Durvalumab-induced myocarditis, myositis, and myasthenia gravis: a case report

J Med Case Rep. 2021 May 31;15(1):278. doi: 10.1186/s13256-021-02858-7.

Abstract

Background: Immune checkpoint inhibitors are effective therapies for a wide range of malignancies. Their increased use has led to a wide range of immune-related adverse effects including skin, gastrointestinal, pulmonary, endocrine, cardiac, and neurologic complications.

Case presentation: We present the case of a 72-year-old Caucasian man with non-small cell lung cancer who was admitted for dyspnea after two cycles of durvalumab. He was found to have significantly elevated levels of serum creatinine kinase and troponin with a negative cardiac catheterization. During his hospitalization, he developed progressive dyspnea and new-onset axial weakness, ultimately leading to the diagnosis of durvalumab-induced myocarditis, myasthenia gravis, and myositis.

Conclusion: This is, to our knowledge, the first reported case of anti-programmed cell death ligand 1-induced combination of myocarditis, myasthenia gravis, and myositis. While the use of immunologic agents has resulted in overall improved cancer outcomes, their increased use has led to a vast spectrum of immune-related adverse effects. We review the diagnostic workup and management of patients with these immune-related adverse effects, underscoring the importance of early identification given the potential for rapid deterioration.

Keywords: Adverse effects; Checkpoint inhibitors; Immunotherapy; Myasthenia gravis; Myocarditis; Myositis; Non-small cell lung cancer.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Aged
  • Antibodies, Monoclonal
  • Antineoplastic Agents, Immunological* / adverse effects
  • Carcinoma, Non-Small-Cell Lung*
  • Humans
  • Lung Neoplasms* / drug therapy
  • Male
  • Myasthenia Gravis* / chemically induced
  • Myasthenia Gravis* / drug therapy
  • Myocarditis* / chemically induced
  • Myocarditis* / diagnosis
  • Myocarditis* / drug therapy
  • Myositis* / chemically induced
  • Myositis* / drug therapy

Substances

  • Antibodies, Monoclonal
  • Antineoplastic Agents, Immunological
  • durvalumab