Combining thrombopoietin receptor agonists with immunosuppressive drugs in adult patients with multirefractory immune thrombocytopenia, an update on the French experience

Author:

Crickx Etienne12ORCID,Ebbo Mikael3,Rivière Etienne45,Souchaud‐Debouverie Odile6,Terriou Louis7,Audia Sylvain8,Ruivard Marc910,Asli Bouchra11,Marolleau Jean‐Pierre12,Méaux‐Ruault Nadine13,Gerfaud‐Valentin Mathieu14,Audeguy Philippe15,Hamidou Mohamed16,Corm Selim17,Delbrel Xavier18,Fontan Jean19,Lebon Delphine12,Mausservey Christelle20,Moulis Guillaume2122,Limal Nicolas1,Michel Marc1,Godeau Bertrand1,Mahévas Matthieu12324ORCID

Affiliation:

1. Internal Medicine Department, Centre national de référence des cytopénies auto‐immunes de l'adulte, Hôpital Henri Mondor, Fédération Hospitalo‐Universitaire TRUE InnovaTive theRapy for immUne disordErs, Assistance Publique Hôpitaux de Paris (AP‐HP) Université Paris Est Créteil Créteil France

2. Laboratory of Immunogenetics of Pediatric Autoimmune Diseases, Imagine Institute Université Paris Cité, INSERM UMR U1163 Paris France

3. Internal Medicine Department Hôpital la Timone, Assistance Publique Hôpitaux de Marseille, Aix Marseille Université Marseille France

4. Internal Medicine and Infectious Diseases Unit, Haut‐Leveque Hospital University Hospital Centre of Bordeaux Pessac France

5. INSERM U1034 Bordeaux University Pessac Cedex France

6. Internal Medicine Department CHU de Poitiers Poitiers France

7. Internal Medicine and Clinical Immunology Department Centre de référence des maladies auto‐immunes systémiques rares du nord et nord‐ouest de France (CeRAINO), LIRIC INSERM U995, CHU LILLE Lille France

8. Internal Medicine and Clinical Immunology Department Centre de référence constitutif des cytopénies auto‐immunes, Hôpital François Mitterrand, Centre Hospitalier Universitaire (CHU) Dijon‐Bourgogne Dijon France

9. Internal Medicine Department Estaing University Hospital, CHU Clermont‐Ferrand Clermont‐Ferrand France

10. Université Clermont Auvergne, CHU Clermont‐Ferrand, CNRS, Institut Pascal Clermont‐Ferrand France

11. Internal Medicine Department Sauvegarde Clinic Lyon France

12. Clinical Hematology and Cellular Therapy Department, CHU Amiens‐Picardie EA4666 Equipe Hematim – CURS – UPJV Amiens France

13. Internal Medicine Department Centre Hospitalier Universitaire Jean‐Minjoz Besançon France

14. Internal Medicine Department Hôpital de la Croix‐Rousse, Hospices Civils de Lyon, Université Claude Bernard‐Lyon1 Lyon France

15. Internal Medicine Hôpital Privé Pasteur Évreux France

16. Internal Medicine Department CHU de Nantes Nantes France

17. Clinical Hematology Department Médipole de Savoie Challes‐les‐Eaux France

18. Internal Medicine Department Centre Hospitalier de Pau Pau France

19. Clinical Hematology Department CHU Besançon Besançon France

20. Internal Medicine Department Centre Hospitalier William‐Morey Chalon/Saône France

21. Internal Medicine Department CHU de Toulouse Toulouse France

22. CIC 1436, équipe PEPSS CHU de Toulouse Toulouse France

23. Institut Necker Enfants Malades (INEM), INSERM U1151/CNRS UMS 8253, ATIP‐Avenir Team AI2B Université de Paris Cité, Université Paris‐Est‐Créteil Créteil France

24. INSERM U955, équipe 2 Université Paris‐Est Créteil (UPEC) Créteil France

Abstract

SummaryCombining drugs could be an effective option for treating multirefractory ITP, that is, patients not responding to rituximab, thrombopoietin receptor agonists (TPO‐RA) and splenectomy. We conducted a retrospective, multicenter, observational study including multirefractory ITP patients who received a combination of a TPO‐RA and an immunosuppressive drug. We included 39 patients (67% women, median age 59 years [range 21–96]), with a median ITP duration of 57 months [3–393] and a median platelet count at initiation of 10 × 109/L [1–35]. The combination regimen was given for a median duration of 12 months [1–103] and included eltrombopag (51%) or romiplostim (49%), associated with mycophenolate mofetil (54%), azathioprine (36%), cyclophosphamide (5%), cyclosporin (3%) or everolimus (3%). Overall, 30 patients (77%) achieved at least a response (platelet count ≥30 × 109/L and at least doubling baseline during at least 3 months), including 24 complete responses (platelet count >100 × 109/L during at least 3 months) with a median time to response of 30 days [7–270] and a median duration of response of 15 months [4–63]. Severe adverse event related to ITP treatment was observed in 31%. In conclusion, this study confirms that some patients with multirefractory ITP can achieve long lasting response with this combination.

Publisher

Wiley

Subject

Hematology

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