Osimertinib-Induced Cutaneous Vasculitis Responsive to Low-Dose Dapsone Without Interruption of Anticancer Therapy: A Case Report and Review of the Literature

被引:6
作者
Iriarte, Christopher [1 ,2 ]
Young, Jonathan H. [2 ,3 ]
Rabin, Michael S. [2 ,4 ,5 ]
LeBoeuf, Nicole R. [1 ,2 ,6 ]
机构
[1] Brigham & Womens Hosp, Dept Dermatol, Boston, MA USA
[2] Dana Farber Canc Inst, Ctr Cutaneous Oncol, Boston, MA USA
[3] Harvard Med Sch, Boston, MA USA
[4] Brigham & Womens Hosp, Dept Pathol, Boston, MA USA
[5] Dana Farber Canc Inst, Lowe Ctr Thorac Oncol, Boston, MA USA
[6] Dana Farber Canc Inst, Ctr Cutaneous Oncol, 450 Brookline Ave, Boston, MA 02215 USA
关键词
Cutaneous vasculitis; Osimertinib; Epidermal growth factor receptor inhibitor; Case report; Dapsone; GROWTH-FACTOR RECEPTOR; LEUKOCYTOCLASTIC VASCULITIS;
D O I
10.1016/j.jtocrr.2022.100415
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A 45-year-old woman with a history of lung adenocarci-noma treated with osimertinib developed purpuric plaques and vesicles on the lower extremities after 5 months of therapy. Skin biopsy revealed leukocytoclastic vasculitis (LCV). A workup for systemic involvement was unremark-able. The patient was treated with oral dapsone while continuing osimertinib without interruption. Skin lesions cleared within 2 weeks of therapy with no recurrence after titrating off dapsone. To the best of our knowledge, this is the first reported case of LCV induced by a small-molecule EGFR inhibitor in which therapy was not interrupted. This is also the first reported case treated with dapsone rather than systemic corticosteroids. We suggest consideration of dapsone to treat skin-limited LCV induced by EGFR in-hibitors in patients with lung cancer without features of systemic vasculitis. In addition, this case highlights that it may not be necessary to stop EGFR inhibitor therapy in the absence of severe features such as ulceration, bullae, ne-crosis, or severe pain. Dapsone is an effective targeted therapy for cutaneous LCV that does not globally impair the immune system and may allow for uninterrupted treatment of the underlying malignancy.(c) 2022 The Authors. Published by Elsevier Inc. on behalf of the International Association for the Study of Lung Cancer.This is an open access article under the CC BY-NC-ND li-cense (http://creativecommons.org/licenses/by-nc-nd/ 4.0/).
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页数:4
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