Who We Fund

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

Dana-Farber Cancer Institute

Dr. Romee is a translational physician-scientist at Dana Farber Cancer Institute, Harvard Medical School. His long-term research goals are to translate novel aspects of immunology to improve treatments for patients with advanced cancer. He did his medical training at University of Minnesota and Washington University and was a faculty at Washington University before joining Dana Farber. He is the PI of Romee Lab for NK Cell Gene Manipulation and Therapy (https://romeelab.dana-farber.org) and the focus of his lab is gene editing of the immune cells particularly NK cells to enhance their cancer cell targeting and killing. His work helped describe memory-like NK cells which have enhanced activity against cancer cells and persist for months after their infusion into leukemia patients. He is leading efforts at Dana Farber to develop novel protocols using memory-like NK cells with other immunomodulating agents like checkpoint inhibitors in patients with advanced and otherwise incurable leukemia and solid tumors like Head and Neck Cancer, Ovarian Cancer and Kidney Cancer.

Program Name(s)

Career Development Program

Translational Research Program

Project Title

Cytokine induced memory-like NK cell immunotherapy to target post transplant relapse

Memorial Sloan Kettering Cancer Center

I am a Research Scholar in the laboratory of Dr. Omar Abdel-Wahab at Memorial Sloan Kettering Cancer Center. I obtained my Bachelor’s degree at East China University of Science and Technology and completed my PhD training at the Shanghai Institute of Nutrition and Health in the University of Chinese Academy of Sciences under the mentorship of Dr. Lan Wang. During my graduate studies, I identified an important role of the histone methyltransferase SETD2 in the transformation of patients with myelodysplastic syndromes (MDS) to acute myeloid leukemia (AML). As an LLS Special Fellow, I will focus on developing novel CAR-T cell therapy targeting cell surface expression of the RNA helicase U5 snRNP200. Moreover, I will explore the mechanistic basis for cell surface localization of U5 snRNP200 on AML cells. I hope that my work has immediate therapeutic potential for the future treatment of AML while shedding important novel insights into the pathobiology of AML.

Program Name(s)

Career Development Program

Project Title

Targeting the cell surface U5 snRNP complex as a novel immunotherapy for AML

The University of Melbourne

I am an Assoc. Prof. and Group Leader at the Peter MacCallum Cancer Centre (Peter Mac; Melbourne, Australia). I formed my group in 2018 and my research program is focused upon enhancing the effectiveness of chimeric antigen receptor (CAR) T cells, a form of immune therapy where a patient’s own immune cells are genetically engineered to recognize and kill tumor cells. I have published numerous seminal papers and research metrics place me in the top 1% of researchers in my field. Despite being a PI for just 5 years, I have already led 1 CAR T clinical trial and I am currently developing a second trial with a technology developed in my lab in 2020.

Previously my focus has been on using CAR T to treat cancers such as breast and lung cancer. However, recent clinical data indicates that CAR T cells have significant potential in multiple myeloma. Therefore, this project will be a key strategic enabler, allowing me to apply approaches developed in my lab to this disease.

Program Name(s)

Translational Research Program

Project Title

Exploiting escape from Y-inactivation as a synthetic dependency in MYC-driven lymphoma

Monash University

Professor Jake Shortt is a clinician scientist who is co-appointed by Monash Health as Director of Clinical Haematology and by Monash University as the Head of Haematology Research at the School of Clinical Sciences. Monash Health provides lymphoma services to the largest Australian healthcare network in the Australian state of Victoria. He is also an Honorary Clinical Professor at the Sir Peter MacCallum Department of Oncology, University of Melbourne.

Professor Shortt is group leader of the 'Blood Cancer Therapeutics Laboratory' at Monash, seeking to discover and translate new lymphoma treatments to the clinic. As a clinician scientist his research covers the full translational spectrum from scientific discovery to advanced clinical trials and registry initiatives. For more than a decade his research has focussed on poor-risk lymphoid cancers, particularly those hallmarked by activation of a gene called 'MYC' which features in some of the most aggressive lymphomas.

Program Name(s)

Translational Research Program

Stanford University

Dr. Jaiswal is an assistant professor at Stanford University in the Department of Pathology and Institute for Stem Cell Biology and Regenerative Medicine, where his lab focuses on understanding the biology of the aging blood system. Several years ago, he identified a common, pre-malignant state for blood cancers, termed "clonal hematopoiesis”, by analyzing large human genome sequencing studies. He discovered that clonal hematopoiesis is prevalent in the aging population and increases the risk of not only blood cancers, but also cardiovascular disease and overall mortality. Understanding the biology of these mutations and how they contribute to the development of cancer and other age-related diseases is the current focus of work in the lab. Ultimately, Dr. Jaiswal and his team aim to develop novel therapies that can prevent adverse outcomes due to clonal hematopoiesis.

