The Hematologic Malignancies Program (HMP) is composed of 51 scientists, and clinical investigators from 7 departments at Mayo Clinic in Rochester, MN (MCR), Arizona (MCA), and Florida (MCF). The Program is co- led by Drs. Ansell (MCR), Bergsagel (MCA) and Chanan-Khan (MCF). The HMP aims are to 1) investigate the epidemiology of hematologic malignancies and mechanisms of progression, 2) characterize the molecular and cell biology of hematologic malignancies to identify new therapeutic targets, and 3) develop and test new therapies. To accomplish these aims, the HMP is organized into 4 disease groups (DGs) that are composed of basic and translational research scientists, hematopathologists, and clinicians. The DGs meet weekly or biweekly to discuss research results, clinical trial activities, and requests for use of biobank samples and ensure that research is meeting the needs of the patients in our catchment area. Annual peer-reviewed direct funding to HMP members is $4.6M, with 93% from the National Cancer Institute. This includes 2 SPOREs (Lymphoma and Multiple Myeloma), 15 R01s, 2 R41s, 1 R21, 1 U54, 5 Multiple Myeloma Research Foundation and 2 Leukemia and Lymphoma Society grants. Since 2012, the HMP has recruited 10 new scientists who focus on key research areas ranging from cell signaling to cancer survivorship. Major scientific contributions by the HMP since 2012 include a major role in the approval of nivolumab in Hodgkin lymphoma, leadership in genome wide association studies (GWAS) identifying susceptibility loci in large cell lymphoma, leadership in trials establishing the role of ibrutinb in CLL, and leadership in trials including bortezomib in frontline therapy for multiple myeloma. The HMP continues to have a robust clinical trials program that enrolls over 500 patients each year to therapeutic clinical trials. Members have contributed 1172 publications to the literature since 2013, 43% of which are intraprogrammatic and 30% interprogrammatic. HMP members have extensive collaborations with members in the Gene and Virus Therapy, Experimental Therapeutics, and Genetic Epidemiology and Risk Assessment Programs. HMP members make extensive use of numerous Shared Resources, with substantial use of Biospecimens Accessioning & Processing, Biostatistics, and Pharmacy. Significant institutional and philanthropic (Predolin Foundation) support continues for HMP-related research. In the next funding period, we will mentor young investigators and focus on developing tools to integrate genomic information into the individual care plans for our patients.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA015083-47
Application #
10113611
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
1997-04-25
Project End
2024-02-29
Budget Start
2021-03-01
Budget End
2022-02-28
Support Year
47
Fiscal Year
2021
Total Cost
Indirect Cost
Name
Mayo Clinic, Rochester
Department
Type
DUNS #
006471700
City
Rochester
State
MN
Country
United States
Zip Code
55905
Langlais, Blake T; Geyer, Holly; Scherber, Robyn et al. (2018) Quality of life and symptom burden among myeloproliferative neoplasm patients: do symptoms impact quality of life? Leuk Lymphoma :1-7
Yang, Ju Dong; Addissie, Benyam D; Mara, Kristin C et al. (2018) GALAD Score for Hepatocellular Carcinoma Detection in Comparison to Liver Ultrasound and Proposal of GALADUS Score. Cancer Epidemiol Biomarkers Prev :
Kurmi, Kiran; Hitosugi, Sadae; Yu, Jia et al. (2018) Tyrosine Phosphorylation of Mitochondrial Creatine Kinase 1 Enhances a Druggable Tumor Energy Shuttle Pathway. Cell Metab 28:833-847.e8
O'Mara, Tracy A; Glubb, Dylan M; Amant, Frederic et al. (2018) Identification of nine new susceptibility loci for endometrial cancer. Nat Commun 9:3166
Wallace, Sumer K; Halverson, Jessica W; Jankowski, Christopher J et al. (2018) Optimizing Blood Transfusion Practices Through Bundled Intervention Implementation in Patients With Gynecologic Cancer Undergoing Laparotomy. Obstet Gynecol 131:891-898
Shrestha, Shikshya; Zhang, Cheng; Jerde, Calvin R et al. (2018) Gene-Specific Variant Classifier (DPYD-Varifier) to Identify Deleterious Alleles of Dihydropyrimidine Dehydrogenase. Clin Pharmacol Ther 104:709-718
Hu, G; Dasari, S; Asmann, Y W et al. (2018) Targetable fusions of the FRK tyrosine kinase in ALK-negative anaplastic large cell lymphoma. Leukemia 32:565-569
Geller, James I; Fox, Elizabeth; Turpin, Brian K et al. (2018) A study of axitinib, a VEGF receptor tyrosine kinase inhibitor, in children and adolescents with recurrent or refractory solid tumors: A Children's Oncology Group phase 1 and pilot consortium trial (ADVL1315). Cancer 124:4548-4555
Luchtel, Rebecca A; Dasari, Surendra; Oishi, Naoki et al. (2018) Molecular profiling reveals immunogenic cues in anaplastic large cell lymphomas with DUSP22 rearrangements. Blood 132:1386-1398
Oishi, Naoki; Brody, Garry S; Ketterling, Rhett P et al. (2018) Genetic subtyping of breast implant-associated anaplastic large cell lymphoma. Blood 132:544-547

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