4.2 Article

Allogeneic Hematopoietic Stem Cell Transplantation for Relapsed/Refractory Acute Myeloid Leukemia: A Single-Centre Experience

Journal

CLINICAL LYMPHOMA MYELOMA & LEUKEMIA
Volume 23, Issue 1, Pages 28-39

Publisher

CIG MEDIA GROUP, LP
DOI: 10.1016/j.clml.2022.08.014

Keywords

AML; Allogeneic stem cell transplantation; Allo-HSCT; r; rAML; refractory; relapsed AML

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This study analyzed the safety and efficacy of allogenic stem cell transplantation in patients with relapsed/refractory acute myeloid leukemia (r/r AML). The results showed that secondary AML and the number of pretransplantation treatment lines increased the risk of disease progression, while chronic graft versus host disease (cGVHD) had the opposite effect. The study emphasized the importance of early transplantation for r/r AML patients, even after unsatisfactory induction.
We present our single-center data on the safety and efficacy of allogenic stem cell transplantation in the r/r AML. The retrospective analysis included 64 patients. Our results confirm that secondary AML and the number of pretransplantation treatment lines increased the risk of progression, cGVHD showed the opposite effect. We confirm that patients with r/r AML should be transplanted as soon as possible, even after the first unsatisfactory induction.Introduction: Patients with relapsed/refractory acute myeloid leukemia (r/r AML) are characterized as having a poor prognosis. The only viable option of treatment for these patients is allogenic stem cell transplantation (allo-HSCT). Therefore, we have attempted to analyse factors related to both the disease itself and the transplantation procedure that could have an influence on the improvement of outcomes in this group of patients. Patients and methods: Sixty-four patients with r/r AML underwent allo-HSCT at our center in 2012 to 2021. Fifty-two had active disease at the beginning of theallo-HSCT procedure, with amedian number of blasts in bone marrow (BM) of 18, and 12 had therapeutic aplasia after the last reinduction (blasts < 5% in BM). Results: The probability of overall survival (OS) at 2 years was 25%. The median follow-up for survivors was 21.5 months. Progression-free survival (PFS) estimates were above 46%. The main cause of death was disease progression (49%). A statistically significant effect on premature death was reported for the diagnosis of secondary AML (sAML) and cytomelovirus (CMV) reactivation post allo-HSCT. On the other hand, chronic graft versus host disease (cGVHD) decreased the risk of disease progression. sAML and CMV reactivation were found to have opposite effects.

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