Program Name(s)

Discovery

Project Title

Uncovering the role of TCL1A as a driver of clonal hematopoiesis and hematological malignancies

Dr. Manabu Fujisawa received M.D. from Kyushu University in Fukuoka, Japan. Motivated by the experience as a hematologist having treated many patient with treatment-resistant disease, Dr. Fujisawa conducted a clinical study on clonality and clinical progression in multiple myeloma in Kameda Medical Center, Chiba. Dr. Fujisawa then began his basic research at University of Tsukuba in 2016, where he received PhD under the supervision of Pr. Mamiko Sakata-yanagimoto. Pr. Sakata’s lab focused on clonal hematopoiesis and malignant lymphoma, which Dr. Fujisawa studied the function of clonal hematopoietic-derived immune cells in the tumor microenvironment. In 2022, Dr. Fujisawa joined the laboratory of Pr. Christian Steidl in Lymphoid Cancer Research at the BC Cancer Research Centre in Vancouver, Canada, as a postdoctoral fellow.

Program Name(s)

Career Development Program

Project Title

Spatial architecture and malignant cell characterization of nodular lymphocyte-predominant Hodgkin lymphoma

Dana-Farber Cancer Institute

Dr. Lindsley is an Assistant Professor of Medicine at Harvard Medical School and Dana-Farber Cancer Institute. He received his M.D. and Ph.D. in Immunology from Washington University School of Medicine, then completed a residency in internal medicine at Brigham and Women’s Hospital and a fellowship in oncology at the Dana-Farber Cancer Institute. He is a member of the MDS Genetics Subcommittee for the NIH National MDS Study, NHLBI Trans-Omics for Precision Medicine Steering Committee, and the International Working Group for Prognosis in MDS (IWG-PM) molecular committee. The primary focus of his laboratory is the biology and treatment of myeloid malignancies. His genetic studies have led to new genomic models of leukemia classification and MDS outcome after stem cell transplantation. His laboratory uses mouse and cell line models to dissect the mechanistic basis of genetic cooperation during myeloid disease progression, with a specific focus on leukemia initiation in patients with predisposition syndromes and mutations that cause epigenetic alterations.

Program Name(s)

Career Development Program

Project Title

Genetic pathways of myeloid transformation and treatment response

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

Washington University in St. Louis

John F. DiPersio MD, PhD is the Golman Professor of Medicine and Director of The Center for Gene and Cellular Immunotherapy at the Washington University School of Medicine. His research has focused on targeting key elements of the hematopoietic niche for optimal stem cell mobilization and chemosensitization, mitigating GvHD in T cell replete transplants, understanding the genomic alterations in AML, and developing and testing in the clinic novel therapeutics and immuno-therapeutics, including cellular therapies, for the treatment of AML, ALL, T/B-NHL and multiple myeloma. Dr. DiPersio was instrumental in the development and FDA approval of Plerixafor, Motixafortide, and Ruxolitinib. He is the recipient of multiple awards and was past president of the ASTCT and member of the NCI Board of Scientific Counselors. He has authored or co-authored more than 490 publications, is a co-founder of two companies (WUGEN and Magenta) and holds multiple patents.

Program Name(s)

Translational Research Program

Project Title

KT1, a novel NK trispecific antibody for the treatment of AML and MDS

Columbia University Medical Center

Dr. Doulatov is an Associate Professor at the University of Washington. His laboratory investigates how normal hematopoietic stem cells (HSCs) transform into blood cancers. As an undergraduate at UCLA with Dr. Jeff Miller, he discovered a new class of retroelements. As a Ph.D. student with Dr. John Dick at the University of Toronto, he helped establish the “roadmap” of the human HSC and progenitor hierarchy. As a postdoctoral fellow with Dr. George Daley at Harvard, he identified methods to promote HSC development from induced pluripotent stem cells (iPSCs). These advances have enabled the use of iPSCs as a platform for disease modeling and drug screens, leading to the discovery of a drug for inherited anemia. The Doulatov laboratory is using human iPSCs and HSCs to discover how oncogenic mutations cooperate to transform normal stem cells into leukemias. His long-term goal is to develop treatments that target malignant stem cells leading to lasting remissions for patients.

Program Name(s)

Career Development Program

Project Title

Modeling and targeting leukemic transformation of human hematopoietic stem cells

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)