To Evaluate the Effect of Therapy With IT MTX on the Disease Course of Patients With Progressive MS Clinical Trial
Official title:
Intrathecal Methotrexate for Progressive Multiple Sclerosis: An Open Label Single Arm Study
Multiple sclerosis (MS) is characterized pathologically by demyelination, axonal loss, and
glial scar formation. Clinically, most patients have a relapsing-remitting course of MS
(RRMS) that over time may become progressive without remissions - a secondary progressive MS
(SPMS). About 15% of patients have a progressive course from onset which is called primary
progressive (PP).
Currently, there is no approved treatment for PPMS and for SPMS only therapy with
mitoxantrone showed mild effect. Thus, more effective therapies need to be developed for
treatment of SPMS and PPMS.
Methotrexate (MTX), an anti-metabolite, has been in clinical use since 1948 when it was
found to produce temporary remission of acute childhood leukemia.
There are accumulating evidences that in progressive MS patients there are follicular
lymphoid structures in the meninges and in the Virchow-Robin spaces. Therefore, intrathecal
therapy may target the pathological follicular lymphoid activity.
The safety of intrathecal MTX (ITMTX) has been demonstrated by its widespread use in
treating lymphoproliferative diseases and leptomeningeal metastases. Sadik et. Al. reported
about the feasibility and safety of using intrathecal methotrexate (ITMTX) as a treatment
for unresponsive patients with progressive forms of MS. In their open label study they found
that ITMTX may have a beneficial effect in progressive forms of MS and that it was well
tolerated with no serious adverse events.
The investigators aim is to evaluate the efficacy , safety and tolerability of intrathecal
methotrexate administration every 3 months in progressive 30 patients with progressive MS.
The investigators will evaluate clinical, laboratory evaluation of the blood and
cerebrospinal fluid as well as the MRI scans of the participants. Each patient will be
treated 4 times for 1 year with the option to continue for another 1 more year with the same
protocol.
Protocol Intrathecal Methotrexate for Progressive Multiple Sclerosis: An Open Label Single
Arm Study
Introduction Multiple sclerosis (MS) is characterized pathologically by demyelination,
axonal loss, and glial scar formation. Clinically, most patients have a relapsing-remitting
course of MS (RRMS) that over time may become progressive without remissions - a secondary
progressive MS (SPMS). About 15% of patients have a progressive course from onset which is
called primary progressive (PP) (1). In the past decades, several treatments have been
approved mainly for the use in RRMS.
Treatments for SPMS may be still effective for the early phase of this course, but it become
ineffective for the later phase of SPMS (2,3) For PPMS, there is currently no approved
treatment. Thus, more effective therapies need to be developed for treatment of SPMS and
PPMS.
Methotrexate (MTX), an anti-metabolite, has been in clinical use since 1948 when it was
found to produce temporary remission of acute childhood leukemia. Methotrexate irreversibly
binds to and inhibits dihydrofolate reductase, inhibiting the formation of reduced folate,
and thymidylate synthetase, resulting in inhibition of purine and thymidylic acid synthesis,
thus interfering with DNA synthesis, repair, and cellular replication.
Because of its indirect immunosuppressive effects, MTX is used in treating autoimmune
conditions such as rheumatoid arthritis and psoriasis (4). Low dose oral MTX (7.5 mg weekly)
was found to be mildly effective, in slowing the deterioration in patients with SPMS (5).
There are accumulating evidences that in progressive MS patients there are follicular
lymphoid structures in the meninges and in the Virchow-Robin spaces (8). These follicles are
enriched in lymphocytes and dendritic cells which may drive the CNS inflammatory responses
in the disease. This CNS restricted immune response may be unaffected by systemic
immunomodulation and immunosuppressive therapies. Therefore, intrathecal therapy may target
the pathological follicular lymphoid activity.
