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与厄洛替尼治疗相关的皮肤白细胞破碎性血管炎:一例报告并文献复习

Cutaneous leukocytoclastic vasculitis associated with erlotinib treatment: A case report and review of the literature.

作者信息

Fekete Gyula László, Fekete László

机构信息

Dermatology Clinic, University of Medicine and Pharmacy, 540530 Târgu Mureş, Romania.

CMI Dermamed, 540530 Târgu Mureş, Romania.

出版信息

Exp Ther Med. 2019 Feb;17(2):1128-1131. doi: 10.3892/etm.2018.6988. Epub 2018 Nov 19.

Abstract

Erlotinib is a targeted anticancer therapy used for treating epidermal growth factor receptor (EGFR) mutation positive lung cancer in advanced stage as well as for other malignancies. The most common cutaneous side effect of erlotinib, are well documented; however the number of reports regarding cutaneous leukocytoclastic vasculitis (CLCV) are limited. We report a case, a 58-year-old, 60 kg weight, non-smoking woman suffering of lung adenocarcinoma and brain metastases treated with erlotinib monotherapy with 150 mg/day dose, who presents cutaneous leukocytoclastic vasculitis after 8 months of initiating the treatment. The administration of the drug was discontinued and oral prednisolone treatment was introduced at 1 mg/kg body weight dose for two weeks, decreasing the dose with 5 mg, at every 3 days. The treatment was combined with topical potent steroid and antibiotic therapy used once, daily. The lesions cleared within 7 weeks without recurrence. The treatment with erlotinib was restarted after 14 days with a lower dose of 100 mg/day. The skin lesions have not occurred anymore. Unfortunately the evolution was unfavorable, our patient died 3 months after the vasculitis healing, due to the complications of new metastases that occurred. This may indicate the inefficiency of erlotinib. The late onset of 240 days of the vasculitis and the presumed inefficiency of the drug lead to the speculation that the appearance of cutaneous vasculitis could be a worsening clinical marker of the tumor response. This limited number of cases precludes any meaningful interpretation of data about the erlotinib induced cutaneous vasculitis. Further investigations are needed to assess cutaneous vasculitis.

摘要

厄洛替尼是一种靶向抗癌疗法,用于治疗晚期表皮生长因子受体(EGFR)突变阳性肺癌以及其他恶性肿瘤。厄洛替尼最常见的皮肤副作用已有充分记录;然而,关于皮肤白细胞破碎性血管炎(CLCV)的报告数量有限。我们报告一例,一名58岁、体重60公斤、不吸烟的女性,患有肺腺癌和脑转移瘤,接受厄洛替尼单药治疗,剂量为每日150毫克,在开始治疗8个月后出现皮肤白细胞破碎性血管炎。停用该药,开始口服泼尼松龙治疗,剂量为1毫克/公斤体重,持续两周,每3天剂量减少5毫克。治疗联合每日一次使用的强效局部类固醇和抗生素疗法。皮损在7周内消退且未复发。14天后以较低剂量每日100毫克重新开始使用厄洛替尼治疗。皮肤病变未再出现。不幸的是,病情发展不利,我们的患者在血管炎愈合3个月后因新转移灶出现的并发症死亡。这可能表明厄洛替尼无效。血管炎240天的迟发以及该药可能的无效性导致推测皮肤血管炎的出现可能是肿瘤反应恶化的临床标志物。这一有限的病例数排除了对厄洛替尼诱发皮肤血管炎数据进行任何有意义解读的可能性。需要进一步研究来评估皮肤血管炎。

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