My current research agenda falls into two main areas. The first area is my focus on a population-based approach to examining the quality of care for women with breast cancer. The second area is the evaluation of online communication and service tools to improve the quality of cancer early detection initiatives in primary care settings. My research agenda over the next five years will extend my current work in several ways. First, I plan to expand my current SEER-based population research program to address the quality of care for women with breast cancer. This will include: 1) additional population-based studies of determinants and outcomes of other potentially marginalized patient populations;and 2) population-based intervention studies to improve communication, treatment processes and outcomes for women with breast cancer. Second, I will build and evaluate novel online communication and service tools for patients and providers to improve cancer screening processes and outcomes in primary care settings. The goals of my mentoring plan are 1) to increase the quantity and quality of NIH investigator-initiated proposals in oncology health services research from the University of Michigan;2) to foster interest in oncology-related health services research by fellows and junior investigators through my leadership on clinical training programs at the University of Michigan;and 3) recruit new investigators to the medical school focused on health services research in oncology. In order to address the goals above I will lead the following initiatives: 1) to obtain intramural and extramural funding to recruit and support clinician investigators and non-clinician research scientists in oncology health services research;2) to personally mentor these investigators towards a successful career;3) to develop and direct educational programs to support this area of research;and 4) to coordinate efforts in this area across professional schools at Michigan. The structure, process and outcomes of my personal mentoring program are described in detail in the application.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Scientist Award (K05)
Project #
5K05CA111340-04
Application #
7925637
Study Section
Special Emphasis Panel (ZCA1-RTRB-L (J1))
Program Officer
Perkins, Susan N
Project Start
2006-09-21
Project End
2012-08-31
Budget Start
2010-09-01
Budget End
2011-08-31
Support Year
4
Fiscal Year
2010
Total Cost
$105,620
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Griggs, Jennifer J; Hamilton, Ann S; Schwartz, Kendra L et al. (2017) Discordance between original and central laboratories in ER and HER2 results in a diverse, population-based sample. Breast Cancer Res Treat 161:375-384
Jagsi, Reshma; Li, Yun; Morrow, Monica et al. (2015) Patient-reported Quality of Life and Satisfaction With Cosmetic Outcomes After Breast Conservation and Mastectomy With and Without Reconstruction: Results of a Survey of Breast Cancer Survivors. Ann Surg 261:1198-206
Jagsi, Reshma; Griffith, Kent A; Kurian, Allison W et al. (2015) Concerns about cancer risk and experiences with genetic testing in a diverse population of patients with breast cancer. J Clin Oncol 33:1584-91
Friese, Christopher R; Martinez, Kathryn A; Abrahamse, Paul et al. (2014) Providers of follow-up care in a population-based sample of breast cancer survivors. Breast Cancer Res Treat 144:179-84
Jagsi, Reshma; Hawley, Sarah T; Abrahamse, Paul et al. (2014) Impact of adjuvant chemotherapy on long-term employment of survivors of early-stage breast cancer. Cancer 120:1854-62
Morrow, Monica; Li, Yun; Alderman, Amy K et al. (2014) Access to breast reconstruction after mastectomy and patient perspectives on reconstruction decision making. JAMA Surg 149:1015-21
Jagsi, Reshma; Pottow, John A E; Griffith, Kent A et al. (2014) Long-term financial burden of breast cancer: experiences of a diverse cohort of survivors identified through population-based registries. J Clin Oncol 32:1269-76
Friese, Christopher R; Pini, T May; Li, Yun et al. (2013) Adjuvant endocrine therapy initiation and persistence in a diverse sample of patients with breast cancer. Breast Cancer Res Treat 138:931-9
Pini, T May; Hawley, Sarah T; Li, Yun et al. (2012) The influence of non-clinical patient factors on medical oncologists' decisions to recommend breast cancer adjuvant chemotherapy. Breast Cancer Res Treat 134:867-74
Jagsi, Reshma; Abrahamse, Paul; Hawley, Sarah T et al. (2012) Underascertainment of radiotherapy receipt in Surveillance, Epidemiology, and End Results registry data. Cancer 118:333-41

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