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

Systemic sclerosis cancer infections mycophenolate mofetil persistence rescue strategy safety

Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
30 Sep 2024
Historique:
received: 03 07 2024
revised: 28 08 2024
accepted: 17 09 2024
medline: 30 9 2024
pubmed: 30 9 2024
entrez: 30 9 2024
Statut: aheadofprint

Résumé

Mycophenolate mofetil (MMF) is a mainstay for the treatment of systemic sclerosis (SSc). The occurrence and implications of MMF-related adverse events 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, adverse events (AEs) and treatment options used after discontinuation. 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. 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. 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.

Sections du résumé

BACKGROUND BACKGROUND
Mycophenolate mofetil (MMF) is a mainstay for the treatment of systemic sclerosis (SSc). The occurrence and implications of MMF-related adverse events 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, adverse events (AEs) and treatment options used after discontinuation.
METHODS 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 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 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.

Identifiants

pubmed: 39348184
pii: 7796566
doi: 10.1093/rheumatology/keae532
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Enrico De Lorenzis (E)

Unit of Rheumatology, Catholic University of the Sacred Heart, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Scleroderma Program, Leeds Institute of Rheumatic and Musculoskeletal Diseases, University of Leeds, Leeds, United Kingdom.

Gerlando Natalello (G)

Unit of Rheumatology, Catholic University of the Sacred Heart, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

Greta Pellegrino (G)

Rheumatology Unit, Department of Clinical Internal, Anesthesiological and Cardiovascular Sciences, Sapienza University of Rome, Rome, Italy.

Lucrezia Verardi (L)

Unit of Rheumatology, Catholic University of the Sacred Heart, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

Veronica Batani (V)

Unit of Immunology, Rheumatology, Allergy and Rare Diseases, IRCCS San Raffaele Hospital, Milan, Italy.

Gemma Lepri (G)

Rheumatology Unit, Department of Clinical and Experimental Medicine, University of Florence, Florence, Italy.

Stefano Stano (S)

Rheumatology Unit, Department of Emergency and Organs Transplantation, Università degli Studi di Bari Aldo Moro, Bari, Italy.

Giuseppe Armentano (G)

Scleroderma Clinic, Dip. Reumatologia, ASST G. Pini-CTO, Università degli Studi di Milano.

Marco De Pinto (M)

Department of Rheumatology, University of Modena and Reggio Emilia, Modena, Italy.

Francesca Motta (F)

Rheumatology and Clinical Immunology, IRCCS Humanitas Research Hospital, Rozzano, Italy.
Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy.

Stefano Di Donato (S)

Scleroderma Program, Leeds Institute of Rheumatic and Musculoskeletal Diseases, University of Leeds, Leeds, United Kingdom.

Vishal Kakkar (V)

Scleroderma Program, Leeds Institute of Rheumatic and Musculoskeletal Diseases, University of Leeds, Leeds, United Kingdom.

Silvia Fiore (S)

Unit of Rheumatology, Catholic University of the Sacred Heart, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

Ilaria Bisconti (I)

Rheumatology Unit, Department of Clinical Internal, Anesthesiological and Cardiovascular Sciences, Sapienza University of Rome, Rome, Italy.

Corrado Campochiaro (C)

Unit of Immunology, Rheumatology, Allergy and Rare Diseases, IRCCS San Raffaele Hospital, Milan, Italy.

Laura Cometi (L)

Rheumatology Unit, Department of Clinical and Experimental Medicine, University of Florence, Florence, Italy.

Antonio Tonutti (A)

Rheumatology and Clinical Immunology, IRCCS Humanitas Research Hospital, Rozzano, Italy.

Amalia Spinella (A)

Department of Rheumatology, University of Modena and Reggio Emilia, Modena, Italy.

Simona Truglia (S)

Rheumatology Unit, Department of Clinical Internal, Anesthesiological and Cardiovascular Sciences, Sapienza University of Rome, Rome, Italy.

Silvia Cavalli (S)

Scleroderma Clinic, Dip. Reumatologia, ASST G. Pini-CTO, Università degli Studi di Milano.

Maria De Santis (M)

Rheumatology and Clinical Immunology, IRCCS Humanitas Research Hospital, Rozzano, Italy.
Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy.

Dilia Giuggioli (D)

Department of Rheumatology, University of Modena and Reggio Emilia, Modena, Italy.

Nicoletta Del Papa (N)

Scleroderma Clinic, Dip. Reumatologia, ASST G. Pini-CTO, Università degli Studi di Milano.

Serena Guiducci (S)

Rheumatology Unit, Department of Clinical and Experimental Medicine, University of Florence, Florence, Italy.

Fabio Cacciapaglia (F)

Rheumatology Unit, Department of Emergency and Organs Transplantation, Università degli Studi di Bari Aldo Moro, Bari, Italy.

Giacomo De Luca (G)

Unit of Immunology, Rheumatology, Allergy and Rare Diseases, IRCCS San Raffaele Hospital, Milan, Italy.

Fiorenzo Iannone (F)

Rheumatology Unit, Department of Emergency and Organs Transplantation, Università degli Studi di Bari Aldo Moro, Bari, Italy.

Valeria Ricceri (V)

Rheumatology Unit, Department of Clinical Internal, Anesthesiological and Cardiovascular Sciences, Sapienza University of Rome, Rome, Italy.

Marco Matucci Cerinic (M)

Unit of Immunology, Rheumatology, Allergy and Rare Diseases, IRCCS San Raffaele Hospital, Milan, Italy.

Maria Antonietta D'Agostino (MA)

Unit of Rheumatology, Catholic University of the Sacred Heart, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

Francesco Del Galdo (F)

Scleroderma Program, Leeds Institute of Rheumatic and Musculoskeletal Diseases, University of Leeds, Leeds, United Kingdom.

Silvia Laura Bosello (SL)

Unit of Rheumatology, Catholic University of the Sacred Heart, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

Classifications MeSH