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Methotrexate dosage reduction in patients with rheumatoid arthritis beginning therapy with infliximab: the Infliximab
R M Fleischmann1, S B Cohen, L W Moreland
1Radiant Research--Dallas, University of Texas, Southwestern Medical Center at Dallas, Dallas, TX 75235, USA. royfleischmann@radiantresearch.com
Objective:
Infliximab plus methotrexate (MTX) is approved for the treatment of rheumatoid arthritis (RA). Based on the benefit/risk profile of this combination therapy, lower doses of MTX would be preferable when infliximab efficacy can be maintained. We evaluated the ability of patients receiving infliximab plus MTX to achieve and maintain a clinical response while the dose of MTX was tapered.
Methods:
Infliximab infusions were administered at a minimum dosage of 3 mg/kg at 8-week intervals (following three loading doses at weeks 0, 2, and 6) to patients who had an inadequate response to MTX. MTX tapering was initiated at week 22 or later when at least a 40% improvement in the combined tender and swollen joint count was achieved; dosages were reduced by 5 mg every 8 weeks to a protocol-specified minimum dosage of 5 mg per week. If the required dosage of MTX after a flare was greater than the baseline dosage, the patient was considered a treatment failure.
Results:
Of the 210 patients enrolled, 159 (76%) achieved a 40% or better improvement in the combined tender and swollen joint count and had their MTX doses tapered. In these 159 responders, the median (mean) dose of MTX was reduced from 15 (16.5) mg per week at baseline to 5 (7.1) mg per week at week 54. From the time of initial response, 79% of these patients had a zero- or a one-vial increase in infliximab, corresponding to an approximate dose increase of 1 mg/kg, through week 54.
Conclusion:
Approximately 75% of the patients participating in this trial achieved at least a 40% reduction in the combined swollen and tender joint count (correlating with an American College of Rheumatology 20% [ACR20] response in 83% of patients) while reducing the mean MTX dose by 57%.
Insights
Reducing methotrexate doses in rheumatoid arthritis patients on infliximab maintained treatment efficacy. This approach allowed for a significant decrease in methotrexate dosage while preserving clinical response, demonstrating a favorable benefit/risk profile.
Area of Science:
- Rheumatology
- Immunology
- Pharmacology
Background:
- Infliximab combined with methotrexate (MTX) is a standard treatment for rheumatoid arthritis (RA).
- Optimizing the benefit/risk profile of this combination therapy is desirable.
- Lowering MTX dosage while maintaining infliximab efficacy could improve patient outcomes.
Purpose of the Study:
- To assess the feasibility of maintaining clinical response in RA patients treated with infliximab and MTX while tapering the MTX dose.
- To evaluate the long-term efficacy and safety of reduced MTX dosages in this patient population.
Main Methods:
- Patients with inadequate response to MTX received infliximab infusions (3 mg/kg at 8-week intervals).
- MTX tapering began at week 22 or later upon achieving at least a 40% improvement in joint counts.
- MTX doses were reduced by 5 mg every 8 weeks to a minimum of 5 mg/week; treatment failure was defined by increased MTX requirement post-flare.
Main Results:
- 159 out of 210 patients (76%) achieved a 40% or greater improvement and underwent MTX tapering.
- The median MTX dose decreased from 15 mg/week to 5 mg/week by week 54.
- 79% of these responders required only a minimal increase (0-1 vial) in infliximab dosage through week 54.
Conclusions:
- Approximately 75% of RA patients achieved significant clinical improvement (40% joint count reduction, correlating to 83% ACR20 response) with reduced MTX doses.
- This study demonstrates that mean MTX dosage can be reduced by 57% while maintaining infliximab efficacy.
- Tapering MTX in RA patients on infliximab is a viable strategy to optimize treatment and potentially reduce toxicity.
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