Who We Fund

University of Miami

Dr. Nimer has cared for patients with MDS, AML, multiple myeloma, and lymphoma for over three decades. This melding of clinical studies and care, with both basic laboratory and translational studies, reflects the fundamental focus of his career. Since coming to the University of Miami-Miller School of Medicine in 2012 and assuming the Directorship of the Sylvester Comprehensive Cancer Center, the center received the prestigious National Cancer Institute designation in July 2019. In November 2019, Dr. Nimer was named the inaugural Oscar de la Renta Endowed Chair in Cancer Research. He has been elected to the American Society of Clinical Investigators and the Association of American Physicians. He is a Fellow of the American College of Physicians and serves on the editorial board of several medical journals. In April 2021, Dr. Nimer was inducted into the Academy of Science, Engineering, and Medicine of Florida. Dr. Nimer is also the Chairman of the Myelodysplastic Syndrome Foundation, and the Chairman of the Medical Advisory Board of Gabrielle's Angel Foundation for Cancer Research.

Program Name(s)

Specialized Center of Research Program

Interventional Epigenetics in Myeloid Malignancies

Emory University

Dr. Porter is an Associate Professor of Pediatrics and holds the Paul Amos Chair for Pediatric Oncology Research. He is a pediatric hematologist-oncologist and directs a lab in which they study molecular and cellular mechanisms of leukemogenesis, with the goal of developing novel therapeutic strategies. Most recently, they have been studying how leukemia cells influence the microenvironment to promote immune evasion. For example, they found that IL-12 overcomes calcineurin-dependent immune evasion by leukemia cells. Collaboratively, they designed BiTEokines to deliver IL-12 to the immune synapse of T cells and leukemia cells, supported by a DOD award (CA180783). They have also found that B cell malignancies express high levels of Siglec15, a newly identified immune checkpoint, and that inhibition of Siglec15 promotes immune clearance of malignant B cells in vivo. Thus, they are uniquely positioned to further develop Siglec15 as a therapeutic target for leukemia and lymphoma.

Program Name(s)

Translational Research Program

Project Title

Targeting Siglec15 to promote immune response to malignant B cells

Dana-Farber Cancer Institute

I graduated from Columbia College of Physicians & Surgeons, where I stayed for Internal Medicine residency training/chief residency before moving to Boston for fellowship training in hematology/oncology at Dana-Farber/Mass General Cancer Center. I stayed on as faculty in the lymphoma program at Dana-Farber and am now an Assistant Professor of Medicine at Harvard Medical School.  My research interests are in the clinical and translational study of immunotherapies for lymphoma, with a particular interest in cellular immunotherapies. I also serve as the Medical Director of the Immune Effector Cell Therapy program at Dana-Farber, which houses our commercial and research cell therapy programs across the Institute.  I am the principal investigator of industry-sponsored and investigator-initiated clinical trials involving cellular therapies for lymphoma, and lead retrospective and translational studies to identify mechanisms of response and resistance to these therapies.

Program Name(s)

Career Development Program

Project Title

CAR T-cell therapy in central nervous system (CNS) lymphoma: a study in safety and efficacy and a model in which to study mechanisms of neurotoxicity

Dana-Farber Cancer Institute

Nicoletta Cieri is a Postdoctoral Research Fellow at Dana-Farber Cancer Institute. Before joining DFCI, Nicoletta obtained her MD degree summa cum laude and mention of honor, PhD in Cellular and Molecular Biology and Clinical Specialization in Hematology summa cum laude from San Raffaele University, Italy, in 2010, 2014 and 2020, respectively. Nicoletta's research interests include genomics, proteomics, immunology and gene therapy applied to the field of onco-hematology. She is committed to define how to manipulate the immune response to recognize and eradicate hematological malignancies, while mitigating detrimental effects such as graft-versus-host disease, off-target toxicities and immune overactivation. Honors include Jon J. Van Rood Award and Basic Science Award from the European Bone Marrow Transplantation Society, Mundipharma Hematology Award from the Italian Society of Hematology, AACR-Incyte Immuno-Oncology Research Fellowship, and Helen Gurley Brown Fellowship.

