Sintilimab-induced inflammatory myopathy in a patient with esophageal cancer: a case report

Front Immunol. 2023 Oct 18:14:1253463. doi: 10.3389/fimmu.2023.1253463. eCollection 2023.

Abstract

The use of immune checkpoint inhibitors (ICIs) has shown remarkable efficacy in the treatment of various malignancies, significantly reshaping cancer treatment. However, as a result of the widespread use of ICIs, several immune-related adverse events (iRAEs) have emerged, some of which can be rare and potentially fatal. In this paper, we reported the earliest case of Sintilimab used in the treatment of esophageal cancer with severe inflammatory myopathy (involving the cardiac, respiratory, and skeletal muscles)in China. This patient was an elderly female who presented to our institution with progressive limb weakness and ptosis. Prior to the onset of symptoms, the patient had undergone a radical esophagectomy for esophageal cancer, experienced several cycles of of radiotherapy and chemotherapy, as well as two doses of Sintilimab treatment. Shortly after initiating immunotherapy, the patient developed symptoms including bilateral ptosis, limb weakness, and difficulty swallowing and breathing. The levels of creatine kinase and troponin I in the patient's blood were significantly elevated, and positive results were observed for anti-skeletal and anti-cardiac muscle antibodies, indicating that the patient might be developing ICIs-related inflammatory myopathy. Fortunately, the patient responded well to treatment including corticosteroids, plasmapheresis, intravenous immunoglobulin, and other supportive therapies. Here, we discuss the incidence, mechanisms, and management strategies of fatal iRAEs. Early detection and timely intervention may be critical in reducing the incidence and mortality rates of iRAEs and improving patient outcomes.

Keywords: PD-1; Sintilimab; immune checkpoint inhibitors; immune-related adverse events; inflammatory myopathy.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Antibodies, Monoclonal, Humanized / adverse effects
  • Esophageal Neoplasms* / drug therapy
  • Esophageal Neoplasms* / etiology
  • Female
  • Humans
  • Immunotherapy / adverse effects
  • Immunotherapy / methods
  • Myositis* / chemically induced
  • Myositis* / diagnosis
  • Myositis* / drug therapy

Substances

  • sintilimab
  • Antibodies, Monoclonal, Humanized

Grants and funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.