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

Paul Richardson, MD is the Clinical Program Leader and Director of Clinical Research at the Jerome Lipper Multiple Myeloma Center at Dana-Farber Cancer Institute, and the RJ Corman Professor of Medicine at Harvard Medical School. A leading authority in the treatment of multiple myeloma, Paul Richardson, MD has been instrumental in advancing novel therapies that have transformed patient outcomes. His work has been central to the development and approval of groundbreaking agents, including thalidomide, lenalidomide, bortezomib, pomalidomide, panobinostat, elotuzumab, daratumumab, and more recently, ixazomib, selinexor, and mezigdomide. Paul Richardson, MD has led numerous pivotal trials that have reshaped standards of care, most notably the VISTA trial, which established bortezomib-based therapy as frontline treatment, and the international DETERMINATION study, which helped define the role of autologous stem cell transplantation in the era of novel agents. His research integrates translational science with clinical innovation, exploring combinations of small molecules, targeted therapies, and immunotherapeutics to optimize outcomes for patients across the spectrum of multiple myeloma. In addition to his research, Paul Richardson, MD is deeply committed to patient care and mentorship. He has authored or co-authored hundreds of peer-reviewed publications, reviews, and book chapters, and is widely recognized as an educator and thought leader in hematology-oncology. His contributions have been honored with numerous awards, including recognition for excellence in teaching, clinical research, and innovation in cancer care. Through his leadership, Paul Richardson, MD continues to advance the field of myeloma therapy while improving the lives of patients worldwide.

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

Catherine Broome, MD is a Professor of Medicine in the Division of Hematology and Oncology at MedStar Georgetown University Hospital in Washington, DC. She is board certified in internal medicine, hematology, and medical oncology and has been on staff at the Georgetown Lombardi Comprehensive Cancer Center for over a decade, where she specializes in benign hematology. Dr. Broome's clinical expertise includes cold agglutinin disease, autoimmune hemolytic anemia, immune thrombocytopenia, paroxysmal nocturnal hemoglobinuria, hemophagocytic lymphohistiocytosis, and pure red cell aplasia. She is actively involved in clinical research and routinely offers patients access to clinical trials focused on rare and complex hematologic disorders. In addition to her clinical work, Dr. Broome serves as an associate professor in the Department of Medicine at Georgetown University and is engaged in the education and mentorship of trainees. She also participates in institutional safety and quality initiatives across MedStar Health. This session will provide clinical updates in cold agglutinin disease, focusing on diagnostic nuances, evolving disease classification, and emerging therapeutic strategies. Emphasis will be placed on practical management considerations and individualized patient care in this complement mediated hemolytic anemia.

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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Program details coming soon

Upcoming Scientific Conferences

American Society of Transplantation and Cellular Therapy (ASTCT) Conference

February 4-7, 2026
Salt Palace Convention Center, Salt Lake City, Utah, USA

The premier international meeting on transplantation and cellular therapy, uniting thousands of clinicians, researchers, and industry leaders to advance blood and marrow transplantation and cellular immunotherapy.

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Hemostasis & Thrombosis Research Society (HTRS) 2026 Scientific Symposium

March 11-13 2026
Loews Coronado Bay Resort, Coronado, California, USA

A global event for experts in thrombosis, hemostasis, and vascular biology, featuring plenaries, workshops, and networking opportunities.

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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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Latest Live Webinars

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.

POST ASH 2023 Annual Meeting
01:03:04
ASH
October 4, 2025

POST ASH 2023 Annual Meeting

This session featuring Yu-Min Shen, MD; Ibrahim Ibrahim, MD; and Taha Bat, MD, offered a comprehensive analysis of key hematology advances presented at the 2023 ASH Annual Meeting, with a special focus on bone marrow failure syndromes such as aplastic anemia (AA), paroxysmal nocturnal hemoglobinuria (PNH), and related clonal disorders. The panel emphasized how the field is rapidly shifting toward precision medicine, integrating molecular diagnostics and immune characterization into everyday clinical decision-making. A central theme was the expanding therapeutic landscape beyond traditional immunosuppressive therapy (IST). Emerging data on novel complement inhibitors, thrombopoietin receptor agonists, and targeted immune modulatorsare redefining treatment pathways and allowing for individualized regimens based on patient-specific molecular profiles and risk factors. The experts discussed how these developments may reduce relapse rates, delay clonal evolution, and improve quality of life for patients. Another focal point was the timing and optimization of hematopoietic stem cell transplantation (HSCT). The panelists noted that earlier consideration of HSCT—particularly in younger, high-risk, or treatment-refractory patients—can lead to superior survival outcomes. Advances in donor matching, reduced-intensity conditioning, and supportive care are making transplant a safer and more accessible option worldwide. The discussion also highlighted the growing role of genomic testing in identifying patients at risk for clonal progression to myelodysplastic syndromes (MDS) or acute myeloid leukemia (AML). Routine incorporation of NGS panels, flow cytometry, and cytogenetic studies was encouraged to guide prognosis and therapeutic selection. Finally, the panel addressed real-world barriers to adopting these novel therapies, including cost, access, and health equity challenges. They stressed the importance of multidisciplinary collaboration and data sharing to ensure that innovation translates into measurable improvements in patient outcomes globally. Overall, the session reflected the momentum in translational hematology, bridging laboratory discoveries with clinical practice, and underscored the collective effort to refine diagnosis, enhance treatment precision, and improve long-term survivorship in bone marrow failure disorders.