Crohn's Disease Clinical Trial
Official title:
Phase 4, Open Lable Non Randomized un Controlled Study. Salvage Therapy With High/Low Methotrexate for Loss of Response to Infliximab Dose Escalation
The goal of the present study is to evaluate if addition of methotrexate can restore
remission after loss of response to infliximab after dose escalation.
another goal is to evaluate if low dose methotrexate can maintain remission achieved by
regular dose methotrexate by 6 months.
Background: IFX mono-therapy became the method of choice for treatment in pediatric CD,
though this strategy has been called into question due to frequent loss of response to IFX
requiring dose escalation of IFX or decreased intervals of IFX( up to 40% during the first
year) (1). This loss of response has been attributed to development of ATIs and low trough
levels of IFX, which can develop after the first infusions. This loss of response will often
occur in patients with prior azathioprine exposure (2,3,4).
Currently , the first step during loss of response to infliximab in children is dose
escalation either by decreasing the interval between infusions or doubling the dose. However,
patients with persistent antibodies or high titers are likely to fail even with dose
escalation. The Sonic trial clearly demonstrated that combination therapy with a thiopurine
may be more effective than Anti TNF alpha monotherapy (2). Ben Horin et al demonstrated that
antidrug antibodies can be reversed and improved anti TNF trough levels obtained by adding an
immunomodulator to failed monotherapy due to an antidrug antibody (3).
We have previously shown that in patients with a previous loss of response to two biologics
leading to cessation of both biologics can respond to reinduction with adalimumab and
methotrexate . Among 12 patients (10 children and two adults) , 6 obtained complete
remission. We subsequently lowered the does in several patients without loss of response, and
tried stopping methotrexate in 3 patients. All 3 patients relapsed within months of complete
cessation of methorexate.In this previous study we took two separate actions that restored
response, re-induction and methotrexate therapy. In the current proposal we will take
patients that are on escalated therapy and just add methotrexate, in order to evaluate if
adding methotrexate once weekly can restore response after loss of response to infliximab
after failed dose escalation.It is important to note that methotrexate does not increase the
risk of malignancy as co-therapy as far as we know.
Methods: It is a prospective open label phase 4, non randomized uncontrolled study in a small
cohort of patients to evaluate if addition of methotrexate can restore remission after loss
of response to infliximab after dose escalation in paediatric patients.
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