Who We Fund

University of Virginia

I am currently the Director of the Comprehensive Cancer Center at University of Virginia. I was also founding Director of Penn State Cancer Institute. I had excellent training at the Fred Hutchinson Cancer Research Center under Nobel Laureate, E.D. Thomas, and served on its faculty for many years. I was instrumental in discovering a new hematologic malignancy which I termed large granular lymphocyte (LGL) leukemia. My career path has been a testament to translational research as a vehicle to directly improve disease management and patient outcomes. I also have extensive leadership experience in team science, exemplified by my current NCI P01 funding. Since my discovery of LGL leukemia, I have consistently been at the forefront of translational research into this disease and have built an entire Program at the University of Virginia dedicated to helping improve outcomes for patients with this disease, which includes the LGL Leukemia Registry with >2,100 consented participants.

Program Name(s)

Translational Research Program

Project Title

Epigenetic Therapy and Nano-Drug Development for Large Granular Lymphocyte Leukemia

Josep Carreras Leukemia Research Institute

Dr. Melnick is a recognized leader in the fields of hematologic malignancies and cancer epigenetics. Among his major contributions are the first large-scale epigenomic studies in humans, which demonstrated that aberrant epigenetic programming is a hallmark of cancer and that epigenetic diversity is a key determinant of tumor fitness and poor clinical outcomes. These findings led to important mechanistic insights—for example, how mutations in IDH1 and IDH2 disrupt the epigenome through the production of an aberrant oncometabolite, and how mutations in TET2, WT1, IDH1/2, and FLT3 promote leukemogenesis through cooperative epigenetic reprogramming. This was the basis for him receiving the ASH Beutler Award for Outstanding Translational Research in 2020.  Dr. Melnick has played a foundational role in establishing the importance of epigenetic dysfunction in lymphomagenesis, elucidating the mechanistic roles of chromatin modifiers such as EZH2, CREBBP, EP300, KDM1A, KMT2D, HIST1H1, BTG1, ARID1A, TBL1XR1, and TET2. He has also pioneered studies on nuclear topology and its role in regulating the humoral immune response and the malignant transformation of B cells. In the therapeutic arena, Dr. Melnick has developed novel targeted therapies against key lymphoma oncoproteins such as BCL6, SIRT3, and MALT1, and has helped define the rationale for additional targets, including EZH2. Several of these therapeutic approaches have received FDA approval or progressed to phase III clinical trials. He has authored more than 350 scientific publications, held numerous national leadership roles, organized prominent scientific conferences, and devoted extensive effort to mentoring trainees and junior faculty—many of whom now lead distinguished careers in basic and translational research. Dr. Melnick serves on the Board of Directors of both the Blood Cancer United and the Lymphoma Research Foundation. He also has extensive experience initiating and leading multi-center and international research consortia, and is currently the Principal Investigator of several program grants, including two active Blood Cancer United SCOR and RAFL programmatic grants.  He recently took on the position of the Josep Carreras Institute in Barcelona, a unique, free-standing institute focused exclusively on Blood Cancer research, leveraging a diverse and highly accomplished team of cutting-edge basic, translational and clinical scientists. With expertise in many disciplines including epigenetics, immunology, stem cell biology, metabolism, genetics, cell biology and many others, the team integrates artificial intelligence and state-of-the-art preclinical facilities to lead the world in curing Blood Cancers.  The institute is located in Barcelona, which has become one of the top hotspots for biomedicine and biotech in Europe.

Program Name(s)

Research Accelerator for Follicular Lymphoma

Project Title

The ERADICATE follicular lymphoma consortium: accelerating improved outcomes for FL patients

Houston Methodist Research Institute

My research focuses on the translation of bench works into new therapeutic approaches/strategies for multiple myeloma and other blood cancers. One of my research goals is to study the mechanism underlying the pathogenesis of myeloma and its associated tumor microenvironment. I have been investigating the interaction of myeloma cells with bone marrow adipocytes, bone cells, and the signaling pathways associated with obesity, inflammation, chemo-, immune-therapeutic resistance, and bone disease, which are the major hurdles in treating myeloma. As a PI, I have managed many projects funded by extramural grants, private funds, and industry alliances. Some highlights include the NIH/NCI R01s and funding received from ASH and ACS. I have an excellent publication track record with peer-review articles that are in top-tier journals with high impact factors (e.g. Cell Metabolism, Science Translational Medicine, Cancer Cell). My research experience shows my capacity to be a PI for this Project.

