| Literature DB >> 30658222 |
Robert Zeiser1, Dietrich W Beelen2, Wolfgang Bethge3, Martin Bornhäuser4, Gesine Bug5, Andreas Burchert6, Maximilian Christopeit7, Justus Duyster8, Jürgen Finke8, Armin Gerbitz9, Jan Henning Klusmann10, Guido Kobbe11, Michael Lübbert8, Carsten Müller-Tidow12, Uwe Platzbecker13, Wolf Rösler14, Martin Sauer15, Christoph Schmid16, Thomas Schroeder11, Mathias Stelljes17, Nicolaus Kröger7, Lutz P Müller18.
Abstract
The curative potential of allogeneic hematopoietic cell transplantation (allo-HCT) in the treatment of acute myelogenous leukemia (AML) and myelodysplastic syndrome (MDS) relies mainly on the graft-versus-leukemia effect. Relapse after allo-HCT occurs in a considerable proportion of patients and has a dismal prognosis, with still very limited curative potential. This review provides an overview of the established and evolving approaches to preventing or treating relapse of AML and MDS after allo-HCT, in the context of novel insight into the biology of relapse. Established prophylactic measures to prevent relapse include optimized conditioning and graft-versus-host disease (GVHD) prophylaxis, as well as donor lymphocyte infusion (DLI) for high-risk patients; novel immunomodulatory interventions and maintenance approaches are still experimental. Improved diagnostics can detect persistent or recurring disease at a molecular level, enabling early preemptive interventions. Established options include hypomethylating agents and DLI. Standard treatments for hematologic relapse include chemotherapy, cessation of immunosuppressive treatment, and DLI. Experimental approaches include molecular targeted therapies, novel immunomodulatory treatments, and second allo-HCT. For all interventions, the potential risks, including occurrence of GVHD, must be weighed against the benefits individually in each patient. Concurrently, prevention and treatment of relapse after allo-HCT remain challenging and unmet medical needs.Entities:
Keywords: Acute myelogenous leukemia; Allogeneic hematopoietic stem cell transplantation; Myelodysplastic syndrome; Relapse
Year: 2019 PMID: 30658222 DOI: 10.1016/j.bbmt.2019.01.016
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742