PROTOCOL REVIEW AND MONITORING SYSTEM (Core-361) ABSTRACT The Protocol Review and Monitoring System (PRMS) of the University of Colorado Cancer Center (UCCC) is an integral component of the clinical research performed at the UCCC consortium. This component was disapproved in 2011 and subsequently re-engineered by a new chair, Jonathan Gutman MD, Associate Professor in the Department of Medicine and a clinical investigator in allogeneic stem cell transplantation for hematologic malignancies. These efforts led to re-approval by the NCI in June 2015. PRMS functions for cancer clinical trials across the UCCC consortium include: 1) review of scientific merit prior to submission to an IRB; 2) assessment of study priority and feasibility, and 3) monitoring of intervention trials for accrual and scientific progress. The PRMS collaborates with, but operates independently of the IRB and the UCCC Data and Safety Monitoring Committee (DSMC). The PRMS is comprised of two committees, the PRMS-Executive Committee (PRMS-EC) and the PRMS-Scientific Review Committee (PRMS-SRC). Members of these committees reflect the breadth and diversity of disciplines of UCCC. The PRMS-EC and PRMS-SRC meet on alternating weeks resulting in efficient disposition and flow of protocols. The PRMS-EC assesses prioritization and feasibility of protocols and grants expedited approval if appropriate. Evaluation of scientific merit is performed by the PRMS- SRC. New protocol submissions to PRMS are reviewed with differing levels of intensity depending on the type of protocol. Institutional and industry intervention trials receive the most comprehensive review before being approved to submit to the IRB. Once a protocol is activated, the PRMS-EC monitors scientific progress. PRMS- EC membership includes the PRMS chair, deputy chair, PRMS administrator and all disease site leaders. Inclusion of disease site leaders ensures that larger scope issues ? prioritization, feasibility, and progress ? are continuously revisited by those responsible for leading clinical research in their respective areas. The PRMS- SRC provides focused, well documented scientific reviews of institutional and industry intervention protocols. PRMS-SRC membership includes the PRMS chair, deputy chair, PRMS administrator, biostatisticians and a diverse group of investigators from all oncologic disciplines. Since 2013, PRMS has reviewed and prioritized 397 intervention studies. 25% (98) were NCTN or external peer reviewed studies that received a feasibility and prioritization review only. The remaining 75% were institutional (45) and industry (255) studies. Of the institutional studies, 7 (16%) were disapproved. During this same period 67 six month low accrual warning letters, 39 ten month low accrual warning letters, and 42 twelve month low accrual warning letter were issued for intervention studies and 35 were closed by PRMS for a lack of progress or closed voluntarily by the PI following receipt of letters from PRMS. During the next grant period PRMS will continue to apply a careful evaluation of feasibility and prioritization and perform a rigorous review of scientific merit to ensure that UCCC investigators open studies that are scientifically meritorious, feasible to complete, and meet the priorities of the UCCC.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA046934-32
Application #
9867673
Study Section
Subcommittee H - Clinical Groups (NCI)
Project Start
Project End
Budget Start
2020-02-01
Budget End
2021-01-31
Support Year
32
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Colorado Denver
Department
Type
DUNS #
041096314
City
Aurora
State
CO
Country
United States
Zip Code
80045
Oweida, Ayman; Phan, Andy; Vancourt, Benjamin et al. (2018) Hypofractionated Radiotherapy Is Superior to Conventional Fractionation in an Orthotopic Model of Anaplastic Thyroid Cancer. Thyroid 28:739-747
Gadalla, Shahinaz M; Wang, Tao; Loftus, David et al. (2018) No association between donor telomere length and outcomes after allogeneic unrelated hematopoietic cell transplant in patients with acute leukemia. Bone Marrow Transplant 53:383-391
Ghosh, Moumita; Miller, York E; Nakachi, Ichiro et al. (2018) Exhaustion of Airway Basal Progenitor Cells in Early and Established Chronic Obstructive Pulmonary Disease. Am J Respir Crit Care Med 197:885-896
Helfrich, Barbara A; Gao, Dexiang; Bunn Jr, Paul A (2018) Eribulin inhibits the growth of small cell lung cancer cell lines alone and with radiotherapy. Lung Cancer 118:148-154
Gavin, Kathleen M; Kohrt, Wendy M; Klemm, Dwight J et al. (2018) Modulation of Energy Expenditure by Estrogens and Exercise in Women. Exerc Sport Sci Rev 46:232-239
Cao, Yu; Green, Katherine; Quattlebaum, Steve et al. (2018) Methylated genomic loci encoding microRNA as a biomarker panel in tissue and saliva for head and neck squamous cell carcinoma. Clin Epigenetics 10:43
Conroy, Shannon M; Shariff-Marco, Salma; Yang, Juan et al. (2018) Characterizing the neighborhood obesogenic environment in the Multiethnic Cohort: a multi-level infrastructure for cancer health disparities research. Cancer Causes Control 29:167-183
Bagati, Archis; Bianchi-Smiraglia, Anna; Moparthy, Sudha et al. (2018) FOXQ1 controls the induced differentiation of melanocytic cells. Cell Death Differ 25:1040-1049
Tuttle, Kathryn D; Krovi, S Harsha; Zhang, Jingjing et al. (2018) TCR signal strength controls thymic differentiation of iNKT cell subsets. Nat Commun 9:2650
Keysar, Stephen B; Eagles, Justin R; Miller, Bettina et al. (2018) Salivary Gland Cancer Patient-Derived Xenografts Enable Characterization of Cancer Stem Cells and New Gene Events Associated with Tumor Progression. Clin Cancer Res 24:2935-2943

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