Reprint

AML in the Molecular Age: From Biology to Clinical Management

Edited by
September 2018
208 pages
  • ISBN978-3-03897-280-8 (Paperback)
  • ISBN978-3-03897-281-5 (PDF)

This book is a reprint of the Special Issue AML in the Molecular Age: From Biology to Clinical Management that was published in

Medicine & Pharmacology
Public Health & Healthcare
Summary

In this Special Issue, we aim to discuss important scientific and clinical ongoing activities in AML. Scientific subjects will include articles concerning the molecular abnormalities, epigenetic mechanisms of disease/therapy as well as the role of the immune system in AML. Very interesting and uncommon subjects will include discussions of extramedullary disease and evaluations of the central nervous system by various imaging techniques. Experts will describe the role of hypomethylating agents in the management of AML and currently emerging and promising investigational therapies. Specifics of treament of pediatric and younger patients with AML. Clinical success relies greatly on supportive therapy, and we will discuss supportive therapy, including infection prophylaxis. Allogeneic hematopoietic stem cell transplantation remains the most effective measure for curing aggressive AML, and a variety of topics will be considered: donor selection, age of recipient, which has been increasing seemingly without limit; therefore, recipient/donor assessments are more important than ever in the aging population. Alternative donor use (e.g., cord blood and haploidentical individuals) has been increasing dramatically; when and who should be considered, what is being investigated? With significant changes occurring with respect to both donors and recipients, the pros and cons of using of anti-thymocyte globulin use in conditioning regimens will be also described.

Format
  • Paperback
License
© 2019 by the authors; CC BY license
Keywords
acute myeloid leukemia; FLT3; tyrosine kinase inhibitors; clinical trials; AML; azacitidine; decitabine; hypomethylating agents; elderly; epigenetics; pediatric AML; clinical management; cytogenetics; molecular aberrations; acute myeloid leukemia; adolescent and young adults; treatment; acute myeloid leukemia (AML); gene mutation; FLT3-ITD; NPM1; CEBPA; AML; CD34+ selection; T-cell depletion; graft-versus-host disease; hematopoietic stem cell transplantation; acute myeloid leukemia; targeted therapy; differentiation; 1,25-dihydroxyvitamin D3; mitogen-activated kinases; AML; targeted therapies; rational combinations; HDAC inhibitors; CDK inhibitors; proteasome inhibitors; checkpoint abrogators; apoptosis; BH3-mimetics; Mcl-1; salvage therapy; leukemia; neoplasm metastasis; AML; relapse; AML; acute myeloid leukemia; leukemia; myeloid sarcoma; extramedullary disease; chloroma; intracranial; central nervous system; brain; spine; AML; alternative donor; UCB; Haploidentical; Transplantation