Evidence map›Paper›PMID 42264879›Full record

ArticleRMD open2026

Safety and effectiveness of tocilizumab in systemic sclerosis: a multicentre French-Italian study.

Giulia Buonsante, Giacomo De Luca, Elena Marazzi, Fabio Cacciapaglia, Maria Grazia Lazzaroni, Marco De Pinto, Devis Benfaremo, Valentina Longo, Carlo Iandoli, Giovanna Cuomo and 20 more

Abstract readMulticenter Study
In one paragraph

Article in RMD open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

30 authors.

Giulia BuonsanteIRCCS and INFLAGE San Raffaele Hospital, Vita-Salute San Raffaele University, Milan, Italy.
Giacomo De LucaUnit of Immunology, Rheumatology, Allergy, and Rare Diseases (UnIRAR), San Raffaele Hospital, Milan, Italy.
Elena MarazziSC Reumatologia, Università di Pavia, Pavia, Italy.
Fabio CacciapagliaRheumatology Unit, Department of Precision and Regenerative Medicine and Ionian Area, Università degli Studi di Bari Aldo Moro, Bari, Italy.ORCID http://orcid.org/0000-0001-7479-4462
Maria Grazia LazzaroniRheumatology and Clinical Immunology, ASST Spedali Civili di Brescia, Brescia, Italy.ORCID http://orcid.org/0000-0002-1860-6866
Marco De PintoRheumatology, University of Modena and Reggio Emilia, Modena, Italy.ORCID http://orcid.org/0000-0002-0947-8663
Devis BenfaremoScienze Cliniche e Molecolari, Università Politecnica delle Marche, Ancona, Italy.
Valentina LongoScleroderma Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Carlo IandoliDepartment of Precision Medicine, University of Campania Luigi Vanvitelli, Caserta, Italy.
Giovanna CuomoDepartment of Precision Medicine, University of Campania Luigi Vanvitelli, Caserta, Italy.
Anna CuberliUnit of Rheumatology, Universita degli Studi di Padova Scuola di Medicina e Chirurgia, Padua, Italy.
Elisabetta ZanattaDIMED, Universita degli Studi di Padova Dipartimento di Medicina, Padova, Italy.ORCID http://orcid.org/0000-0002-4845-5413
Alain LescoatInternal Medicine, CHU de Rennes, Rennes, France.ORCID http://orcid.org/0000-0003-2081-8558
Silvia Bellando-RandoneDepartment of Experimental and Clinical Medicine, University of Florence, Firenze, Italy.
Giorgia TrignaniGaetano Pini-CTO, Milan, Italy.
Serena GuiducciDepartment of Experimental and Clinical Medicine, University of Florence, Firenze, Italy.
Lorenzo BerettaFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Gianluca MoronciniScienze Cliniche e Molecolari, Università Politecnica delle Marche, Ancona, Italy.
Dilia GiuggioliUniversity of Modena and Reggio Emilia, Modena, Italy.
Paolo AiròRheumatology and Clinical Immunology, ASST Spedali Civili di Brescia, Brescia, Italy.
Florenzo IannoneRheumatology Unit, Department of Precision and Regenerative Medicine and Ionian Area, Università degli Studi di Bari Aldo Moro, Bari, Italy.ORCID http://orcid.org/0000-0003-0474-5344
Veronica CodulloSC Reumatologia, Università di Pavia, Pavia, Italy.
Silvia Laura BoselloRheumatology, Università Cattolica del Sacro Cuore Facoltà di Medicina e Chirurgia, Rome, Italy.
Nicoletta Del PapaScleroderma Clinic, Gaetano Pini-CTO, Milan, Italy.ORCID http://orcid.org/0000-0003-1549-8852
Marie-Elise TruchetetRhumatologie, CHU Bordeaux GH Pellegrin, Bordeaux, France.ORCID http://orcid.org/0000-0001-8045-0180
Jerome AvouacDepartment of Rheumatology, Université Paris Cité, Cochin Institute, Paris, France.ORCID http://orcid.org/0000-0002-2463-218X
Lorenzo DagnaUnit of Immunology, Rheumatology, Allergy, and Rare Diseases (UnIRAR), San Raffaele Hospital, Milan, Italy.ORCID http://orcid.org/0000-0002-7428-315X
Marco Matucci-CerinicIRCCS and INFLAGE San Raffaele Hospital, Vita-Salute San Raffaele University, Milan, Italy.ORCID http://orcid.org/0000-0002-9324-3161
Yannick AllanoreDepartment of Rheumatology, Université Paris Cité, Cochin Institute, Paris, France yannick.allanore@aphp.fr.
Corrado CampochiaroIRCCS and INFLAGE San Raffaele Hospital, Vita-Salute San Raffaele University, Milan, Italy.ORCID http://orcid.org/0000-0001-6806-3794

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTocilizumab (TCZ) has shown beneficial effects on interstitial lung disease (ILD) in systemic sclerosis (SSc). We aimed to assess the real-life safety and effectiveness of TCZ on several SSc-related domains using data from a French-Italian multicentre cohort.

methodsWe conducted a retrospective analysis of patients with SSc treated with TCZ across 15 referral centres. The following clinical data were collected at 12 months before TCZ initiation, at baseline and at 12 and 24 months of treatment: modified Rodnan skin score (mRSS), pulmonary function tests, Disease Activity Score in 28 joints using C reactive protein, digital ulcers and cardiac biomarkers. ILD progression was defined as a decline ≥5 in %predicted forced vital capacity (%pFVC) over 12±3 months.

results197 patients were included (88% female; median age 57 years; median disease duration 9 years); 67% were antitopoisomerase I positive. TCZ monotherapy was used in 29% of cases, methotrexate was the most frequent combined treatment (35%). In SSc-associated ILD, %pFVC declined significantly from -12 months to baseline (81% to 77%; p=0.003). On TCZ introduction, %pFVC stabilised and the proportion of progressors declined from 43% to 24% (p=0.015). Among diffuse cutaneous patients, mRSS decreased significantly at 12 and 24 months. Digital ulcers, arthritis activity and cardiac biomarkers also improved. Infections were the most frequent adverse events (22.8%). TCZ was discontinued in 32% of patients, mainly for inefficacy. Pulmonary arterial hypertension and older age predicted TCZ failure, whereas elevated CRP predicted better response.

conclusionsIn this large real-life cohort, TCZ was safe and associated with consistent benefits across different domains, supporting its role as a potential disease-modifying treatment in selected patients with SSc.

Indexed as

Antibodies, Monoclonal, HumanizedScleroderma, SystemicAdultAgedBiomarkersDisease ProgressionFemaleFranceHumansItalyLung Diseases, InterstitialMaleMiddle AgedRespiratory Function TestsRetrospective StudiesTreatment OutcomeAntibodies, Monoclonal, HumanizedBiomarkerstocilizumabDMARDLung Diseases, InterstitialScleroderma, SystemicSystemic Sclerosis

Identifiers

PMID42264879
PMCPMC13264945

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.