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How I approach hematopoietic stem cell transplantation for CML in a TKI world.

Blood 2026 Vol.147(4) p. 357-368

Chalandon Y, Simonetta F, Masouridi-Levrat S

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After the introduction of tyrosine kinase inhibitors (TKIs), the number of patients undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT) for chronic phase chronic myeloid leukemia

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APA Chalandon Y, Simonetta F, Masouridi-Levrat S (2026). How I approach hematopoietic stem cell transplantation for CML in a TKI world.. Blood, 147(4), 357-368. https://doi.org/10.1182/blood.2024026512
MLA Chalandon Y, et al.. "How I approach hematopoietic stem cell transplantation for CML in a TKI world.." Blood, vol. 147, no. 4, 2026, pp. 357-368.
PMID 40354577

Abstract

After the introduction of tyrosine kinase inhibitors (TKIs), the number of patients undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT) for chronic phase chronic myeloid leukemia (CP-CML) has dramatically decreased. Imatinib was the first TKI introduced into the clinical arena, predominantly used in the first-line setting. In cases of insufficient response, resistance, or intolerance, patients with CML can subsequently be treated with a second-, third-, or fourth-generation TKI. However, despite the approval of first-, second-, third-, and fourth-generation TKIs, allo-HSCT still remains indicated for a minority of patients with CML. Here, we discuss the indications in the era of TKIs through different cases representing the clinical situations for which allo-HSCT remains the best option. We also propose our transplant strategy to decrease transplant-related morbidity, particularly graft-versus-host disease, and mortality in the particular context of CML, a disease that is one of the most sensitive to immune cellular therapy, allowing the use of a combination of donor lymphocyte infusion and TKIs for posttransplant molecular progression.

MeSH Terms

Humans; Hematopoietic Stem Cell Transplantation; Protein Kinase Inhibitors; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Male; Graft vs Host Disease; Female; Adult; Middle Aged; Transplantation, Homologous