on our pilot workwith an emphasis on personalized medicine for colorectal and breast cancer.Our objective is to develop an evidence base on personalized medicine technologies, using genomics, forcolorectal and breast cancer.
The Specific Aims are to:
Aim 1 : Identify, describe, and assess available data sources for the evidence base on colorectal and breastcancer personalized medicine interventions.
Aim 2 : Conduct case studies of personalized medicine technologies for colorectal and breast cancer thatfocus on clinical applications, economics, policy and regulatory issues and provide findings on keytechnologies and supplement detailed case studies with ongoing horizon scans of personalized medicinetechnology.
Aim 3 : Systematically review data needed for Program Projects: evaluations of clinical applications, includingutilization data and studies of patients' and providers' preferences, and economic evaluations ofpersonalized medicineAim 4: Evaluate the policy implications of findings, including: what is known about personalized medicineinnovations; how and why personalized medicine innovations get (or not get) to be adopted; and thepotential or actual value and societal impact of personalized medicine innovations.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
1P01CA130818-01A1
Application #
7515633
Study Section
Special Emphasis Panel (ZCA1-RPRB-7 (M1))
Project Start
2008-07-01
Project End
2011-06-30
Budget Start
2008-09-16
Budget End
2009-08-31
Support Year
1
Fiscal Year
2008
Total Cost
$43,354
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143
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Weitzel, Jeffrey N; Clague, Jessica; Martir-Negron, Arelis et al. (2013) Prevalence and type of BRCA mutations in Hispanics undergoing genetic cancer risk assessment in the southwestern United States: a report from the Clinical Cancer Genetics Community Research Network. J Clin Oncol 31:210-6

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