Life (Basel, Switzerland) · 2026
Adverse Respiratory Reactions to Tyrosine Kinase Inhibitors: A Disproportionality Analysis of Spontaneous Reports from European Countries.
СтатьяНазвание и аннотация: Перевод пока не подготовлен
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Ammendolia Ilaria, Mannucci Carmen, Esposito Emanuela, Calapai Gioacchino, Currò Mariaconcetta, Midiri Paola, Mondello Cristina, Cancellieri Antonino, Cardia Luigi, Calapai Fabrizio
Аннотация
BACKGROUND: The tyrosine kinase inhibitors (TKIs) asciminib, bosutinib, dasatinib, imatinib, nilotinib, and ponatinib have been approved for chronic myelogenous leukemia (CML) therapy. However, pharmacovigilance reports associated with these drugs are neither consistent nor homogenous, with reports of pulmonary toxicity, which could limit their utilization. To better clarify TKIs' pulmonary risk, we used the European database EudraVigilance to conduct a study on adverse events suspected to be caused by the TKIs asciminib, bosutinib, dasatinib, imatinib, nilotinib, and ponatinib when used for CML therapy.
METHODS: Suspected adverse reactions to TKIs in the EudraVigilance database (2020-2024) coming from European countries and the United Kingdom were analyzed and compared through a disproportionality analysis.
RESULTS: The most frequent alerts concerned the respiratory disorders "pleural effusion" (PE) and "pulmonary arterial hypertension" (PAH) in relation to dasatinib and bosutinib use. Among the TKIs, the prescription of dasatinib is associated with a higher occurrence of PE and PAH, while the prescription of bosutinib induces PE at a minor frequency that nonetheless carries a significant risk for PAH, occurring more often in women.
CONCLUSIONS: The results indicate that respiratory disorders induced by the TKIs dasatinib and bosutinib need to be diagnosed in a timely manner, and suggest that caution should be taken when prescribing these TKIs to patients affected by CML and pulmonary comorbidities.
METHODS: Suspected adverse reactions to TKIs in the EudraVigilance database (2020-2024) coming from European countries and the United Kingdom were analyzed and compared through a disproportionality analysis.
RESULTS: The most frequent alerts concerned the respiratory disorders "pleural effusion" (PE) and "pulmonary arterial hypertension" (PAH) in relation to dasatinib and bosutinib use. Among the TKIs, the prescription of dasatinib is associated with a higher occurrence of PE and PAH, while the prescription of bosutinib induces PE at a minor frequency that nonetheless carries a significant risk for PAH, occurring more often in women.
CONCLUSIONS: The results indicate that respiratory disorders induced by the TKIs dasatinib and bosutinib need to be diagnosed in a timely manner, and suggest that caution should be taken when prescribing these TKIs to patients affected by CML and pulmonary comorbidities.