The safety of intrathecal MTX (ITMTX) has been demonstrated by its widespread use in
treating lymphoproliferative diseases and leptomeningeal metastases (9). Sadik et. Al.
reported about the feasibility and safety of using intrathecal methotrexate (ITMTX) as a
treatment for unresponsive patients with progressive forms of MS (10). In their open label
study they found that ITMTX may have a beneficial effect in progressive forms of MS and that
it was well tolerated with no serious adverse events.
In the Last year the investigators have treated 8 patients with IT MTX according to the
proposed protocol. Until now these patients receive 1-3 therapies of IT MTX without
significance adverse event. The adverse event was were reported were: fatigue for several
days post therapy and mild headache.
Objective The investigators aim is to evaluate the efficacy , safety and tolerability of
intrathecal methotrexate administration in progressive MS patients.
Methods Study Population 30 progressive MS patients Inclusion Criteria
- Age 18-750 years
- Clinically definite diagnosis of MS according to McDonald criteria 2010.
- Progressive disease form defined by confirmed expanded disability status scale (EDSS)
progression without relapse by at least 0.5 point or greater in the six months prior to
enrollment.
Exclusion criteria
- Pregnancy
- Active infection
- Significant associated medical condition such as malignancy, heart disease or
concurrent other autoimmune condition.
- Known allergy to MTX.
- WBC<4000 cells/µL
- Lym<800 cells/µL
- Treated with fingolimod or natalizumab 3 months prior to enrollment
Treatment The physician will administer 12.5 mg of MTX diluted to a concentration of up to 4
mg/mL in 0.9 percent sodium chloride with 4 mg Dexamethasone via lumbar puncture needle.
These doses are standard doses of IT treatment with MTX.
Treatments will be scheduled 3 months apart for 1 year .A tota of 4 treatments in a 1 year.
A CBC with differential will be obtained before each treatment to assess the level of
hematological suppression.
Evaluation A. Patients will be evaluated every 3 months by a physician other then their
treating physician with the following: Kurtzke Expanded Disability Status Scale (EDSS). 25
FW , 9 PHT, Symbol Digit Modalities Test (SDMT), fatigue scale (FSS) and depression scale
(BDI). In each of the visits the patient will be asked about adverse events (AE) and will be
instructed to report us every AE/ medical complain he will experience between visits.
AEs will be followed until resolution or through completion of the study, whichever comes
first. All Serious adverse events (SAEs) will be followed until event resolution, until the
condition stabilizes, until the event is otherwise explained, or until the subject is lost
to follow-up. The investigator is responsible for ensuring that follow-up includes any
supplemental investigations as may be reasonably indicated to elucidate the nature and/or
causality of the SAE. Any follow-up information regarding SAEs must be reported to the
Helsinki committee within 24 hours.
Treatment The physician will administer 12.5 mg of MTX diluted to a concentration of up to 4
mg/mL in 0.9 percent sodium chloride with 4 mg Dexamethasone via lumbar puncture needle.
These doses are standard doses of IT treatment with MTX.
Treatments will be scheduled 3 months apart for 1 year .A tota of 4 treatments in a 1 year.
A CBC with differential will be obtained before each treatment to assess the level of
hematological suppression.
Laboratory test After obtaining informed consent to perform the procedure, a physician will
perform a lumbar puncture with a 25 gauge needle and cerebrospinal fluid (CSF) sample will
be obtained and analyze for parameters including cell count and differential, protein and
glucose concentration, oligoclonal bands, IgG concentration, cellular analysis by flow
cytometry for CD3+, CD20+, CD14+ cell subsets, and measurement of several soluble mediators
such as: CXCL13, CD23, light chains, TNFa, IFNg, IL-17, IL-2, IL-10, BDNF and Neurofilaments
will be studied by ELISA
MRI scan Brain MRI scan will be done within 1 week before each treatment. The MRI protocol
includes the following sequences: T1, T2, FLAIR, T1 will gadolinium, DTI.
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Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment