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Brain Arterial DiseaseBioMAVNCT06494358

Liquid Biopsies for the Detection of Somatic Mutations in bAVMs

An observational study of Brain Arterial Disease, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

"Personalized medicine has revolutionized patient care, particularly in oncology. Brain arteriovenous malformations (bAVMs) are abnormal vessels located on the surface of the brain or within the brain parenchyma, causing abnormal communication between arterial and venous networks, without the interposition of the… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Brain Arterial Disease
What is being tested?
liquid biopsies and surgery specimen analysis
How many people
50 participants
Where
1 siteFrance
Study dates
1 Apr 2025to 1 Dec 2027
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Adult, Older adult

Study population: The population consists of patients aged 18 years or older with a bAVM, for whom treatment by microsurgery with preoperative embolization at Pitié-Salpêtrière Hospital was decided upon in a multidisciplinary consultation meeting.

Who may be able to join

None listed.

Who cannot join

  • Extra-cerebral arteriovenous malformations
  • Under legal protection (guardianship/curators, etc.)
  • Pregnancy
  • Not eligible for combined treatment (embolization followed by surgery)

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Frederic Clarençon, MD,PhD contact

0033 1 42 16 35 99

frederic.clarencon@aphp.fr

France1 site, 1 recruiting
  • Unité de neuroradiologie interventionnelle, hôpital Pitié-Salpêtrière

    Paris, 75571

    Frédéric - CLARENÇON, 01 42 16 35 99, frederic.clarencon@aphp.fr

    Julien Burel, julen.burel@aphp.fr

    Recruiting

Other trials in France

About this study

Official title: Liquid Biopsies for the Detection of Somatic Mutations in Brain Arteriovenous Malformations

"Personalized medicine has revolutionized patient care, particularly in oncology. Brain arteriovenous malformations (bAVMs) are abnormal vessels located on the surface of the brain or within the brain parenchyma, causing abnormal communication between arterial and venous networks, without the interposition of the capillary bed. The main risk of these malformations is rupture, leading to intracranial bleeding, which can cause severe sequelae or even death. bAVMs (except those of clearly identified genetic origin [< 5%], such as mutations associated with Rendu-Osler disease) have long been considered non-genetic in origin.

However, somatic genetic mutations activating the RAS/RAF/MEK/ERK (MAPK) signaling pathway have recently been identified in surgical specimens of bAVMs. Additionally, targeted inhibition of this pathway is effective in treating these malformations in animals and appears to be effective in extracranial arteriovenous malformations, particularly superficial ones.

Read more

Next-generation sequencing of circulating DNA on liquid biopsies is a promising and minimally invasive approach to studying the presence of mutations in arteriovenous malformations.

The treatment of a bAVM aims to obliterate the malformation to prevent or avoid the risk of hemorrhage. It may involve several therapeutic modalities: microsurgery, endovascular embolization, and radiosurgery. These treatments can be combined, and microsurgery is often preceded by pre-surgical embolization, aimed at reducing the hemorrhagic risk of the intervention. However, these are invasive treatments, not without risk.

The identification of mutations through liquid biopsies could enable the development of non-invasive targeted therapies against these bAVMs.

This research aims to identify somatic genetic mutations activating the MAPK signaling pathway in bAVMs. These mutations have already been identified in surgical specimens. This research aims to evaluate the diagnostic performances of liquid biopsies (detection of genetic mutations in blood samples, i.e., circulating DNA), with the gold standard being the detection of the same mutations in surgical specimens."

Read the detailed description

"Description of Domain Knowledge Personalized medicine has revolutionized patient care, especially in oncology. Brain arteriovenous malformations (bAVMs) are abnormal vessels located on the brain's surface or within the cerebral parenchyma, abnormally connecting the arterial and venous networks without the intermediary of the capillary bed. The primary risk of these malformations is rupture, leading to intracranial bleeding, which can cause severe sequelae or even death. bAVMs (excluding those of clearly identified genetic origin [< 5%], such as mutations associated with Rendu-Osler disease) have long been considered non-genetic in origin.

However, somatic genetic mutations activating the RAS/RAF/MEK/ERK (MAPK) signaling pathway have recently been identified in surgical specimens of bAVMs [1]. Moreover, targeted inhibition of this pathway is effective in treating these malformations in animal models [2] and seems effective in extracranial arteriovenous malformations, particularly superficial ones [3].

Next-generation sequencing of circulating DNA on liquid biopsies is a promising new approach, allowing for a non-invasive study of mutations in arteriovenous malformations [4].

The treatment of a bAVM aims to obliterate the malformation to prevent or mitigate hemorrhagic risk. Several therapeutic modalities can be used: microsurgery, endovascular embolization, and radiosurgery. These treatments can be combined, with microsurgery often preceded by pre-surgical embolization to reduce the hemorrhagic risk of the intervention. However, these treatments are invasive and not without risk [5].

The identification of mutations through liquid biopsies would enable the development of non-invasive targeted therapies against these bAVMs [6].

Description of the Population to be Studied and Justification for Their Choice The population consists of patients aged 18 years or older with a bAVM, for whom treatment by microsurgery with preoperative embolization at Pitié-Salpêtrière Hospital was decided upon in a multidisciplinary consultation meeting.

