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Pre-Existing Autoimmune Disease Increases the Risk of Cardiovascular and Noncardiovascular Events After Immunotherapy.
Lee, Charlotte; Drobni, Zsofia D; Zafar, Amna; Gongora, Carlos A; Zlotoff, Daniel A; Alvi, Raza M; Taron, Jana; Rambarat, Paula K; Schoenfeld, Sara; Mosarla, Ramya C; Raghu, Vineet K; Hartmann, Sarah E; Gilman, Hannah K; Murphy, Sean P; Sullivan, Ryan J; Faje, Alexander; Hoffmann, Udo; Zhang, Lili; Mayrhofer, Thomas; Reynolds, Kerry L; Neilan, Tomas G.
Afiliação
  • Lee C; Division of Cardiology, Columbia University Irving Medical Center, NewYork-Presbyterian Hospital, New York, New York, USA.
  • Drobni ZD; Cardiovascular Imaging Research Center, Department of Radiology and Division of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Zafar A; Heart and Vascular Center, Semmelweis University, Budapest, Hungary.
  • Gongora CA; Division of Cardiovascular Diseases and Hypertension, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.
  • Zlotoff DA; Cardiovascular Imaging Research Center, Department of Radiology and Division of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Alvi RM; Division of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Taron J; Cardiovascular Imaging Research Center, Department of Radiology and Division of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Rambarat PK; Department of Radiology, University Hospital Freiburg, Freiburg, Germany.
  • Schoenfeld S; Department of Internal Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Mosarla RC; Division of Rheumatology, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Raghu VK; Division of Cardiology, New York University, New York, New York, USA.
  • Hartmann SE; Cardiovascular Imaging Research Center, Department of Radiology and Division of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Gilman HK; Cardiovascular Imaging Research Center, Department of Radiology and Division of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Murphy SP; Cardiovascular Imaging Research Center, Department of Radiology and Division of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Sullivan RJ; Division of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Faje A; Division of Oncology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Hoffmann U; Division of Endocrinology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Zhang L; Cardiovascular Imaging Research Center, Department of Radiology and Division of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Mayrhofer T; Department of Cardiology, Department of Medicine, Montefiore Medical Center, Bronx, New York, USA.
  • Reynolds KL; Cardiovascular Imaging Research Center, Department of Radiology and Division of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Neilan TG; Division of Oncology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
JACC CardioOncol ; 4(5): 660-669, 2022 Dec.
Article em En | MEDLINE | ID: mdl-36636443
ABSTRACT

Background:

The use of immune checkpoint inhibitors (ICI) is associated with cardiovascular (CV) events, and patients with pre-existing autoimmune disease are at increased CV risk.

Objectives:

The aim of this study was to characterize the risk for CV events in patients with pre-existing autoimmune disease post-ICI.

Methods:

This was a retrospective study of 6,683 patients treated with ICIs within an academic network. Autoimmune disease prior to ICI was confirmed by chart review. Baseline characteristics and risk for CV and non-CV immune-related adverse events were compared with a matched control group (11 ratio) of ICI patients without autoimmune disease. Matching was based on age, sex, history of coronary artery disease, history of heart failure, and diabetes mellitus. CV events were a composite of myocardial infarction, percutaneous coronary intervention, coronary artery bypass graft, stroke, transient ischemic attack, deep venous thrombosis, pulmonary embolism, or myocarditis. Univariable and multivariable Cox proportional hazards models were used to determine the association between autoimmune disease and CV events.

Results:

Among 502 patients treated with ICIs, 251 patients with and 251 patients without autoimmune disease were studied. During a median follow-up period of 205 days, there were 45 CV events among patients with autoimmune disease and 22 CV events among control subjects (adjusted HR 1.77; 95% CI 1.04-3.03; P = 0.0364). Of the non-CV immune-related adverse events, there were increased rates of psoriasis (11.2% vs 0.4%; P < 0.001) and colitis (24.3% vs 16.7%; P = 0.045) in patients with autoimmune disease.

Conclusions:

Patients with autoimmune disease have an increased risk for CV and non-CV events post-ICI.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: JACC CardioOncol Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: JACC CardioOncol Ano de publicação: 2022 Tipo de documento: Article