Eosinophilic Fasciitis Following Checkpoint Inhibitor Therapy: Four Cases and a Review of Literature

Author:

Chan Karmela Kim1,Magro Cynthia2,Shoushtari Alexander3,Rudin Charles3,Rotemberg Veronica3,Rossi Anthony3,Lezcano Cecilia4,Carrino John5,Fernandez David1,Postow Michael A.3,Apollo Arlyn3,Lacouture Mario E.3,Bass Anne R.1

Affiliation:

1. Department of Medicine, Hospital for Special Surgery, New York, New York, USA

2. Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York, USA

3. Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA

4. Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York, USA

5. Department of Radiology, Hospital for Special Surgery, New York, New York, USA

Abstract

Abstract Background 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. Case Presentation 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. Conclusion 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.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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