The choice of this particular population (patients treated with embolization followed by surgery) is justified by the need to obtain the gold standard diagnosis on a surgical specimen for the primary evaluation criteria of the study.

Some patients, whose initial decision in the multidisciplinary consultation was treatment by microsurgery with preoperative embolization, will undergo complete embolization. These patients will not have surgery, and the initially planned surgery will be canceled subsequently. These patients will only be included in the analysis of certain secondary outcome criteria. This accounts for about half of the patients.

In total, there will be 25 patients for the primary evaluation criteria and about twice as many for the secondary evaluation criteria.

Description of Research Elements The research focuses on identifying somatic genetic mutations activating the RAS/RAF/MEK/ERK (MAPK) signaling pathway in brain arteriovenous malformations. These mutations have already been identified in surgical specimens. This research aims to evaluate the diagnostic performance of liquid biopsies (search for genetic mutations on blood samples, i.e., circulating DNA search), with the gold standard being the search for the same mutations on surgical specimens.

These liquid biopsies will be performed during the embolization procedure by arterial sampling near the malformation and on peripheral venous blood (no additional procedure compared to usual care). A blood sample taken from the artery immediately adjacent to the nidus (2 mL) will use the aspirated blood to check the microcatheter's patency, according to standard care procedures (normally not conserved sample), and two other blood samples will be taken from a peripheral vein [one at the beginning of the embolization procedure (10 mL) and one at the end of the embolization procedure (10 mL)] via the venous catheter used by the anesthesia team as part of standard care. This tube taken at the end of the procedure is justified by the hypothesis of the release of mutated cells linked to embolization.

Thus, for the research, there will be 1 tube of 2 mL (arterial sample near the nidus, collected as part of standard care but conserved for research) and 2 tubes of 10 mL (peripheral blood sampled from the care catheter), in addition to the samples taken as part of standard care during the embolization procedure.

Primary Objective To study the diagnostic performance of 1) liquid biopsies on the artery near the nidus and 2) liquid biopsies on peripheral veins for identifying somatic genetic mutations in bAVMs compared to the gold standard diagnosis on a surgical specimen.

Secondary Objectives

  • Evaluate the prevalence of genetic mutations identified on surgical specimens.
  • Evaluate the prevalence of genetic mutations identified by liquid biopsies on the artery near the nidus.
  • Evaluate the prevalence of genetic mutations identified by liquid biopsies on peripheral veins.
  • Evaluate the general characteristics of patients (age, gender, mode of presentation) for each identified mutation.
  • Evaluate imaging characteristics of bAVMs for each identified mutation. Number of Participating Centers Monocentric study
  • Recruiting center: Interventional Neuroradiology Unit, Pitié-Salpêtrière Hospital"
Being tested
liquid biopsies and surgery specimen analysis
Keywords
brain arteriovenous malformation, liquid biopsies
Medical subject headings
Intracranial Arterial Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • liquid biopsies and surgery specimen analysisOther

    liquid biopsies and surgery specimen analysis

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Study of the diagnostic performance of 1) liquid biopsies on the artery in the immediate vicinity of the nidus, 2) liquid biopsies on the peripheral vein, for the detection of somatic genetic mutations in cAVMs

    • Sensitivity / Specificity / Positive Predictive Value / Negative Predictive Value Compared with the gold standard: detection of mutations on surgical specimens

    Measured: 30 months

Secondary outcomes (5)
  1. - Prevalence of mutations on surgical specimens

    Measured: 30 months

  2. - Prevalence of mutations on the artery in the immediate vicinity of the nidus

    Measured: 30 months

  3. - Prevalence of peripheral vein mutations

    Measured: 30 months

  4. - General patient characteristics for each of the mutations identified

    Measured: 30 months

  5. - Imaging characteristics of cAVMs for each of the mutations identified

    Measured: 30 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Jul 2024
  2. Study start1 Apr 2025
  3. Primary completion1 Dec 2027 (estimated)
  4. Study completion1 Dec 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
50 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06494358
Sponsor's protocol ID
APHP240718
Acronym
BioMAV
Status last verified
Aug 2026
First submitted
2 Jul 2024
Last updated
31 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: The procedures carried out with the French data privacy authority (CNIL, Commission nationale de l\&#39;informatique et des libertés) do not provide for the transmission of the database, nor do the information and consent documents signed by the patients. Consultation by the editorial board or interested researchers of individual participant data that underlie the results reported in the article after deidentification may nevertheless be considered, subject to prior determination of the terms and conditions of such consultation and in respect for compliance with the applicable regulations.

Questions about this trial

What is this clinical trial studying?

An observational study of Brain Arterial Disease, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 0 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 31 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Frederic Clarençon, MD,PhD (0033 1 42 16 35 99, frederic.clarencon@aphp.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Study of the diagnostic performance of 1) liquid biopsies on the artery in the immediate vicinity of the nidus, 2) liquid biopsies on the peripheral vein, for the detection of somatic genetic mutations in cAVMs (time frame: 30 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 Aug 2026.

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