Program Name(s)

Translational Research Program

Project Title

Targeting acetyl-CoA synthetase 2 to remodel obesity-evoked inflammatory microenvironment in myeloma

University of Fribourg

Nicola Vannini after his MSc degree in Biological Sciences obtained at the University of Parma, moved to La Jolla (CA) where he worked for two years at the Burnham Institute in the laboratory of Prof. John C. Reed studying the metabolic basis of cardiac aging. He completed his PhD at the National Institute for Cancer Research in Genova (Italy) under the supervision of Prof. Adriana Albini, where he worked on nutritional interventions to prevent tumor progression. After his PhD he moved to EPFL (Lausanne, Switzerland) in the laboratory directed by Prof. Matthias Lütolf and Prof. Olaia Naveiras at the EPFL, where he developed targeted metabolic interventions to boost hematopoietic recovery.

Since March 2016 Nicola Vannini is group leader at the Ludwig Cancer Institute at the University of Lausanne . His primary research goals are the understanding of metabolic changes occurring during aging in the hematopoietic and immune compartments and their impact on cancer immunotherapy.

Program Name(s)

Translational Research Program

Project Title

Mitochondrial reprogramming to restore age-driven dysfunction in T cell and boost CAR-T cell therapy

Stanford

I am a hematologist/oncologist specializing in the treatment of multiple myeloma and related disorders. I am an Associate Professor in the Division of BMT/ Cell Therapy Division at Stanford University. I lead the Myeloma Disease Focused Group and am the Associate Director for Clinical Research for the Division. I have a broad research portfolio that includes clinical trials of novel therapies in myeloma, translational and outcomes research. I have a special focus on immunotherapy related research and am the principal investigator of several clinical trials of CAR-T cell therapy and bispecific antibodies in myeloma. I also co-lead a multi-center consortium of academic medical centers in the US collaborating to generate insights from real-world application of CAR-T therapy and bispecific antibodies in myeloma. I am actively involved with cooperative groups and professional societies, including holding leadership positions with the goal of advancing treatment of hematological disorders.

Program Name(s)

Career Development Program

Project Title

Improving Immunotherapy in Multiple Myeloma Through Innovative Clinical Trials, Real-World Evidence and Correlative Research

Washington University in St. Louis

Stefan Tarnawsky, M.D.; Ph.D. is a Hematology/Oncology fellow and junior physician scientist at the Washington University School of Medicine in Saint Louis, MO. His research focus is understanding the origin of myeloid blood cancers. His graduate work at Indiana University with Dr. Merv Yoder and Dr. Rebecca Chan focused on the prenatal origin of childhood blood cancers. This work led to a F30 award from the NHLBI and three first-author research publications, including one in the Journal of Clinical Investigations. Currently, under the mentorship of Dr. Matt Walter, M.D., Stefan studies how splicing factor gene mutations dysregulate blood cell growth. He thereby aims to identify novel therapies for the ~50% of myelodysplastic syndrome patients and ~20% of acute myeloid leukemia patients that have these mutations. His career goal is to continue this research focus as an independent investigator studying and treating blood cancer patients at an academic medical center.

Program Name(s)

Career Development Program

Project Title

The Role of TP53 in Mutant U2AF1 Myelodysplastic Syndromes

Weill Cornell Medicine

Ramon Massoni-Badosa, PhD is a graduate of Pompeu Fabra University, Barcelona in 2023, and his PhD focused on applying single-cell genomics technologies to benchmark the effect of sample preservation in single-cell RNA-seq data (Massoni-Badosa R. Genome Biol 2020), create a single-cell-driven atlas of cell types in human tonsils (Massoni-Badosa R., Immunity in press), and track the clonal evolution of CLL to Richter's syndrome (Nadeu,* Royo,* Massoni-Badosa*, Playa-Albinyana*, Garcia-Torre* Nat Med 2022). As highlighted in these three publications, he has gained extensive experience in large-scale single-cell multi-omics projects, as well as in combining computational and biological knowledge to gain biological and clinical insights. During his postdoc in the ten Hacken and Landau labs, Ramon will leverage his expertise to improve the mechanistic understanding of Richter’s syndrome, with the ultimate goal of identifying new targets to treat this incurable disease.

Program Name(s)

Career Development Program

Project Title

Uncovering MGA-driven epigenetic reprogramming in Richter's syndrome

The University of North Carolina at Chapel Hill

Adam Palmer is an Assistant Professor of Pharmacology at the University of North Carolina at Chapel Hill and a member of the UNC Lineberger Comprehensive Cancer Center. His research combines laboratory experiments, data analysis, and computer modeling to understand how combinations of cancer medicines work together, particularly curative treatments for aggressive lymphomas. Dr Palmer has developed computer models that predict the clinical effectiveness of drug combinations from how well the individual drugs work, and is now applying these methods to make combination therapies for blood cancers more effective and tolerable. Previously he completed undergraduate training in biochemistry, chemistry, and physics at the University of Adelaide, Australia, earned his PhD in Systems Biology from Harvard University studying antibiotic resistance, and conducted postdoctoral research on cancer pharmacology at Harvard Medical School.

