L'Orphelin Jean-Matthieu
Department of Dermatology, Caen-Normandie University Hospital, Avenue de la Côte de Nacre, 14003 Caen, France.
Ther Adv Hematol. 2024 Mar 6;15:20406207241235777. doi: 10.1177/20406207241235777. eCollection 2024.
Mogamulizumab is a monoclonal antibody that binds to C-C chemokine receptor 4 (CCR4), initiating antibody-dependent cellular cytotoxicity. CCR4 is highly expressed in the cutaneous T-cell lymphoma subtypes mycosis fungoides and Sézary syndrome (SS), and mogamulizumab has been shown to be effective in patients with these conditions who were refractory to at least one prior systemic treatment. One of the more common adverse events encountered with mogamulizumab is rash, which may mimic disease progression and lead to premature discontinuation. Moreover, there has been some evidence to suggest that mogamulizumab-associated rash (MAR) is associated with improved outcomes in some patients, particularly those with SS. This report presents the case of a 72-year-old woman with SS, which manifested with macular and papular lesions and abnormal blood cytometry, who was treated with mogamulizumab after failure of bexarotene and photopheresis combination therapy. She achieved a complete response (CR), but experienced lymphopenia associated with histologically proven eosinophilic folliculitis (EF) of the scalp and alopecia. The EF responded well to initial topical corticosteroids, defined by regression of erythema and pustular involvement and reduction in pruritus-like symptoms, but without hair regrowth. Mogamulizumab was withdrawn after 32 cycles, but CR was maintained. To date, EF persists in the form of diffuse erythema without pustules or pruritus. A link between cluster of differentiation 4 lymphopenia and EF has previously been established; therefore, EF should be considered in patients who develop rash and lymphopenia while receiving treatment with mogamulizumab. MAR has been associated with clinical response to mogamulizumab, and this case report adds to the evidence that EF may also be associated with sustained clinical response following treatment cessation. However, regular monitoring is required to prevent a relapse of SS. Prospective studies are needed to confirm whether such an association between EF and CR following mogamulizumab exists.
莫加穆利单抗是一种单克隆抗体,可与C-C趋化因子受体4(CCR4)结合,引发抗体依赖性细胞毒性。CCR4在皮肤T细胞淋巴瘤亚型蕈样肉芽肿和塞扎里综合征(SS)中高度表达,并且已证明莫加穆利单抗对至少一种先前全身治疗难治的这些病症患者有效。莫加穆利单抗较常见的不良事件之一是皮疹,其可能模仿疾病进展并导致过早停药。此外,有一些证据表明,莫加穆利单抗相关皮疹(MAR)在一些患者中,特别是SS患者中与改善的预后相关。本报告介绍了一名72岁SS女性患者的病例,该患者表现为黄斑和丘疹性病变以及血细胞计数异常,在贝沙罗汀和光分离置换联合治疗失败后接受莫加穆利单抗治疗。她达到了完全缓解(CR),但经历了淋巴细胞减少症,并伴有经组织学证实的头皮嗜酸性毛囊炎(EF)和脱发。EF对初始外用皮质类固醇反应良好,表现为红斑和脓疱受累消退以及瘙痒样症状减轻,但无毛发再生。32个周期后停用莫加穆利单抗,但维持了CR。迄今为止,EF以无脓疱或瘙痒的弥漫性红斑形式持续存在。先前已确立分化簇4淋巴细胞减少与EF之间的联系;因此,在接受莫加穆利单抗治疗时出现皮疹和淋巴细胞减少的患者中应考虑EF。MAR与莫加穆利单抗的临床反应相关,本病例报告补充了证据,表明EF也可能与停药后的持续临床反应相关。然而,需要定期监测以防止SS复发。需要进行前瞻性研究以确认莫加穆利单抗治疗后EF与CR之间是否存在这种关联。