Treatment of Brain AVMs (TOBAS) Study

Study Purpose

The objectives of this study and registry are to offer the best management possible for patients with brain arteriovenous malformations (AVMs) (ruptured or unruptured) in terms of long-term outcomes, despite the presence of uncertainty. Management may include interventional therapy (with endovascular procedures, neurosurgery, or radiotherapy, alone or in combination) or conservative management. The trial has been designed to test a) whether medical management or interventional therapy will reduce the risk of death or debilitating stroke (due to hemorrhage or infarction) by an absolute magnitude of about 15% (over 10 years) for unruptured AVMs (from 30% to 15%); and, b) to test if endovascular treatment can improve the safety and efficacy of surgery or radiation therapy by at least 10% (80% to 90%). As for the nested trial on the role of embolization in the treatment of Brain AVMs by other means: the pre-surgical or pre-radiosurgery embolization of cerebral AVMs can decrease the number of treatment failures from 20% to 10%. In addition,embolization of cerebral AVMs can be accomplished with an acceptable risk, defined as permanent disabling neurological complications of 8%.

Recruitment Criteria

Accepts Healthy Volunteers

Healthy volunteers are participants who do not have a disease or condition, or related conditions or symptoms

No
Study Type

An interventional clinical study is where participants are assigned to receive one or more interventions (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.


An observational clinical study is where participants identified as belonging to study groups are assessed for biomedical or health outcomes.


Searching Both is inclusive of interventional and observational studies.

Interventional
Eligible Ages 5 Years and Over
Gender All
More Inclusion & Exclusion Criteria

Inclusion Criteria:

  • - Any patient with a brain AVM.

Exclusion Criteria:

  • - Hemorrhagic presentation with mass effect requiring surgical management.
In these cases, if a residual AVM is found after the initial surgery, the patient could then be a candidate for TOBAS.

Trial Details

Trial ID:

This trial id was obtained from ClinicalTrials.gov, a service of the U.S. National Institutes of Health, providing information on publicly and privately supported clinical studies of human participants with locations in all 50 States and in 196 countries.

NCT02098252
Phase

Phase 1: Studies that emphasize safety and how the drug is metabolized and excreted in humans.

Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition) and additional safety data.

Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs.

Phase 4: Studies occurring after FDA has approved a drug for marketing, efficacy, or optimal use.

N/A
Lead Sponsor

The sponsor is the organization or person who oversees the clinical study and is responsible for analyzing the study data.

Centre hospitalier de l'Université de Montréal (CHUM)
Principal Investigator

The person who is responsible for the scientific and technical direction of the entire clinical study.

Daniel Roy, MD
Principal Investigator Affiliation CHUM-Montreal
Agency Class

Category of organization(s) involved as sponsor (and collaborator) supporting the trial.

Other
Overall Status Recruiting
Countries Brazil, Canada, Chile, Colombia, France, United States
Conditions

The disease, disorder, syndrome, illness, or injury that is being studied.

Unruptured Brain Arteriovenous Malformation, Ruptured Brain Arteriovenous Malformation, Arteriovenous Malformations, AVM, BAVM
Additional Details

