Duke Medical Center is currently completing its third 5-year grant cycle as a member of Cancer and Leukemia Group B (CALGB). Throughout Duke's involvement with CALGB this institution has consistently been one of the top institutions in overall patient accrual and was recognized in 2000 and 2001 as being the leading institution both in terms of patient accrual from the main member institution as well as from a growing affiliate network. Data quality for this large number of patients both at Duke and across the affiliate network has been excellent. This high level of commitment of patient resources to cooperative group activities both intramurally and extramurally is matched by a high level of scientific participation by Duke faculty across the disease and modality committees of CALGB. Particular areas of strength include Breast Cancer and Correlative Studies, Cancer in the Elderly and Health Outcome, Leukemia/Lymphoma and Transplant, and Respiratory Cancer, Thoracic Surgery, and Correlative Studies. Pilot work in these areas has led to group wide protocols within CALGB during the current grant cycle with several concepts and proposals already developed for the next study period. Additional faculty recruitment will further expand the scientific impact of Duke within CALGB. Furthermore, the Duke Oncology Network of rural oncology clinics staffed by Duke faculty and research personnel will enhance enrollment of a more diverse population of patients on clinical trials. The success that Duke has had within CALGB in terms of scientific participation, patient accrual, and data quality stem from a longstanding commitment for the Cancer Center to clinical research and cooperative group activities. Both intramural and extramural clinical trial participation is coordinated through centralized clinical trials offices, housed within the Duke Cancer Center. The organizational structure has been developed and refined over the last 15 years under the direction of Dr. Jeffrey Crawford, who serves both as the Principal Investigator for CALGB activities, as well as Director for clinical research for the Duke Comprehensive Cancer Center. This organizational structure is further strengthened by close interaction with the CALGB Biostatistics and Data Management Center, which is headquartered at Duke under the direction of Dr. Stephen George, who is also the Director of Biostatistics for the Duke Cancer Center. As a leading institution within CALGB activities over the last 15 years, Duke is looking forward to funding support appropriate to our current and growing level of patient accrual and scientific involvement in CALGB trials during the next grant cycle.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Cooperative Clinical Research--Cooperative Agreements (U10)
Project #
5U10CA047577-20
Application #
7253895
Study Section
Subcommittee G - Education (NCI)
Program Officer
Mooney, Margaret M
Project Start
1988-04-01
Project End
2009-03-31
Budget Start
2007-06-27
Budget End
2008-03-31
Support Year
20
Fiscal Year
2007
Total Cost
$160,142
Indirect Cost
Name
Duke University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Morrison, Vicki A; McCall, Linda; Muss, Hyman B et al. (2018) The impact of actual body weight-based chemotherapy dosing and body size on adverse events and outcome in older patients with breast cancer: Results from Cancer and Leukemia Group B (CALGB) trial 49907 (Alliance A151436). J Geriatr Oncol 9:228-234
Innocenti, Federico; Jiang, Chen; Sibley, Alexander B et al. (2018) Genetic variation determines VEGF-A plasma levels in cancer patients. Sci Rep 8:16332
Li, Megan; Mulkey, Flora; Jiang, Chen et al. (2018) Identification of a Genomic Region between SLC29A1 and HSP90AB1 Associated with Risk of Bevacizumab-Induced Hypertension: CALGB 80405 (Alliance). Clin Cancer Res 24:4734-4744
Freedman, Rachel A; Seisler, D K; Foster, J C et al. (2017) Risk of acute myeloid leukemia and myelodysplastic syndrome among older women receiving anthracycline-based adjuvant chemotherapy for breast cancer on Modern Cooperative Group Trials (Alliance A151511). Breast Cancer Res Treat 161:363-373
Bluethmann, Shirley M; Alfano, Catherine M; Clapp, Jonathan D et al. (2017) Cognitive function and discontinuation of adjuvant hormonal therapy in older breast cancer survivors: CALGB 369901 (Alliance). Breast Cancer Res Treat 165:677-686
Ellis, Matthew J; Suman, Vera J; Hoog, Jeremy et al. (2017) Ki67 Proliferation Index as a Tool for Chemotherapy Decisions During and After Neoadjuvant Aromatase Inhibitor Treatment of Breast Cancer: Results From the American College of Surgeons Oncology Group Z1031 Trial (Alliance). J Clin Oncol 35:1061-1069
Doostan, Iman; Karakas, Cansu; Kohansal, Mehrnoosh et al. (2017) Cytoplasmic Cyclin E Mediates Resistance to Aromatase Inhibitors in Breast Cancer. Clin Cancer Res 23:7288-7300
Mandelblatt, Jeanne S; Cai, Ling; Luta, George et al. (2017) Frailty and long-term mortality of older breast cancer patients: CALGB 369901 (Alliance). Breast Cancer Res Treat 164:107-117
Freedman, Rachel A; Foster, Jared C; Seisler, Drew K et al. (2017) Accrual of Older Patients With Breast Cancer to Alliance Systemic Therapy Trials Over Time: Protocol A151527. J Clin Oncol 35:421-431
Himelstein, Andrew L; Foster, Jared C; Khatcheressian, James L et al. (2017) Effect of Longer-Interval vs Standard Dosing of Zoledronic Acid on Skeletal Events in Patients With Bone Metastases: A Randomized Clinical Trial. JAMA 317:48-58

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