Ault Patricia S, Rose PharmD John, Nodzon PhD Lisa A, Kaled Elizabeth S
MD Anderson Cancer Center, University of Texas, Houston, Texas.
Pfizer Inc, Collegeville, Pennsylvania.
J Adv Pract Oncol. 2016 Mar;7(2):160-175. doi: 10.6004/jadpro.2016.7.2.3. Epub 2016 Mar 1.
The past decade has witnessed great advances in the treatment of chronic myeloid leukemia (CML), brought about in large part by the development of BCR-ABL tyrosine kinase inhibitors (TKIs). Bosutinib joins the armamentarium of approved TKIs for the treatment of chronic phase (CP), accelerated phase (AP), and blast phase (BP) Philadelphia chromosome (Ph)-positive CML resistant to or intolerant of prior therapy. Bosutinib has an adverse-event (AE) profile distinct from that of other TKIs. Diarrhea is the predominant toxicity associated with bosutinib treatment; other commonly reported nonhematologic AEs include rash and liver enzyme elevations. Cardiac events, fluid retention, and electrolyte abnormalities are infrequent. Optimal response to bosutinib requires adherence, which depends, in part, upon optimal management of associated toxicities. The oncology clinician can facilitate this process by providing patient education, timely patient follow-up, and close monitoring to promptly identify and manage AEs. Thus, optimal patient management requires a thorough and current understanding of toxicity profiles and AE management paradigms. This review provides an overview of bosutinib safety data derived from ongoing clinical trials and offers practical clinical strategies currently used to manage toxicities associated with bosutinib treatment in patients with Ph-positive CP, AP, and BP CML.
在过去十年中,慢性髓性白血病(CML)的治疗取得了巨大进展,这在很大程度上归功于BCR-ABL酪氨酸激酶抑制剂(TKIs)的发展。博舒替尼加入了已获批的TKIs药物库,用于治疗慢性期(CP)、加速期(AP)和急变期(BP)对先前治疗耐药或不耐受的费城染色体(Ph)阳性CML。博舒替尼的不良事件(AE)谱与其他TKIs不同。腹泻是与博舒替尼治疗相关的主要毒性;其他常见的非血液学AE包括皮疹和肝酶升高。心脏事件、液体潴留和电解质异常并不常见。对博舒替尼的最佳反应需要坚持用药,这部分取决于对相关毒性的最佳管理。肿瘤临床医生可以通过提供患者教育、及时的患者随访和密切监测来迅速识别和管理AE,从而促进这一过程。因此,最佳的患者管理需要对毒性谱和AE管理模式有全面且最新的了解。本综述概述了来自正在进行的临床试验的博舒替尼安全性数据,并提供了目前用于管理Ph阳性CP、AP和BP CML患者中与博舒替尼治疗相关毒性的实用临床策略。