Prevalence of autoimmune diseases in thymic epithelial tumors (TET) insights from RYTHMIC.

Author:

Benitez Jose Carlos1,Boucher Marie Eve2,Dansin Eric3,Kerjouan Mallorie4,Mazieres Julien5,Pichon Eric6,Thillays Francois7,Falcoz Pierre-Emmanuel8,Roch Benoit9,Oulkhouir Youssef10,Fabien Calcagno11,Thiberville Luc12,Clément Duchene Christelle13,Morin Franck14,Missy Pascale14,Thomas Pascal Alexandre15,Maury Jean-Michel16,Molina Thierry17,Girard Nicolas16,Besse Benjamin18

Affiliation:

1. Gustave Roussy, Villejuif, Paris, YT, France;

2. Medical Oncology Department, Gustave Roussy, Villejuif, France;

3. Centre Oscar Lambret, Lille, France;

4. CHU Rennes, Rennes, France;

5. IUCT, CHU de Toulouse, Toulouse, France;

6. Centre Hospitalier Universitaire Tours, Tours, France;

7. ICO René Gauducheau, Pays-De-La-Loire, France;

8. Centre Hospitalier Universitaire de Strasbourg, Strasbourg, France;

9. Centre Hospitalier Universitaire de Montpellier, Montpellier, France;

10. Centre Hospitalier Universitaire de Caen, Caen, France;

11. IRFC-CHRU Besançon, Besançon, France;

12. Centre Hospitalier Unversitaire Rouen, Rouen, France;

13. Institut de Cancérologie de Lorraine, Nancy, France;

14. Intergroupe Francophone de Cancérologie Thoracique, Paris, France;

15. Centre Hospitalier Universitaire Marseille, Marseille, France;

16. Institut Curie, Paris, France;

17. APHP, Paris, France;

18. Gustave Roussy Université Paris Sud, Villejuif, France;

Abstract

9073 Background: TET are associated with autoimmune disorders (AID) in up to 30% of patients (pts). However, there have been wide variations in the reported prevalence of AID in TET pts in small single-center series. RYTHMIC (Réseau tumeurs THYMiques et Cancer) is a French network mandated to systematically discuss every case of TET. We aimed to describe the prevalence of AID in a large French population. Methods: RYTHMIC database, hosted by IFCT (Intergroupe Francophone de Cancérologie Thoracique), prospectively includes all consecutive pts with a diagnosis of TET discussed in French national or regional tumor boards. We analyzed epidemiologic, clinical and pathological characteristics of pts with TET’s related AID. Results: From January 2012 to December 2019, 2909 pts were included in the database. The mean age at diagnosis of TET was 54 and 52% were male. In the overall population, Masaoka Koga stages were well balanced with 12.6% (n = 187) stage I, 8.8% (n = 131) stage IIa, 8.4% (n = 124) stage IIb, 11.1% (n = 164) stage III and 8.5% (n = 125) stage IV. There were 364 (12.5%) events of AID in 302 pts. 62 pts (17%) had more than 1 AID. Among the events, 236 were myasthenia gravis (MG) (64.8%), 19 Hypo-gammaglobulinemia syndrome (5.2%), 15 pure red cell aplasia (4.1%), 18 thyroiditis (4.9%) and 16 systemic erythematous lupus (4.4%). Diagnosis of AID was mostly done at tumor diagnosis (n = 239, 65.7%) but some patient had AID diagnosed before diagnosis (n = 67, 18.4%) or during follow up (n = 32, 8.8%). Among pts presenting AID, B2 was the most common subtype (n = 133, 36.5%). The incidence of AID per subtype was as follow: A (n = 10/81, 12.3%), AB (n = 48/225, 21.3%), B1 (n = 35/130, 26.9%), B2 (n = 133/295, 45.0%), B3 (n = 46/113, 40.7%), thymic carcinoma (n = 16/275, 5.8%). Conclusions: The prevalence of AID in pts with TET was 12.5%, > 40% in B2 and B3 subtypes. Diagnosis of AID can be delayed compared to the diagnosis of TET. Immunotherapy indication should be carefully assessed in pts with TET other than thymic carcinoma.

Funder

None

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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