Coronary Toxicities of Anti-PD-1 and Anti-PD-L1 Immunotherapies: a Case Report and Review of the Literature and International Registries.
Marion FerreiraEric PichonDelphine CarmierEmilie BouquetCécile PageotTheodora Bejan-AngoulvantMarion CampanaEmmanuelle VermesSylvain Marchand-AdamPublished in: Targeted oncology (2019)
Immunotherapy medications that target programmed death 1 protein (PD-1) and programmed death-ligand 1 (PD-L1), such as nivolumab, pembrolizumab, and atezolizumab, are currently used in the first- or second-line treatment of non-small cell lung cancers, among other indications. However, these agents are associated with immune-related side effects, the most common of which are endocrinopathies, colitis, hepatitis, and interstitial pneumonitis. In contrast, coronary toxicities are rarely reported and remain poorly understood. Here, we describe the case of a patient who developed an acute coronary syndrome when treated with nivolumab as second-line therapy for metastatic pulmonary adenocarcinoma. A review of the literature, the French pharmacovigilance registry, and the World Health Organization pharmacovigilance database led to the identification of four cases of patients with coronary manifestations attributable to anti-PD1 immunotherapy (with no reported cases of patients undergoing anti-PD-L1 immunotherapy), which we describe herein. The potential mechanisms causing adverse coronary reactions to this type of therapy, which is used to treat lung cancer as well as other solid and hematological neoplastic diseases, are also discussed.
Keyphrases
- coronary artery
- coronary artery disease
- acute coronary syndrome
- adverse drug
- patients undergoing
- squamous cell carcinoma
- aortic stenosis
- percutaneous coronary intervention
- magnetic resonance
- small cell lung cancer
- pulmonary hypertension
- case report
- drug induced
- stem cells
- risk assessment
- rheumatoid arthritis
- bone marrow
- radiation therapy
- advanced non small cell lung cancer
- climate change
- ejection fraction
- transcatheter aortic valve replacement
- antiplatelet therapy
- idiopathic pulmonary fibrosis
- interstitial lung disease
- epidermal growth factor receptor
- amino acid
- combination therapy