Impact of imatinib treatment on renal function in chronic myeloid leukaemia patients
Jazyk angličtina Země Austrálie Médium print-electronic
Typ dokumentu časopisecké články, metaanalýza
Grantová podpora
LTC20031
INTER-EXCELLENCE Grant
CZ.02.2.69/0.0/0.0/18_053/0016952
Masarykova Univerzita
JH/RO/OO/2020/12
Sun Pharma
PubMed
34894374
DOI
10.1111/nep.14014
Knihovny.cz E-zdroje
- Klíčová slova
- cancer, chronic kidney disease, chronic myeloid leukaemia, imatinib, meta-analysis, tyrosine kinase inhibitors,
- MeSH
- chronická myeloidní leukemie * chemicky indukované farmakoterapie MeSH
- chronická nemoc MeSH
- imatinib mesylát škodlivé účinky MeSH
- inhibitory proteinkinas škodlivé účinky MeSH
- ledviny fyziologie MeSH
- lidé MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- metaanalýza MeSH
- Názvy látek
- imatinib mesylát MeSH
- inhibitory proteinkinas MeSH
BACKGROUND: Recently, multiple epidemiological studies have linked imatinib with the alteration of renal function in chronic myeloid leukaemia (CML) patients. This meta-analysis aimed to summarize the impact of imatinib use on renal function in CML patients. METHODS: A systematic search was conducted on MEDLINE and Embase to identify articles assessing the impact of imatinib exposure on renal function in CML patients. The risk of bias was assessed using the Newcastle-Ottawa scale (NOS). Two authors independently performed literature-screening, risk of bias and data extraction. The risk of renal dysfunction (chronic kidney disease or acute kidney injury) among imatinib users was computed as the primary outcome of interest. The certainty of findings was assessed using the grading of recommendations assessment, development and evaluation (GRADE) criteria. RESULTS: A total of nine articles qualified for inclusion in the systematic review, of which four articles were eligible for meta-analysis. Based on the scoring on NOS, majority of the included studies were found to be of moderate risk of bias. Majority of the studies (n = 6) reported significantly (p < .05) decrease in estimated glomerular filtration rate (eGFR) after imatinib treatment. The risk of developing renal dysfunction (chronic kidney disease or acute kidney injury) was found to be significantly higher in imatinib users as compared to other tyrosine kinase inhibitor (TKI) users with a pooled relative risk of 2.70 (95% CI: 1.49-4.91). Sensitivity analysis also revealed a consistently high risk of renal dysfunction with imatinib use. GRADE criteria revealed low certainty of evidence. CONCLUSION: This meta-analysis found an increased risk of renal dysfunction in imatinib users compared to other TKI users.
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