PROJECT-002 - LEUKEMIA RESEARCH PROGRAM (LR) PROJECT SUMMARY / ABSTRACT The Leukemia Research (LR) Program within The Ohio State University Comprehensive Cancer Center (OSUCCC) is co-led by two physician scientists; Drs. John C. Byrd and Michael R. Grever who bring together 34 peer-reviewed funded members from 9 Departments and 5 Colleges (Engineering, Pharmacy, Medicine, Veterinary Medicine, and Arts & Sciences). The program is focused on the etiology, pathogenesis, prognosis, and treatment of leukemia with emphasis on acute myeloid leukemia (AML), human T-cell lymphotrophic virus l (HTLV-1) leukemia, large granular lymphocyte leukemia, hairy cell leukemia and chronic lymphocytic leukemia (CLL). LR Program-wide seminars, retreats, and disease-specific meetings provide an avenue for interaction among scientists and physicians to improve the quality of scientific discovery made through research. The LR Program integrates the use of novel technologies and translational and clinical support personnel provided through OSUCCC shared resources to facilitate impactful discoveries that ultimately have the potential to change the lives of patients with leukemia. LR Program discoveries span diagnostics through therapeutics, many of which are actively tested in both investigator initiated clinical trials and also NCI sponsored Phase I and II as well as cooperative group trials where our members have prominent leadership roles.
The Specific Aims of LR Program include: 1) to integrate genetic, epigenetic, RNA/protein, non-coding RNAs, biochemical and immunosuppressive features of leukemic cells in order to enhance risk stratification and target identification; and 2) to foster preclinical and clinical development of epigenetic, targeted molecular, and immunologic therapeutics directed at the causes of leukemic transformation and progression. LR Program members have published 557 manuscripts of which 48% are inter-programmatic, 53% are intra- programmatic, 61% are multi-institutional; total collaborative publications are 93%. The Program has $8.7M in annual direct costs of peer-reviewed funding of which $6.1M (70%) is from the NCI, including strong programmatic funding in basic, translational, and clinical research. With regard to translational research, in five years the LR Program members have accrued 1,660 patients to interventional clinical trials, 100% of which were therapeutic accruals, and of those, 989, or 60%, were placed on investigator-initiated trials. Of the 1,660 patients accrued, 1,495 or 90% were on Phase I/II trials. LR Program members have led the development of two therapeutic agents (ibrutinib and idelalisib) that were recently FDA approved for leukemia. Additionally, LR Program members have developed two novel diagnostic tests that are now utilized in clinical practice. Our future plans consist of targeted recruitment, continued enhancement of collaborative efforts, better molecular classification of both AML and CLL for improvement in targeted therapies, and moving a number of preclinical and clinical observations onto novel clinical trials.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA016058-43
Application #
9632737
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2018-12-01
Budget End
2019-11-30
Support Year
43
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Ohio State University
Department
Type
DUNS #
832127323
City
Columbus
State
OH
Country
United States
Zip Code
43210
Sharpnack, Michael F; Chen, Bin; Aran, Dvir et al. (2018) Global Transcriptome Analysis of RNA Abundance Regulation by ADAR in Lung Adenocarcinoma. EBioMedicine 27:167-175
Tanaka, Ichidai; Sato, Mitsuo; Kato, Toshio et al. (2018) eIF2?, a subunit of translation-initiation factor EIF2, is a potential therapeutic target for non-small cell lung cancer. Cancer Sci 109:1843-1852
Slayton, William B; Schultz, Kirk R; Kairalla, John A et al. (2018) Dasatinib Plus Intensive Chemotherapy in Children, Adolescents, and Young Adults With Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia: Results of Children's Oncology Group Trial AALL0622. J Clin Oncol 36:2306-2314
Bassett, Emily A; Palanichamy, Kamalakannan; Pearson, Mitchell et al. (2018) Calpastatin phosphorylation regulates radiation-induced calpain activity in glioblastoma. Oncotarget 9:14597-14607
Trn?ný, Marek; Verhoef, Gregor; Dyer, Martin Js et al. (2018) A phase II multicenter study of the anti-CD19 antibody drug conjugate coltuximab ravtansine (SAR3419) in patients with relapsed or refractory diffuse large B-cell lymphoma previously treated with rituximab-based immunotherapy. Haematologica 103:1351-1358
Bishop, Erin A; Java, James J; Moore, Kathleen N et al. (2018) Surgical outcomes among elderly women with endometrial cancer treated by laparoscopic hysterectomy: a NRG/Gynecologic Oncology Group study. Am J Obstet Gynecol 218:109.e1-109.e11
Kim, Miriam Y; Yu, Kyung-Rok; Kenderian, Saad S et al. (2018) Genetic Inactivation of CD33 in Hematopoietic Stem Cells to Enable CAR T Cell Immunotherapy for Acute Myeloid Leukemia. Cell 173:1439-1453.e19
Malpeli, Giorgio; Barbi, Stefano; Tosadori, Gabriele et al. (2018) MYC-related microRNAs signatures in non-Hodgkin B-cell lymphomas and their relationships with core cellular pathways. Oncotarget 9:29753-29771
Niemas-Teshiba, Risa; Matsuno, Ryosuke; Wang, Larry L et al. (2018) MYC-family protein overexpression and prominent nucleolar formation represent prognostic indicators and potential therapeutic targets for aggressive high-MKI neuroblastomas: a report from the children's oncology group. Oncotarget 9:6416-6432
Li, Jingyi; Xu, Jie; Abruzzo, Lynne V et al. (2018) Acute myeloid leukemia with t(4;12)(q12;p13): an aggressive disease with frequent involvement of PDGFRA and ETV6. Oncotarget 9:10987-10994

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