Cardiac Angiosarcoma International Registry

Recruiting now

Conditions studied: Cardiac Angiosarcoma

In brief

Primary cardiac angiosarcomas (PCA) are highly aggressive malignant heart tumors arising from the endothelial cells (ECs) lining the blood vessels of the heart and account for approximately 25%-30% of all primary cardiac malignancies. It is considered to be the most fatal and aggressive primary cardiac malignancy. This international registry aims to establish a large multicenter database of patients with cardiac angiosarcoma. Our objectives are: 1. Collect clinical data, including demographics, medical history, treatments, and outcomes, to build a comprehensive database. 2. Analyze data to evaluate and identify genetic, environmental, or lifestyle risk factors for cardiac angiosarcoma. 3. Evaluate the effectiveness of various treatments (surgery, chemotherapy, immunotherapy, radiation) to inform best practices. 4. Develop evidence-based guidelines and recommendations for prevention, diagnosis, treatment, and management based on registry data.

Key facts

Study ID

NCT06715579

Run by

Immune Oncology Research Institute

People needed

500

Starts

2025-05-01

Expected to finish

2035-05-01

Last updated by the study team

2026-02-18

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Histological Confirmation: A confirmed diagnosis of cardiac angiosarcoma through histopathological examination, including subtypes such as hemangiosarcoma and epithelioid hemangiosarcoma.
• Diagnosis Timing: Eligible patients must have been diagnosed between January 2015 and January 2035.
• Geographical Representation: Participants should be from diverse geographical locations to ensure a comprehensive understanding of the disease across different populations.
• Treatment Status: Patients who have received any treatment (surgery, chemotherapy, immunotherapy or radiation) for cardiac angiosarcoma may be included to evaluate treatment outcomes.
• Informed Consent: For prospective patients, informed consent must be obtained before they are included in the registry.
• Clinical Data Availability: Relevant clinical data, including demographics, tumor characteristics (size, location), treatment regimens, and outcomes, must be available for analysis.
• Follow-Up Willingness: Participants should be willing to undergo follow-up assessments as part of the registry's data collection efforts.

You may not qualify if…

• Patients who decline to provide informed consent.
• Cases where cardiac involvement is secondary to another primary malignancy

Where it is running

• Yeolyan Hematology and Oncology Center — Yerevan, Armenia (enrolling)

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.