The Hematological Malignancies Program (HMP) continues a long tradition of leukemia and lymphoma research in the St. Jude Children's Research Hospital Comprehensive Cancer Center (SJCCC), facilitating interdisciplinary collaborations among basic, translational and clinical research investigators. The HMP has 27 Full members, and one Associate (junior mentored) member, drawn from seven departments. The overall goal of the Program is to advance cures for children with leukemia, while minimizing acute and long-term side effects of therapy. To this end, the Program conducts multi-disciplinary research across the full spectrum of basic science, translational and clinical research: (1) Basic Science Research within the HMP aims to identify and characterize the key genetic alterations that underlie childhood hematological malignancies, and to determine the potential of these alterations to serve as therapeutic targets. This group also studies the biology of bone marrow transplantation. (2) Translational Research focuses on defining genetic determinants of disease risk, drug pharmacology; efficacy and toxicity. This group also builds on genomic and transplant discoveries made in the Basic Science Group to develop innovative tools to classify leukemia, detect minimal residual disease, and treat hematologic malignancies. (3) Clinical Research within the HMP serves as the final step to translate basic science discoveries to the clinic. To this end the group conducts large, single-institution or multi-center clinical trials to advance cures for childhood leukemia, including trials of molecular targeted and cell transplant-based therapies. Members also collaborate with experts in the Cancer Prevention and Control Program to define and mitigate treatment late effects. For many years the members of the HMP have played leading and collaborative roles in the national consortia including the NCI-Children's Oncology Group (COG). The HMP benefits from strong extramural funding that totals $14.3 million in cancer-related awards ($10.4 million peer-reviewed; $3.9 million non-peer reviewed sources). The HMP is also a highly productive Program, publishing 469 manuscripts during the last funding period (30%, intraprogrammatic; 28%, interprogrammatic).

Public Health Relevance

Leukemia is the most common pediatric malignancy, accounting for one third of all childhood cancers. Despite steady increases in the overall cure rate for leukemias, significant numbers of children still suffer relapsed or refractory disease, and many have unacceptable treatment-related toxicities. Therefore, by translating basic understanding of leukemia biology to the clinic, the HMP strives to improve the use of existing therapies, discover new treatments for resistant disease, and reduce late effects of therapy.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA021765-38
Application #
9228958
Study Section
Subcommittee A - Cancer Centers (NCI-A)
Project Start
Project End
Budget Start
2017-03-01
Budget End
2018-02-28
Support Year
38
Fiscal Year
2017
Total Cost
$657,292
Indirect Cost
$291,113
Name
St. Jude Children's Research Hospital
Department
Type
Independent Hospitals
DUNS #
067717892
City
Memphis
State
TN
Country
United States
Zip Code
38105
Shadrick, William R; Slavish, Peter J; Chai, Sergio C et al. (2018) Exploiting a water network to achieve enthalpy-driven, bromodomain-selective BET inhibitors. Bioorg Med Chem 26:25-36
Ramsey, Laura B; Balis, Frank M; O'Brien, Maureen M et al. (2018) Consensus Guideline for Use of Glucarpidase in Patients with High-Dose Methotrexate Induced Acute Kidney Injury and Delayed Methotrexate Clearance. Oncologist 23:52-61
Churchman, Michelle L; Qian, Maoxiang; Te Kronnie, Geertruy et al. (2018) Germline Genetic IKZF1 Variation and Predisposition to Childhood Acute Lymphoblastic Leukemia. Cancer Cell 33:937-948.e8
Hatfield, M Jason; Binder, Randall J; Gannon, Rowan et al. (2018) Potent, Irreversible Inhibition of Human Carboxylesterases by Tanshinone Anhydrides Isolated from Salvia miltiorrhiza (""Danshen""). J Nat Prod 81:2410-2418
Vo, BaoHan T; Kwon, Jin Ah; Li, Chunliang et al. (2018) Mouse medulloblastoma driven by CRISPR activation of cellular Myc. Sci Rep 8:8733
Drummond, Catherine J; Hanna, Jason A; Garcia, Matthew R et al. (2018) Hedgehog Pathway Drives Fusion-Negative Rhabdomyosarcoma Initiated From Non-myogenic Endothelial Progenitors. Cancer Cell 33:108-124.e5
Jones, Conor M; Baker, Justin N; Keesey, Rachel M et al. (2018) Importance ratings on patient-reported outcome items for survivorship care: comparison between pediatric cancer survivors, parents, and clinicians. Qual Life Res 27:1877-1884
Huang, I-Chan; Brinkman, Tara M; Mullins, Larry et al. (2018) Child symptoms, parent behaviors, and family strain in long-term survivors of childhood acute lymphoblastic leukemia. Psychooncology 27:2031-2038
Huang, I-Chan; Klosky, James L; Young, Chelsea M et al. (2018) Misclassification of self-reported smoking in adult survivors of childhood cancer. Pediatr Blood Cancer 65:e27240
Mandrell, Belinda N; Avent, Yvonne; Walker, Breya et al. (2018) In-home salivary melatonin collection: Methodology for children and adolescents. Dev Psychobiol 60:118-122

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