ClinicalTrials.gg
RecruitingNCT06715579CAIRUpdated Feb 18, 2026

Cardiac Angiosarcoma International Registry

An observational study in Cardiac Angiosarcoma, sponsored by Immune Oncology Research Institute. Recruiting at 1 site in Armenia. Per ClinicalTrials.gov, last updated 2026-02-18.

Sponsored by Immune Oncology Research Institute · Observational

From the registry’s dates

  • Started May 2025; still recruiting 1 year 6 months later.
Study type
Observational
Model
Case-only
Time perspective
Other
Enrollment
500
Sex
All
01

Study summary

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.
Read the detailed description

Primary cardiac angiosarcoma arises directly within the heart, unlike secondary cardiac tumors that originate from elsewhere in the body. While it predominantly affects the right side of the heart, particularly the right atrium, it can also impact other cardiac chambers and structures. The characteristic feature of cardiac angiosarcoma is the rapid formation of abnormal blood vessels that invade the myocardium, leading to the destruction of healthy heart tissue.The five-year survival rate for patients with primary cardiac angiosarcoma (PCA) is reported to be around 14%. In contrast, familial variants of this malignancy exhibit even more severe outcomes, with a mean survival rate of only 4 months.

Establishing an international registry for cardiac angiosarcomas is crucial for several reasons:

  • The registry will facilitate a comprehensive understanding of the clinical characteristics, treatment responses, and outcomes associated with cardiac angiosarcoma. By collecting data from diverse populations, researchers can identify patterns and factors that influence survival rates. It is crucial to better understand the growth rates and risk factors associated with cardiac angiosarcoma and to make the disease more manageable.
  • The international registry will enable the latest advancements in oncology and related medical fields to be incorporated into clinical practice. It will provide a platform for developing and conducting clinical trials aimed at improving treatment strategies and increasing survival rates for patients with cardiac angiosarcoma.
  • Finally, with data from various institutions and countries, the registry will promote collaboration among healthcare professionals, researchers, and institutions dedicated to improving outcomes for patients with this rare malignancy.

Creating an international registry for cardiac angiosarcoma is crucial for better understanding this aggressive cancer. It will help address the rising cancer burden and support research and treatment advancements that could improve patient survival rates and prevention.

The following data will be collected through questionnaires:

  1. Patient characteristics
  2. Characteristics of Primary Cardiac Angiosarcomas
  3. Details of the diagnosis and treatment
  4. Complications and late effects of treatment
  5. Outcomes and follow-up information

Quality control and data management will be done by the Immune Oncology Research Institute.

02

Conditions studied

  • Cardiac Angiosarcoma

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Keywords

  • Cardiac Angiosarcoma
  • Angiosarcoma
  • Hemangiosarcoma
  • Epithelioid Hemangiosarcoma
  • Primary Cardiac Sarcoma
03

In context

Hemangiosarcoma

99 studies on the registry are indexed under Hemangiosarcoma; 16 are open to participants now.

Browse Hemangiosarcoma studies →

Lead sponsor

Immune Oncology Research Institute is the lead sponsor of 6 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All patients diagnosed with Cardiac Angiosarcoma

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 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.
  • : 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.

Exclusion criteria

Exclusion Criteria:

  • Patients who decline to provide .
  • Cases where cardiac involvement is secondary to another primary
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

05

Study design

Observational model
Case-only
Time perspective
Other
Enrollment
500 participants (estimated)
Target follow-up
5 Years
Patient registry
Yes
06

What researchers measure

Primary outcomes

  1. 6-month overall survival

    Time frame: 6 months

Secondary outcomes

  1. 1-year overall survival

    Time frame: 1 year

  2. 6-month progression free survival

    Time frame: 6 months

  3. 1-year progression free survival

    Time frame: 1 year

  4. 3-year progression free survival

    Time frame: 3 years

  5. 6-month event-free survival

    Time frame: 6 months

  6. 1-year event-free survival

    Time frame: 1 year

  7. 3-year event-free survival

    Time frame: 3 years

  8. Complete remission rate

    Time frame: 5 years

07

Study locations

1 of 1 sites recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started May 2025 (actual). Primary completion is estimated for May 2035, 120 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 28, 2024
First posted
Dec 4, 2024
StartActual
May 1, 2025
Primary completionEst.
May 2035
CompletionEst.
May 2035
Last update
Feb 18, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06715579
Lead sponsor
Immune Oncology Research Institute
Responsible party
Sponsor
First posted
Dec 4, 2024
Start date
May 1, 2025
Primary completion
May 2035 (estimated)
Completion
May 2035 (estimated)
Last update
Feb 18, 2026

Study contacts

Aharon Tsaturyan, MD
Contact
aharon3tsaturyan@gmail.com
+374 99190152
Shushan Hovsepyan, MD
principal investigator · Immune Oncology Research Institute, Yerevan, Armenia
Amalya Sargsyan, MD
study chair · Immune Oncology Research Institute, Yerevan, Armenia
Ruzanna Papyan, MD
study director · Immune Oncology Research Institute, Yerevan, Armenia

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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