Program Name(s)

Career Development Program

Project Title

TCR-like CARs targeting GvL mHAgs for the treatment of post-transplant AML 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

University of Manchester

Sam Butterworth joined the University of Manchester as a Senior Lecturer in Medicinal Chemistry in November 2016. Prior to this he worked at the University of Birmingham from 2013 and at AstraZeneca from 2005-2013. During this time he has been accountable for chemistry strategy and delivery for all phases of drug discovery projects from target review and hit generation, through to lead optimisation and pre-clinical development. His work at AstraZeneca led to the development of a targeted anti-cancer agent osimertinib that was approved by the FDA in November 2015, and along with his colleagues Sam has been recognised for this work through the 2017 RSC Malcolm Campbell Award and the 2018 ACS Heroes of Chemistry award. Since returning to academia he has established national and international collaborations focussing on translation research, predominantly in Oncology, and has been awarded >£8M translational funding as PI.

Program Name(s)

CMML Initiative

Project Title

Development of peptide-drug conjugates for the treatment of Chronic Myelomonocytic Leukaemia (CMML)

Vanderbilt University Medical Center

Dr. Savona is the Head of Hematology, Cellular Therapy and Stem Cell Transplant, the Beverly and George Rawlings Director of Hematologic Malignancies Research, and Professor of Internal Medicine and Cancer Biology at Vanderbilt University.

He is a physician scientist specializing in the development of experimental therapies for myeloid malignancies. He has led development and approval of several novel treatments targeting the proteosome, BCL2 family proteins, PI3 kinase delta, the JAK/STAT pathway, and various epigenetic agents. He studies clonal hematopoiesis (CH) and experimental opportunities to alter the progression of CH to myeloid neoplasia and/or vascular disease. He has been involved medical research for over 20 years and has published over 100 manuscripts in major academic journals including: Cancer Discovery, Journal of Clinical Oncology, Nature Medicine, Blood, Cell Stem Cell, Lancet Oncology, Lancet Haematology, JAMA, and Nature Reviews.

He is a veteran of Operation Iraqi Freedom/Operation Enduring Freedom for the USAF.

Program Name(s)

Career Development Program

IMPACT

Project Title

Manipulation of cell fate in myeloid disease

Reaching out to underserved & minority patients with hematological diseases in the southeastern US

University of Cambridge

George Vassiliou is Professor of Hematological Medicine, Director of the Blood Cancer United/Blood Cancer UK Specialist Center of Research (SCOR) in Myeloid Cancer Prevention and Co-lead of the Hematological Malignancies Virtual Institute at the University of Cambridge. He is also an Honorary Consultant Hematologist at Cambridge University Hospitals, where he founded and leads Europe’s first clonal hematopoiesis clinic. 

He studies the pre-clinical evolution, molecular pathogenesis and treatment of myeloid cancers. Highlights of his work include the co-discovery of the shared precursor of myeloid cancers, clonal hematopoiesis (CH), the description of its lifelong natural history and the first demonstration that individuals at risk of these cancers can be identified years in advance, opening the prospect of their prevention. He also developed the first genomic diagnostic tools for myeloid cancers, discovered mechanisms of how they develop and identified hundreds of potential treatment targets using the first genome-wide CRISPR genetic screen in any human cancer. His work has led to development of new treatments, including METTL3 inhibitors that are now in clinical trials against acute myeloid leukemia.

In recognition of his work, he was elected a Fellow of the Academy of Medical Sciences and awarded the European Haematology Association Research Excellence Award in 2026.

Program Name(s)

Specialized Center of Research Program

Project Title

Development of a clinical program for myeloid cancer prevention

City of Hope National Medical Center

Dr. Siddiqi is an associate professor in the Department of Hematology/Hematopoietic Cell Transplantation and Director of the chronic lymphocytic leukemia (CLL) program at COH. As an active member of the Toni Stephenson Lymphoma Center and the Immunotherapy Center at COH, she has been the institutional and, for some studies, national principal investigator of many phase 1, 2 and 3 clinical trials involving novel targeted therapies and cellular therapeutics such as chimeric antigen receptor (CAR) T cells in CLL and non-Hodgkin lymphomas. She works closely with Cancer Therapy Evaluation Program (CTEP), cooperative groups, and pharmaceutical companies on important clinical trials in order to bring novel, potentially lifesaving, therapeutics to our patients. As of June 1, 2021, she will be the Lymphoma Medical Director at the Irvine campus, set up open August 2022, which puts her in an ideal position to open impactful hematology clinical trials at CAN sites, starting with Orange county.

