Management and Risk Factors for Pleural Effusion in Japanese Patients with Chronic Myeloid Leukemia Treated with First-line Dasatinib in Real-world Clinical Practice.
chronic myeloid leukemia
dasatinib
management of adverse event
pleural effusion
Journal
Internal medicine (Tokyo, Japan)
ISSN: 1349-7235
Titre abrégé: Intern Med
Pays: Japan
ID NLM: 9204241
Informations de publication
Date de publication:
15 Nov 2023
15 Nov 2023
Historique:
medline:
17
11
2023
pubmed:
3
4
2023
entrez:
2
4
2023
Statut:
ppublish
Résumé
Objective Pleural effusion (PE) is a common adverse event that occurs during dasatinib therapy for chronic myeloid leukemia (CML). However, the pathomechanism of PE and appropriate management of Asian patients with CML have not been elucidated. This study investigated the incidence rate, risk, and appropriate management of PE in Asian patients with CML treated with dasatinib. Methods We retrospectively collected data on patients in the chronic phase of CML who received first-line dasatinib therapy and were registered in the CML-Cooperative Study Group database. Patients We identified 44 cases of PE in a series of 89 patients and analyzed previously reported risk factors and effective management of PE. Results A univariate analysis revealed that age, diabetes mellitus, chronic renal failure, hypertension, the history of cardiovascular events, and dasatinib dose were significantly associated with PE. A multivariate analysis revealed that age ≥65 years old was the only independent risk factor for PE. Dasatinib dose reduction and switching to a tyrosine kinase inhibitor showed a statistically significant difference in effectively reducing PE volume compared to single diuretic use. Conclusion Although further studies are warranted, our observations showed that advanced age is a significant risk factor for PE, and tyrosine kinase inhibitor dose reduction or replacement of dasatinib may be an effective management strategy for PE in Asian CML patients who received first-line treatment with dasatinib in real-world clinical practice.
Identifiants
pubmed: 37005261
doi: 10.2169/internalmedicine.1611-23
pmc: PMC10713361
doi:
Substances chimiques
Dasatinib
RBZ1571X5H
Protein Kinase Inhibitors
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
3299-3303Références
J Clin Oncol. 2018 Jan 20;36(3):231-237
pubmed: 29091516
Am J Hematol. 2016 Sep;91(9):869-74
pubmed: 27192969
Leuk Lymphoma. 2014 Sep;55(9):2093-100
pubmed: 24289108
J Clin Oncol. 2017 Jan 20;35(3):298-305
pubmed: 28095277
J Clin Invest. 2016 Sep 1;126(9):3207-18
pubmed: 27482885
J Clin Oncol. 2016 Aug 20;34(24):2851-7
pubmed: 27325849
Leukemia. 2016 Aug;30(8):1648-71
pubmed: 27121688
J Cancer Res Clin Oncol. 2018 May;144(5):945-954
pubmed: 29468438
Leukemia. 2016 May;30(5):1044-54
pubmed: 26837842
Br J Haematol. 2021 Jul;194(2):393-402
pubmed: 34195988
J Clin Oncol. 2016 Jul 10;34(20):2333-40
pubmed: 27217448
Clin Pharmacol. 2013 Jun 10;5:85-97
pubmed: 23788844
Blood. 2011 Jul 21;118(3):686-92
pubmed: 21536864
N Engl J Med. 2017 Mar 9;376(10):917-927
pubmed: 28273028
Blood. 2013 Aug 8;122(6):872-84
pubmed: 23803709
Ann Hematol. 2018 Jan;97(1):95-100
pubmed: 28971265
Lancet Haematol. 2021 Dec;8(12):e902-e911
pubmed: 34826413
Bone Marrow Transplant. 2013 Mar;48(3):452-8
pubmed: 23208313