Relapsed and refractory AML is a very difficult clinical problem, and there is currently no unified and efficient treatment plan.

Relapsed and refractory AML is a very difficult clinical problem, and there is currently no unified and efficient treatment plan.

Relapsed and refractory acute myeloid leukemia (AML) presents one of the most formidable challenges in oncology, lacking a unified and efficient treatment strategy. Dr. Johannes Schetelig, Head of the Cell Therapy Unit at the Technical University of Dresden and Chair of the Clinical Trials Unit within the DKMS, offers invaluable insights into the complexities and evolving approaches in managing this condition. From the nuances of defining refractory AML at various stages to the critical decision-making involved in stem cell transplantation, Dr. Schetelig's expertise sheds light on current practices and future directions. This article delves into the multifaceted strategies for treating relapsed and refractory AML, focusing on patient suitability for stem cell transplantation, predictive clinical characteristics for better outcomes, and proactive measures to prevent relapse post-transplantation. 
VLA-4 Agonists – Enhancing Hematopoietic Stem Cell Engraftment, Accelerating Immune Reconstitution, and Increasing Treatment Success Rates for Patient

VLA-4 Agonists – Enhancing Hematopoietic Stem Cell Engraftment, Accelerating Immune Reconstitution, and Increasing Treatment Success Rates for Patient

Hematopoietic stem cell transplantation (HSCT) is an effective, and often the only, curative treatment for malignant hematological diseases such as leukemia. Key steps that impact the success of the transplantation include stem cell engraftment and the reconstitution of immune functions. From April 14 to 17, 2024, the 50th European Society for Blood and Marrow Transplantation (EBMT) annual meeting was grandly held in Glasgow, UK. The conference focused on the latest advancements in stem cell transplantation and cell therapy, driving better clinical outcomes for patients with hematological diseases. At this conference, a team led by Professor Xianmin Song from Shanghai First People's Hospital presented an oral report titled "VLA-4 Agonists Promote Engraftment and Cellular Immune Reconstitution in Allogeneic Hematopoietic Stem Cell Transplantation," which garnered widespread attention. Professor Song was specially invited to our live interview room to share the main findings of his research and provide a detailed explanation of the latest developments in the critical steps of allogeneic stem cell transplantation: graft engraftment and immune reconstitution.
EBMT 2024 | Professor Qingxiao Song: PI3Kδ Inhibitors Show High Potential in the Treatment of cGVHD

EBMT 2024 | Professor Qingxiao Song: PI3Kδ Inhibitors Show High Potential in the Treatment of cGVHD

Chronic graft-versus-host disease (cGVHD) is a clinical syndrome occurring after allogeneic hematopoietic stem cell transplantation (allo-HSCT), where the recipient’s organs are attacked by donor-derived lymphocytes during the reconstitution of the donor's immune system. This includes both classic cGVHD and overlapping syndromes and is one of the main complications of transplantation, with an incidence rate of 30% to 70%. The mechanisms behind cGVHD are complex, its clinical manifestations diverse, and the individual differences significant. The course of the disease can be prolonged and persistent; if not properly diagnosed and treated, it can severely affect the patient's quality of life and long-term survival. With the introduction of guidelines, there are now standardized diagnostic criteria and first-line treatment protocols for cGVHD, but there is still no consensus on second-line treatments. PI3Kδ inhibitors, which interfere with the proliferation and survival of lymphocytes by inhibiting the activity of the PI3Kδ enzyme and thus suppress tumor growth, have not only introduced new drugs and strategies for non-Hodgkin's lymphoma but have also shown therapeutic potential in the treatment of GVHD. At the recent 50th European Society for Blood and Marrow Transplantation (EBMT) annual meeting, a basic study from the Second Affiliated Hospital of Army Medical University was selected for an oral presentation (Abstract No: OS7-05) [1], showcasing the activity of PI3Kδ inhibitors in the treatment of cGVHD. "Oncology Frontier - Hematology Frontier" has invited Professor Qingxiao Song from The Second Affiliated Hospital of Army Medical University (Xinqiao Hospital) to interpret and comment on this research for our readers.there is still no consensus on second-line treatments. PI3Kδ inhibitors, which interfere with the proliferation and survival of lymphocytes by inhibiting the activity of the PI3Kδ enzyme and thus suppress tumor growth, have not only introduced new drugs and strategies for non-Hodgkin's lymphoma but have also shown therapeutic potential in the treatment of GVHD. At the recent 50th European Society for Blood and Marrow Transplantation (EBMT) annual meeting, a basic study from the Second Affiliated Hospital of Army Medical University was selected for an oral presentation (Abstract No: OS7-05) [1], showcasing the activity of PI3Kδ inhibitors in the treatment of cGVHD. "Oncology Frontier - Hematology Frontier" has invited Professor Qingxiao Song from The Second Affiliated Hospital of Army Medical University (Xinqiao Hospital) to interpret and comment on this research for our readers.
EBMT Interview | The Latest Advances and Challenges in Bispecific Antibody Treatment for Lymphoma

EBMT Interview | The Latest Advances and Challenges in Bispecific Antibody Treatment for Lymphoma

Monoclonal antibody-based targeted therapy has significantly improved treatment options for cancer patients. In recent years, advancements in protein engineering have led to the development of bispecific antibodies (BsAbs), marking a paradigm shift in antibody construction usage. BsAbs, recognized for their higher therapeutic response, resistance barrier, and fewer adverse reactions, have caught significant attention in the academic world. The next wave of "bispecific or multispecific antibodies" is also on the horizon. At the 50th European Society for Blood and Marrow Transplantation (EBMT) Annual Meeting, Professor Maria Gomes Da Silva from the Portuguese Oncology Institute delivered an insightful report on the latest advances in BsAb treatments for lymphoma. "Oncology Frontier - Hematology Frontier" invited Professor Da Silva to share the latest developments and challenges in this field with our readers.
EBMT Spotlight Interview | Professor Li Chunfu: Improved TCRαβ-T Cell Depleted Hematopoietic Stem Cell Transplantation (TDH) for Treating Severe Thalassemia

