Who We Fund

Washington University in St. Louis

Dr. Challen is currently an Associate Professor in the Division of Oncology at Washington University School of Medicine (St. Louis). His laboratory research is at the interface of stem cell biology and blood cancer, and aims to determine how disruption of the epignenome changes the fate of HSCs and ultimately leads to the development of hematopoietic disorders. He was the first to describe how mutations in the gene DNMT3A regulates the balance of HSC self-renewal and differentiation as a first step to development of AML. His lab aims to develop mutation-specific therapies to inhibit CH clones as a mechanism of blood cancer prevention.

Dr. Challen is investigating how mutations in genes that alter the epigenome alter the function of blood-forming hematopoietic stem cells (HSCs), leading to a condition known as clonal hematopoiesis (CH) and predispose for future development of blood diseases such as myelodysplastic syndromes (MDS), acute myeloid leukemia (AML)and T-cell acute lymphoblastic leukemia (T-ALL).

Program Name(s)

Career Development Program

Translational Research Program

Project Title

Synergism of cell-intrinsic and cell-extrinsic factors in the clonal evolution of pre-malignant HSCs

Precision Medicine For DNMT3A-Mutant T-cell ALL

University of California San Diego

Dr. Su is Professor of Obstetrics, Gynecology and Reproductive Science in the Division of Reproductive Endocrinology and Infertility at the University of California, San Diego, where she directs the Oncofertility Program. Dr. Su completed residency in obstetrics and gynecology, fellowship in reproductive endocrinology, and Master’s of Science in Clinical Epidemiology at the University of Pennsylvania, as well as implementation science training through NCI’s Training in Dissemination and Implementation Research in Cancer Program. Dr. Su is a physician scientist who conducts patient oriented research on reproductive health in young cancer survivors. Through innovative observational and interventional studies, team-based science, and community engagement, Dr. Su’s studies focus on estimating reproductive risks after cancer, implementing evidence-based practices, and improving equity in reproductive health care delivery, funded by NCI, NICHD, American Cancer Society, and Robert Wood Johnson Foundation. Recent work on health policies as an intervention to improve access to care suggest that state-level fertility preservation benefit mandates are not working as intended. This team with existing collaborations and complementary methodologic and clinical expertise will use national administrative data to estimate the impact of mandated insurance benefits on fertility preservation utilization and affordability, in order to inform future federal and state laws and regulations.

Program Name(s)

Equity in Access

Project Title

Impact of State Health Insurance Mandates on Affordability and Utilization of Fertility Preservation in Adolescent and Young Adults with Blood Cancers

Boston Children's Hospital

George Q. Daley, MD, PhD is Dean, Caroline Shields Walker Professor of Medicine, and Professor of Biological Chemistry and Molecular Pharmacology at Harvard Medical School. His research has focused on stem cell and cancer biology, with an emphasis on hematopoietic development and diseases of the bone marrow, blood and immune system. Daley earned his AB and MD degrees from Harvard and a PhD in biology from MIT. He has been a trainee, fellow and staff physician at the Massachusetts General Hospital, Brigham and Women’s Hospital, Dana Farber Cancer Institute and Boston Children’s Hospital. Prior to becoming Dean at HMS, he was an investigator of the Howard Hughes Medical Institute and Director of the Pediatric Stem Cell Transplantation Program of the Dana Farber Cancer Institute and Boston Children’s Hospital. He is an elected member of the National Academy of Medicine and the American Association of Arts and Sciences.

Program Name(s)

Translational Research Program

Project Title

Pluripotent Stem Cell-derived CAR-T and CAR-NK Cells for Immunotherapy of Leukemia and Lymphoma

TAP Partner

Rgenta Therapeutics is developing a pipeline of oral, small-molecule RNA-targeting medicines with an initial focus on oncology and neurological disorders. Rgenta has a proprietary platform to mine the massive genomics data to identify targetable RNA processing events and to design small-molecule glues to modulate the interactions among the spliceosome, regulatory proteins, and RNAs. 

Rgenta is working closely with TAP to further develop RNA-targeting molecules by supporting preclinical studies with the goal of moving towards clinical development in hematological malignancies. 

Program Name(s)

Therapy Acceleration Program

Project Title

Supporting development of RNA-targeting molecules for blood cancers

The Brigham and Women’s Hospital

My scientific background involves the functional characterization of rare immune cells called dendritic cells in advanced melanoma patients. These cells are master regulators of immunity and are responsible for orchestrating anti-cancer responses driven by effector cells called T cells. My PhD focused on patients who received immunotherapy via antibodies that reinvigorate the immune system, also known as immune checkpoint inhibitors. I collected patient blood samples before and during treatment, and found that a critical subtype of dendritic cell is numerically and functionally impaired in patients who did not respond to immunotherapy compared to those who responded. In my current lab, I leveraged my experience in immune cell research and now study how a novel drug combination can be used to target and kill acute myeloid leukemia (AML) cells. This innovative approach targets two biologically important processes within a cell – the protein-making machinery and the control of cell death.

