Giant-cell arteritis associated with ...
Type de document :
Article dans une revue scientifique: Lettre à l'éditeur
PMID :
URL permanente :
Titre :
Giant-cell arteritis associated with myelodysplastic syndrome: french multicenter case control study and literature review
Auteur(s) :
Roupie, Anne Laure [Auteur]
CHU Saint-Antoine [AP-HP]
De Boysson, Hubert [Auteur]
CHU Caen
Thietart, Sara [Auteur]
CHU Saint-Antoine [AP-HP]
Carrat, Fabrice [Auteur]
Institut Pierre Louis d'Epidémiologie et de Santé Publique [iPLESP]
Seguier, Julie [Auteur]
CHU Marseille
Terriou, Louis [Auteur]
Lille Inflammation Research International Center - U 995 [LIRIC]
Versini, Mathilde [Auteur]
Centre Hospitalier Universitaire de Nice [CHU Nice]
Queyrel, Viviane [Auteur]
Centre Hospitalier Universitaire de Nice [CHU Nice]
Groh, Matthieu [Auteur]
Hôpital Foch [Suresnes]
Benhamou, Ygal [Auteur]
CHU Rouen
Maurier, Francois [Auteur]
Decaux, Olivier [Auteur]
Centre Hospitalier Universitaire de Rennes [CHU Rennes] = Rennes University Hospital [Pontchaillou]
D'Aveni, Maud [Auteur]
Service d'Hématologie [CHRU Nancy]
Rossignol, Julien [Auteur]
Institut Gustave Roussy [IGR]
Galland, Joris [Auteur]
Solary, Eric [Auteur]
Institut Gustave Roussy [IGR]
Willems, Lise [Auteur]
Hôpital Cochin [AP-HP]
Schleinitz, Nicolas [Auteur]
CHU Marseille
Ades, Lionel [Auteur]
Hopital Saint-Louis [AP-HP] [AP-HP]
Dellal, Azeddine [Auteur]
Groupe Hospitalier Intercommunal Le Raincy-Montfermeil
Samson, Maxime [Auteur]
CHU Dijon
Aouba, Achille [Auteur]
CHU Caen
Fenaux, Pierre [Auteur]
Hopital Saint-Louis [AP-HP] [AP-HP]
Fain, Olivier [Auteur]
CHU Saint-Antoine [AP-HP]
Mekinian, Arsene [Auteur]
CHU Saint-Antoine [AP-HP]
CHU Saint-Antoine [AP-HP]
De Boysson, Hubert [Auteur]
CHU Caen
Thietart, Sara [Auteur]
CHU Saint-Antoine [AP-HP]
Carrat, Fabrice [Auteur]
Institut Pierre Louis d'Epidémiologie et de Santé Publique [iPLESP]
Seguier, Julie [Auteur]
CHU Marseille
Terriou, Louis [Auteur]
Lille Inflammation Research International Center - U 995 [LIRIC]
Versini, Mathilde [Auteur]
Centre Hospitalier Universitaire de Nice [CHU Nice]
Queyrel, Viviane [Auteur]
Centre Hospitalier Universitaire de Nice [CHU Nice]
Groh, Matthieu [Auteur]
Hôpital Foch [Suresnes]
Benhamou, Ygal [Auteur]
CHU Rouen
Maurier, Francois [Auteur]
Decaux, Olivier [Auteur]
Centre Hospitalier Universitaire de Rennes [CHU Rennes] = Rennes University Hospital [Pontchaillou]
D'Aveni, Maud [Auteur]
Service d'Hématologie [CHRU Nancy]
Rossignol, Julien [Auteur]
Institut Gustave Roussy [IGR]
Galland, Joris [Auteur]
Solary, Eric [Auteur]
Institut Gustave Roussy [IGR]
Willems, Lise [Auteur]
Hôpital Cochin [AP-HP]
Schleinitz, Nicolas [Auteur]
CHU Marseille
Ades, Lionel [Auteur]
Hopital Saint-Louis [AP-HP] [AP-HP]
Dellal, Azeddine [Auteur]
Groupe Hospitalier Intercommunal Le Raincy-Montfermeil
Samson, Maxime [Auteur]
CHU Dijon
Aouba, Achille [Auteur]
CHU Caen
Fenaux, Pierre [Auteur]
Hopital Saint-Louis [AP-HP] [AP-HP]
Fain, Olivier [Auteur]
CHU Saint-Antoine [AP-HP]
Mekinian, Arsene [Auteur]
CHU Saint-Antoine [AP-HP]
Titre de la revue :
Autoimmunity Reviews
Nom court de la revue :
Autoimmun Rev
Numéro :
19
Date de publication :
2020-02
ISSN :
1873-0183
Mot(s)-clé(s) en anglais :
Myelodysplastic syndrome
Giant cell arteritis
Outcome
Giant cell arteritis
Outcome
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
BACKGROUND: Myelodysplastic syndromes (MDS) and MDS/myeloproliferative neoplasms (MDS/MPN) can be associated with giant cell arteritis (GCA). In this nationwide study by the "French Network of dysimmune disorders associated ...
