Efficacy and safety of two rituximab biosimilars for treating immune thrombocytopenia: a reference-product matched study.

Fiche publication

Date publication

décembre 2023

Journal

Platelets

Auteurs

Membres identifiés du Cancéropôle Est :
Pr BONNOTTE Bernard

Tous les auteurs :
Mageau A, Bonnotte B, Ebbo M, Dossier A, Galicier L, Souchaud-Debouverie O, Orvain C, Gerfaud-Valentin M, Gobert D, Riviere E, Audia S, Mahevas M, Michel M, Viallard JF, Godeau B

Lien Pubmed

https://www.ncbi.nlm.nih.gov/pubmed/37128870

Résumé

The emergence of rituximab biosimilars offers the prospect of significant savings to the healthcare system. However, these drugs have never been evaluated for treating immune thrombocytopenia (ITP). This was an observational, matched study. We included adults who received a rituximab biosimilar for ITP. Each rituximab-naïve biosimilar patient was matched with two controls from the historic ITP-ritux registry. For non-naïve patients, we compared the response to the biosimilar with that observed with the reference product. Response status was defined according to international criteria. We included 107 patients; 55 receiving Rixathon™ and 52 Truxima™. Three months after the first infusion of rituximab biosimilars, the overall response rate was 47/74 (63.5%) versus 76/142 (53.5%) for the matched controls receiving the reference product ( = .13). The 3-month overall response rate was 76.5% for Rixathon™ versus 51.5% for the matched control group ( = .01) and 21/40 (52.5%) for Truxima™ versus 41/74 (55.4%) for the matched controls ( = .81). For non-naïve patients, the response pattern was similar to that observed previously with the reference product. Safety was analogous to that observed with the reference product. Rituximab biosimilars seemed safe and effective for ITP treatment.