Sam Butterworth
CMML
Sam Butterworth, PhD
Manchester,
United Kingdom
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)
Manyi Wei
acute megakaryoblastic leukemia
Manyi Wei, PhD
New Haven, CT
United States
Yale
Dr. Manyi Wei gained his B.S. degree at China Pharmaceutical University in Nanjing. Subsequently, he completed his Ph.D. training in Cell Biology at the Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences. During his Ph.D. research, Dr. Wei focused on the regulatory role of long non-coding RNA in gene expression and its impact on neuronal function. Dr. Wei has always nurtured a particular interest in understanding and developing novel treatment for leukemia. After his Ph.D. training, Dr. Wei joined the laboratory of Dr. Stephanie Halene at Yale Cancer Center and Yale University School of Medicine. He immediately began exciting work on RNA modifications and their functions in the initiation and progression of acute myeloid leukemia and myelodysplastic syndromes and importantly on novel therapeutic approaches exploiting cell intrinsic and extrinsic effects of targeted inhibitors of RNA methylation. His goal is to contribute to the cure of leukemia.
Program Name(s)
Career Development Program
Project Title
Daniel Herranz
T-ALL
Daniel Herranz, PharmD, PhD
New Brunswick, NJ
United States
Rutgers University
A PharmD by training, I then obtained my PhD guided by Dr. Manuel Serrano at the CNIO studying Sirt1 role in metabolism and cancer, which led to 4 first-author and 1 corresponding papers, plus 11 co authorships. Next, I joined the Ferrando Lab at Columbia University where I published two seminal papers identifying a NOTCH1-driven Myc enhancer critical for T-cell development and leukemia, and dissecting the role of cancer metabolism in the resistance to anti-NOTCH1 therapy. I started my independent career at Rutgers in July 2017. In these 4 years, I have established a highly successful and productive laboratory, as reflected by the multiple funding sources obtained (including R01, ACS or AACR grants, among others), as well as by the publication of 3 corresponding author studies: a Blood Cancer Discovery paper identifying an enhancer of PTEN in leukemia; a Leukemia paper describing the antileukemic effects of SHMT inhibition; and a Blood paper describing the therapeutic effects of mitochondrial uncoupling in T-ALL.
Program Name(s)
Career Development Program
Project Title
Therapeutic exploitation of novel mouse models and metabolic interventions in leukemia
Fenghuang Zhan
Myeloma and bone disease
Fenghuang Zhan, MD, PhD
Little Rock, AR
United States
University of Arkansas for Medical Sciences
Fenghuang (Frank) Zhan, MD & PhD, is a Professor of Medicine and the Research Director of Myeloma Center at University of Arkansas for Medical Sciences (UAMS). Frank’s research focuses on identifying treatment approaches to overcome drug resistance in multiple myeloma (MM) by using genomic, genetic, and immunological tools from a very large database of clinical samples and mouse models. Frank has published more than 170 peer reviewed papers. Many of his publications appeared in prestigious journals such as Science, NEJM, Cancer Cell, Blood, and J Clin Invest. As a principal investigator (PI), he has received many grants from the Multiple Myeloma Research Foundation (MMRF), Blood Cancer United and NIH-NCI, etc. Frank received his PhD in Cancer Molecular Genetics and was then trained as a postdoctoral fellow and junior faculty at UAMS. Prior he returned to UAMS, he was an Associate Professor in the University of Utah, and then a Professor in the University of Iowa.
Program Name(s)
Translational Research Program
Project Title
Toward improvement of BCMA/CST6-CAR-T therapy to target both myeloma cells and bone resorption
Grant Challen
preleukemia, leukemia
Grant Challen, PhD
St. Louis, MO
United States
Washington University in St. Louis
Dr. Challen is currently an Associate Professor in the Division of Oncology at Washington University School of Medicine (St. Louis). His laboratory research is at the interface of stem cell biology and blood cancer, and aims to determine how disruption of the epignenome changes the fate of HSCs and ultimately leads to the development of hematopoietic disorders. He was the first to describe how mutations in the gene DNMT3A regulates the balance of HSC self-renewal and differentiation as a first step to development of AML. His lab aims to develop mutation-specific therapies to inhibit CH clones as a mechanism of blood cancer prevention.
Dr. Challen is investigating how mutations in genes that alter the epigenome alter the function of blood-forming hematopoietic stem cells (HSCs), leading to a condition known as clonal hematopoiesis (CH) and predispose for future development of blood diseases such as myelodysplastic syndromes (MDS), acute myeloid leukemia (AML)and T-cell acute lymphoblastic leukemia (T-ALL).
Program Name(s)
Career Development Program
Translational Research Program
Project Title
Synergism of cell-intrinsic and cell-extrinsic factors in the clonal evolution of pre-malignant HSCs
Shazia Nakhoda
Equity in Access
Shazia Nakhoda, MD
Philadelphia, PA
United States
Fox Chase Cancer Center
Dr. Nakhoda is a clinician-scientist in the department of hematology/oncology at Fox Chase Cancer Center. She serves as steering committee member for the Leukemia & Lymphoma Society supported Philadelphia Lymphoma rounds and is a panelist on the NCCN Guidelines for Chronic Lymphocytic Leukemia. She has a research focus on improving tolerability of lymphoma and leukemia directed therapies in elderly patients and those with medical comorbidities, actively running an investigator-initiated study evaluating methods to improve methotrexate toxicity in this population. She is well suited to serve as primary investigator for this proposed project having served as local site PI for several multi-institutional investigational studies in lymphoma and with now 6 years of malignant hematology experience serving the Philadelphia area, first as hematology/oncology fellow at Temple University Hospital System and FCCC and now as an assistant professor at Fox Chase.
