Patterns and organ treatment response of Erdheim-Chester disease with cardiac involvement

Hui-Lei Miao1,2, Long Chang1,3, He Lin1

  • 1Department of Hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.

Insights

Erdheim-Chester disease (ECD) heart response was evaluated using pericardial effusion and metabolic indicators. BRAF inhibitors showed promise in improving cardiac response in ECD patients.

Area of Science:

  • Cardiology
  • Oncology
  • Rare Diseases

Background:

  • Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis with poorly understood cardiac manifestations.
  • Cardiac involvement in ECD can significantly impact patient prognosis and treatment strategies.

Purpose of the Study:

  • To evaluate the cardiac response in a large cohort of Erdheim-Chester disease patients.
  • To assess the correlation between pericardial effusion and metabolic responses in cardiac involvement.
  • To investigate the impact of BRAF inhibitors on cardiac response in ECD.

Main Methods:

  • Retrospective analysis of clinical data from 40 ECD patients with cardiac involvement (2010-2023).
  • Assessment of heart response integrating pericardial effusion and metabolic responses.
  • Evaluation of imaging and metabolic response rates and correlation analysis.

Main Results:

  • 86% of evaluable patients achieved a heart response, with 24% complete response (CR) and 62% partial response (PR).
  • Significant correlation found between pericardial effusion response and cardiac metabolic response (r=0.73, p<0.001).
  • Patients receiving BRAF inhibitors demonstrated improved heart response (p=0.037) irrespective of treatment line.

Conclusions:

  • This study pioneers the evaluation of ECD heart response using combined pericardial effusion and metabolic indicators.
  • A significant correlation exists between pericardial effusion and cardiac metabolic response in ECD.
  • BRAF inhibitors may enhance cardiac response in Erdheim-Chester disease patients.
Abstract

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