Jacobs Joshua A, Jahangir Eiman, Ryan John J
Department of Pharmacy University of Utah Health Salt Lake City Utah USA.
Division of Cardiovascular Medicine, Department of Medicine Vanderbilt University Nashville Tennessee USA.
Pulm Circ. 2022 May 11;12(2):e12075. doi: 10.1002/pul2.12075. eCollection 2022 Apr.
Protein kinase inhibitors (PKIs) have been implicated in pulmonary vascular toxicities including risk factors for at least three of the five World Health Organization groups of pulmonary hypertension (PH). These toxicities include direct drug-induced pulmonary arterial hypertension, an increase in cardiomyopathies, and an increase in interstitial lung disease. On- and off-target toxicities are common within multitargeted PKIs leading to cardiopulmonary toxicities. This review highlights the incidence, possible mechanisms, and management strategies for each group of possible PKI-induced PH. Future identification and clarification of protein kinase pathways for both mechanisms of toxicity and pathophysiology for PH could lead to improvements in patient care in oncology and pulmonary vascular diseases.
蛋白激酶抑制剂(PKIs)与肺血管毒性有关,包括世界卫生组织五个肺动脉高压(PH)组别中至少三组的风险因素。这些毒性包括直接药物诱发的肺动脉高压、心肌病增加以及间质性肺病增加。多靶点PKIs中,脱靶毒性和靶向毒性都很常见,会导致心肺毒性。本综述重点介绍了每组可能由PKI诱发的PH的发生率、可能机制及管理策略。未来,明确毒性机制和PH病理生理学的蛋白激酶途径,可能会改善肿瘤学和肺血管疾病患者的护理。