The Cancer Research of Kansas (CR Kansas) NCORP, formerly the Wichita Community Clinical Oncology (WCCOP), established and funded by the National Cancer Institute (NCI) in 1983, continued in 1987 (for 3 years), in 1990 (for 5 years), in 1995 (for 5 years), in 2000 (for 5 years), in 2005 (for 5 years), and 2010 (for 5 years). The WCCOP was a citywide cooperative program of the two major community hospitals and most of the Wichita oncologists. CR Kansas is a program, which will provide clinical trial access to a large portion ofthe state, including three community hospitals and most of the state's oncologists. Wichita is located n the center of the United States. It has the largest population center between Kansas City, 200 mile to the northeast, Denver, Colorado, 600 miles to the northwest, and Oklahoma City, 160 miles to the south. The presence of the CCOP/NCORP in Wichita brings the benefits of clinical research to patients in Wichita and its catchment area of south central, southwest and northeast Kansas - an ara that would otherwise be underserved because of its remote distance from the larger comprehensive cancer centers. CR Kansas consortium is in the process of developing a collaborative continuum of care that connects CR Kansas and community resources to deliver patient-centered, clinically integrated care for oncology patients, while demonstrating excellence in safety, quality and reducig avoidable costs. This collaboration will develop a coalition between practitioners across the stateof Kansas and Northern Oklahoma, including oncologists, primary care, surgeons, etc., that will provid an overall continuum of care from screening and prevention services through diagnosis, treatment an follow-up. CR Kansas aims to bring the state of Kansas community together in improving the overall f cancer care statewide. The CR Kansas National Community Oncology Research Program plans to continue an annual accrual of 200 credits on treatment protocols and 400 new credits on cancer control protocols using the eight research bases: NRG, SWOG, ECOG-ACRIN, Alliance, Wake Forest, University of Rochester, M.D. Anderson CCOP, SunCoast, as well as the Cancer Trials Support Unit.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Clinical Research Cooperative Agreements - Single Project (UG1)
Project #
1UG1CA189808-01
Application #
8789455
Study Section
Special Emphasis Panel (ZCA1-RTRB-E (M1))
Program Officer
Whitman, Cynthia B
Project Start
2014-08-01
Project End
2019-07-31
Budget Start
2014-08-01
Budget End
2015-07-31
Support Year
1
Fiscal Year
2014
Total Cost
$1,700,000
Indirect Cost
$251,959
Name
Via Christi Regional Medical Center
Department
Type
DUNS #
056577646
City
Wichita
State
KS
Country
United States
Zip Code
67214
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Hussain, Maha; Tangen, Catherine M; Thompson Jr, Ian M et al. (2018) Phase III Intergroup Trial of Adjuvant Androgen Deprivation With or Without Mitoxantrone Plus Prednisone in Patients With High-Risk Prostate Cancer After Radical Prostatectomy: SWOG S9921. J Clin Oncol 36:1498-1504
Wagner, Lynne I; Zhao, Fengmin; Goss, Paul E et al. (2018) Patient-reported predictors of early treatment discontinuation: treatment-related symptoms and health-related quality of life among postmenopausal women with primary breast cancer randomized to anastrozole or exemestane on NCIC Clinical Trials Group (CCTG Breast Cancer Res Treat 169:537-548
Persky, Daniel O; Li, Hongli; Rimsza, Lisa M et al. (2018) A phase I/II trial of vorinostat (SAHA) in combination with rituximab-CHOP in patients with newly diagnosed advanced stage diffuse large B-cell lymphoma (DLBCL): SWOG S0806. Am J Hematol 93:486-493
Durie, Brian G M; Hoering, Antje; Abidi, Muneer H et al. (2017) Bortezomib with lenalidomide and dexamethasone versus lenalidomide and dexamethasone alone in patients with newly diagnosed myeloma without intent for immediate autologous stem-cell transplant (SWOG S0777): a randomised, open-label, phase 3 trial. Lancet 389:519-527
Flaig, Thomas W; Plets, Melissa; Hussain, Maha H A et al. (2017) Abiraterone Acetate for Metastatic Prostate Cancer in Patients With Suboptimal Biochemical Response to Hormone Induction. JAMA Oncol 3:e170231

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