New drugs before, during, and after hematopoietic stem cell transplantation for patients with acute myeloid leukemia

Loading...
Thumbnail Image

Date

Journal Title

Journal ISSN

Volume Title

Publisher

Ferrata Storti Foundation

Abstract

The treatment of acute myeloid leukemia (AML) has evolved over the past few years with the advent of next-generation sequencing. Targeted therapies alone or in combination with low-dose or high-intensity chemotherapy have improved the outcome of patients with AML treated in the frontline and relapsed/refractory settings. Despite these advances, allogeneic stem cell transplantation (allo-HCT) remains essential as consolidation therapy following frontline treatment in intermediate- and adverse-risk and relapsed/refractory disease. However, many patients relapse, with limited treatment options, hence the need for post-transplant strategies to mitigate relapse risk. Maintenance therapy following allo-HCT was developed for this specific purpose and can exploit either a direct anti-leukemia effect and/or enhance the bona fide graft-versus-leukemia effect without increasing the risk of graft-versus-host disease. In this paper, we summarize novel therapies for AML before, during, and after allo-HCT and review ongoing studies. ©2023 Ferrata Storti Foundation Published under a CC BY-NC license.

Description

Keywords

Graft vs host disease, Graft vs leukemia effect, Hematopoietic stem cell transplantation, High-throughput nucleotide sequencing, Humans, Leukemia, myeloid, acute, Azacitidine, Busulfan, Cladribine, Crenolanib, Cytarabine, Daunorubicin, Enasidenib, Fludarabine, Gemtuzumab, Glasdegib, Histone deacetylase inhibitor, Idarubicin, Isocitrate dehydrogenase inhibitor, Ivosidenib, Magrolimab, Midostaurin, Palbociclib, Quizartinib, Sorafenib, Treosulfan, Venetoclax, Vincristine, Acute graft versus host disease, Acute myeloid leukemia, Allogeneic hematopoietic stem cell transplantation, Allogeneic stem cell transplantation, Antileukemic activity, Carcinogenesis, Cytogenetics, Event free survival, Graft versus leukemia effect, Human, Myelodysplastic syndrome, Overall survival, Phase 1 clinical trial (topic), Phase 2 clinical trial (topic), Phase 3 clinical trial (topic), Review, Adverse event, Genetics, Graft versus host reaction, High throughput sequencing

Citation

Endorsement

Review

Supplemented By

Referenced By