Moffitt Cancer Center, Tampa, FL 33612, USA.
J Clin Nurs. 2010 May;19(9-10):1207-18. doi: 10.1111/j.1365-2702.2009.03167.x. Epub 2010 Mar 16.
To review the use of second-line tyrosine kinase inhibitors in patients with chronic myeloid leukaemia (CML) and provide recommendations for managing adverse events (AEs) to maximise patient benefit.
Treatment of CML has been revolutionised with the advent of tyrosine kinase inhibitors (TKIs) that target the breakpoint cluster region-Abelson (BCR-ABL) kinase. Imatinib is the only first-line TKI currently available for the treatment of CML; however, intolerance and resistance remain significant clinical challenges. The approved second-line treatment options for CML are dasatinib, nilotinib or escalated-dose imatinib.
Review article.
Searches of PubMed, ASCO and ASH electronic databases for relevant search terms were performed between July 2008-January 2009.
Dasatinib has no cross-intolerance with imatinib, and the most frequent AEs (cytopenias and pleural and pericardial effusions) can generally be managed by dose interruption and reduction. Nilotinib has a high degree of haematologic cross-intolerance with first-line imatinib. As might be expected, high-dose imatinib has the potential for more severe AEs than standard-dose imatinib.
There are known safety issues inherent to each TKI and close monitoring by nursing staff is necessary to identify and effectively manage AEs.
All three TKIs have demonstrated potential for fluid retention and cardiotoxicity. Nurses should be aware of how these AEs manifest and intervene appropriately. The safety profiles of these TKIs clearly differs and it is important to consider factors such as comorbidities when making treatment decisions.
回顾慢性髓性白血病(CML)患者二线酪氨酸激酶抑制剂的应用,并提供管理不良反应(AE)的建议,以最大程度地提高患者的获益。
酪氨酸激酶抑制剂(TKI)的出现彻底改变了 CML 的治疗,这些 TKI 靶向断裂点簇区-Abelson(BCR-ABL)激酶。伊马替尼是目前唯一可用于治疗 CML 的一线 TKI;然而,不耐受和耐药仍然是重大的临床挑战。CML 的批准二线治疗选择是达沙替尼、尼洛替尼或高剂量伊马替尼。
综述文章。
在 2008 年 7 月至 2009 年 1 月期间,在 PubMed、ASCO 和 ASH 电子数据库中对相关检索词进行了检索。
达沙替尼与伊马替尼无交叉不耐受,最常见的不良反应(血细胞减少症、胸腔和心包积液)通常可以通过中断和减少剂量来管理。尼洛替尼与一线伊马替尼具有高度的血液学交叉不耐受。正如预期的那样,高剂量伊马替尼比标准剂量伊马替尼更有可能出现严重的不良反应。
每种 TKI 都存在固有安全性问题,护理人员需要密切监测,以识别和有效管理不良反应。
三种 TKI 都有潜在的液体潴留和心脏毒性。护士应了解这些不良反应的表现,并进行适当干预。这些 TKI 的安全性特征明显不同,在做出治疗决策时,考虑合并症等因素很重要。