Comparative study of micro-transplantation from HLA fully mismatched unrelated and partly matched related donors in acute myeloid leukemia.
Kai-Xun HuXin DuMei GuoChang-Lin YuJian-Hui QiaoQi-Yun SunHong-Li ZuoBo CaiYa-Jing HuangHui-Sheng AiZheng DongYi WangPublished in: American journal of hematology (2020)
Micro-transplantation (MST) by chemotherapy, combined with granulocyte colony-stimulating factor-mobilized peripheral blood stem cell (GPBSC) infusion, from an HLA partial matched related donor has shown some encouraging effective therapy for acute myeloid leukemia (AML). However, the outcome of human leukocyte antigen (HLA) fully mismatched unrelated donor-derived MST in such patients is still unknown. In the present study, we compared the efficacy of HLA fully mismatched unrelated donor-derived MST, and partly matched related donor-derived MST, in AML of 126 patients from two centers in China, These patients, aged 16 to 65 years, were given three or four courses of MST, which consisted of a high dosage cytarabine followed by GPBSC from unrelated donor or related donor. There was a statistically significant difference in 3-year leukemia-free survival (LFS) and 3-year overall survival (OS) between the unrelated and the related group. The non-treatment-related mortality (NRM) rates of patients, and other adverse complications, were no different in the two groups. In conclusion, unrelated donor-derived MST is believed to be a safe treatment, with efficacy similar to or higher than related donor-derived MST. This result provides support for the potential of MST for expanding the donor selection. However, the specific mechanism of action needs further study.
Keyphrases
- acute myeloid leukemia
- end stage renal disease
- peripheral blood
- chronic kidney disease
- ejection fraction
- stem cells
- newly diagnosed
- mesenchymal stem cells
- radiation therapy
- acute lymphoblastic leukemia
- high dose
- allogeneic hematopoietic stem cell transplantation
- cardiovascular events
- cardiovascular disease
- locally advanced
- low dose
- combination therapy