HemeHub

Committed to Hematology

A leading resource for advancing care and knowledge in hematological disorders. We provide case-based learning resources, targeted training, conference insights, and case reviews, connecting professionals and trainees with top experts in hematology.

STRATEGIC PARTNERSHIPS

Texas OncologyUnited Porphyria AssociationWhitetulip Health Foundation

Upcoming Live Webinars

Live webinar

Ayalew Tefferi, MD is a professor of Hematology and Medicine at Mayo Clinic and a distinguished physician specializing in the pathophysiology, natural history, and treatment of chronic myeloproliferative neoplasms (MPNs), including polycythemia vera, essential thrombocythemia, and primary myelofibrosis. He completed his MD at the University of Athens Medical School, followed by a residency in internal medicine at St. Joseph Hospital in Chicago, IL. Ayalew Tefferi, MD then completed his residency in hematology and fellowship in hematology at the Mayo Clinic Graduate School of Biomedical Sciences, Mayo Clinic College of Medicine and Science. His research encompasses both database and laboratory-based studies, aiming to develop new therapeutic drugs for these conditions. Ayalew Tefferi, MD meticulously analyzes clinical and laboratory risk factors predictive of patient outcomes in MPNs, such as fibrotic transformation, leukemic transformation, and overall survival. He utilizes disease-specific clinical databases, with data collected over several decades, to identify these risk factors. Additionally, he has led extensive research in genetic and mutational profiling of MPNs, resulting in the creation of genetic and clinical-molecular prognostic models, which are now integral to contemporary clinical care for patients with MPNs. He has spearheaded numerous clinical trials, contributing to the licensing of several drugs for MPNs in the U.S. Notable therapeutic agents include ruxolitinib and momelotinib for the treatment of myelofibrosis. Ayalew Tefferi, MD has also conducted pioneering studies on rare MPNs, including systemic mastocytosis, eosinophilic conditions, histiocytic disorders, and hemophagocytic lymphohistiocytosis. Chronic myeloproliferative neoplasms are a group of relatively uncommon diseases with poorly understood clinical and biological features, and the only curative treatment is stem cell transplantation. Ayalew Tefferi, MD's research has significantly enhanced the understanding of these diseases, identified critical patient characteristics, and developed new treatments. His work is widely adopted by MPN experts and incorporated into international guidelines. His studies on rare MPNs have also advanced disease biology understanding and informed rational treatment strategies. Ayalew Tefferi, MD is deeply committed to improving patient care by educating other healthcare professionals and sharing his extensive knowledge and expertise in the field of hematology.

Live webinar

Mrinal S. Patnaik, MBBS is a physician scientist in the Division of Hematology within the Department of Internal Medicine at Mayo Clinic in Rochester, Minnesota. He serves as Chair of the Acute Leukemia and Myeloid Neoplasms Group in Rochester and is the Scientific Director of the Epigenetics Developmental Laboratory and the Epigenomics Program. He is actively involved in the Mayo Clinic Comprehensive Cancer Center and the Bone Marrow Transplant Program. Dr. Patnaik’s clinical and research expertise centers on precision genomics and epigenetics, with a focus on myeloid neoplasms and bone marrow failure syndromes. He directs the Mayo Clinic Clonal Hematopoiesis Clinic, the Bone Marrow Failure Syndrome Clinic, and the Short Telomere Clinic. His primary clinical interests include chronic myelomonocytic leukemia, myelodysplastic syndromes, myeloproliferative neoplasms, hereditary predisposition syndromes, and short telomere syndromes. He performs allogeneic stem cell transplantation and integrates genomic risk stratification into therapeutic decision making. Board certified in internal medicine and hematology by the American Board of Internal Medicine, Dr. Patnaik completed his residency and hematology oncology fellowship training at Mayo Clinic. He is recognized for excellence in education and mentorship, including induction into the Mayo Fellows Association Teacher of the Year Hall of Fame and receipt of the Internal Medicine Residents Outstanding Teaching Award. This session will provide a comprehensive clinical update in chronic myelomonocytic leukemia, highlighting key aspects of diagnosis, risk assessment, and current treatment approaches. Emphasis will be placed on practical management strategies, evolving therapeutic options, and individualized patient care to support informed decision making in the management of CMML.

