Who We Fund

Dana-Farber Cancer Institute

Dr. Odejide is a health services researcher, a hematologic oncologist at the Dana-Farber Cancer Institute, and an Assistant Professor of Medicine at Harvard Medical School. Her research aims to improve outcomes and care delivery for patients with blood cancers throughout their disease trajectory. A substantial proportion of her work has focused on improving end-of-life (EOL) care for this patient population. For example, her work demonstrated that EOL quality measures developed for patients with solid malignancies are also applicable for patients with blood cancers (JCO, 2016). She also has extensive experience using insurance claims-based data (Medicare and Private) to identify potential solutions to improve EOL care. Dr. Odejide is interested in translating her work to impact policy. For example, she synthesized findings from her research and that of others to propose potential policy solutions to reduce barriers to high-quality EOL care for patients with blood cancers (JAMA, 2016). Her research was also part of the body of work used to support the American Society of Hematology 2019 policy statement to address barriers to high-quality hospice services for patients with blood cancers.

Program Name(s)

Equity in Access

Project Title

Health Insurance and End-of-Life Care for People with Hematologic Malignancies

Weill Cornell Medicine

Dr. Cerchietti is physician scientist dedicated to translational research in hematology oncology. His lab conduct mechanistic studies on the genetic, metabolic, and epigenetic regulation of lymphoma and microenvironment cells. Therapeutic approaches developed from his lab have been successfully translated to patients in investigator-initiated to cooperative group phase 3 clinical trials. Dr. Cerchietti also developed biomarkers to improve the precision of these interventions. Successfully translated research includes the concept of epigenetic priming to improve chemotherapy and immunotherapy as well as the discovering of the mechanism of action of XPO1 inhibitors in lymphomas contributing to gain FDA approval. A major focus of his lab is the study of the microenvironment to provide novel therapeutic targets as well as patient selection biomarkers (the “LME” classification) to improve the precision of therapies and increase disease curability.

Program Name(s)

Translational Research Program

Project Title

Targeting the microenvironment to increase immunity and immunotherapy response in DLBCL

University of Colorado Denver, Anschutz Medical Campus

I am a scientist of Indian origin who moved to the US upon completion of a Master’s in Pharmaceutical Biotechnology degree. I obtained my PhD in Cancer Biology from the University of Alabama at Birmingham, in the laboratory of Dr. Rob Welner. My PhD project focused on identifying basic mechanisms of drug resistance in blood cancer stem cells. This work culminated in 4 first author and 9 co-author publications. To gain experience in translational research, grant writing and mentoring, I am pursuing postdoctoral studies with Dr. Craig Jordan at the University of Colorado Anschutz Medical Campus. Here, I am leveraging my training in blood cancer and stem cell biology to identify new approaches for targeting malignant stem cells in myelodysplastic syndrome. This training will help me achieve my long-term goal of establishing an independent translational research program to improve outcomes for blood cancer patients and mentor students interested in pursuing a blood cancer research career.

Program Name(s)

Career Development Program

Project Title

Nicotinamide metabolism is essential for myelodysplastic syndrome stem and progenitor cell function and survival

Perelman School of Medicine at the University of Pennsylvania

Dr. Garfall is a hematologist-oncologist specializing in the care of multiple myeloma patients and research on new multiple myeloma therapies. He is a member of the Abramson Cancer Center at the University of Pennsylvania, where he is an Assistant Professor of Medicine. Dr. Garfall completed his undergraduate studies at Princeton University, medical school at New York University, residency in internal medicine at Brigham & Women’s Hospital, and hematology/oncology fellowship at Penn. Dr. Garfall’s research focuses on immunotherapy. He has conducted clinical trials with CAR T cells and bispecific antibodies for multiple myeloma. He is specifically interested on developing new approaches to prevent relapse in multiple myeloma patients.

