CANCER BIOSTATISTICS SHARED RESOURCE ABSTRACT The Cancer Biostatistics Shared Resource (CB) provides state-of-the-art biostatistics and research design to support clinical, translational, laboratory, and population sciences investigators at Huntsman Cancer Institute (HCI). CB provides expert consulting for researchers, from formulation of research objectives to study design, analysis, development of novel methods, interpretation, and dissemination of results. CB includes nine statisticians with specialized cancer expertise targeting Cancer Center members? current and anticipated future needs, including clinical trial design, cancer epidemiology, causal inference, longitudinal data analysis, predictive modeling, meta-analysis, and Bayesian techniques. CB contributes significantly to the success of HCI?s Research Programs and progress toward HCI?s strategic objectives by ensuring timely, rigorous, and appropriate statistical methods are used in design, analysis, and interpretation of research data. Established in 1996, CB is directed by Kenneth Boucher, PhD, and Benjamin Haaland, PhD.
The aims of the Resource are: 1) to provide state-of-the-art biostatistics and research design support to HCI clinical, translational, laboratory, and population sciences investigators; and 2) to support the scientific research objectives of the Cancer Center by applying biostatistical methods for team science grants, high-impact research, and clinical trials in a high- quality, cost-effective manner. Access to CB is afforded equally to all HCI researchers. CB enhances scientific interactions and productivity at HCI by ensuring rigorous study design, accurate, reproducible, and transparent data analysis, and valid results. In the current funding period, CB has contributed to >140 publications and 39 funded grants, including two U01s, a U54, a Patient-Centered Outcomes Research Institute (PCORI) grant, and a Breakthrough Funding Award. CB currently participates in more than 26 HCI investigator-initiated clinical trials (IITs) and has been involved in the design or analysis of 117 proposed clinical trials since 2014. CB members are actively involved in a broad spectrum of projects of particular relevance to our catchment area, including rural/frontier cancer disparities, treatment and prevention of melanoma, and care standards for lung cancer. CB adds value to HCI research by solidifying research questions; improving study design, conduct, and power; and utilizing rigorous, reproducible, and high-quality statistical techniques. CB works closely with other HCI Shared Resources to ensure best statistical practices in multi-resource projects. Similarly, CB works closely with the HCI Clinical Trials Office to ensure appropriate methods are used in design, monitoring, and analysis of HCI IITs. The full spectrum of HCI?s mission is impacted by CB, from understanding cancer?s beginnings, to creation and improvement of cancer treatments, to understanding cancer risk, prevention, and care.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA042014-31
Application #
9935884
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2020-04-01
Budget End
2021-03-31
Support Year
31
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Utah
Department
Type
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Vahrenkamp, Jeffery M; Yang, Chieh-Hsiang; Rodriguez, Adriana C et al. (2018) Clinical and Genomic Crosstalk between Glucocorticoid Receptor and Estrogen Receptor ? In Endometrial Cancer. Cell Rep 22:2995-3005
Gupta, Sumati; Albertson, Daniel; Gaston, David et al. (2018) Comprehensive Genomic Sequencing of Urothelial Tumors Identifies Rare SMARCB1 (INI-1)-Deficient Carcinomas of the Urinary System. Clin Genitourin Cancer 16:e373-e382
Yazdimamaghani, Mostafa; Moos, Philip J; Ghandehari, Hamidreza (2018) Global gene expression analysis of macrophage response induced by nonporous and porous silica nanoparticles. Nanomedicine 14:533-545
Al-Agha, Abdulmoein Eid; Ahmed, Ihab Abdulhamed; Nuebel, Esther et al. (2018) Primary Ovarian Insufficiency and Azoospermia in Carriers of a Homozygous PSMC3IP Stop Gain Mutation. J Clin Endocrinol Metab 103:555-563
Petersen, Jenna; Koptiuch, Cathryn; Wu, Yelena P et al. (2018) Patterns of family communication and preferred resources for sharing information among families with a Lynch syndrome diagnosis. Patient Educ Couns 101:2011-2017
Flack, Caralyn E; Parkinson, John S (2018) A zipped-helix cap potentiates HAMP domain control of chemoreceptor signaling. Proc Natl Acad Sci U S A 115:E3519-E3528
Pishas, Kathleen I; Drenberg, Christina D; Taslim, Cenny et al. (2018) Therapeutic Targeting of KDM1A/LSD1 in Ewing Sarcoma with SP-2509 Engages the Endoplasmic Reticulum Stress Response. Mol Cancer Ther 17:1902-1916
Blackburn, Brenna E; Ganz, Patricia A; Rowe, Kerry et al. (2018) Reproductive and gynecological complication risks among thyroid cancer survivors. J Cancer Surviv 12:702-711
Wu, Yelena P; Aspinwall, Lisa G; Nagelhout, Elizabeth et al. (2018) Development of an Educational Program Integrating Concepts of Genetic Risk and Preventive Strategies for Children with a Family History of Melanoma. J Cancer Educ 33:774-781
Kim, Hyung-Seok; McKnite, Autumn; Xie, Yuanyuan et al. (2018) Fibronectin type III and intracellular domains of Toll-like receptor 4 interactor with leucine-rich repeats (Tril) are required for developmental signaling. Mol Biol Cell 29:523-531

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