Sustained Remission Without Corticosteroids among Patients with Pemphigus Who Had Rituximab as First-Line Therapy: Follow-Up of the Ritux 3 Trial

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Tedbirt, Billal | Maho-Vaillant, Maud | Mignard, Claire | Golinski, Marie Laure | Calbo, Sébastien | Joly, Pascal | Hébert, Vivien | Houivet, Estelle | Prost-Squarcioni, Catherine | Caux, Frédéric | Alexandre, Marina | Musette, Philippe | Labeille, Bruno | Picard-Dahan, Catherine | Chaby, Guillaume | Richard, Marie Aleth | Tancrede-Bohin, Emmanuelle | Duvert-Lehembre, Sophie | Delaporte, Emmanuel | Bernard, Philippe | Ingen-Housz-Oro, Saskia | Vabres, Pierre | Quereux, Gaëlle | Dupuy, Alain | Debarbieux, Sébastien | Avenel-Audran, Martine | D Incan, Michel | Bédane, Christophe | Bénéton, Nathalie | Jullien, Denis | Dupin, Nicolas | Misery, Laurent | Machet, Laurent | Beylot-Barry, Marie | Dereure, Olivier | Sassolas, Bruno | Benichou, Jacques

Edité par CCSD ; American Medical Association -

International audience. © 2024 American Medical Association. All rights reserved.Importance: The Ritux 3 trial demonstrated the short-term efficacy and safety of first-line treatment with rituximab compared with a standard corticosteroid regimen in pemphigus. No data on the long-term follow-up of patients who received rituximab as first line are available. Objective: To assess the long-term efficacy and safety of the Ritux 3 treatment regimen. Design, Setting, and Participants: This 7-year follow-up study of the Ritux 3 trial included patients with pemphigus from 25 dermatology departments in France from January 1, 2010, to December 31, 2015. Exposure: Patients were initially randomized in the rituximab plus prednisone group or prednisone-alone group. Main outcomes and measures: The primary outcome was the 5- and 7-year disease-free survival (DFS) without corticosteroids, assessed by Kaplan-Meier curves. Secondary outcomes were occurrence of relapse, occurrence of severe adverse events (SAEs), and evolution of antidesmoglein (Dsg) antibody enzyme-linked immunosorbent assay values to predict long-term relapse. Results: Of the 90 patients in the Ritux 3 trial, 83 were evaluated at the end of follow-up study visit (44 in the rituximab plus prednisone group; 39 in the prednisone-alone group) with a median (IQR) follow-up of 87.3 (79.1-97.5) months. Forty-three patients (93%) from the rituximab plus prednisone and 17 patients (39%) from the prednisone-alone group had achieved complete remission without corticosteroids at any time during the follow-up. Patients from the rituximab group had much longer 5- and 7-year DFS without corticosteroids than patients from the prednisone-alone group (76.7% and 72.1% vs 35.3% and 35.3%, respectively; P <.001), and had about half the relapses (42.2% vs 83.7%; P <.001). Patients who received rituximab as second-line treatment had shorter DFS than patients treated as first line (P =.007). Fewer SAEs were reported in the rituximab plus prednisone group compared with the prednisone-alone group, 31 vs 58 respectively, corresponding to 0.67 and 1.32 SAEs per patient, respectively (P =.003). The combination of anti-Dsg1 values of 20 or more IU/mL and/or anti-Dsg3 values of 48 or more IU/mL yielded 0.83 positive predictive value and 0.94 negative predictive value to predict long-term relapse. Conclusions and Relevance: In this secondary analysis of the Ritux 3 trail, first-line treatment of patients with pemphigus with the Ritux 3 regimen was associated with long-term sustained complete remission without corticosteroid therapy without any additional maintenance infusion of rituximab.

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