EBMT Spotlight Interview | Professor Li Chunfu: Improved TCRαβ-T Cell Depleted Hematopoietic Stem Cell Transplantation (TDH) for Treating Severe Thalassemia

Hematopoietic stem cell transplantation is a common and effective treatment in the field of hematology. As techniques have matured, stem cell transplantation not only serves as a treatment for malignant blood diseases such as leukemia but also offers a new solution for curing thalassemia. The 50th European Society for Blood and Marrow Transplantation (EBMT) Annual Meeting took place in Glasgow, UK, from April 14th to 17th, 2024. The conference highlighted the latest advancements in stem cell transplantation and cellular therapies, pushing hematologic patients towards better clinical outcomes. At this meeting, Professor Li Chunfu from the Gaobo Medical (Hematology) Guangdong Research Center and Southern Chunfu (Children’s) Hematology Institute delivered an excellent oral presentation on the modified TCRαβ-T cell depleted hematopoietic stem cell transplantation (TDH) for treating severe thalassemia. "Oncology Frontier - Hematology Frontier" invited Professor Li to share his insights and experiences regarding transplantation treatments for thalassemia with our readers.
EBMT Interview Spotlight | Latest Advances and Challenges in CAR-T Therapy for Acute Lymphoblastic Leukemia (ALL)

EBMT Interview Spotlight | Latest Advances and Challenges in CAR-T Therapy for Acute Lymphoblastic Leukemia (ALL)

Acute Lymphoblastic Leukemia (ALL) is a malignant neoplastic disease that originates from B-cell or T-cell lymphocytes and proliferates abnormally in the bone marrow. In recent years, immunotherapy has made significant strides in the field of ALL, including breakthroughs in treatments such as Chimeric Antigen Receptor T-cell (CAR-T) therapy, bispecific antibodies, and antibody-drug conjugates (ADC). The 50th European Society for Blood and Marrow Transplantation (EBMT) annual meeting took place in Glasgow, UK, from April 14 to 17, 2024. At the conference, Professor Peter Bader from the Department of Stem Cell Transplantation, Immunology, and Intensive Care Medicine at the University Hospital Frankfurt, Germany, delivered a special report on the current application of CAR-T therapy in ALL patients. Hematology Frontier invited Professor Bader to share the latest progress and challenges in CAR-T therapy in the field of ALL with a wide audience.
EBMT Interview Spotlight | Future Landscape of Multiple Myeloma Treatment: Cell Therapy vs. Transplantation

EBMT Interview Spotlight | Future Landscape of Multiple Myeloma Treatment: Cell Therapy vs. Transplantation

Multiple myeloma is a clonal plasma cell proliferative disorder that has seen significant therapeutic advancements over the past few decades due to deepening biological research. With the development of proteasome inhibitors, immunomodulatory drugs, monoclonal antibodies, Chimeric Antigen Receptor T-cell (CAR-T) therapy, and other new drugs, the survival and prognosis for patients with multiple myeloma have undergone milestone changes. From April 14 to 17, 2024, the 50th European Society for Blood and Marrow Transplantation (EBMT) annual meeting was held in Glasgow, UK. At the conference, Professor Reuben Benjamin from King's College Hospital in London gave a special report on the clinical application and future prospects of hematopoietic stem cell transplantation and CAR-T cell therapy in multiple myeloma patients. Hematology News invited Professor Benjamin to share his insights with a broad audience.
Professor Jun Ma: Fruitful Updates to the 2024 CSCO Lymphoma Treatment Guidelines | 2024 CSCO Guidelines Conference

Professor Jun Ma: Fruitful Updates to the 2024 CSCO Lymphoma Treatment Guidelines | 2024 CSCO Guidelines Conference

Lymphoma has become the most prevalent malignant hematological tumor in China. Enhancing the standardized diagnosis and treatment of lymphoma is crucial for improving cure rates. The "Chinese Society of Clinical Oncology (CSCO) Lymphoma Treatment Guidelines" are updated annually and play a significant role in promoting standardized care for lymphoma. At the recent 2024 CSCO Guidelines Conference, the 2024 edition of the CSCO Lymphoma Treatment Guidelines was released as scheduled. To better understand the key updates in the 2024 edition, "Oncology Frontier - Hematology Frontier" invited Professor Jun Ma, Director of the Harbin Institute of Hematology Oncology, to discuss the current status of lymphoma diagnosis and treatment in China, and to share the significance and highlights of the new guidelines.
 Professor Tiejun Gong: Striving for Excellence, 2024 CSCO Guidelines on Malignant Hematology with a Focus on Leukemia | 2024 CSCO Guidelines Conference

 Professor Tiejun Gong: Striving for Excellence, 2024 CSCO Guidelines on Malignant Hematology with a Focus on Leukemia | 2024 CSCO Guidelines Conference

The 2024 China Clinical Oncology Society (CSCO) Guidelines Conference was held in Jinan on April 26-27, 2024. As always, the conference updated and released multiple CSCO cancer treatment guidelines. Professor Tiejun Gong, Deputy Director of the Harbin Institute of Hematologic Oncology, gave an insightful interpretation of the leukemia section in the "2024 CSCO Guidelines on Malignant Hematology." After the conference, "Oncology Frontier - Hematology Frontier" invited Professor Gong to introduce the characteristics and updates in leukemia treatment in the 2024 CSCO Malignant Hematology Guidelines, discuss current challenges in leukemia treatment, and express his views on potential improvements.