Program Name(s)

Career Development Program

Project Title

Cotargeting oncogenic protein translation and apoptosis in acute myeloid leukemia

Children's Research Institute

Dr. Bollard received her medical degree at the University of Otago. She is board certified both in pediatrics and hematology. She is currently the Bosworth Chair for Cancer Biology, the Director of the Center for Cancer and Immunology Research, and the Director of the Program for Cell Enhancement and Technologies for Immunotherapy (CETI) at Children’s National Health System. She is a Professor of Pediatrics and of Microbiology, Immunology, and Tropical Medicine at The George Washington University and the Associate Center Director for Translational Research and Innovation at the GW Cancer Center. Dr. Bollard is a member of the American Society for Clinical Investigation (ASCI) and is the current President of the Foundation for the Accreditation of Cellular Therapy (FACT). She is currently Editor in Chief of Blood Advances. She has over 200 peer reviewed publications. Her bench and translational research focuses on improving outcomes for patients after hematopoietic stem cell transplantation and on the development of novel cell therapies for cancer and virus-associated diseases.

Program Name(s)

Translational Research Program

T cells with native and chimeric receptors against multiple tumor targets for acute myeloid leukemia

The University of Sydney

I am Head of the Cancer and Stem Cell Laboratory, and my research has been focused on leukemia stem cell biology and targeted therapies in the past 15 years. I have an extensive background in leukemia research, with specific training and expertise in stem cell biology, patient-derived preclinical models, CRISPR-genome editing, and single-cell multi-omics. As PI on several NHMRC-funded grants, I laid the groundwork for the proposed research by uncovering new therapeutic targets and mechanisms, and by establishing partnerships with industry that will enable personalized therapies into clinical application. I successfully administered the projects (e.g. staffing, research protections, timeline, budget), collaborated with researchers, and produced publications from each project in leading scientific journals (e.g. Cancer Cell, Blood). The current application builds logically on my prior work. I have the expertise, leadership, and motivation necessary to successfully carry out this project.

Program Name(s)

Translational Research Program

Project Title

Strategic combinations to overcome therapeutic resistance and relapse in acute myeloid leukemia

Washington University in St. Louis

Dr. Fehniger is a physician-scientist that leads a research program focused on translational NK cell biology and therapy. His group pioneered studies characterizing memory-like (ML) NK cell biology and activity against AML and has led clinical trials advancing ML NK cell adoptive therapy for both adult and pediatric patients. Dr. Fehniger is director of the Biologic Therapies Core Facility and Laboratory Director of the Center for Gene and Cellular Immunotherapy. His team developed the platform and protocols for production of GMP grade ML NK cells for use in academic clinical trials. His lab performs correlative immunology to understand ML NK cell biology and identify mechanisms of resistance to NK cells in patients. Dr. Fehniger has extensive experience in human NK cell biology, flow and mass cytometry, single cell analysis, and immunotherapy. For the proposed clinical trial, Dr. Fehniger will work with clinical co-investigators in pediatric and adult stem cell transplant programs.

Program Name(s)

Academic Clinical Trials Program (ACT)

Project Title

NK cell immunotherapy to reduce relapse after haploidentical transplant for high-risk pediatric AML

University of Florida

Despite Hodgkin lymphoma’s (HL) favorable prognosis, Black and Hispanic patients have worse survival rates compared to White patients. Insurance status and non-White race and ethnicity are associated with the inequitable receipt of optimal treatments, as well as survivorship care. Patients’ decision-making experiences with their clinicians influence cancer care, and shared decision-making (SDM) is central to patient-centered care when patients have multiple treatment options. However, in hematologic cancer care, many physicians underestimate patient preference for SDM, and HL survivors report minimal involvement in decision-making about their treatment and care.

Program Name(s)

Equity in Access

Project Title

Insurance Inequities in Hodgkin Lymphoma Treatment and Survivorship in the Southeast

Memorial Sloan Kettering Cancer Center

Coming soon.

Program Name(s)

Specialized Center of Research Program

Project Title

Translational Discovery in Peripheral T-Cell Lymphomas

Columbia University Medical Center

I am a pediatric oncologist and health outcomes researcher at Columbia University Irving Medical Center. My research aims to identify how social determinants of health drive care and outcomes in children, adolescents, and young adults (AYA) with leukemia and lymphoma. At Columbia, I am the institutional Principal Investigator for the Dana-Farber Cancer Institute ALL Consortium and I serve on the Children’s Oncology Group Hodgkin Lymphoma (HL) Steering Committee. In these roles I participate in the design and implementation of new clinical trials, and in the development of embedded health services studies. My recent work includes a series of large-scale analyses (using clinical trials and population data) evaluating outcomes by race/ethnicity and age in ALL and HL. Increasingly, I am working to identify barriers to clinical trial participation among diverse populations, and on leveraging the clinical trial infrastructure to collect prospective data on social determinants of health.

Program Name(s)

Career Development Program

Project Title

Leveraging cancer registries, clinical trials, and community partnerships to address disparities in pediatric, adolescent, and young adult lymphoma

University of California, San Francisco

Program Name(s)

Translational Research Program

Project Title

Towards Risk-Adapted Therapeutic Strategies in CNS Lymphoma