Program Name(s)

Academic Clinical Trials Program (ACT)

Translational Research Program

Project Title

Limited-duration bispecific antibody therapy for multiple myeloma

Anti-Sox2 immunotherapy to prevent multiple myeloma relapse

NYU Grossman School of Medicine

Dr. Wendy Béguelin is a basic and translational research scientist working in the field of lymphoma epigenetics. She obtained her degree of Biology at the University of Buenos Aires, Argentina, where she received extensive training in the investigation of cell biology and signal transduction with studies on epigenetic gene regulation and transcription factor binding. As a postdoctoral scientist at Weill Cornell Medical College, under the mentorship of Prof. Ari Melnick she has identified novel epigenetic and transcriptional mechanisms that contribute to B-cell differentiation and lymphomagenesis. She has studied the biological and transcriptional mechanisms of action of Polycomb proteins in germinal center B-cells and lymphomas derived from germinal centers. As Assistant Professor, Dr. Béguelin is committed to a career in basic/translational cancer research, bringing new ideas into the field of epigenetic control of lymphomagenesis and making discoveries that can be translated from the diagnostic and therapeutic standpoints.

Program Name(s)

Translational Research Program

Project Title

Discovery and therapeutic targeting of novel mechanisms driving Double Hit Lymphomas

Columbia

I am an Associate Professor in Pediatric Hematology Oncology and Director of the Pediatric Immunotherapy Program at Columbia University. My work focuses on advancing immune therapies (CAR T cells) for children with cancer. I recently transitioned from Stanford University (2013–2025), where I led early first-in-human CAR T cell trials and helped deliver over 250 CAR-therapies to children with advanced cancer. Recognizing a major gap in data sharing, I founded the Pediatric Real-world CAR Consortium, a collaboration of over 50 pediatric oncology centers that enables large-scale data and sample sharing. Through this effort, we have identified predictors of survival and toxicity, modifiable treatment factors that impact survival, and informed international clinical trials. Given the recent approval of CAR T cells, long-term outcomes remain poorly understood. Our next goal is to study survivorship, late effects, and strategies to improve cure rates while reducing toxicity.

Program Name(s)

Dare to Dream

Project Title

Establishing longitudinal outcomes and clinical prognosticators in pediatric and young adult B-ALL after commercially available CD19-CAR T cells

University of Colorado Denver, Anschutz Medical Campus

Dr. Daniel Pollyea has received degrees from the University of Chicago Pritzker School of Medicine and Stanford University. He served as Chief Medical Resident at Cook County Hospital in Chicago. He has been the Principal Investigator for multiple early-phase clinical trials and been involved in the clinical development and approval of four drugs for acute myeloid leukemia (AML). He has published over 100 peer-reviewed papers, spoken to audiences around the world about this work, and is currently the Chair of the National Comprehensive Cancer Network (NCCN) Guidelines Committee on AML. His work involves developing ways to target leukemia stem cells in patients with AML and myelodysplastic syndrome (MDS). Eradication can result in deep and durable remissions, or even cures. His team’s efforts have involved identifying vulnerabilities in the ways that leukemia stem cells process energy. These weaknesses can be specifically exploited with novel drug therapies, and Dr. Pollyea is focused on developing and running clinical trials that use these agents to target these weaknesses.

Program Name(s)

Career Development Program

Targeting Leukemia Stem Cells in the Clinical Setting: The Development of A Comprehensive Program

Dana-Farber Cancer Institute

Margaret Shipp, MD, is Chief of the Division of Hematologic Neoplasia at Dana-Farber Cancer Institute and a Professor of Medicine at Harvard Medical School. Her research focuses on the clinical and molecular heterogeneity of the large B-cell lymphomas (LBCLs) and Hodgkin lymphomas. Dr. Shipp has led efforts to define molecular signatures of LBCLs and Hodgkin lymphomas, identify biologically distinct subsets of these diseases, and characterize associated rational treatment targets including modulators of the host anti-tumor immune response.

Program Name(s)

Translational Research Program

Project Title

Analysis and Targeting of Tumor-Associated Monocytes/Macrophages that Inhibit PD-1 Blockade

University of Perugia. Department of Medicine and Surgery

Dr. Enrico Tiacci is a physician scientist who established an independent translational and clinical research program in leukemias and lymphomas at the University and Hospital of Perugia, where he is Associate Professor of Hematology. His most relevant scientific contributions to pathogenesis, diagnosis and therapy of blood cancers span Hodgkin lymphoma, acute myeloid leukemia and, within the field of HCL, include the discovery of BRAF mutation as the genetic cause of this disease, its diagnostic exploitation and its therapeutic targeting in the clinic, which radically changed the understanding of HCL and considerably improved its treatment. For his achievements (mostly published in the highly influential New England Journal of Medicine), Dr. Tiacci received several prestigious national and international prizes as well as scientific grants from the most competitive international research agencies, including the European Research Council and Blood Cancer United.