Lire la suite >BACKGROUND: Myelodysplastic syndromes (MDS) and MDS/myeloproliferative neoplasms (MDS/MPN) can be associated with giant cell arteritis (GCA). In this nationwide study by the "French Network of dysimmune disorders associated with hemopathies" (MINHEMON) the objective was to evaluate characteristics, treatment and outcome of GCA MDS-MDS/MPN. METHODS: Retrospective analysis of patients that presented a MDS or MDS/MPN associated with GCA. Treatment efficiency, relapse-free and overall survival of GCA MDS-MDS/MPN were compared to GCA alone. RESULTS: Twenty-one patients with GCA MDS-MDS/MPN were included with median age 76 [42-92], M/F ratio 2.5, 8 MDS with multilineage dysplasia (38%), 4 chronic myelomonocytic leukemia (19%), at low or intermediate risk according to IPPS and IPSS-R. The prevalence of headaches, jaw claudication and anterior ischemic optic neuropathy was significantly lower in patients with GCA MDS-MDS/MPN compared to idiopathic GCA (14.3%, 0% and 0% versus 30%, 25%, and 25%, respectively; p < .05). Other clinical and histology findings were similar. All GCA patients received steroid therapy as first-line treatment. Complete or partial response was observed in 14 GCA MDS-MDS/MPN patients (66.7%), of whom 6 (28.6%) received combined immunosuppressive therapies (versus 10% of idiopathic GCA; p = .07). Relapse incidence was similar in the two groups. Steroid dependence was more frequent among GCA MDS-MDS/MPN patients (12 (57%) versus 18 (22.5%); p < .05). Relapse-free and steroid-free survivals were significantly decreased in GCA MDS-MDS/MPN patients (log rank 0.002 and 0.049 respectively), but not overall survival. CONCLUSIONS: Characteristics of GCA MDS-MDS/MPN seem different than idiopathic GCA, with a distinct clinical phenotype and poorer outcome with a higher risk of steroid dependence and relapse.Lire moins >
Lire la suite >BACKGROUND: Myelodysplastic syndromes (MDS) and MDS/myeloproliferative neoplasms (MDS/MPN) can be associated with giant cell arteritis (GCA). In this nationwide study by the "French Network of dysimmune disorders associated with hemopathies" (MINHEMON) the objective was to evaluate characteristics, treatment and outcome of GCA MDS-MDS/MPN. METHODS: Retrospective analysis of patients that presented a MDS or MDS/MPN associated with GCA. Treatment efficiency, relapse-free and overall survival of GCA MDS-MDS/MPN were compared to GCA alone. RESULTS: Twenty-one patients with GCA MDS-MDS/MPN were included with median age 76 [42-92], M/F ratio 2.5, 8 MDS with multilineage dysplasia (38%), 4 chronic myelomonocytic leukemia (19%), at low or intermediate risk according to IPPS and IPSS-R. The prevalence of headaches, jaw claudication and anterior ischemic optic neuropathy was significantly lower in patients with GCA MDS-MDS/MPN compared to idiopathic GCA (14.3%, 0% and 0% versus 30%, 25%, and 25%, respectively; p < .05). Other clinical and histology findings were similar. All GCA patients received steroid therapy as first-line treatment. Complete or partial response was observed in 14 GCA MDS-MDS/MPN patients (66.7%), of whom 6 (28.6%) received combined immunosuppressive therapies (versus 10% of idiopathic GCA; p = .07). Relapse incidence was similar in the two groups. Steroid dependence was more frequent among GCA MDS-MDS/MPN patients (12 (57%) versus 18 (22.5%); p < .05). Relapse-free and steroid-free survivals were significantly decreased in GCA MDS-MDS/MPN patients (log rank 0.002 and 0.049 respectively), but not overall survival. CONCLUSIONS: Characteristics of GCA MDS-MDS/MPN seem different than idiopathic GCA, with a distinct clinical phenotype and poorer outcome with a higher risk of steroid dependence and relapse.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
CHU Lille
Inserm
Université de Lille
Inserm
Université de Lille
Date de dépôt :
2024-01-30T10:28:17Z
2024-04-03T16:48:27Z
2024-04-03T16:48:27Z