Intracranial arteriovenous malformations (AVMs) are relatively uncommon but increasingly discovered lesions that can lead to significant neurological disability or death.1 Population-based data suggest that the annual incidence of discovery of a symptomatic AVM is approximately 1.1 per 100 000 population.7. AVMs commonly present following an intracranial hemorrhage or seizure, although with contemporary brain imaging techniques, an increasing number of incidental lesions are found.2.Intracranial AVMs are typically diagnosed before the age of 40 years old, with more than 50% of patients presenting following an intracranial hemorrhage, the most feared sequelae of harbouring an AVM.3 An AVM-related seizure is reported as the presenting feature in 20-25% of cases4, 5 and although these can sometimes be successfully managed with anti-epileptic agents, some AVMs lead to intractable seizures in spite of medication. Other presentations include headaches, focal neurological deficits, or pulsatile tinnitus.1.The available natural history studies indicate an overall risk of initial hemorrhage of approximately 2% to 4% per year, although the long-term consequences in terms of the probability of death or long-term disability following intracranial hemorrhage remains unclear.6-8 Mortality from the first hemorrhage has been reported to occur between 10-30% of patients with a ruptured AVM, although some more recent data suggest that the mortality rate may be lower and only 10-20% of survivors have long-term disability.9-11 Hemorrhagic presentation is considered the most reliable risk factor for a repeat hemorrhage.6, 8 Unfortunately, the natural history data available is not of sufficient quality (Level V) to support making management recommendations. Over the last decade, there have been substantial developments in the management of intracranial AVMs. There has been an evolution of microsurgical as well as endovascular and radiosurgical techniques to treat these lesions. As the management options have evolved, individual and combined modality treatment protocols have been developed in different institutions for the management of AVMs. Current interventional therapy for brain arteriovenous malformations (BAVMs) is varied and includes open neurosurgical resection, radiosurgery, and endovascular management, either alone or in combination. The choice of management is largely dependent on the decisions of the local physicians that make up the treatment team, and a recent survey has demonstrated substantial variability in decision-making for almost all AVMs.12.Interventional therapies, when they are performed, are assumed to decrease the risk of initial or subsequent hemorrhage and therefore lead to better long-term outcomes, an assumption that has yet to be proven. Although the question of which AVM treatment modality is the most appropriate first choice (surgery, radiosurgery, or embolization) remains controversial, consensus can be reached in several circumstances. Surgical evacuation of a hematoma exerting significant mass effect is an uncontested appropriate management, although many patients with a hemorrhagic presentation do not necessarily meet this threshold for surgical indication. Almost all other management choices remain debatable.13, 14 A systematic review has proposed that approximately 7.1% of surgical candidates, 6.6% of endovascular candidates, and 5.1% of radiosurgical candidates were facing permanent neurological deficits after treatment.15 The epidemiological study of Davies et al, using the Nationwide Inpatient Sample (NIS) data base and surrogates such as location at discharge, showed worse outcomes for surgical and endovascular management of both ruptured and unruptured AVMs.16.Current choices of interventional therapy for brain arteriovenous malformations are varied, with decisions made on a case-by-case basis, by the local clinical team. Often these decisions will change as the results of one particular attempted treatment modality become available. All interventional therapies are performed with the assumption that they will decrease the risk of initial or subsequent hemorrhage and lead to better long-term patient outcomes. Despite these laudable goals, there is no reliable evidence that interventional management of unruptured bAVMs is beneficial, and in patients judged to need interventional therapy, such as those patients presenting with ruptures, there is no randomized evidence that embolization is beneficial. Although no clinical trial data exist on the effect of interventional therapy even after AVM hemorrhage, the most contentious issue at present is whether interventional therapy should be considered for patients with incidentally discovered AVMs, whose lesions have not bled. In patients with unruptured AVMs, the best management strategy remains unknown, and interventions should be proposed only in the context of a randomized trial. The potential role of embolization: Although endovascular AVM embolization can occasionally eradicate lesions without surgery or radiation therapy in selected cases, and although embolization may potentially improve the safety and efficacy of surgical or radiosurgical treatments in some other cases, it remains a contentious issue whether it is worth accepting the additional risks of endovascular treatment for a greater overall benefit for patients with brain AVMs that are treatable by surgery or radiation therapy. Some series have reported satisfactory results.20 It is possible that the overall morbidity and mortality of the combined interventional management strategy is increased when embolization is added to a surgical or radiosurgical procedure.17 Therefore, pre-surgical or pre-radiosurgical embolization can be offered, but only as a randomized allocation between embolization and no embolization, within the context of a trial. Primary objective: In the spirit of care trials, the primary objective of the trial and accompanying registry is to offer the best management possible for patients with brain AVMs (ruptured or unruptured) in terms of long-term outcomes, despite the presence of uncertainty. Management may include interventional therapy (neurosurgery, or radiosurgery, alone or in combination, with or without endovascular procedures, alone or combined) or conservative management. An expert multidisciplinary study group will review patients on an individual basis to determine eligibility for the trial or registry parts of the study. The trial has been designed to test whether conservative management or interventional therapy will reduce the risk of disabling stroke or death. Secondary objectives: To determine if interventional management is effective in the prevention of neurological events during 10 years. To determine the morbidity and mortality related to therapy. To follow-up and record the neurological events and the neurological status of all patients with brain AVMs recruited and managed in our institutions, regardless of management strategy chosen. Hypotheses.A) Randomized comparison of interventional treatment and conservative management: Primary hypothesis: Treatment of cerebral AVMs can decrease the number of disabling neurological events caused by the presence of the AVM (excluding peri-operative complications) from 30 to 15% within 10 years. (n = 266 minima) Secondary hypothesis: Treatment of cerebral AVMs can be accomplished with an acceptable up-front risk, defined as the occurrence of a permanent disabling neurological complication in less than 15% of patients) B) Nested trial on the Role of embolization in the treatment of Brain AVMs by other means Primary hypothesis: Pre-surgical or pre-radiosurgery embolization of cerebral AVMs can decrease the number of treatment failures (failure to achieve angiographic cure) from 20% to 10% (n= 440). Secondary hypothesis: Embolization of cerebral AVMs can be accomplished with an acceptable risk, defined as permanent disabling neurological complications of 8% (3.4 to 12.6%, 95% C.I.). The study design is a prospective, multi-center, randomized, controlled trial and registry. Treatment assignment will not be masked; Interim study results will be kept confidential. The primary outcome is the composite event of death from any cause or disabling stroke (hemorrhage or infarction revealed by imaging and resulting in mRS >2). Functional outcome status will be measured by the Rankin Scale, a widely used outcome measure for stroke. The secondary measures of outcome include adverse events, ruptures, and angiographic occlusion of the lesion.

