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

机译:Osimertinib:肺癌患者的一种新型皮肤病性不良事件概况

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Abstract 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. Implications for Practice Appropriate prevention and management of dermatologic adverse events (dAEs) associated with the use of epidermal growth factor receptor‐tyrosine kinase inhibitors (EGFR‐TKIs) may help patients to continue therapy and lessen any negative impact on their quality of life. EGFR‐TKIs are frequently associated with acneiform rash, pruritus, xerosis, and paronychia; however, dAEs associated with third‐generation EGFR‐TKIs are lower in frequency and severity. Before therapy, health care providers should discuss the potential osimertinib‐associated dAEs and encourage patients to report their dAEs. Patients should also be educated on prophylactic measures to minimize the severity of dAEs and the importance of adherence to the treatment regimen.
机译:摘要皮肤病学不良事件(DAES)与使用表皮生长因子受体 - 酪氨酸激酶抑制剂(EGFR-TKI)治疗是常见的。第一代和第二代药剂(Erlotinib,Gefitinib和Afatinib)经常与痤疮皮疹,瘙痒,血症和Paronychia相关;这些DAE的发病率和表征已经很好地描述。然而,有证据表明DAE配置文件与第三代EGFR-TKI不同。在此,我们描述了与第三代EGFR-TKI相关的DAE,以及我们对OSIMERTINIB的第三代EGFR-TKI相关的DAE,由美国食品和药物管理局治疗转移性,EGFR T790M突变阳性非小型在疾病的患者中患者进行细胞肺癌,在预科治疗疗法中进行。还提出了来自我们的两位机构的患者患者的案例摘要。总体而言,证据表明,Osimertinib与比第一代和第二代EGFR-TKI的严重和更少的频繁的DAE相关,因此有一个不同的方法是有必要的。最后,我们在通常使用第一代和第二代EGFR-TKIS的那些上下文中概述了OSIMERTINIB的DAE管理方法。对实践的影响适当预防和治疗与使用表皮生长因子受体 - 酪氨酸激酶抑制剂(EGFR-TKIS)相关的皮肤病学不良事件(DAE)可以帮助患者继续治疗并减少对其生活质量的任何负面影响。 EGFR-TKIS经常与痤疮皮疹,瘙痒,血症和帕隆尼亚有关;然而,与第三代EGFR-TKI相关的DAES频率和严重程度较低。在治疗前,医疗保健提供者应讨论潜在的Osimertinib相关的Daes并鼓励患者报告他们的Daes。患者还应接受预防措施的教育,以尽量减少Daes的严重程度以及依从治疗方案的重要性。

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