De novosubacute cutaneous lupus erythematosus-like eruptions in the setting of programmed death-1 or programmed death ligand-1 inhibitor therapy: clinicopathological correlation

被引:17
作者
Bui, A. N. [1 ]
Hirner, J. [2 ]
Singer, S. B. [1 ]
Eberly-Puleo, A. [3 ]
Larocca, C. [2 ]
Lian, C. G. [4 ]
LeBoeuf, N. R. [2 ,3 ]
机构
[1] Harvard Med Sch, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Dept Dermatol, 75 Francis St, Boston, MA 02115 USA
[3] Dana Farber Brigham & Womens Canc Ctr, Dept Dermatol, Ctr Cutaneous Oncol, 450 Brookline Ave, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Dept Pathol, 75 Francis St, Boston, MA 02115 USA
关键词
D O I
10.1111/ced.14449
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Immune checkpoint inhibitors (ICI) may cause eruptions resembling cutaneous autoimmune diseases. There are six cases of immunotherapy-associated subacute cutaneous lupus erythematosus (SCLE) in the literature. We present details of five patients referred to the Skin Toxicity Program at the Dana-Farber Cancer Institute/Brigham and Women's Cancer Center who developedde novoimmunotherapy-associated SCLE-like eruptions, along with clinicopathological correlation and highlight potential mechanistic features and important diagnostic points. Two patients were maintained on topical corticosteroids, antihistamines and photoprotection. One had complete clearance and two had improvement with addition of hydroxychloroquine. Four patients continued their immunotherapy uninterrupted, while one had immunotherapy suspended for a month before restarting at full dose. Histopathologically, this series illustrates the temporal evolution of ICI-induced immune cutaneous reactions with SCLE subtype. Looking beyond the universally present lichenoid infiltrate, features of evolving SCLE were evident. We hypothesize that programmed death-1 blockade may induce immunological recognition of previously immunologically tolerated drug antigens, leading to epitope spreading and the SCLE phenotype.
引用
收藏
页码:328 / 337
页数:10
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