Teclistamab in relapsed or refractory AL amyloidosis, a multinational retrospective case series

Author:

Forgeard Nathalie1,ELESSA Dikelele1ORCID,Carpinteiro Alexander2ORCID,Belhadj Karim3ORCID,Minnema Monique C.4ORCID,Roussel Murielle5ORCID,Huart Antoine6,Javaugue Vincent7,Pascal Laurent8ORCID,Royer Bruno9,Talbot Alexis1,Gounot Romain10,Hegenbart Ute11ORCID,Schonland Stefan12ORCID,Karlin Lionel13,Harel Stephanie14,Kastritis Efstathios15ORCID,Bridoux Frank7,Jaccard Arnaud16ORCID,Arnulf Bertrand1

Affiliation:

1. Université Paris Cité, France

2. University Hospital Essen, Essen, Germany

3. Hopital Henri Mondor, Creteil, France

4. UMC Utrecht, Utrecht, Netherlands

5. University Hospital Limoges

6. University Hospital of Toulouse, Toulouse, France

7. CHU Poitiers, POITIERS, France

8. GHICL, Lille, France

9. Hopital Saint Louis, APHP, paris, France

10. Hôpital Henri Mondor, Créteil, France

11. University Hospital, Heidelberg, Germany

12. University Hospital Heidelberg, Heidelberg, Germany

13. Hôpital Lyon Sud, Pierre-benite, France

14. APHP Hôpital Saint Louis, Paris, France

15. Department of Clinical Therapeutics, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece

16. CHU Limoges, Limoges, France

Abstract

Teclistamab shows promising results in R/R AL amyloidosis, with VGPR or better in 88% of patients and involved FLC < 10 mg/L in 76%. We observed a 35% rate of severe infections and no cardiac or kidney related events.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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