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Myasthenia gravis, myositis and myocarditis: a fatal triad of immune-related adverse effect of immune checkpoint inhibitor treatment
  1. Biji Soman1,
  2. Maria Cecilia Dias2,
  3. Syed Azhar J Rizvi2 and
  4. Attila Kardos1,3
  1. 1Department of Cardiology, Milton Keynes University Hospital, Milton Keynes, UK
  2. 2Department of Oncology, Milton Keynes University Hospital, Milton Keynes, UK
  3. 3Faculty of Medicine and Health Sciences, The University of Buckingham, Buckingham, UK
  1. Correspondence to Professor Attila Kardos; attila.kardos{at}cardiov.ox.ac.uk

Abstract

Pembrolizumab, a humanised monoclonal antibody and immune checkpoint inhibitor (ICI) that blocks programmed death receptor 1 and its ligands, is an effective immunotherapy for malignancies such as melanoma, lung, head and neck, cancers, and Hodgkin’s lymphoma. It has an overall response rate between 73% and 83%, with complete response rate of 27%–30%. It is well tolerated with minor side effects in 70% of cases characterised by fatigue, rash, pruritus and diarrhoea. In rare cases, more serious and life-threatening complications can occur at a rate of 0.3%–1.3%. We report a case of a woman in her 70s with non-small-cell lung cancer treated with ICI. She presented to the emergency department with left-sided ptosis and muscle weakness 3 weeks of her first dose of pembrolizumab infusion as a treatment plan of her cancer. She was diagnosed with myasthenia gravis, myocarditis and myositis as ICI-induced immune-related adverse effects resistant to medical intervention. We wish to raise awareness of the triad of life-threatening complication of ICI therapy that accounts for 30%–50% of fatal complications.

  • Cancer - see Oncology
  • Cancer intervention
  • Cardiovascular system
  • Malignant disease and immunosuppression
  • Lung cancer (oncology)

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Footnotes

  • Contributors MCD was in charge of the patient's daily care; MCD and BS drafted the MS with the critical appraisal of the final draft. BS sought consent from the patient’s relative. AK has been involved in patient care as well as generated the composite figures and the diagram of the proposed pathomechanism for the MS and codrafted and finalised the MS and is responsible for the submission and correspondence. SAJR was responsible for the patient’s initial diagnosis and care and reviewed the final draft of the manuscript.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Case reports provide a valuable learning resource for the scientific community and can indicate areas of interest for future research. They should not be used in isolation to guide treatment choices or public health policy.

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.