Clinical and immunological features of patients with cancer-associated systemic sclerosis: An observational study.


Journal

Joint bone spine
ISSN: 1778-7254
Titre abrégé: Joint Bone Spine
Pays: France
ID NLM: 100938016

Informations de publication

Date de publication:
05 2023
Historique:
received: 21 07 2022
revised: 14 01 2023
accepted: 15 02 2023
medline: 12 5 2023
pubmed: 27 2 2023
entrez: 26 2 2023
Statut: ppublish

Résumé

Clinical and immunological features of patients with cancer-associated systemic sclerosis: an observational study. Several studies have reported an increased incidence of cancer in patients with systemic sclerosis (SSc). The presence of RNA polymerase III antibodies (anti-RNA Pol 3) associates with an increased risk of cancer, but other risk factors need yet to be identified. We aimed to assess clinical and immunological predictive factors of cancer-associated SSc to guide clinicians when setting up selective cancer screening. We conducted a monocentric, retrospective, observational study of SSc patients with and without associated malignancy. Clinical, laboratory and imaging data were collected, as well as SSc treatment. Subgroup analyses were performed according to the type of cancer and the time of diagnosis. Of 464 SSc patients, 74 (16%) had cancer, with breast (n=26) and lung cancer (n=13) being the most frequent. Diagnosis of cancer was made less than 3 years before or after SSc diagnosis for 23 patients (31%). In a multivariate analysis, anti-RNA Pol 3 and anti-SSA antibodies were significantly associated with an increased overall risk of cancer with an odds ratio (OR) of 4.12 (95% CI [1.6-10.7]; P<0.01) and 2.43 (95% CI [1.1-5.4]; P<0.05), respectively. Age at diagnosis of SSc and delay from the SSc diagnosis were also independent risk factors of cancer. Interstitial lung disease and anti-topoisomerase antibodies were associated with an increased risk of lung cancer and cancer occuring more than three years after SSc diagnosis. In addition to anti-RNA Pol 3 antibodies, anti-SSA antibodies associated with an increased risk of cancer in SSc patients. Interstitial lung disease was a risk factor specifically for lung cancer and cancers diagnosed more than 3 years after SSc diagnosis. For these patients, a systematic and regular cancer screening should be considered.

Identifiants

pubmed: 36842760
pii: S1297-319X(23)00034-9
doi: 10.1016/j.jbspin.2023.105555
pii:
doi:

Substances chimiques

Autoantibodies 0

Types de publication

Observational Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

105555

Informations de copyright

Copyright © 2023 Société française de rhumatologie. Published by Elsevier Masson SAS. All rights reserved.

Auteurs

Léa Lopez (L)

Department of Rheumatology, National Reference Center for Systemic Autoimmune Rare Diseases, Bordeaux University Hospital, Hôpital Pellegrin, place Amélie-Raba-Léon, Bordeaux, France.

Thomas Barnetche (T)

Department of Rheumatology, National Reference Center for Systemic Autoimmune Rare Diseases, Bordeaux University Hospital, Hôpital Pellegrin, place Amélie-Raba-Léon, Bordeaux, France.

Gael Galli (G)

Department of Internal Medicine, National Reference Center for Systemic Autoimmune Rare Diseases, Bordeaux University Hospital, Hôpital Haut Lévêque, Pessac, France.

Julien Seneschal (J)

Department of Dermatology, Bordeaux University Hospital, Hôpital Saint-André, Bordeaux, France.

Elodie Blanchard (E)

Department of Pneumology, Bordeaux University Hospital, Hôpital Haut Leveque, Pessac, France.

Emilie Shipley (E)

Department of Rheumatology, Hôpital de Dax, boulevard Yves-du-Manoir, Dax, France.

Jean-Luc Pellegrin (JL)

Department of Internal Medicine, National Reference Center for Systemic Autoimmune Rare Diseases, Bordeaux University Hospital, Hôpital Haut Lévêque, Pessac, France.

Estibaliz Lazaro (E)

Department of Internal Medicine, National Reference Center for Systemic Autoimmune Rare Diseases, Bordeaux University Hospital, Hôpital Haut Lévêque, Pessac, France.

Joel Constans (J)

Department of Vascular Medicine, Bordeaux University Hospital, Hôpital Saint-André, Bordeaux, France.

Pierre Duffau (P)

Department of Internal Medicine, Bordeaux University Hospital, Hôpital Saint-André, Bordeaux, France.

Thierry Schaeverbeke (T)

Department of Rheumatology, National Reference Center for Systemic Autoimmune Rare Diseases, Bordeaux University Hospital, Hôpital Pellegrin, place Amélie-Raba-Léon, Bordeaux, France; CNRS, Immunoconcept, UMR 5164, Bordeaux University, 146, rue Léo-Saignat, 33076 Bordeaux, France.

Christophe Richez (C)

Department of Rheumatology, National Reference Center for Systemic Autoimmune Rare Diseases, Bordeaux University Hospital, Hôpital Pellegrin, place Amélie-Raba-Léon, Bordeaux, France; CNRS, Immunoconcept, UMR 5164, Bordeaux University, 146, rue Léo-Saignat, 33076 Bordeaux, France.

Marie Kostine (M)

Department of Rheumatology, National Reference Center for Systemic Autoimmune Rare Diseases, Bordeaux University Hospital, Hôpital Pellegrin, place Amélie-Raba-Léon, Bordeaux, France; CNRS, Immunoconcept, UMR 5164, Bordeaux University, 146, rue Léo-Saignat, 33076 Bordeaux, France.

Marie-Elise Truchetet (ME)

Department of Rheumatology, National Reference Center for Systemic Autoimmune Rare Diseases, Bordeaux University Hospital, Hôpital Pellegrin, place Amélie-Raba-Léon, Bordeaux, France; CNRS, Immunoconcept, UMR 5164, Bordeaux University, 146, rue Léo-Saignat, 33076 Bordeaux, France. Electronic address: marie-elise.truchetet@chu-bordeaux.fr.

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Classifications MeSH