Arms & Interventions

Arms

Active Comparator: Interventional therapy

Interventional therapies include: neurosurgery (surgical resection when the lesion is considered by a multidisciplinary team to be safely 'operable'); radiation therapy (when the AVM is smaller than 3 cm, and considered to not be safely 'operable'); radiosurgery, alone or in combination, with or without endovascular procedure; curative embolization (when the lesion is considered curable by embolization). Patients with AVMs that the multidisciplinary team judges could potentially benefit from endovascular treatment prior to surgical resection or radiation therapy will then also be pre-randomly allocated to embolization or to no embolization.

No Intervention: Conservative management (medical management)

The conservative, or medical management arm, involves pharmacological therapy as deemed appropriate for medical symptoms as determined by the treating investigator. Should patients in the conservative management arm develop hemorrhage or infarction related to their AVM, they then potentially become candidates for interventional therapy.

Interventions

Procedure: - Neurosurgery

Surgical resection to be used when the lesion is considered by a multidisciplinary team to be safely 'operable'.

Radiation: - Radiation therapy

when the AVM is smaller than 3 cm, and considered to not be safely 'operable'.

Procedure: - Embolization

Curative embolization, when the lesion is considered curable by embolization.

Contact a Trial Team

If you are interested in learning more about this trial, find the trial site nearest to your location and contact the site coordinator via email or phone. We also strongly recommend that you consult with your healthcare provider about the trials that may interest you and refer to our terms of service below.

Mayo Clinic in Jacksonville FL, Jacksonville, Florida

Status

Recruiting

Address

Mayo Clinic in Jacksonville FL

Jacksonville, Florida,

Site Contact

Rabih Tawk, MD

[email protected]

514-890-8000

Boston Medical Center, Boston, Massachusetts

Status

Recruiting

Address

Boston Medical Center

Boston, Massachusetts, 02118

Site Contact

Thanh Nguyen, MD

[email protected]

514-890-8000

Albuquerque, New Mexico

Status

Recruiting

Address

University of New Mexico Health Sciences Center

Albuquerque, New Mexico, 87131

Site Contact

Andrew Carlson, MD

[email protected]

514-890-8000

International Sites

Hospital Geral de Fortaleza, Fortaleza, Brazil

Status

Recruiting

Address

Hospital Geral de Fortaleza

Fortaleza, ,

Site Contact

Iuri Martins, MD

[email protected]

514-890-8000

Universidade Federal de Sǎo Paulo, São Paulo, Brazil

Status

Recruiting

Address

Universidade Federal de Sǎo Paulo

São Paulo, ,

Site Contact

Luciana Alves Oliveira Silva, MD

[email protected]

514-890-8000

University of Alberta Hospital, Edmonton, Alberta, Canada

Status

Recruiting

Address

University of Alberta Hospital

Edmonton, Alberta,

Site Contact

Tim Darsaut, MD, PhD

[email protected]

514-890-8000

Klink, Ruby, Montreal, Quebec, Canada

Status

Recruiting

Address

Klink, Ruby

Montreal, Quebec, H2L 4M1

Site Contact

Ruby Klink, PhD

[email protected]

5148908000 #27235

Instituto de Neurocirugia Dr. A. Asenjo, Santiago, Chile

Status

Recruiting

Address

Instituto de Neurocirugia Dr. A. Asenjo

Santiago, ,

Site Contact

Rodrigo Rivera Miranda, MD

[email protected]

514-890-8000

Universidad Autonoma de Bucaramanga, Bucaramanga, Colombia

Status

Recruiting

Address

Universidad Autonoma de Bucaramanga

Bucaramanga, ,

Site Contact

Daniel Eduardo Mantilla Garcia, MD

[email protected]

514-890-8000

Brest, Bretagne, France

Status

Recruiting

Address

CHRU de Brest (Brest University Hospital)

