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 #
5P30CA021765-39
Application #
9439721
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2018-03-01
Budget End
2019-02-28
Support Year
39
Fiscal Year
2018
Total Cost
Indirect Cost
Name
St. Jude Children's Research Hospital
Department
Type
DUNS #
067717892
City
Memphis
State
TN
Country
United States
Zip Code
38105
Dove, Austin P; Manole, Bogdan-Alexandru; Wakefield, Daniel V et al. (2018) Managing local-regional failure in children with high-risk neuroblastoma: A single institution experience. Pediatr Blood Cancer 65:e27408
Kurmasheva, Raushan T; Kurmashev, Dias; Reynolds, C Patrick et al. (2018) Initial testing (stage 1) of M6620 (formerly VX-970), a novel ATR inhibitor, alone and combined with cisplatin and melphalan, by the Pediatric Preclinical Testing Program. Pediatr Blood Cancer 65:
Chamdine, Omar; Elhawary, Ghada Ahmad Saad; Alfaar, Ahmad Samir et al. (2018) The incidence of brainstem primitive neuroectodermal tumors of childhood based on SEER data. Childs Nerv Syst 34:431-439
Heitzer, Andrew M; Ashford, Jason M; Harel, Brian T et al. (2018) Computerized assessment of cognitive impairment among children undergoing radiation therapy for medulloblastoma. J Neurooncol :
Robinson, Katherine M; Yang, Wenjian; Haidar, Cyrine E et al. (2018) Concordance between glucose-6-phosphate dehydrogenase (G6PD) genotype and phenotype and rasburicase use in patients with hematologic malignancies. Pharmacogenomics J :
Teitz, Tal; Fang, Jie; Goktug, Asli N et al. (2018) CDK2 inhibitors as candidate therapeutics for cisplatin- and noise-induced hearing loss. J Exp Med 215:1187-1203
Binder, Randall J; Hatfield, M Jason; Chi, Liying et al. (2018) Facile synthesis of 1,2-dione-containing abietane analogues for the generation of human carboxylesterase inhibitors. Eur J Med Chem 149:79-89
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
Donohoe, Clare; Bosi, Judy K; Sykes, April et al. (2018) Clinical Characteristics of Children and Adolescents Undergoing Hematopoietic Cell Transplantation Who Develop Oral Mucositis. Oncol Nurs Forum 45:457-462
Green, Daniel M; Wang, Mingjuan; Krasin, Matthew J et al. (2018) Serum ALT elevations in survivors of childhood cancer. A report from the St. Jude Lifetime Cohort Study. Hepatology :

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