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CASE REPORT
New drugs and new toxicities: pembrolizumab-induced myocarditis
  1. Faisal Inayat1,
  2. Muhammad Masab2,
  3. Sorab Gupta2,
  4. Waqas Ullah3
  1. 1 Allama Iqbal Medical College, Lahore, Pakistan
  2. 2 Einstein Medical Center, Philadelphia, Pennsylvania, USA
  3. 3 University of Arizona, Tucson, Arizona, USA
  1. Correspondence to Dr Waqas Ullah, waqasullah.dr{at}gmail.com

Summary

Pembrolizumab is an immune checkpoint inhibitor that significantly improves clinical outcomes in numerous solid organ malignancies. Despite successful therapeutic responses, this new drug comes with a constellation of adverse reactions. Herein, we chronicle the case of a patient with metastatic non-small-cell lung cancer treated with pembrolizumab. After two cycles, he developed new-onset dyspnoea on exertion. Electrocardiogram showed idioventricular rhythm with diffuse ST-segment elevations. Echocardiography revealed severe biventricular cardiac dysfunction. Based on diagnostic workup and exclusion of probable aetiologies, the patient was diagnosed with pembrolizumab-induced myocarditis. The treatment was initiated with corticosteroids and guideline-conform heart failure therapy. He demonstrated a marked clinical response with resolution of congestive heart failure symptoms. This article summarises the clinical evidence regarding the epidemiology, pathophysiology, clinical features, diagnostic modalities and management of patients with pembrolizumab-associated myocarditis. In addition, it highlights that programmed death receptor-1 inhibition can cause a spectrum of autoimmune adverse events requiring clinical monitoring and periodic screenings.

  • oncology
  • chemotherapy

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Footnotes

  • Contributors FI: designed the study, performed the literature review, drafted the manuscript, formulated the data table, revised the manuscript critically for important intellectual content, and gave the final approval for the version published. MM: wrote the case presentation. SG: contributed to the discussion. WU: reviewed the manuscript.

  • Competing interests None declared.

  • Patient consent Obtained.

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