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Osimertinib: A Novel Dermatologic Adverse Event Profile in Patients with Lung Cancer

机译:Osimertinib:肺癌患者的新型皮肤病学不良事件

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摘要

Dermatologic adverse events (dAEs) are common with the use of epidermal growth factor receptor‐tyrosine kinase inhibitor (EGFR‐TKI) therapy. First‐ and second‐generation agents (erlotinib, gefitinib, and afatinib) are frequently associated with acneiform rash, pruritus, xerosis, and paronychia; the incidence and characterization of these dAEs have been well described. However, there is evidence that the dAE profile is different with third‐generation EGFR‐TKIs. Herein, we describe the dAEs associated with third‐generation EGFR‐TKIs and our clinical experience with osimertinib, a third‐generation EGFR‐TKI approved by the U.S. Food and Drug Administration for the treatment of metastatic, EGFR T790M mutation‐positive non‐small cell lung cancer in patients whose disease has progressed on or after EGFR‐TKI therapy. Case summaries of patients from two of our institutions who received osimertinib and were referred to a dermatologist for dAEs are also presented. Overall, the evidence suggests that osimertinib is associated with less severe and less frequent dAEs than first‐ and second‐generation EGFR‐TKIs and that therefore a different approach is warranted. Finally, we outline dAE management approaches for osimertinib in the context of those typically employed with first‐ and second‐generation EGFR‐TKIs.
机译:皮肤不良反应(dAE)在使用表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)治疗时很常见。第一和第二代药物(厄洛替尼,吉非替尼和阿法替尼)通常与痤疮样皮疹,瘙痒,干燥症和甲沟炎有关;这些dAE的发生率和特征已得到很好的描述。但是,有证据表明,第三代EGFR-TKIs的dAE谱有所不同。本文中,我们描述了与第三代EGFR-TKI相关的dAE,以及我们在osimertinib方面的临床经验,osimertinib是美国食品药品监督管理局批准用于治疗转移性EGFR T790M突变阳性的非小剂量的第三代EGFR-TKI在EGFR-TKI治疗中或治疗后疾病发展的患者中发生细胞肺癌。还介绍了来自我们两家机构的接受奥西替尼治疗并转介给皮肤科医师进行dAE治疗的患者的病例摘要。总体而言,有证据表明,与第一代和第二代EGFR-TKIs相比,奥西替尼与dAE的严重性和频率较低有关,因此有必要采用不同的方法。最后,在第一代和第二代EGFR-TKI通常采用的背景下,我们概述了osimertinib的dAE管理方法。

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