Departments of Dermatology.
Oncology.
Melanoma Res. 2019 Jun;29(3):338-341. doi: 10.1097/CMR.0000000000000587.
Checkpoint blockade immunotherapy has revolutionized the treatment of advanced melanoma, with impressive survival benefits attained through upregulation of the anticancer immune response. Blockade of regulatory checkpoint molecules can, however, also result in aberrant immune activation leading to undesirable inflammation and autoimmunity. Although many genetic determinants have been described in patients with primary autoimmune diseases, it is uncertain whether patients developing autoimmune skin disease as an adverse effect of anti-PD-1 therapy share the same genetic risks. Furthermore, it is also unclear whether treatment with these agents can result in the unveiling of underlying 'silent' autoimmunity resulting in chronic inflammatory disease. We report three cases of cutaneous lupus associated with pembrolizumab therapy for advanced melanoma. One patient had a previous diagnosis of histologically proven discoid lupus erythematosus, well-controlled without treatment for over 2 years, which flared on first exposure to pembrolizumab. The remaining two patients had no previous history of autoimmune disease; both developed cutaneous eruptions, histologically and immunohistologically, in keeping with subacute cutaneous lupus following treatment with pembrolizumab. Our report bolsters what is currently an exceedingly small body of evidence documenting the development of cutaneous lupus in the setting of pembrolizumab therapy. Our third case specifically documents an otherwise unreported severe reflare of previously diagnosed, quiescent discoid lupus erythematosus in the setting of pembrolizumab, vividly highlighting the potential for autoimmune and specifically, lupus reactivation in the setting of anti-PD-1 therapy.
检查点阻断免疫疗法彻底改变了晚期黑色素瘤的治疗方法,通过上调抗癌免疫反应,取得了令人印象深刻的生存获益。然而,抑制调节性检查点分子也可能导致异常的免疫激活,导致不良的炎症和自身免疫。尽管在原发性自身免疫性疾病患者中已经描述了许多遗传决定因素,但尚不确定作为抗 PD-1 治疗不良反应而发生自身免疫性皮肤病的患者是否具有相同的遗传风险。此外,这些药物的治疗是否会导致潜在的“沉默”自身免疫被揭示,从而导致慢性炎症性疾病,目前也尚不清楚。我们报告了三例与 pembrolizumab 治疗晚期黑色素瘤相关的皮肤狼疮病例。一名患者既往有组织学证实的盘状红斑狼疮诊断,未经治疗已超过 2 年,在首次接触 pembrolizumab 时病情加重。其余两名患者无自身免疫性疾病既往史;两名患者均在接受 pembrolizumab 治疗后出现皮肤发疹,组织学和免疫组织化学检查均符合亚急性皮肤狼疮。我们的报告支持了目前极少量的证据,这些证据记录了 pembrolizumab 治疗中出现皮肤狼疮。我们的第三个病例特别记录了在 pembrolizumab 治疗中,先前诊断的静止性盘状红斑狼疮严重复发的情况,这突出了在抗 PD-1 治疗中发生自身免疫和狼疮再激活的潜在可能性。