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Pharmacologic Therapies to Prevent Relapse of Acute Myeloid Leukemia After Allogeneic Hematopoietic Stem Cell Transplantation
- Source :
- Frontiers in Oncology, Frontiers in Oncology, Vol 10 (2020)
- Publication Year :
- 2020
-
Abstract
- Relapse is the main cause of mortality in patients with acute myeloid leukemia (AML) after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Adverse cytogenetic or molecular risk factors, as well as refractory disease or persistent measurable residual disease (MRD) at the time of transplantation are associated with an increased risk of recurrence. Salvage therapy for AML relapse after allo-HSCT is often limited to chemotherapy, donor lymphocyte infusions and/or second transplants and is rarely successful. Effective post-transplant preventive intervention in high risk AML may be crucial. The most frequent and promising approach is the use of post-transplant maintenance with hypomethylating agents or with FLT3 tyrosine kinase inhibitors when the target is present. Moreover, IDH1/IDH2 inhibitors and BCL-2 inhibitors in combination with other strategies are promising approaches in the maintenance setting. Here we summarize the current knowledge about the preemptive and prophylactic use of pharmacologic agents after allo-HSCT to prevent relapse of AML.
- Subjects :
- 0301 basic medicine
Oncology
Cancer Research
medicine.medical_specialty
Lymphocyte
medicine.medical_treatment
Salvage therapy
Disease
Hematopoietic stem cell transplantation
Review
acute myeloid leukemia
lcsh:RC254-282
IDH2
stem cell transplantation
03 medical and health sciences
0302 clinical medicine
prevention
Internal medicine
hemic and lymphatic diseases
medicine
allogeneic
relapse
Chemotherapy
hypomethylating agents
business.industry
Myeloid leukemia
lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
Transplantation
030104 developmental biology
medicine.anatomical_structure
surgical procedures, operative
030220 oncology & carcinogenesis
business
Subjects
Details
- ISSN :
- 2234943X
- Volume :
- 10
- Database :
- OpenAIRE
- Journal :
- Frontiers in oncology
- Accession number :
- edsair.doi.dedup.....c047486c108d4e76ac28b4b7500699fc