Central Vein Sign: a Diagnostic Biomarker in Multiple Sclerosis

Multiple Sclerosis Clinical Trial

— CAVS-MS  

Official title:

Central Vein Sign: a Diagnostic Biomarker in Multiple Sclerosis

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT04495556
• Other study ID #: 20-063
• Secondary ID: 1U01NS116776-01
• Status: Active, not recruiting
• Start date: September 11, 2020
• Est. completion date: June 2024

Study information

• Verified date: March 2024
• Source: The Cleveland Clinic
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The need for improved diagnostic methods in Multiple Sclerosis (MS) is widely recognized. Although Magnetic Resonance Imaging (MRI) is a longstanding tool for detecting MS lesions, diagnostic inaccuracies persist. Up to 20% of people diagnosed with MS (1 in 5) are later found not to have the disease. This is highly consequential, as more than two-thirds of misdiagnosed patients are unnecessarily exposed to risks from disease-modifying therapies, which in rare cases can be life-threatening. Moreover, the current standard in MS diagnosis - the McDonald criteria, which combine clinical symptoms and MRI findings - were developed from studies in people with typical clinical presentations of MS. This reduces the specificity of these criteria, rendering them uninformative for the nearly half of MS patients who present to neurologists with atypical or nonclassical symptoms. Timeliness of MS diagnosis is also key, as diagnostic delay is common in cases of relapsing-remitting MS and can carry severe and lifelong consequences. The CentrAl Vein Sign in MS (CAVS-MS) study has been designed to assess whether Central Vein Sign (CVS) criteria can help address some of these unmet diagnostic needs. It will specifically explore the role of presentation type by enrolling a mixed population of patients with typical clinical presentations (n = 200) and those with atypical presentations, including suggestive MRI findings in the absence of neurologic symptoms (n = 200) across North America.

Description:

The CentrAl Vein Sign in MS (CAVS-MS) study seeks to answer whether the central vein sign (CVS) can be used as a sensitive and specific diagnostic marker for a diagnosis of MS. The study will investigate the CVS in a mixed population of participants with typical and atypical clinical presentations including radiological presentations without neurological symptoms. The CVS is proposed as a diagnostic biomarker with improved sensitivity for a diagnosis of MS, while retaining diagnostic specificity - all in an-easy-to use diagnostic test that can be applied in patients with both typical and atypical disease presentation. There is extensive research demonstrating the ability of the CVS criteria to discriminate MS lesions from common mimickers, such as vascular disease and migraine. However, the CVS has mainly been applied in cross- sectional studies. In addition, the majority of these studies have focused analysis primarily on patients presenting with typical clinical events of demyelination (i.e. a classic Clinically Isolated Syndrome (CIS)). This study will evaluate CVS criteria prospectively in individuals with typical and atypical MS presentations. Aim 1 will examine sensitivity and specificity of CVS criteria in conjunction with, and separate from, the McDonald Criteria. Aim 2 will examine CVS in a population where McDonald criteria explicitly cannot be applied. Because the likelihood of MS is lower in this group, the focus will be on specificity, which is where the unmet need exists. Although current MS diagnostic criteria are sensitive in most typical cases, the use of the CVS may hasten diagnosis in patients with low lesion numbers and those without dissemination in time. In the past, studies that informed revision of the diagnostic criteria used "clinically definite MS" (defined as two separate clinical events) as the definitive determination of a diagnosis. In the current treatment era, however, clinically definite MS is less relevant, since most patients will be diagnosed after a first clinical event (relapse) and will go on to start treatment prior to even having a second relapse. For this reason, the 2017 McDonald Criteria is being used as the "gold standard" for the proposed study. Importantly, in the current study the CVS will be applied in a population where the McDonald Criteria are not applicable (atypical presentations) and where currently a significant unmet clinical need exists. Because the studies that informed the diagnostic criteria did not include patients presenting with atypical syndromes, such patients are not covered in the McDonald Criteria path, but are frequently given a diagnosis of MS on the basis of MRI findings. To address this limitation, the presence of CVS as a predictor of development of future clinical events will be examined, within a 24- month period, that would satisfy the 2017 McDonald Criteria. Thus, the results of this study will have a significant impact on both improving sensitivity in those presenting with typical presentations and providing a specific test for MS in those with atypical presentations, thereby avoiding unnecessary costs associated with misdiagnosis. The investigators will leverage the North American Imaging in Multiple Sclerosis Cooperative (NAIMS) to conduct a multicenter study, based on an initial cross-sectional pilot study using the CVS criteria as a diagnostic biomarker for MS. Patients will be enrolled when presenting to an MS center for diagnostic referral, and they will undergo follow-up at prespecified intervals for 24 months. Brain MRI will be performed at baseline and 24 months, with scans scored on the basis of CVS criteria. T2-weighted fluid-attenuated inversion recovery (FLAIR) imaging will be combined with T2*-weighted segmented echo-planar imaging to enable simultaneous identification of white matter lesions and venous structures. The primary objective is to determine whether use of CVS criteria allows for an earlier accurate diagnosis of MS in patients who do not meet the McDonald criteria at baseline. The aim is to show that the CVS is a simple and reliable diagnostic biomarker that will show an increase in sensitivity while preserving specificity. Secondary objectives include the following: - Determining concordance of CVS criteria and the McDonald criteria among patients meeting McDonald criteria at baseline. - Determining whether use of CVS criteria improves diagnostic specificity for MS in people presenting with atypical symptoms. - Determining whether the CVS predicts development of clinical MS in individuals with suggestive radiologic findings but no symptoms. The researchers will also begin exploratory studies of optimal methods for integrating CVS findings into MS diagnostic criteria, along with any resulting healthcare-related cost savings. These initial exploratory analyses will be important to how readily positive findings about the utility of CVS criteria can impact clinical practice. The ultimate goal is to have the CVS incorporated into the MS diagnostic criteria.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 420
• Est. completion date: June 2024
• Est. primary completion date: June 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