Brest, Bretagne, 29609

Site Contact

Elsa Magro, MD

[email protected]

514-890-8000

Besançon, France

Status

Recruiting

Address

Centre Hospit Régional Universitaire de Besançon

Besançon, , 25030

Site Contact

Alessandra Biondi, MD

[email protected]

514-890-8000

Bordeaux, France

Status

Recruiting

Address

Centre Hospitalier Universitaire de Bordeaux

Bordeaux, , 33000

Site Contact

Xavier Barreau, MD

[email protected]

514-890-8000

Centre Hospitalier Universitaire de Caen, Caen, France

Status

Recruiting

Address

Centre Hospitalier Universitaire de Caen

Caen, , 14033

Site Contact

Patrick Courtheoux, MD

[email protected]

514-890-8000

CHU Clermont-Ferrand, Clermont-Ferrand, France

Status

Recruiting

Address

CHU Clermont-Ferrand

Clermont-Ferrand, ,

Site Contact

Emmanuel Chabert, MD

[email protected]

514-890-8000

CHU Dijon Bourgogne, Dijon, France

Status

Recruiting

Address

CHU Dijon Bourgogne

Dijon, ,

Site Contact

Frédéric Ricolfi, MD

[email protected]

514-890-8000

Hôpital Bicêtre AP-HP, Le Kremlin-Bicêtre, France

Status

Recruiting

Address

Hôpital Bicêtre AP-HP

Le Kremlin-Bicêtre, , 94270

Site Contact

Laurent Spelle, MD

[email protected]

514-890-8000

CHU Limoges, Limoges, France

Status

Recruiting

Address

CHU Limoges

Limoges, , 87042

Site Contact

Charble Mounayer, MD

[email protected]

514-890-8000

Centre Hospitalier Universitaire de Lyon, Lyon, France

Status

Recruiting

Address

Centre Hospitalier Universitaire de Lyon

Lyon, , 69002

Site Contact

Isabelle Pelissou-Guyotat, MD

[email protected]

514-890-8000

Marseille, France

Status

Recruiting

Address

Assistance Publique - Hôpitaux de Marseille

Marseille, , 13005

Site Contact

Pierre-Hugues Roche, MD

[email protected]

514-890-8000

Montpellier, France

Status

Recruiting

Address

Centre Hospitalier Universitaire de Montpellier

Montpellier, , 34000

Site Contact

Vincent Costalat, MD

[email protected]

514-890-8000

Nancy, France

Status

Recruiting

Address

Centre Hospitalier Régional Universitaire de Nancy

Nancy, , 54035

Site Contact

Serge Bracard, MD

[email protected]

514-890-8000

Nantes, France

Status

Recruiting

Address

Centre Hospitalier Universitaire de Nantes

Nantes, , 44093

Site Contact

Hubert Desal, MD

[email protected]

514-890-8000

Hôpital Universitaire Pitié-Salpêtrière, Paris, France

Status

Recruiting

Address

Hôpital Universitaire Pitié-Salpêtrière

Paris, , 75013

Site Contact

Philippe Cornu, MD

[email protected]

514-890-8000

Fondation Ophtalmologique Rothschild, Paris, France

Status

Recruiting

Address

Fondation Ophtalmologique Rothschild

Paris, , 75019

Site Contact

Michel Piotin, MD

[email protected]

514-890-8000

Centre Hospitalier Sainte-Anne, Paris, France

Status

Recruiting

Address

Centre Hospitalier Sainte-Anne

Paris, , 75674

Site Contact

Denis Trystram, MD

[email protected]

514-890-8000

Rennes, France

Status

Recruiting

Address

Centre Hospitalier Universitaire de Rennes

Rennes, , 35033

Site Contact

Xavier Morandi, MD

[email protected]

514-890-8000

Rouen, France

Status

Recruiting

Address

Centre Hospitalier Universitaire Hôpitaux de Rouen

Rouen, , 76130

Site Contact

Christine Papagiannaki, MD

[email protected]

514-890-8000

Strasbourg, France

Status

Recruiting

Address

Les Hôpitaux Universitaires de Strasbourg

Strasbourg, , 67200

Site Contact

François Proust, MD

[email protected]

514-890-8000

Toulouse, France

Status

Recruiting

Address

Centre Hospitalier Universitaire de Toulouse

Toulouse, , 70034

Site Contact

Christophe Cognard, MD

[email protected]

514-890-8000

Tours, France

Status

Recruiting

Address

Centre Hospitalier Régional Universitaire de Tours

Tours, , 37000

Site Contact

Denis Herbreteau, MD

[email protected]

514-890-8000

Stay Informed & Connected