Department of Medicine, Hospital for Special Surgery, New York, New York, USA.
Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York, USA.
Oncologist. 2020 Feb;25(2):140-149. doi: 10.1634/theoncologist.2019-0508. Epub 2019 Oct 15.
Checkpoint inhibitor therapy is widely known to cause a number of immune-related adverse events. One rare adverse effect that is emerging is eosinophilic fasciitis, a fibrosing disorder causing inflammatory infiltration of subcutaneous fascia. It is characterized clinically by edema and subsequent induration and tightening of the skin and subcutaneous tissues. The condition is rare, yet at our institutions we have seen four cases in the past 3 years. We describe our 4 cases and review 11 other cases reported in the literature.
We present four cases of eosinophilic fasciitis following treatment with programmed cell death protein 1 or programmed cell death-ligand 1 blockade. All patients had extremity involvement with characteristic skin changes ranging from peripheral edema to induration, tightening, and joint limitation. The patients had varying degrees of peripheral eosinophilia. In two of our patients, the diagnosis was made by full-thickness skin biopsy showing lymphocytic infiltration of the subcutaneous fascia, with CD4+ T cells predominating in one case and CD8+ T cells in the other. In the other two cases, the diagnosis was made on the basis of characteristic imaging findings in the context of clinical features consistent with the diagnosis. All four patients were treated with glucocorticoids with varying degrees of success; immunotherapy had to be discontinued in all four. Patients with advanced melanoma who experienced this adverse effect had either a partial response or a complete response to therapy.
Eosinophilic fasciitis can occur as a result of checkpoint inhibitor therapy. Although a tissue diagnosis is the gold standard, imaging studies may facilitate the diagnosis in the presence of consistent clinical features, but a degree of suspicion is key to recognizing the condition early. Therapy requires a collaborative approach by oncology, rheumatology, and dermatology; physical therapy is an important adjunct in treatment. For advanced melanoma, it may be a good prognostic indicator.
It is important for clinicians to recognize that eosinophilic fasciitis is a potential immune-related adverse event (irAE) as a consequence of immune checkpoint inhibitor therapy. The presentation is quite stereotypical; the diagnosis can be made by imaging in the absence of a full-thickness skin biopsy. Early intervention is important to limit morbidity. This irAE may be a good prognostic sign among patients with melanoma.
众所周知,检查点抑制剂疗法会引起许多免疫相关的不良反应。一种新出现的罕见不良反应是嗜酸性筋膜炎,这是一种纤维性疾病,导致皮下筋膜的炎症浸润。其临床特征为水肿,随后皮肤和皮下组织出现硬结和紧绷。这种情况很少见,但在过去 3 年中,我们医院已发现 4 例。我们描述了这 4 例病例,并回顾了文献中报告的 11 例其他病例。
我们报告了 4 例接受程序性细胞死亡蛋白 1 或程序性细胞死亡配体 1 阻断治疗后发生的嗜酸性筋膜炎病例。所有患者均有四肢受累,皮肤改变特征性,从周围水肿到硬结、紧绷和关节受限不等。患者有不同程度的外周血嗜酸性粒细胞增多。在我们的 2 例患者中,通过全层皮肤活检做出诊断,显示皮下筋膜的淋巴细胞浸润,1 例以 CD4+T 细胞为主,另 1 例以 CD8+T 细胞为主。在另外 2 例患者中,根据临床特征一致的情况下的特征性影像学表现做出诊断。所有 4 例患者均接受糖皮质激素治疗,疗效不一;所有患者均不得不停止免疫治疗。患有晚期黑色素瘤并发生这种不良反应的患者对治疗有部分反应或完全反应。
嗜酸性筋膜炎可由检查点抑制剂治疗引起。虽然组织学诊断是金标准,但在存在一致的临床特征的情况下,影像学研究可能有助于诊断,但早期识别该疾病需要高度怀疑。治疗需要肿瘤学、风湿病学和皮肤病学的协作方法;物理治疗是治疗的重要辅助手段。对于晚期黑色素瘤,它可能是一个良好的预后指标。
临床医生认识到,嗜酸性筋膜炎是免疫检查点抑制剂治疗的潜在免疫相关不良事件(irAE)是很重要的。其表现相当典型;在没有全层皮肤活检的情况下,可通过影像学诊断。早期干预对于限制发病率很重要。这种 irAE 可能是黑色素瘤患者的一个良好预后标志。