Inclusion criteria for participants with typical presentations will include:

1. Age 18 to 65 inclusive

2. Referral to a study academic site for a clinical suspicion of MS

3. Onset with typical symptom onset including: acute unilateral optic neuritis, double vision due to an internuclear ophthalmoplegia or sixth nerve palsy, facial sensory loss or trigeminal neuralgia in a young adult (<40 years of age), cerebellar ataxia and nystagmus, partial myelopathy, sensory symptoms in a CNS pattern, Lhermitte's symptom, asymmetric limb weakness, urge incontinence or erectile dysfunction, or other neurological presentation considered to be typical by the site investigator.

4. Able to provide written informed consent to participate in the study

5. For participants referred for clinical suspicion of multiple sclerosis who had workup prior to referral or who are taking disease-modifying therapies for MS, digital availability of diagnostic cranial MRI with gadolinium within 3 months of initial symptoms

6. Onset of typical neurological symptoms within 10 years of screening.

Inclusion criteria for participants with atypical presentations will include:

1. Age 18 to 65 inclusive

2. Referral to a study academic site for a suspicion of MS

3. Onset with atypical onset including: bilateral optic neuritis or unilateral optic neuritis with a poor visual recovery, complete gaze palsy or fluctuating ophthalmoparesis, intractable nausea, vomiting, or hiccups, complete transverse myelopathy with bilateral motor and sensory involvement, encephalopathy, subacute cognitive decline, headache or meningismus, isolated fatigue or asthenia, constitutional symptoms, other clinical presentations considered atypical by the site investigator (examples include: vague or patchy sensory symptoms, pain, short lasting bilateral blurred vision, etc.), or absence of clinical symptoms with MRI features suggestive of MS

4. Able to provide written informed consent to participate in the study

5. For participants referred for clinical suspicion of multiple sclerosis who had workup prior to referral or who are taking disease-modifying therapies for MS, digital availability of diagnostic cranial MRI with gadolinium within 3 months of initial symptoms

6. Onset of atypical neurological symptoms within 10 years of screening. Exclusion Criteria:

Exclusion criteria for both typical and atypical populations will include:

1. Contraindication to MRI studies; metal or metal implants incompatible with MRI

2. Inability to tolerate MRI due to claustrophobia or known excessive movement (e.g. tremor)

3. Contraindication to use of gadolinium containing contrast agents (allergy or renal failure)

4. Treatment with systemic corticosteroids in the 4 weeks preceding enrollment.

Related Conditions & MeSH terms

• Multiple Sclerosis
• Sclerosis

Intervention

Diagnostic Test:
• MRI
The study will include MRI at baseline (first study visit) and month 24 (final study visit). MRI at month 24 (end of study) will be used to determine McDonald Criteria and final review of CVS.

Locations

Country	Name	City	State
Canada	St. Michael's Hospital of Unity Health Toronto	Toronto	Ontario
United States	University of Colorado	Aurora	Colorado
United States	The University of Texas at Austin	Austin	Texas
United States	Johns Hopkins University	Baltimore	Maryland
United States	University of Vermont	Burlington	Vermont
United States	Cleveland Clinic Foundation	Cleveland	Ohio
United States	Cedars-Sinai Medical Center	Los Angeles	California
United States	University of Southern California	Los Angeles	California
United States	Yale University	New Haven	Connecticut
United States	University of Pennsylvania	Philadelphia	Pennsylvania
United States	Washington University in St. Louis	Saint Louis	Missouri

Sponsors (5)