Program Name(s)

IMPACT

Project Title

Establishing Hematology Clinical Trial Hubs within the City of Hope Community and Affiliate Network

The University of Texas MD Anderson Cancer Center

Dr. Robert Orlowski, the Principal Investigator of this proposal, serves as the Florence Maude Thomas Cancer Research Professor and Director of the Myeloma Section at The University of Texas MD Anderson Cancer Center, and is the Deputy Chair of the Department of Lymphoma & Myeloma. Also, Dr. Orlowski serves as the Chair of the SWOG Barlogie/Salmon Myeloma Committee, which is part of the National Clinical Trials Network that conducts studies to advance novel therapies for myeloma, and to expand our understanding of its biology. In the laboratory arena, Dr. Orlowski is a physician scientist whose focus has been on bench-to-bedside research that develops and validates novel therapies to improve patient outcomes, and focuses on drug resistance mechanisms that may serve as predictive biomarkers for response. His past work has included leading roles in the development of the proteasome inhibitors bortezomib and carfilzomib, as well as the monoclonal antibodies daratumumab and elotuzumab.

Program Name(s)

Specialized Center of Research Program

Translational Research Program

Project Title

SCOR in High-Risk Plasma Cell Dyscrasias

Targeting HSP70 to Immune Effector Cells to Overcome the Immune Suppressive Myeloma Microenvironment

Cincinnati Children’s Hospital Medical Center

I am an Assistant Professor at Cincinnati Children's Hospital Medical Center. My areas of research interest include drug development and signaling with focus on small GTPases. My research is both basic and translational.

My research efforts encompass several methodologies, including structural biology, biophysical and biochemical studies, cellular functional assays, and ultimately, identifying small molecule compounds that bind to and modulate GTPase signaling in in vivo pre-clinical models of cancer.

RAC GTPases are key regulators of cell growth. By reorganizing the actin cytoskeleton, RAC plays a key role in cancer cell metastasis. It is also involved in mechanisms of resistance to therapies. My lab's goal is to inhibit RAC in leukemia by understanding the molecular mechanisms driving its hyperactivity.

One of my lab’s groundbreaking discoveries is the identification of a small molecule inhibitor of VAV3, a RAC activator. Current research studies the efficacy of VAV3 inhibition in models of relapsed/recurrent leukemia.

Program Name(s)

Translational Research Program

Project Title

Overcoming RAS-driven Mechanisms of Resistance in Leukemia

St. Jude Children's Research Hospital

Dr. John Crispino is Chief of the Division of Experimental Hematology at St. Jude Children’s Research Hospital. He received his PhD from MIT for research on the mechanisms of RNA splicing performed in the laboratory of Dr. Phillip Sharp and then performed post-doctoral hematology research at Harvard Medical School with Dr. Stuart Orkin. Dr. Crispino and members of his laboratory have made many important contributions to improve our understanding of the mechanisms of normal and aberrant blood development. Currently, his research is focused on the role of GATA1 in blood cell development, mechanisms of leukemogenesis in children with Down syndrome and the characterization of genetic changes that drive malignant progression of MDS and MPN. He has authored over 170 manuscripts, with recent papers in Cancer Discovery, Journal of Clinical Investigation, and Blood. Dr. Crispino is a recent Associate Editor of Blood, on the editorial boards of Leukemia and Blood Cancer Journal and past chair of an NIH study section.

Program Name(s)

Special Grants

Specialized Center of Research Program

Project Title

Aberrant Megakaryopoiesis in the MPNs

Understanding Leukemia in Children with Down Syndrome to Develop Better Therapies