Girard Nicolas, Audigier-Valette Clarisse, Cortot Alexis B, Mennecier Bertrand, Debieuvre Didier, Planchard David, Zalcman Gérard, Moro-Sibilot Denis, Cadranel Jacques, Barlési Fabrice
Department of Respiratory Medicine and Thoracic Oncology, Hôpital Louis Pradel, Hospices Civils de Lyon, Claude Bernard University Lyon 1, Lyon, France.
Expert Rev Anticancer Ther. 2015 Feb;15(2):225-33. doi: 10.1586/14737140.2014.986103. Epub 2014 Nov 21.
Crizotinib (XALKORI™, Pfizer) is a tyrosine kinase inhibitor targeting ALK, MET and ROS1, currently approved for the treatment of adults with ALK-rearranged non-small-cell lung cancer. Optimizing the management of frequent crizotinib-related adverse events is crucial to ensure its continuous administration and reproduce the response and survival rates reported in clinical trials. Here, we propose some practical measures, which are mostly derived from the recommendations given to the investigators of the PROFILE 1001, 1005, 1007 and 1014 trials and are based on experience and scientific findings regarding the management of these disorders. While visual disturbances or bradycardia are frequent but benign, the severity of the cardiac and hepatic adverse events requires special attention potential to QT interval prolongations and to the monitoring of electrolyte levels and liver function, taking into account potential drug-drug interactions.
克唑替尼(XALKORI™,辉瑞公司)是一种靶向ALK、MET和ROS1的酪氨酸激酶抑制剂,目前已被批准用于治疗ALK重排的非小细胞肺癌成人患者。优化对克唑替尼相关常见不良事件的管理对于确保其持续给药以及重现临床试验中报告的缓解率和生存率至关重要。在此,我们提出一些实用措施,这些措施大多源自对PROFILE 1001、1005、1007和1014试验的研究者的建议,并基于有关这些疾病管理的经验和科学发现。虽然视觉障碍或心动过缓很常见但为良性,但心脏和肝脏不良事件的严重程度需要特别关注,考虑到潜在的药物相互作用,要注意QT间期延长的可能性以及监测电解质水平和肝功能。