Long-term outcome of autologous haematopoietic stem cell transplantation in patients with systemic sclerosis: a comparison with patients treated with rituximab and with traditional immunosuppressive agents.


Journal

Arthritis research & therapy
ISSN: 1478-6362
Titre abrégé: Arthritis Res Ther
Pays: England
ID NLM: 101154438

Informations de publication

Date de publication:
23 Oct 2024
Historique:
received: 29 04 2024
accepted: 25 09 2024
medline: 24 10 2024
pubmed: 24 10 2024
entrez: 24 10 2024
Statut: epublish

Résumé

Autologous haematopoietic stem cell transplantation (AHSCT) is more effective than conventional immunosuppressive therapies (CIT) in improving the outcome of patients with rapidly progressive diffuse cutaneous systemic sclerosis (dcSSc). So far, there is still a paucity of data comparing AHSCT with rituximab (RTX). Aim of the study is to retrospectively compare, in patients with dcSSc, the effectiveness of AHSCT with that of RTX and CIT. Thirty-five dcSSc AHSCT-treated patients were compared with 29 and 36 matched cases treated with RTX and CIT, respectively. The patients were followed up for 5 years by assessing selected outcome measures every year. Overall survival, modified Rodnan skin score (mRSS), lung function tests (FVC and DLCO), and the revised EUSTAR Activity Index (REAI) were the outcome measures chosen to evaluate the therapy efficacy. AHSCT was significantly more effective than RTX and CIT in prolonging survival, inducing a rapid reduction of the mRSS and REAI and maintaining the baseline level of lung function tests for a longer time. RTX therapy was also superior to CIT in reducing REAI, mRSS and in saving lung function. AHSCT is more effective than both RTX and CIT in prolonging survival and inducing prolonged remission in patients with rapidly progressive dcSSc.

Sections du résumé

BACKGROUND BACKGROUND
Autologous haematopoietic stem cell transplantation (AHSCT) is more effective than conventional immunosuppressive therapies (CIT) in improving the outcome of patients with rapidly progressive diffuse cutaneous systemic sclerosis (dcSSc). So far, there is still a paucity of data comparing AHSCT with rituximab (RTX). Aim of the study is to retrospectively compare, in patients with dcSSc, the effectiveness of AHSCT with that of RTX and CIT.
METHODS METHODS
Thirty-five dcSSc AHSCT-treated patients were compared with 29 and 36 matched cases treated with RTX and CIT, respectively. The patients were followed up for 5 years by assessing selected outcome measures every year. Overall survival, modified Rodnan skin score (mRSS), lung function tests (FVC and DLCO), and the revised EUSTAR Activity Index (REAI) were the outcome measures chosen to evaluate the therapy efficacy.
RESULTS RESULTS
AHSCT was significantly more effective than RTX and CIT in prolonging survival, inducing a rapid reduction of the mRSS and REAI and maintaining the baseline level of lung function tests for a longer time. RTX therapy was also superior to CIT in reducing REAI, mRSS and in saving lung function.
CONCLUSION CONCLUSIONS
AHSCT is more effective than both RTX and CIT in prolonging survival and inducing prolonged remission in patients with rapidly progressive dcSSc.

Identifiants

pubmed: 39444017
doi: 10.1186/s13075-024-03408-4
pii: 10.1186/s13075-024-03408-4
doi:

Substances chimiques

Rituximab 4F4X42SYQ6
Immunosuppressive Agents 0

Types de publication

Journal Article Comparative Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

182

Informations de copyright

© 2024. The Author(s).

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Auteurs

Nicoletta Del Papa (N)

Scleroderma Clinic, UOC Clinica Reumatologica, ASST Pini-CTO, Milano, Italy. nicoletta.delpapa@asst-pini-cto.it.

Silvia Cavalli (S)

Scleroderma Clinic, UOC Clinica Reumatologica, ASST Pini-CTO, Milano, Italy.
Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milano, Italy.

Andrea Rindone (A)

Scleroderma Clinic, UOC Clinica Reumatologica, ASST Pini-CTO, Milano, Italy.
Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milano, Italy.

Francesco Onida (F)

Department of Oncology and Onco-Hematology, Università degli Studi di Milano, Milano, Italy.
Ospedale Fatebenefratelli e Oftalmico, Oncoematologia, Milano, Italy.

Giorgia Saporiti (G)

Hematology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milano, Italy.

Antonina Minniti (A)

Scleroderma Clinic, UOC Clinica Reumatologica, ASST Pini-CTO, Milano, Italy.
Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milano, Italy.

Maria Rosa Pellico (MR)

Scleroderma Clinic, UOC Clinica Reumatologica, ASST Pini-CTO, Milano, Italy.
Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milano, Italy.

Claudia Iannone (C)

Scleroderma Clinic, UOC Clinica Reumatologica, ASST Pini-CTO, Milano, Italy.
Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milano, Italy.

Giorgia Trignani (G)

Scleroderma Clinic, UOC Clinica Reumatologica, ASST Pini-CTO, Milano, Italy.
Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milano, Italy.

Nicoletta D'Angelo (N)

Scleroderma Clinic, UOC Clinica Reumatologica, ASST Pini-CTO, Milano, Italy.
Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milano, Italy.

Manuel Sette (M)

Scleroderma Clinic, UOC Clinica Reumatologica, ASST Pini-CTO, Milano, Italy.
Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milano, Italy.

Raffaella Greco (R)

Unit of Hematology and Bone Marrow Transplantation, IRCCS San Raffaele Hospital, Vita- Salute San Raffaele University, Milano, Italy.

Claudio Vitali (C)

Rheumatology Outpatient Clinic, Mater Domini Humanitas Hospital, Castellanza, Italy.

Roberto Caporali (R)

Scleroderma Clinic, UOC Clinica Reumatologica, ASST Pini-CTO, Milano, Italy.
Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milano, Italy.

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