Efficacy and Cardiovascular Adverse Events of Long-term Treatment with Tyrosine Kinase Inhibitors for Chronic Myeloid Leukemia: A Report from the Nagasaki CML Study Group.
adverse event
cardiovascular disease
chronic myeloid leukemia
tyrosine kinase inhibitor
Journal
Internal medicine (Tokyo, Japan)
ISSN: 1349-7235
Titre abrégé: Intern Med
Pays: Japan
ID NLM: 9204241
Informations de publication
Date de publication:
15 Jul 2021
15 Jul 2021
Historique:
pubmed:
23
2
2021
medline:
17
7
2021
entrez:
22
2
2021
Statut:
ppublish
Résumé
Objective The standard treatment for chronic myeloid leukemia (CML) is the continuous use of tyrosine kinase inhibitors (TKIs), which results in a favorable prognosis for the majority of patients. Recent studies have identified cardiovascular diseases (CVDs) as late adverse events (AEs) related to TKIs. In this study, we evaluated the long-term efficacy and AEs of TKIs, focusing on CVDs. Methods We performed a retrospective survey of CML patients (diagnosed from 2001 to 2016) treated with TKIs in Nagasaki Prefecture. Clinical data were obtained from their medical records. We analyzed the survival, estimated cumulative incidence of CVDs, and risk factors for CVD among CML patients treated with TKIs. Results The overall survival rate of 264 CML patients treated with TKIs (median age 58 years old) was 89.6% [95% confidence interval (CI), 84.9-92.9%], and 80.5% (95% CI, 73.4-85.9%) at 5 and 10 years after the CML diagnosis, respectively. CVD events occurred in 26 patients (9.8%, median age 67.5 years old) with a median 65.5 months of TKI treatment. The cumulative incidences at 2 and 5 years was 2.4% (95% CI, 1.0-4.8%) and 5.2% (95% CI, 2.8-8.6%), respectively. Hypertension and a high SCORE chart risk at the diagnosis of CML were associated with CVD events during TKI treatment. Conclusion TKI treatment contributed to the long-term survival of CML patients in Nagasaki Prefecture in a "real-world" setting, but the incidence of CVDs seemed to be increased in these patients. A proper approach to managing risk factors for CVD is warranted to reduce CVD events during TKI treatment.
Identifiants
pubmed: 33612681
doi: 10.2169/internalmedicine.6620-20
pmc: PMC8355380
doi:
Substances chimiques
Protein Kinase Inhibitors
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
2207-2216Références
Int J Hematol. 2018 Feb;107(2):185-193
pubmed: 28929332
J Clin Oncol. 2017 Jan 20;35(3):298-305
pubmed: 28095277
Am J Hematol. 2011 Jul;86(7):533-9
pubmed: 21538470
N Engl J Med. 2017 Mar 9;376(10):917-927
pubmed: 28273028
Ann Hematol. 2018 Nov;97(11):2081-2088
pubmed: 29946911
Eur Heart J. 2003 Jun;24(11):987-1003
pubmed: 12788299
Int J Hematol. 2019 Apr;109(4):426-439
pubmed: 30762219
Int J Hematol. 2009 Apr;89(3):319-325
pubmed: 19266256
Leuk Res. 2014 Jan;38(1):76-83
pubmed: 24262285
Lancet. 2015 Apr 11;385(9976):1447-59
pubmed: 25484026
Blood Adv. 2019 Mar 26;3(6):851-861
pubmed: 30885996
Leukemia. 2016 May;30(5):1044-54
pubmed: 26837842
Int J Hematol. 2020 Sep;112(3):268-291
pubmed: 32783166
J Clin Oncol. 2016 Jul 10;34(20):2333-40
pubmed: 27217448
Blood Cancer J. 2018 Dec 2;8(10):91
pubmed: 30504932
Lancet Oncol. 2010 Nov;11(11):1029-35
pubmed: 20965785
Bone Marrow Transplant. 2013 Mar;48(3):452-8
pubmed: 23208313
N Engl J Med. 2003 Mar 13;348(11):994-1004
pubmed: 12637609
Int J Hematol. 2007 Feb;85(2):132-9
pubmed: 17321991
Ann Intern Med. 2016 Aug 2;165(3):161-6
pubmed: 27295519
JAMA Oncol. 2016 May 1;2(5):625-632
pubmed: 26847662