Lead Sponsor	Collaborator
The Cleveland Clinic	Cedars-Sinai Medical Center, National Institute of Neurological Disorders and Stroke (NINDS), National Institutes of Health (NIH), University of Pennsylvania

Countries where clinical trial is conducted

United States,  Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Economics outcomes	Health care expenditures will be measured using Healthcare Resource Utilization (HRU) forms. Total costs for patients over the 24-month follow up period will be assessed using information from all 5 study visits. At each encounter, patients will report emergency care visits and inpatient hospitalizations which have occurred within the past 6-months. Costs accrued over each 6-month period will be used to estimate overall 24-month costs.	Done at all 5 study visits - baseline, month 6, month 12, month 18 and month 24.
Primary	MRI Outcomes	MRI will be done to assess sensitivity and specificity of the CVS for multiple sclerosis.; MRI will be done at baseline or start of the study and at month 24, end of study. Central veins will be counted and lesions will be considered CVS+ using specified criteria. CVS will be determined using Select6, Select3*, and automated lesion analysis with inclusion and exclusion of periventricular lesions.	Change assessed over 24 months. First scan at baseline (first study visit) and the second scan at 24 months or the last study visit.
Secondary	Clinical Outcomes - McDonald Criteria 2017	Determination of a diagnosis of MS using the McDonald Criteria 2017 will be conducted by a central adjudication committee. McDonald diagnostic criteria for MS are clinical, radiographic, and laboratory criteria used in the diagnosis of multiple sclerosis. Members of the adjudication committee will separately review the clinical data, laboratory testing, and study MRIs of each participant at baseline, 12 months, and 24 months.	McDonald criteria will be reviewed at baseline, month 12 and month 24 visits.
Secondary	Clinical Outcomes - Relapses	Relapses will be assessed at every study visit after baseline to look for disease progression and disability. Proportion of people who do not have clinical relapses of MS at 24 months, will help us determine if CVS yields specificity for MS among individuals with atypical presentation.	Relapses will be assessed at month 6, month 12, month 18 and month 24.
Secondary	Clinical Outcomes - Lab results - Cerebrospinal Fluid Testing	Lab results will be collected at every study visit whenever available. May include recording of: cerebrospinal fluid testing (CSF).	Lab results will be collected at baseline, month 6, month 12, month 18 and month 24.
Secondary	Lab results - Neuromyelitis Optica Antibodies (NMO-IgG)	Lab results will be collected at every study visit whenever available. May include recording of: neuromyelitis optica antibodies (NMO-IgG).	Lab results will be collected at baseline, month 6, month 12, month 18 and month 24.
Secondary	Lab results - Myelin oligodendrocyte glycoprotein (MOG) testing.	Lab results will be collected at every study visit whenever available. May include recording of: myelin oligodendrocyte glycoprotein (MOG) testing.	Lab results will be collected at baseline, month 6, month 12, month 18 and month 24.
Secondary	Patient reported Outcomes - Change in Neuro-QoL (Quality of Life in Neurological disorders) using Neuro-QoL short forms to assess Physical Domains, from baseline to month 24.	The Neuro-QoL (short forms) instrument will be used to measure quality of life as related to neurological disease.; 11 subscales, each is scored separately, there is no composite score.; Physical Domains include: Upper Extremity Function (Fine Motor, ADL), Lower Extremity Function (Mobility), Fatigue, and Sleep Disturbance.	Assessed over 24 months. Neuro-QoL at baseline, month 12 and month 24 study visits.
Secondary	Change in Neuro-QoL using Neuro-QoL short forms to assess Mental Domains, from baseline to month 24	The Neuro-QoL (short forms) instrument will be used to measure quality of life as related to neurological disease.; 11 subscales, each is scored separately, there is no composite score.; Mental Domains include: Cognition Function, Stigma, Anxiety, Depression and Positive Affect and Well-being.	Assessed over 24 months. Neuro-QoL at baseline, month 12 and month 24 study visits.
Secondary	Change in Neuro-QoL using Neuro-QoL short forms to assess Social Domains, from baseline to month 24	The Neuro-QoL (short forms) instrument will be used to measure quality of life as related to neurological disease.; 11 subscales, each is scored separately, there is no composite score.; Social Domains include: Ability to Participate in Social Roles and Activities, and Satisfaction with Social Roles and Activities.	Assessed over 24 months. Neuro-QoL at baseline, month 12 and month 24 study visits.
Secondary	Patient reported Outcomes - PDDS (patient determined disease steps)	The PDDS is a patient reported outcome that captures overall MS disability. It will be collected and baseline, month 6, month 12, month 18, and month 24. PDDS scores will be recorded and sustained worsening will be considered for worsening of 1 point or greater confirmed at 3 months.	PDDS will be assessed at all the 5 study visits - baseline, month 6, 12, 18 and 24.