14.0 Abstract: Early Phase Clinical Research Support UMGCC investigator-initiated pilot (pre-Phase I) or Phase I trials that test clinical interventions with a candidate agent or device for the diagnosis, prevention, detection, or treatment of cancer frequently require funding to support research coordination, data management, and regulatory functions. Data from these trial protocols can be used to support later-phase activities with these interventions or as a basis for acquiring funding from other sources to continue the piloted activities. This critical early support provided by Early Phase Clinical Research Support (EPCRS) is necessary to move such trials forward, especially because per-patient costs are not reimbursed. EPCRS funds will be for UMGCC personnel, including research coordinators and data managers, to facilitate innovative clinical investigation efforts. Trials supported by EPCRS will be subject to additional criteria for consideration by the Clinical Research Committee either before their implementation and development or after needs emerge that are not addressed by other sponsoring agencies. The trials will be assigned a priority scale for funding based on how the protocol is significant and innovative in promoting the development of novel cancer diagnosis, treatment, imaging, or prevention strategies and based on evidence that the trial will enable correlative science as a result of EPCRS funding, with translational collaborators and assays in place. During the most recent 5-year funding period, 21 trials were developed by UMGCC investigators within the guidelines for funding through EPCRS. The narrative highlights five protocols recently launched or in development as examples of trials that will benefit from EPCRS in the future. These trials flow from investigator-initiated clinical research or are the logical consequence of an alliance between basic scientists at UMGCC and clinicians well suited to address a translational science goal and are either not incorporated into other grant-supported or Cooperative Group trials of NCI or other funding agencies or have only partial industry support.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA134274-12
Application #
9750159
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2019-08-01
Budget End
2020-07-31
Support Year
12
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Maryland Baltimore
Department
Type
DUNS #
188435911
City
Baltimore
State
MD
Country
United States
Zip Code
21201
Wang, Lei; Felts, Sara J; Van Keulen, Virginia P et al. (2018) Exploring the effect of library preparation on RNA sequencing experiments. Genomics :
Nathenson, Michael J; Barysauskas, Constance M; Nathenson, Robert A et al. (2018) Surgical resection for recurrent retroperitoneal leiomyosarcoma and liposarcoma. World J Surg Oncol 16:203
Sallmyr, Annahita; Tomkinson, Alan E (2018) Repair of DNA double-strand breaks by mammalian alternative end-joining pathways. J Biol Chem 293:10536-10546
Kerr, Candace; Adhikary, Gautam; Grun, Daniel et al. (2018) Combination cisplatin and sulforaphane treatment reduces proliferation, invasion, and tumor formation in epidermal squamous cell carcinoma. Mol Carcinog 57:3-11
Connolly, Sean; Quasi-Woode, Devona; Waldron, Laura et al. (2018) Calcineurin Regulatory Subunit Calcium-Binding Domains Differentially Contribute to Calcineurin Signaling in Saccharomyces cerevisiae. Genetics 209:801-813
Pauza, C David; Liou, Mei-Ling; Lahusen, Tyler et al. (2018) Gamma Delta T Cell Therapy for Cancer: It Is Good to be Local. Front Immunol 9:1305
Wang, Lei; Felts, Sara J; Van Keulen, Virginia P et al. (2018) Integrative Genome-Wide Analysis of Long Noncoding RNAs in Diverse Immune Cell Types of Melanoma Patients. Cancer Res 78:4411-4423
McCusker, Michael G; El Chaer, Firas; Duffy, Alison et al. (2018) Combination of Blinatumomab and Vincristine Sulfate Liposome Injection for Treatment of Relapsed Philadelphia Chromosome Positive B-cell Acute Lymphoblastic Leukemia. Am J Leuk Res 2:
Wang, Junxiang; Zhao, Liang; Ye, Yanfang et al. (2018) Adverse event detection by integrating twitter data and VAERS. J Biomed Semantics 9:19
Furusawa, Aki; Reiser, John; Sadashivaiah, Kavitha et al. (2018) Eomesodermin Increases Survival and IL-2 Responsiveness of Tumor-specific CD8+ T Cells in an Adoptive Transfer Model of Cancer Immunotherapy. J Immunother 41:53-63

Showing the most recent 10 out of 257 publications