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

  • Enrico De Lorenzis
  • , Gerlando Natalello*
  • , Greta Pellegrino
  • , Lucrezia Verardi
  • , Veronica Batani
  • , Gemma Lepri
  • , Stefano Stano
  • , Giuseppe Armentano
  • , Marco De Pinto
  • , Francesca Motta
  • , Stefano Di Donato
  • , Vishal Kakkar
  • , Silvia Fiore
  • , Ilaria Bisconti
  • , Corrado Campochiaro
  • , Laura Cometi
  • , Antonio Tonutti
  • , Amalia Spinella
  • , Simona Truglia
  • , Silvia Cavalli
  • Maria De Santis, Dilia Giuggioli, Nicoletta Del Papa, Serena Guiducci, Fabio Cacciapaglia, Giacomo De Luca, Fiorenzo Iannone, Valeria Ricceri, Marco Matucci Cerinic, Maria Antonietta D'Agostino, Francesco Del Galdo, Silvia Laura Bosello
*Corresponding author
  • University of Rome La Sapienza
  • San Raffaele Scientific Institute
  • University of Florence
  • University of Bari
  • University of Milan
  • University of Modena and Reggio Emilia
  • IRCCS Istituto Clinico Humanitas - Rozzano (Milano)
  • Humanitas University
  • University of Leeds

Research output: Contribution to journalArticle

Abstract

Objectives MMF is a mainstay for the treatment of SSc. The occurrence and implications of MMF-related adverse events (AEs) on drug retention rates in real life remain poorly defined. We aimed to determine the MMF retention rate and to investigate the causes and patterns of discontinuation, AEs and treatment options used after discontinuation.Methods SSc patients who started MMF treatment underwent a retrospective longitudinal assessment for up to 5 years. We documented the incidence, predictors and impacts of MMF treatment on gastrointestinal intolerance, infections, laboratory abnormalities and cancer. Rescue strategies implemented after MMF discontinuation were recorded.Results The 5-year MMF retention rate of 554 patients stood at 70.7%, and 19.6% of them stopped MMF due to AEs. One out of every four patients experienced a dose reduction or discontinuation of MMF due to AEs, with gastrointestinal intolerance being the predominant cause. The 5-year cumulative incidence rates for gastrointestinal intolerance, cancer, severe infections and laboratory toxicity leading to MMF discontinuation were 6.4%, 4.1%, 3.1% and 2.1%, respectively. Lower respiratory tract was the most affected, with bacteria being the predominant causative agent. Intestinal and pulmonary circulation involvement were tied to elevated AE rates and MMF discontinuation. The most common approaches post-MMF cessation were 'watch and wait' and switch to rituximab.Conclusions : MMF use in SSc appears to be limited by the occurrence of AEs, both in terms of persistence and dosing of the drug. Rescue options after MMF discontinuation are limited and many patients remain without immunosuppressant.
Original languageEnglish
Pages (from-to)N/A-N/A
JournalRheumatology
Volume2024
Issue number30
DOIs
Publication statusPublished - 2024

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

All Science Journal Classification (ASJC) codes

  • Rheumatology
  • Pharmacology (medical)

Keywords

  • Systemic sclerosis
  • cancer
  • infections
  • mycophenolate mofetil
  • persistence
  • rescue strategy
  • safety

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