Heamatological malignancies in giant cell arteritis: a French population-based study

Author:

Greigert Hélène123,Mounier Morgane456,Arnould Louis7,Creuzot-Garcher Catherine7,Ramon André8,Martin Laurent9,Tarris Georges9,Ponnelle Tibor10,Audia Sylvain13,Bonnotte Bernard13,Maynadie Marc45611,Samson Maxime13ORCID

Affiliation:

1. Department of Internal Medicine and Clinical Immunology

2. Department of Vascular Medicine, Dijon University Hospital

3. Université Bourgogne Franche-Comté, INSERM, EFS BFC, UMR 1098, RIGHT Interactions Greffon-Hôte-Tumeur/Ingénierie Cellulaire et Génique

4. Dijon-Bourgogne University Hospital, Registre des Hémopathies Malignes de Côte d’Or

5. Université Bourgogne Franche-Comté, INSERM, UMR 1231

6. LabEX LipSTIC, ANR-11-LABX-0021

7. Department of Ophthalmology

8. Department of Rheumatology

9. Department of Pathology, Dijon University Hospital

10. Cypath Pathology Center

11. Department of Biological Hematology, Dijon University Hospital, Dijon, France

Abstract

Abstract Objectives An increased risk of haematological malignancies (HM) has been reported in GCA patients. Our study aimed to investigate the incidence and the type of HM occurring in GCA. Methods All patients with GCA and HM living in Côte d’Or (France) were identified by crossing data from the RHEMCO (Registre des Hémopathies Malignes de Côte d’Or) and those having a positive temporal artery biopsy between 1 January 2001 and 31 December 2018. Results Among 276 biopsy-proven GCA patients, 14 HM were identified in 12 patients (4.3%). In comparison with the general population aged >50 y, the incidence of myeloid HM and myeloproliferative syndromes were increased in GCA patients [standardized incidence ratios (SIR) = 2.71 and 5.16, respectively], with a specific increase in men with GCA (SIR = 4.82 and 9.04, respectively) but not in women. In addition, the study of SIR depending on the chronology between GCA and HM diagnoses suggests that there was an increased risk of developing GCA in men but not in women, after a diagnosis of myeloid HM (SIR = 9.56), especially if it was a MPS (SIR = 17.56). Conclusions Our study shows a particular epidemiology of HM in GCA patients, which is characterized by an increased incidence of myeloid HM, especially MPS, in male GCA patients. The chronology of the diagnoses of GCA and HM raises the hypothesis that clonal hematopoiesis may be implicated in some cases of GCA.

Funder

Funded by French Institut National du Cancer

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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