Live webinar

Saad Z. Usmani, MD, MBA, FACP, FRCP, FASCO is Chief of the Myeloma Service at Memorial Sloan Kettering Cancer Center and a leading international expert in the diagnosis, management, and research of multiple myeloma and other plasma cell disorders. He also serves as Professor of Medicine at Weill Cornell Medical College, Cornell University. Dr. Usmani completed his medical education at Allama Iqbal Medical College, followed by residency training in internal medicine at Sinai Grace Hospital and Wayne State University. He subsequently completed fellowship training in hematology and medical oncology at the University of Connecticut Health Center. Dr. Usmani specializes in the care of patients with multiple myeloma and related plasma cell disorders, including monoclonal gammopathy of undetermined significance (MGUS), smoldering myeloma, and AL amyloidosis. Many of the patients he treats have high risk or difficult to treat disease, and his clinical work focuses on developing individualized treatment strategies that integrate the latest advances in targeted therapy, immunotherapy, and cellular therapy. His expertise also includes bone marrow transplantation and CAR T cell therapy for plasma cell malignancies. His research program focuses on advancing therapeutic strategies for multiple myeloma through clinical trials, immunotherapy development, and the integration of novel treatment approaches. Dr. Usmani has played a key role in the clinical development of several therapies that have received regulatory approval for patients with multiple myeloma and other hematologic malignancies. His work also explores the role of minimal residual disease testing to guide treatment decisions, improve risk stratification, and better understand disease progression from precursor conditions to active myeloma. Dr. Usmani holds numerous leadership roles in international clinical research collaborations and professional societies. He currently serves as Chair of the Myeloma Committee for the Alliance for Clinical Trials in Oncology within the National Clinical Trials Network and is a board member of the International Myeloma Society. His contributions to the field have been recognized through numerous honors, including the Leukemia and Lymphoma Society Career Development Achievement Award, the Celgene Young Investigator Award for Clinical Research in Hematology, and repeated recognition as a Castle Connolly Top Doctor. Through his clinical leadership, research contributions, and educational engagement, Dr. Usmani continues to help shape the evolving landscape of myeloma treatment while advancing care for patients with plasma cell disorders worldwide.

Upcoming Hybrid Events

HemeHub
Hybrid Symposium

HemeHub
Hematology Summit

A premier gathering of minds delivering the latest clinical updates and actionable guidance for the management of complex hematologic diseases.

Location

Dallas–Fort Worth, Texas

Date

October 3, 2026

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Latest Live Webinars

POST ASH 2025 Updates
01:13:53
ASH
January 5, 2026

POST ASH 2025 Updates

In this post-ASH 2025 discussion, Musa Yilmaz, Elif Yilmaz, Adeel Khan, and Taha Bat collectively review major updates from the 2025 American Society of Hematology Annual Meeting, focusing on findings with the greatest relevance to current and future clinical practice in myeloid, marrow failure, lymphoma and myeloma disorders. The speakers synthesize emerging data across hematologic malignancies and bone marrow failure syndromes, highlighting evolving treatment approaches and the growing role of novel and targeted therapies. Throughout the session, each presenter contributes expert perspective on how recent trial results and therapeutic advances may influence real-world decision-making. By emphasizing broader trends—such as personalization of therapy, integration of innovative agents, and thoughtful translation of research into practice—the discussion provides a cohesive and forward-looking overview of where the field of hematology is heading, while identifying ongoing challenges and areas of unmet need.

Hemophilia A
37:26
Bleeding disorders
November 30, 2025

Hemophilia A

In this session, Shannon Meeks, MD, and Ibrahim Ibrahim, MD review current best practices for managing Hemophilia A. They emphasize the move toward individualized, preventive care, noting that well-designed prophylactic therapycan significantly reduce bleeding events and prevent long-term joint damage. The speakers highlight the ongoing need to monitor for complications, particularly inhibitor development and joint deterioration, even with modern treatments. They also stress that optimal outcomes depend on multidisciplinary care, integrating hematology, nursing, physical therapy, and patient-education support to address both clinical and psychosocial needs.

Sickle Cell Disease and Gene Therapy
56:05
Hemolytic disorders
November 30, 2025

Sickle Cell Disease and Gene Therapy

In this session, Thomas Coates, MD and Ibrahim Ibrahim, MD provide an in-depth discussion about the state of gene therapy for sickle cell disease. They outline how gene therapy — by genetically correcting or ameliorating the mutation responsible for SCD in hematopoietic (blood-forming) stem cells — is transitioning from theoretical to actual clinical application. They caution, however, that while gene therapy offers hope for a “cure,” it's not a magic bullet. Concerns remain around long-term safety, durability of therapeutic effects, and equitable access. The speakers stress that even after gene therapy, patients may still require traditional supportive care and monitoring for complications. Finally, they call for strong research infrastructure — including long-term follow-up studies, registries, and multidisciplinary care teams — as critical to properly evaluate and deliver gene therapies to SCD patients.

Upcoming Scientific Conferences

British Society for Haematology (BSH) 66th Annual Scientific Meeting

Apr 19 - 21, 2026
ACC Liverpool, Liverpool, England, United Kingdom

The BSH 66th Annual Scientific Meeting is a key event for hematology professionals, providing the latest research and clinical advances in hematology. It offers educational sessions, networking opportunities, and discussions on the management of hematological conditions.

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American Society of Pediatric Hematology/Oncology (ASPHO) Conference

April 29 -May 2, 2026
Minneapolis Convention Center in Minneapolis, Minnesota, USA

An annual conference dedicated to pediatric hematology and oncology, offering educational sessions, research presentations, and networking opportunities for professionals.

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American Society of Gene & Cell Therapy (ASGCT) Annual Meeting

May 11–15, 2026
Boston Convention and Exhibition Center (BCEC) in Boston, Massachusetts

A leading conference on the latest innovations in gene and cell therapy, highlighting translational research and clinical applications for genetic diseases.

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