Treatment-free remission with first- and second-generation tyrosine kinase inhibitors.
Antineoplastic Agents
/ therapeutic use
Clinical Trials as Topic
Dasatinib
/ therapeutic use
Disease Management
Drug Administration Schedule
Fusion Proteins, bcr-abl
/ antagonists & inhibitors
Gene Expression
Humans
Imatinib Mesylate
/ therapeutic use
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
/ drug therapy
Monitoring, Physiologic
Protein Kinase Inhibitors
/ therapeutic use
Pyrimidines
/ therapeutic use
Remission Induction
Survival Analysis
Treatment Outcome
Journal
American journal of hematology
ISSN: 1096-8652
Titre abrégé: Am J Hematol
Pays: United States
ID NLM: 7610369
Informations de publication
Date de publication:
03 2019
03 2019
Historique:
received:
13
08
2018
revised:
26
10
2018
accepted:
31
10
2018
pubmed:
6
11
2018
medline:
27
12
2019
entrez:
6
11
2018
Statut:
ppublish
Résumé
Chronic myeloid leukemia (CML) has become a chronic disease, for which the chronic phase is manageable with tyrosine kinase inhibitor (TKI) therapy. Patients with optimal responses to TKIs have achieved long-term survival, and treatment-free remission (TFR) has since become an additional treatment goal in CML. In this review, we discuss important factors to consider prior to stopping treatment. In addition, published and presented data with the first-generation TKI imatinib, as well as current clinical trials evaluating TFR with the second-generation TKIs dasatinib and nilotinib, are examined. Results obtained outside of clinical trials have been included as well. Because successful TKI discontinuation depends upon accurate BCR-ABL1 monitoring, emerging technologies are also discussed. Clinical data obtained to date indicate that for many patients who achieve deep molecular response (DMR) on TKI therapy, TFR is a safe treatment goal, and, if the response is lost, patients can expect to regain their responses immediately upon reinitiation of TKI. It is also clear that there remains much room for improvement to make TFR a successful reality for most patients. Data from ongoing trials should help refine decisions as to which patients are the best candidates to attempt TKI discontinuation with safe monitoring in place.
Identifiants
pubmed: 30394563
doi: 10.1002/ajh.25342
pmc: PMC6587857
doi:
Substances chimiques
Antineoplastic Agents
0
BCR-ABL1 fusion protein, human
0
Protein Kinase Inhibitors
0
Pyrimidines
0
Imatinib Mesylate
8A1O1M485B
Fusion Proteins, bcr-abl
EC 2.7.10.2
nilotinib
F41401512X
Dasatinib
RBZ1571X5H
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
346-357Subventions
Organisme : Bristol-Myers Squibb
Pays : International
Informations de copyright
© 2018 The Authors. American Journal of Hematology published by Wiley Periodicals, Inc.
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