Use of thrombopoietin receptor agonists for immune thrombocytopenia in pregnancy: results from a multicenter study

Author:

Michel Marc1,Ruggeri Marco2,Gonzalez-Lopez Tomas Jose3,Alkindi Salam4ORCID,Cheze Stéphane5,Ghanima Waleed67ORCID,Tvedt Tor Henrik Anderson8,Ebbo Mikael9,Terriou Louis10,Bussel James B.11,Godeau Bertrand1

Affiliation:

1. Department of Internal Medicine, National Reference Center for Immune Cytopenias, Henri Mondor University Hospital, Assistance Publique–Hôpitaux de Paris, Université Paris-Est Creteil, Créteil, France;

2. Department of Haematology, S. Bortolo Hospital, Vicenza, Italy;

3. Department of Hematology, Hospital Universitario de Burgos, Burgos, Spain;

4. Department of Haematology, Sultan Qaboos University, Muscat, Oman;

5. Institut d’Hématologie de Basse-Normandie, Centre Hospitalier Universitaire de Caen Normandie, Caen, France;

6. Department of Research, Østfold Hospital Trust, Sarpsborg, Norway;

7. Department of Hematology, Institute of Clinical Medicine, University of Oslo, Oslo, Norway;

8. Section for Hematology, Department of Medicine, Haukeland University Hospital, Bergen, Norway;

9. Department of Internal Medicine, La Timone University Hospital, Assistance Publique–Hôpitaux de Marseille, Aix Marseille Université, Marseille, France;

10. Immuno-Hematology, Hôpital Claude Huriez, Lille, France; and

11. Weill Cornell Medicine, New York, NY

Abstract

Abstract Management of immune thrombocytopenia (ITP) during pregnancy can be challenging because treatment choices are limited. Thrombopoietin receptor agonists (Tpo-RAs), which likely cross the placenta, are not recommended during pregnancy. To better assess the safety and efficacy of off-label use of Tpo-RAs during pregnancy, a multicenter observational and retrospective study was conducted. Results from 15 pregnant women with ITP (pregnancies, n = 17; neonates, n = 18) treated with either eltrombopag (n = 8) or romiplostim (n = 7) during pregnancy, including 2 patients with secondary ITP, were analyzed. Median time of Tpo-RA exposure during pregnancy was 4.4 weeks (range, 1-39 weeks); the indication for starting Tpo-RAs was preparation for delivery in 10 (58%) of 17 pregnancies, whereas 4 had chronic refractory symptomatic ITP and 3 were receiving eltrombopag when pregnancy started. Regarding safety, neither thromboembolic events among mothers nor Tpo-RA–related fetal or neonatal complications were observed, except for 1 case of neonatal thrombocytosis. Response to Tpo-RAs was achieved in 77% of cases, mostly in combination with concomitant ITP therapy (70% of responders). On the basis of these preliminary findings, temporary off-label use of Tpo-RAs for severe and/or refractory ITP during pregnancy seems safe for both mother and neonate and is likely to be helpful, especially before delivery.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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