Program Name(s)

Career Development Program

Project Title

Modeling and analysis of curative combination therapies to advance front-line precision therapy for blood cancers

Fondazione Centro San Raffaele

Dr. Matteo Bellone obtained an M.D. degree (with honors) and was Board Certified in Allergology and Clinical Immunology at the Università degli Studi di Milano, Italy. He had a 3-year post-doctoral training at the University of Minnesota working on autoimmunity with Bianca Conti-Fine. Since the early nineties he has been investigating interactions between cancer and immune cells with discoveries leading to several clinical outputs. He is Head of the Cellular Immunology Unit at Ospedale San Raffaele (Milan, Italy), where he also practices as Clinical Immunologist. He is adjunct professor of Immunology at Università Vita-Salute San Raffaele, Milan, Associate Editor at Frontiers in Immunology and Frontiers in Oncology, and member of several boards serving scientific journals and charities. He is Secretary and Treasurer of the Network Italiano per la BioTerapia dei Tumori (NIBIT), Council Member of the European Network for Cancer Immunotherapy (ENCI), and member of the SIICA, and the AACR.

Program Name(s)

Translational Research Program

Gut microbiota modulation to prevent progression of smoldering multiple myeloma to active disease

Beckman Research Institute of the City of Hope

Stephen J. Forman, MD, is a hematologist-oncologist, international expert in leukemia, lymphoma, and bone marrow transplant (BMT), and pioneer in immunotherapy. Dr. Forman has spent his 45-year career at City of Hope (COH), leading the Department of Hematology for 38 years and directing the Hematology Malignancies Research Institute since 2015. Under his leadership, COH developed one of the world’s largest and most successful BMT centers, which has led to dramatic increase in survival rates for blood cancers. He also directs the T cell Therapeutics Research Laboratories, the goal of which is to develop new ways to use the immune system to fight cancer. In this role, he leads a team of scientists in developing chimeric antigen receptor (CAR)-engineered T cells for treatment of a variety of cancers, including leukemia. Based on this research, Dr. Forman has led the advancement of multiple laboratory discoveries to the clinic, including CD19-directed CAR T cells for adults with leukemia.

Program Name(s)

Academic Clinical Trials Program (ACT)

Project Title

CD19-CAR T cells as Consolidation for Older Adults with Acute Lymphoblastic Leukemia in Remission

University of Colorado Denver, Anschutz Medical Campus

Terry Fry, MD, is a professor of pediatrics, hematology and immunology at the University of Colorado School of Medicine. He is the chair of the Gates Institute Advisory Board and holds the Charles C. Gates Endowed Chair in Regenerative Medicine. He arrived at Colorado in 2018 after serving as head of the Hematologic Malignancies Section in the Pediatric Oncology Branch at the National Institutes of Health (NIH), where he led efforts in cellular immunotherapy for pediatric leukemia. Prior to the NIH, Dr. Fry was chief of Blood and Marrow Transplantation at Children’s National Medical Center in Washington, D.C. His research focuses on the preclinical and clinical development of chimeric antigen receptor T cells for pediatric cancers. He serves on the Committee for Scientific Affairs for the American Society of Hematology, is vice chair for biology in the Cellular Therapy Committee of the Children’s Oncology Group, and was elected into the American Society for Clinical Investigation.

Program Name(s)

Academic Clinical Trials Program (ACT)

Project Title

A phase 1 study of anti-CD64 CAR T cells in patients with venetoclax-refractory myeloid neoplasms

The University of Alabama at Birmingham

Dr. Goyal obtained his medical school diploma from Smt. N.H.L. Municipal Medical College in Ahmedabad, India, in 2011 and moved to the US to complete a residency in Internal Medicine from Creighton University Medical Center, Omaha, Nebraska in 2016. He pursued a fellowship in hematology-oncology from Mayo Clinic, Rochester, Minnesota from 2016-2019. He developed a unique focus in histiocytic neoplasms, including Erdheim-Chester disease, Langerhans cell histiocytosis, and Rosai-Dorfman disease. He conducted multiple studies describing the epidemiology, treatments, and outcomes of patients with histiocytosis and led to the establishment of first of its kind multidisciplinary Histiocytosis Working Group. He has led national and international guidelines on the diagnosis and management of these rare disease entities. He was subsequently recruited to join the Hematology-Oncology division at University of Alabama at Birmingham as an Assistant Professor in 2019 where he launched the Histiocytic Disorder Survivor Study to assess long-term outcomes among individuals with histiocytic neoplasms.

Program Name(s)

Special Grants

A Multi-Center, Multi-National Investigation of Survivorship and Patient-Reported Symptoms in Erdheim-Chester Disease