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Published on: July 18, 2014
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.
Objective:
To evaluate the heart response of Erdheim-Chester disease (ECD) through continuous follow-up within our large cohort, for which there is a lack of understanding.
Methods:
We conducted a retrospective analysis of clinical data from patients with ECD with cardiac involvement diagnosed at our centre between January 2010 and August 2023. We assessed the heart response by integrating pericardial effusion and metabolic responses.
Results:
A total of 40 patients were included, with a median age of 51.5 years (range: 29-66) and a BRAFV600E mutation rate of 56%. The most common imaging manifestations observed were pericardial effusion (73%), right atrium (70%) and right atrioventricular sulcus infiltration (58%). Among 21 evaluable patients, 18 (86%) achieved a heart response including 5 (24%) complete response (CR) and 13 (62%) partial response (PR). The CR rate of pericardial effusion response was 33%, while the PR rate was 56%. Regarding the cardiac mass response, 33% of patients showed PR. For cardiac metabolic response, 32% and 53% of patients achieved complete and partial metabolic response, respectively. There was a correlation between pericardial effusion response and cardiac metabolic response (r=0.73 (95% CI 0.12 to 0.83), p<0.001). The median follow-up was 50.2 months (range: 1.0-102.8 months). The estimated 5-year overall survival was 78.9%. The median progression-free survival was 59.4 months (95% CI 26.2 to 92.7 months). Patients who received BRAF inhibitors achieved better heart response (p=0.037) regardless of treatment lines.
Conclusion:
We pioneered the evaluation of heart response of ECD considering both pericardial effusion and cardiac metabolic response within our cohort, revealing a correlation between these two indicators. BRAF inhibitors may improve heart response, regardless of the treatment lines.
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