Systemic sclerosis & Raynaud's

Long-term retention rate, adverse event temporal patterns and rescue treatment strategies of mycophenolate mofetil in systemic sclerosis: insights from real-life

Rheumatology (Oxford)Published Retrospective cohort study

Authors' conclusion

MMF use in SSc appears to be limited by the occurrence of AEs, both in terms of persistence and dosing of the drug.

Study context

Population
SSc patients who started MMF treatment, real-life setting
Participants
554 patients
Outcome
MMF retention rate
Follow-up
Up to 5 years
Methodological detailslongitudinal, up to 5 years
  • Longitudinal
  • Up to 5 years

Main finding

As reported in the abstract

MMF

70.7%

Observational data: associations, not effects.

Further findings

Post-MMF cessation strategies

Most common approaches were 'watch and wait' and switch to rituximab

Safety

OutcomeValues
MMF discontinuation due to AEsMMF 19.6%

MMF discontinuation due to adverse events (AEs)

One in four patients had dose reduction or discontinuation due to AEs, gastrointestinal intolerance the predominant cause

5-year cumulative incidence of AEs leading to MMF discontinuation · up to 5 years

Gastrointestinal intolerance
6.4%
Cancer
4.1%
Severe infections
3.1%
Laboratory toxicity
2.1%
  • Lower respiratory tract most affected by infection; bacteria predominant

Predictors of AEs and discontinuation

Intestinal and pulmonary circulation involvement tied to elevated AE rates and MMF discontinuation

Original publication

Long-term retention rate, adverse event temporal patterns and rescue treatment strategies of mycophenolate mofetil in systemic sclerosis: insights from real-life. Rheumatology (Oxford). Published 30 September 2024. doi:10.1093/rheumatology/keae532

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