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Debates on the role and timing of allogeneic hemtopoietic stem cell transplantation (HSCT) in acute myelogenous leukemia (AML) have persisted for decades. Time to transplant introduces an immortal time and current treatment algorithm mainly relies on the European LeukemiaNet disease risk classification. Previous studies are also limited to age groups, remission status and other ill-defined parameters. We studied all patients at diagnosis irrespective of age and comorbidities to estimate the cumulative incidence and potential benefit or disadvantage of HSCT in a single center. As a time-dependent covariate, HSCT improved overall survival in intermediate- and poor-risk patients (hazard ratio =0.51; P=0.004). In goodrisk patients only eight were transplanted in first complete remission. Overall, the 4-year cumulative incidence of HSCT was only 21.9% but was higher (52.1%) for patients in the first age quartile (16-57 years old) and 26.4% in older patients (57-70 years old) (P<0.001). It was negligible in patients older than 70 years reflecting our own transplant policy but also barriers to transplantation (comorbidities and remission status). However, HSCT patients need to survive, be considered eligible both by the referring and the HSCT physicians and have a suitable donor to get transplantation. We, thus, comprehensively analyzed the complete decision-making and outcome of all our AML patients from diagnosis to last followup to decipher how patient allocation and therapy inform the value of HSCT. The role of HSCT in AML is shifting with broad access to different donors including haploidentical ones. Thus, it may (or may not) lead to increased numbers of allogeneic HSCT in AML in adults.
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http://dx.doi.org/10.3324/haematol.2023.282729 | DOI Listing |
Allogeneic stem cell transplantation (allo-SCT) is a curative option for acute myelogenous leukemia (AML), but relapse is a challenge. Monitoring minimal residual disease post-transplant through detection of tumor-associated circulating cell-free DNA (TA-cfDNA) in peripheral blood (PB) and bone marrow is an emerging strategy to predict relapse. Persistent mutations in TA-cfDNA may be prognostic indicators of relapse and mortality.
View Article and Find Full Text PDFLeukemia
August 2025
Laboratory of Cell and Developmental Biology, Institute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic.
The acquired JAK2-V617F mutation plays a causal role in myeloproliferative neoplasms (MPN). Weakly activating JAK2 germline variants have been associated with MPN risk, but the underlying mechanisms remain unclear. We previously identified the JAK2-R1063H germline variant, which contributes to hereditary MPN and increased disease severity in essential thrombocythemia.
View Article and Find Full Text PDFEur J Haematol
August 2025
Section for Hematology, Department of Medicine, Haukeland University Hospital, Bergen, Norway.
Objective: Graft-versus-host disease (GVHD) is the most prevalent long-term complication following allogeneic hematopoietic stem cell transplant (allo-HSCT). This study aimed to investigate specific posttransplant metabolic alterations in allo-HSCT recipients with acute myelogenous leukemia (AML) or myelodysplastic neoplasms (MDS).
Methods: We analyzed the global metabolic profile in serum samples from 37 patients at 3 months posttransplantation.
Background: Ponatinib is a third-generation tyrosine kinase inhibitor (TKI) for treatment of chronic myeloid leukemia (CML) and Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL) in patients who fail or are intolerant to a second generation TKI or who carry the mutation.
Method: This is the final analysis of the Belgian ponatinib registry evaluating use of ponatinib in clinical practice, with data available for up to 6 years after reimbursement.
Result: Forty-eight percent of 54 CML and 28% of 29 Ph+ ALL patients had received ≥3 previous TKIs.
Am J Case Rep
August 2025
Department of Academic Affairs and Research, Orlando Regional Healthcare System, Orlando, FL, USA.
BACKGROUND Acute myelogenous leukemia (AML) is a rare, aggressive, disease that requires prolonged treatment. It accounts for a third of all leukemias diagnosed in the United States. A bone marrow biopsy accompanied by histological, cytogenetic, and molecular analysis is essential for the classification of malignancy.
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