Program Name(s)

Hairy Cell Leukemia Research Initiative

Project Title

BRAF inhibition as an alternative to chemotherapy in the treatment strategy of hairy cell leukemia

BRAF and BCL2 coinhibition with vemurafenib and venetoclax as a rational, short, all-oral targeted therapy for relapsed/refractory hairy cell leukemia

Garvan Institute of Medical Research

Peter trained at the University of Wales College of Medicine and Cambridge and Oxford Universities in the UK. In 2003 he joined Sheffield University and became joint Director of the Mellanby Center for Bone Research and Head of Department of Human Metabolism. In 2011 Peter joined the Garvan Institute of Medical Research in Sydney where he is Director of the Cancer Plasticity and Dormancy program. Peter is an international leader in understanding myeloma bone disease. He discovered key molecular pathways that cause myeloma bone disease. This research contributed to development of bone targeted therapies, including anti-RANKL and zoledronic acid, that are now in routine clinical use globally. Peter’s current research is investigating molecular pathways, including the Wnt pathway and sclerostin, that target osteoblasts, restore lost bone, increase bone strength and stop fractures. He is also investigating the role of bone cells in controlling myeloma cell dormancy and disease relapse.

Program Name(s)

Translational Research Program

Project Title

Targeting the Osteogenic Lineage as a Therapeutic Strategy in Multiple Myeloma

The University of Texas MD Anderson Cancer Center

Nitin Jain, MD, is an Associate Professor in the Department of Leukemia at MD Anderson Cancer Center in Houston. He earned his medical degree from the All India Institute of Medical Sciences, New Delhi. He completed Internal Medicine residency at the Medical College of Wisconsin and fellowship in Hematology/Oncology at the University of Chicago. Dr. Jain research interests include new drug development for patients with chronic lymphocytic leukemia (CLL) and acute lymphoblastic leukemia (ALL). Dr. Jain is Principal Investigator of several investigator-initiated phase I-II clinical trials, including combination targeted therapies (ibrutinib and venetoclax) in CLL, checkpoint inhibitors in Richter transformation, novel CD22 antibody drug conjugate in B-ALL, venetoclax + chemotherapy in B- and T-ALL, and off-the-self allogeneic CAR-T in B-ALL. The trial combining ibrutinib and venetoclax was published in New England Journal of Medicine in 2019. He has won many awards including ASCO merit award, Sabin Family Foundation Award in 2018 and MD Anderson Faculty Scholar award in 2020.

Program Name(s)

Career Development Program

Translational Research Program

Project Title

Combination Targeted Therapy in Chronic Lymphocytic Leukemia

LCK-targeted Therapy in T cell Acute Lymphoblastic Leukemia

Emory University

Dr. Jonathon Cohen is an associate professor of hematology/oncology at Emory University and co-directs the lymphoma program at Winship Cancer Institute. He has developed and implemented studies conducted at sites throughout the US and frequently collaborates with colleagues throughout Georgia to offer trials to patients with lymphoma. He is a member of the ECOG-ACRIN Lymphoma Core Committee, Co-Chair of the Hoosier Cancer Research Network Lymphoma Committee, and Co-Chair of the Lymphoma Disease Focus Group of the NCI-funded Experimental Therapeutics Clinical Trials Network Consortium. He also leads national studies evaluating real-world outcomes in lymphoma. He has an active clinical practice providing consultative services for patients throughout Georgia. He has routinely engaged with oncologists throughout the region to promote quality lymphoma care through in-person and virtual educational talks, and through moderation of protocol sessions to develop treatment guidelines.

Program Name(s)

IMPACT

Project Title

Making an IMPACT on hematology care in Georgia: The Georgia Blood Cancer Trials Network (BCTN)