Yubin Zhou
peripheral T cell lymphoma
Yubin Zhou, PhD, MBBS
College Station, TX
United States
Texas A&M Institute of Biosciences and Technology
Dr. Yubin Zhou is a professor of Translational Cancer Research at the Texas A&M University Institute of Biosciences and Technology. He is interested in pioneering chemical and synthetic biology approaches to interrogate tumorigenesis, and developing targeted therapeutics for hematological malignancies. Dr. Zhou received his medical training/internship in internal medicine (1998-2003), and earned his Ph.D. degree in Biochemistry/Virology (2008) from Georgia State University. He thereafter received his postdoctoral training at Harvard Medical School (2008-2010) and then worked as an instructor at La Jolla Institute for Immunology/UCSD (2010-2012). Dr. Zhou was the recipient of the Blood Cancer United Fellow Award, Special Fellow Award, the TAMU Research Excellence Award, the ACS Research Scholar Award, and the Presidential Impact Fellow, Protégé member the Texas Academy of Medicine, Engineering, Science & Technology, and elected Fellow of the American Institute for Medical and Biological Engineering.
Program Name(s)
Translational Research Program
Project Title
Development of mutant GTPase-specific degraders for peripheral T cell lymphoma treatment
Adi Nagler
Bronchiolitis obliterans after transplant
Adi Nagler, PhD
Boston, MA
United States
Dana-Farber Cancer Institute
Dr. Adi Nagler received her Ph.D. at the Weizmann Institute of Science in 2021, under the mentorship of Prof. Yardena Samuels. There, she spearheaded studies that identified intra-tumoral intracellular bacterial peptides eliciting an immune response by melanoma-infiltrating lymphocytes, suggesting a novel source of antigens within tumors (Kalaora & Nagler Nature 2021). As a postdoctoral fellow in Prof. Catherine Wu’s lab, she is studying the impact of the microbiome on T cell response in bronchiolitis obliterans syndrome (BOS) following allogeneic hematopoietic cell transplantation (HCT). She is applying spatial transcriptomics methodology together with characterization of the immunopeptidome of BOS tissue specimens to define the role of bacterial presented peptides in the pathogenesis of this devastating complication of HCT. Overall, her studies aim is to explore the potential link between T cell antigen specificity to these microbial peptides and initiation and propagation of BOS.
Program Name(s)
Career Development Program
Project Title
Nicola Vannini
Aging and CAR-T success
Nicola Vannini, PhD
Fribourg,
Switzerland
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
Julia Paczkowska
immunobiology of Hodgkin's disease
Julia Paczkowska, PhD
Boston, MA
United States
Dana-Farber Cancer Institute
Dr. Julia Paczkowska completed her master’s degree in pharmacy at Poznan University of Medical Science, Poland. Thereafter, she obtained her PhD in medical sciences from the Institute of Human Genetics, Polish Academy of Sciences, Poznan, with a thesis focusing on deregulated transcription factors and microRNAs in the pathogenesis of classic Hodgkin lymphoma. After obtaining her degree, she began her post-doctoral studies in the laboratory of Dr. Margaret Shipp at Dana-Farber Cancer Institute in Boston. Dr. Paczkowska’s postdoctoral research focuses on the immunobiology of classic Hodgkin lymphoma and related B-cell malignancies.
Program Name(s)
Career Development Program
Project Title
Adam de Smith
pediatric ALL and Down Syndrome
Adam de Smith, PhD
Los Angeles, CA
United States
University of Southern California
I am a genetic epidemiologist and Assistant Professor in the Center for Genetic Epidemiology and Department of Population and Public Health Sciences at the USC Keck School of Medicine. During my PhD, my research was focused on genetic variation and its role in human disease, and I received training in genetic epidemiology. Keen to pursue a career in childhood cancer research, I obtained a postdoctoral position at UCSF studying the etiology of acute lymphoblastic leukemia (ALL), the most common childhood cancer. In 2018, I started a faculty position at USC, where I lead epidemiology studies of ALL in high-risk populations, including Hispanic/Latinos and children with Down syndrome. My research has led to several novel discoveries, identifying new genetic risk factors for ALL and shedding light on how Down syndrome increases leukemia risk. Understanding the causes of childhood ALL is my life’s work, with the hope that our discoveries will help to develop precision prevention strategies.
Program Name(s)
Career Development Program
Project Title
Martin Carroll, MD
Philadelphia, PA
United States
Perelman School of Medicine at the University of Pennsylvania
Dr. Carroll is a physician scientist who has been studying leukemia biology for 3 decades. Until recently Dr. Carroll saw patients with blood cancers at the Philadelphia Veterans Administration Hospital but is now focused solely on research to improve therapy for AML. He has performed that research at the Univeristy of Pennsylvania since 1998. Dr. Carroll has had a long term commitment to building tools to enhance the understanding of human AML. These tools have included development of a large tissue bank of patient samples. He has also lead the field in development and application of the study of AML in immunocompromised mice. His work in xenograft AML models lead to the characterization of chemotherapy resistance as not always being dependent on leukemic stem cells but on metabolic adaptations of the cells to chemotherapy. Dr. Carroll has been involved in development of previous novel therapies for AML and continues to focus on developing safer and more effective treatments.
