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奥希替尼的心脏安全性:数据回顾。

Cardiac Safety of Osimertinib: A Review of Data.

机构信息

Department of Cardiology, Division of Internal Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.

Patient Safety, Oncology R&D, AstraZeneca, Cambridge, United Kingdom.

出版信息

J Clin Oncol. 2021 Feb 1;39(4):328-337. doi: 10.1200/JCO.20.01171. Epub 2020 Dec 23.

Abstract

PURPOSE

Osimertinib is a third-generation, CNS-active, irreversible, oral epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) that potently and selectively inhibits both EGFR-TKI-sensitizing and T790M resistance mutations. We assess the cardiac failure risk in patients receiving osimertinib by evaluating the available data.

METHODS

Post hoc analyses of cardiac data from (1) studies in patients with advanced non-small-cell lung cancer, FLAURA (osimertinib, n = 279; comparator EGFR-TKI, n = 277) and AURA3 (osimertinib, n = 279; chemotherapy, n = 140), and (2) a pooled data set of patients treated with osimertinib 80 mg from across the clinical trial program (n = 1,142), including cardiac failure-related adverse events and left ventricular ejection fraction (LVEF) reductions. An LVEF pharmacokinetic or pharmacodynamic analysis of the pooled data set was performed. The sponsor's global safety database was analyzed for cardiac failure-related adverse events, and a literature search was conducted.

RESULTS

Decreases in LVEF from a baseline of ≥ 10 percentage points to an absolute value of < 50% following osimertinib treatment were observed in 8 (3.1%) and 14 (5.5%) patients in FLAURA and AURA3, respectively, and in 35 (3.9%) patients in the pooled population. Most events were asymptomatic and resolved without treatment of the event or osimertinib discontinuation. The pharmacokinetic or pharmacodynamic analysis did not indicate a relationship between exposure to osimertinib and decreases in LVEF from baseline. The database and literature search showed no specific trend or pattern that was suggestive of a safety issue in patients receiving osimertinib.

CONCLUSION

These data do not suggest a causal relationship between osimertinib and cardiac failure. However, because of LVEF decreases that were observed in patients with cardiac risk factors before osimertinib treatment, cardiac monitoring, including an assessment of LVEF at baseline and during osimertinib treatment, is advised.

摘要

目的

奥希替尼是第三代、CNS 活性、不可逆的口服表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI),能够强有力且选择性地抑制 EGFR-TKI 敏感和 T790M 耐药突变。我们通过评估现有数据来评估接受奥希替尼治疗的患者发生心力衰竭的风险。

方法

对晚期非小细胞肺癌患者(1)FLAURA(奥希替尼,n = 279;对照 EGFR-TKI,n = 277)和 AURA3(奥希替尼,n = 279;化疗,n = 140)研究以及(2)来自临床试验计划的奥希替尼 80mg 治疗患者的汇总数据集(n = 1142)的心脏数据进行了事后分析,包括与心力衰竭相关的不良事件和左心室射血分数(LVEF)降低。对汇总数据集进行了 LVEF 药代动力学或药效学分析。分析了赞助商的全球安全性数据库以确定与心力衰竭相关的不良事件,并进行了文献检索。

结果

在 FLAURA 和 AURA3 中,分别有 8(3.1%)和 14(5.5%)名患者在接受奥希替尼治疗后,LVEF 从基线下降≥10 个百分点,绝对值降至<50%,而在汇总人群中,有 35(3.9%)名患者出现这种情况。大多数事件是无症状的,无需治疗事件或停止奥希替尼即可缓解。药代动力学或药效学分析并未表明奥希替尼暴露与从基线开始的 LVEF 降低之间存在关系。数据库和文献检索未显示接受奥希替尼治疗的患者存在安全问题的特定趋势或模式。

结论

这些数据表明奥希替尼与心力衰竭之间没有因果关系。但是,由于在接受奥希替尼治疗之前有心脏危险因素的患者观察到 LVEF 降低,因此建议进行心脏监测,包括在基线和奥希替尼治疗期间评估 LVEF。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e07/8078322/e6642b63adea/jco-39-328-g001.jpg

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