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Use of Tyrosine Kinase Inhibitors to Prevent Relapse After Allogeneic Hematopoietic Stem Cell Transplantation for Patients With Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia: A Position Statement of the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation

Authors :
Jordi Esteve
Arnon Nagler
Fabio Ciceri
Sebastian Giebel
Norbert Claude Gorin
Jan J. Cornelissen
Bipin N. Savani
Oliver G. Ottmann
Frédéric Baron
Christoph Schmid
Eolia Brissot
Anna Czyż
Mohamad Mohty
Giebel, Sebastian
Czyz, Anna
Ottmann, Oliver
Baron, Frederic
Brissot, Eolia
Ciceri, Fabio
Cornelissen, Jan J.
Esteve, Jordi
Gorin, Norbert Claude
Savani, Bipin
Schmid, Christoph
Mohty, Mohamad
Nagler, Arnon
Hematology
Source :
Cancer, 122(19), 2941-2951. John Wiley & Sons Inc.
Publication Year :
2016
Publisher :
John Wiley & Sons Inc., 2016.

Abstract

Allogeneic hematopoietic stem cell transplantation (alloHSCT) is a standard of care for patients with Philadelphia chromosome (Ph)–positive acute lymphoblastic leukemia (ALL). The introduction of tyrosine kinase inhibitors (TKIs) to first-line therapy has improved overall outcomes; however, a significant proportion of patients still relapse after alloHSCT. Posttransplant TKI maintenance was demonstrated to reduce the risk of relapse in a large retrospective study and, therefore, should be considered a valuable option. This consensus paper, written on behalf of the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation, presents an overview of clinical studies on the use of TKIs after alloHSCT and proposes practical recommendations regarding the choice of TKI, treatment timing, and dosage. It is hoped that these recommendations will become the state of art in this field and, more importantly, lead to a reduction of Ph-positive ALL relapse after alloHSCT. Cancer 2016;122:2941-2951. © 2016 American Cancer Society.

Details

ISSN :
10970142, 0008543X, and 29412951
Volume :
122
Issue :
19
Database :
OpenAIRE
Journal :
Cancer
Accession number :
edsair.doi.dedup.....0511c142b5b492d4ab0216d67f7f6657