Program Name(s)
Specialized Center of Research Program
Project Title
Philippe Armand
lymphoma and immunotherapy
Philippe Armand, MD, PhD
Boston, MA
United States
Dana-Farber Cancer Institute
Philippe Armand obtained his MD and PhD (in Biomedical Sciences) from the University of California San Francisco. He completed a residency in Internal Medicine at Brigham and Women’s Hospital in 2004, and a fellowship in Hematology/Oncology at Dana-Farber Cancer Institute (DFCI) in 2007. Since then, he has worked in the Stem Cell Transplantation and Lymphoma Divisions at DFCI. He is currently a Professor of Medicine at Harvard Medical School, an Institute Physician at DFCI, the Harold and Virginia Lash/David Lash Chair in Lymphoma Research, and the Chief of the Division of Lymphoma. His clinical practice is solely focused on patients with lymphoma. His research interests center on the development of novel therapeutics and assays in lymphoma, with a key focus on the translation of local laboratory research to novel clinical trials. He actively mentors many junior investigators, both fellows and junior faculty, in both clinical care and clinical research.
Program Name(s)
Academic Clinical Trials Program (ACT)
Project Title
Bispecific antibody-based frontline therapy for follicular lymphoma
Paolo Caimi
CAR-T clinical trial for CLL
Paolo Caimi, MD
Cleveland, OH
United States
Cleveland Clinic
Paolo Caimi is a physician and clinical investigator at the Cleveland Clinic, where he is also the Associate Bone Marrow Transplant Director for Cellular Therapy. Dr. Caimi completed his medical training at the Pontificia Universidad Catolica de Chile in Santiago, Chile. He finished residency at Johns Hopkins University / Sinai Hospital Residency Program in Internal Medicine followed by a hematology and oncology fellowship at Case Western Reserve University. His clinical focus is on the care of patients with lymphoid malignancies and his research is centered around early phase trials, with an emphasis on phase I trials of cellular therapy.
Program Name(s)
Academic Clinical Trials Program (ACT)
Project Title
BAFF-ligand CAR T-cells and pre-apheresis B-cell lymphodepletion for relapsed/refractory CLL
Ruben Carrasco
Myeloma
Ruben Carrasco, MD PhD
Boston, MA
United States
Dana-Farber Cancer Institute
Dr. Carrasco earned his MD and PhD degrees at the University of Chile. Motivated by his desire to practice medicine at the highest level, he immigrated to the USA and pursued a residency in anatomic pathology at the Massachusetts General Hospital followed by a fellowship in hematopathology at the Brigham and Women’s Hospital. In recognition to his research accomplishments in the field of multiple myeloma (MM) during his postdoctoral training he was recruited to the Dana-Farber Cancer Institute to develop an independent laboratory research program in MM. Dr. Carrasco is current Professor in Pathology at Harvard Medical School. His principal area of excellence is laboratory and clinical investigation focusing on understanding the roles of the Wnt/b-catenin signaling pathway in MM pathogenesis, with the threefold intent of (i) identifying novel therapeutic targets, (ii) developing novel targeted therapies, and (iii) developing animal models for preclinical and clinical intervention.
Program Name(s)
Translational Research Program
Project Title
Developing selective inhibitors of the b-catenin/BCL9 transcriptional complex for myeloma therapy
Mark Murakami
follicular lymphoma
Mark Murakami, MD
Boston, MA
United States
Dana-Farber Cancer Institute
Dr. Mark Murakami is a physician-scientist dedicated to advancing curative treatments for follicular lymphoma. Based in the Division of Hematologic Neoplasia at the Dana-Farber Cancer Institute, Dr. Murakami leads a research group focused on understanding how minute numbers of lymphoma cells survive the initial effect of treatment, persist even when patients are in clinical remission, and later expand to cause relapse. Eradication of these rare cells, called minimal residual disease, is felt to be the key to curing follicular lymphoma. Dr. Murakami has dedicated his career to developing methods for tracking, isolating, and analyzing minimal residual disease and understanding how these cells evade pharmacologic therapy as well as the anti-lymphoma immune response. He uses this information to devise novel treatments for rigorous evaluation – first in the laboratory and eventually in clinical trials run by clinical colleagues – that we hope will cure follicular lymphoma.
Program Name(s)
Translational Research Program
Project Title
Exploiting tumor-immune dynamics to inform curative combination therapy for follicular lymphoma
Daniel Lucas
bone marrow and leukemia biology
Daniel Lucas, PhD
Cincinnati, OH
United States
Cincinnati Children's Hospital Medical Center
Daniel Lucas uses microscopy to understand how blood cells are produced in the marrow of the bone and how leukemia inhibits this process. A native Spaniard, he obtained his PhD in Madrid training with Drs. Antonio Bernad and Luis Blanco. Then he moved to New York for postdoctoral training in Paul Frenette’s lab. There he discovered basic mechanisms through which the nervous system regulates blood cell production. He also identified macrophages and megakaryocytes -two types of cells produced by the blood stem cells- as key regulators of those very same blood stem cells. This was the first demonstration that the stem cells were regulated by their own progeny. He established his own research group at the University of Michigan Medical School before being recruited to Cincinnati Children’s Hospital Medical Center. His group has discovered mechanisms that promote faster blood recovery after transplantation and deciphered how several types of blood cells assemble in the bone marrow.
Program Name(s)
Career Development Program
Project Title
Enrico Tiacci
Hairy cell leukemia
Enrico Tiacci, MD
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