Program Name(s)
Equity in Access
Project Title
Du Wei
Leukemia
Du Wei, PhD, MD
Pittsburg, PA
United States
University of Pittsburgh
My research is centered on pathophysiology of hematologic diseases such as bone marrow failure and leukemia, with specific focus on hematopoietic stem cell (HSC), DNA damage and immune response, and tumor microenvironment. I have been investigating HSC-BM niche interaction and HSC regeneration under conditions of injury and aging; and have identified functional interactions between certain factors implicated in cell proliferation, polarity, adhesion/migration, stem cell metabolism and aging. My work has led to 53 peer-reviewed scientific papers in high-impact scientific journals, including Blood, JCI, Nat Comm and Leukemia. I laid the groundwork for my long-term research by developing cell and animal models as well as effective assays for identifying mechanisms underlying critical hematological diseases as PI on several NIH- and private-funded grants. I am confident that both myself as a PI and my innovative research are highly competitive in future success in grants and publications.
Program Name(s)
Career Development Program
Project Title
Reid Merryman, MD
Boston, MA
United States
Dana-Farber Cancer Institute
Reid Merryman, MD is an Assistant Professor of Medicine at Harvard Medical School, Boston, MA, USA, and a Senior Physician in the Division of Lymphoma at Dana-Farber Cancer institute (DFCI). He received his undergraduate degree from the University of Notre Dame and his medical degree from Harvard Medical School. He completed residency training in internal medicine at Brigham and Women's Hospital and fellowship training in hematology and oncology at DFCI. He serves as the Director of Clinical Research for the Lymphoma Division and as the Director of the Follicular Lymphoma Center and the Marginal Zone Lymphoma Center at DFCI. His research interests include 1) development of novel immune-based treatments in Hodgkin lymphoma and indolent non-Hodgkin lymphoma (NHL) and 2) identification of novel biomarkers (like circulating tumor DNA) to guide response-adapted treatment approaches. He is currently leading 3 investigator-initiated trials testing CD3/CD20 bispecific antibody-based therapeutic approaches for patients with newly diagnosed or relapsed/refractory indolent NHLs.
Program Name(s)
Academic Clinical Trials Program (ACT)
Project Title
Bispecific antibody-based frontline 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
Andrew Lane
BPDCN
Andrew Lane, PhD, MD
Boston, MA
United States
Dana-Farber Cancer Institute
Dr. Lane’s laboratory and translational research focuses on the biology of high-risk blood cancers, including acute myeloid leukemia (AML), myelodysplastic syndrome (MDS), and blastic plasmacytoid dendritic cell neoplasm (BPDCN). His goal is to identify new therapeutic targets and to understand treatment resistance. He is an associate professor of medicine at Harvard Medical School, a physician in the Leukemia Program, and a lab investigator in the Division of Hematologic Neoplasia in the Department of Medical Oncology at the Dana-Farber Cancer Institute. He is director of the BPDCN Center at Dana-Farber. He is also an associate member of the Broad Institute of Harvard and MIT. Dr. Lane received a bachelor’s degree in biomedical engineering from Vanderbilt University, and MD and PhD degrees from Washington University. He completed a residency in internal medicine at Brigham and Women’s Hospital and fellowships in hematology and medical oncology at the Dana-Farber Cancer Institute.
Program Name(s)
Career Development Program
Project Title
Rayne Rouce
Immunotherapy for pediatric, adolescent & young adult patients
Rayne Rouce, MD
Houston, TX
United States
Baylor College of Medicine
Dr. Rouce is a pediatric oncologist and physician scientist whose clinical research focuses on difficult-to-treat blood cancers, specifically how to harness the immune system to attack them. She has spent the past 12 years in the Center for Cell and Gene Therapy at Texas Children’s Hospital leading a research program translating genetically engineered immune cells to first-in-human immunotherapy trials. She has significant experience in every aspect of clinical trial development and in addition to serving as principal investigator on CAR-T trials for blood cancers, has served as Project Leader for projects for the NIH Lymphoma SPORE, Blood Cancer United Specialized Center of Research, and Stand Up to Cancer. She leads health equity and disparities initiatives locally and nationally and is dedicated to addressing access barriers to novel cancer clinical trials for children, adolescents/young adults, underrepresented minorities, patients with limited resources and those with geographic constraints.
Program Name(s)
Academic Clinical Trials Program (ACT)
Project Title
Novel CD7 CAR T-cells for refractory T-cell malignancies affecting pediatric and AYA patients
Ana Vujovic
AML
Ana Vujovic, PhD
Denver, CO
United States
University of Colorado Denver, Anschutz Medical Campus
Ana Vujovic is a postdoctoral research fellow at the University of Colorado Anschutz Medical Campus. She completed her PhD under the mentorship of Dr. Kristin Hope at the University of Toronto and Princess Margaret Cancer Centre, University Health Network, where she studied the role of post-transcriptional regulation in hematopoietic and acute myeloid leukemia (AML) stem cells. Ana joined the laboratory of Dr. Craig T. Jordan in the Spring of 2023, where her postdoctoral studies are focused on investigating metabolic vulnerabilities in AML stem cells and in particular mechanisms that underlie the resistance of these cells to the combination therapy, Venetoclax and Azacitidine (Ven/Aza). The objective of her postdoctoral research is to identify novel therapeutic strategies to uniquely target the metabolic vulnerabilities of Ven/Aza-resistant AML stem cells with the goal of improving AML patient outcomes.
Program Name(s)
Career Development Program