The Application of Personalized Conditioning Regimens in Relapsed/Refractory Acute Myeloid Leukemia Receiving
Shuangzhu Liu1, Biqi Zhou1, Chongsheng Qian1
1National Clinical Research Center for Hematologic Diseases, Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, China.
Objective:
To evaluate the efficacy and safety of personalized conditioning regimens in allogeneic hematopoietic stem cell transplantation (allo-HSCT) for the treatment of relapsed/ refractory acute myeloid leukemia (R/R AML).
Methods:
A retrospective analysis of the clinical data of 14 R/R AML patients who underwent allo-HSCT with a personalized conditioning regimen was conducted.
Results:
Among the 14 patients, there were 8 males and 6 females with a median age of 34.5 years (range 14-56). One patient received a transplant from a fully matched related donor, 2 from unrelated donors, and 12 from haploidentical donors. Prior to transplantation, all patients had a myeloblast percentage greater than 5% before transplantation, with a median myeloblast of 8.5 (6-88)%. Thirteen patients (92.86%) achieved morphologic leukemia-free state (MLFS) after conditioning. All patients achieved successful engraftment and hematopoietic recovery. The median time to neutrophil engraftment was 12 days (range 10-14), and the median time to platelet engraftment was 21.5 days (range 17-29). There was no obvious hepatorenal toxicity during the conditioning, and no mucositis more than grade 2 according to CTCAE 5.0 [1]. Bone marrow biopsies at +30 days post-transplant indicated remission in all cases. Two patients relapsed at 2 and 3 months post-transplant, with 2 dying after relapse. Additionally, 2 patients had CMV infections; 1 became negative after treatment, while the other remained positive and later died due to severe infection. As of the last follow-up, 11 out of 14 patients were alive (with marrow morphology and MRD Continuously negative).
Conclusion:
Allo-HSCT with a personalized conditioning regimen can be considered a treatment option for patients with R/R AML.
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