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Rituximab is an effective treatment in patients with pemphigus vulgaris and demonstrates a steroid-sparing effect.


ABSTRACT: BACKGROUND:Corticosteroids (CS) with or without adjuvant immunosuppressant agents are standard treatment for pemphigus vulgaris (PV). The efficacy of adjuvant therapies in minimizing steroid-related adverse events (AEs) is unproven. OBJECTIVES:To utilize data collected in a French investigator-initiated, phase III, open-label, randomized controlled trial to demonstrate the efficacy and safety of rituximab and seek approval for its use in PV. METHODS:This was an independently conducted post hoc analysis of the moderate-to-severe PV subset enrolled in the Ritux 3 study. Patients were randomized to rituximab plus 0·5 or 1·0 mg kg-1 per day prednisone tapered over 3 or 6 months, or 1·0 or 1·5 mg kg-1 per day prednisone alone tapered over 12 or 18 months, respectively (according to disease severity). The primary end point was complete remission at month 24 without CS (CRoff) for ? 2 months, and 24-month efficacy and safety results were also reported. RESULTS:At month 24, 34 of 38 patients (90%) on rituximab plus prednisone achieved CRoff ? 2 months vs. 10 of 36 patients (28%) on prednisone alone. Median total cumulative prednisone dose was 5800 mg in the rituximab plus prednisone arm vs. 20 520 mg for prednisone alone. Eight of 36 patients (22%) who received prednisone alone withdrew from treatment owing to AEs; one rituximab-plus-prednisone patient withdrew due to pregnancy. Overall, 24 of 36 patients (67%) on prednisone alone experienced a grade 3/4 CS-related AE vs. 13 of 38 patients (34%) on rituximab plus prednisone. CONCLUSIONS:In patients with moderate-to-severe PV, rituximab plus short-term prednisone was more effective than prednisone alone. Patients treated with rituximab had less CS exposure and were less likely to experience severe or life-threatening CS-related AEs. What's already known about this topic? Pemphigus vulgaris (PV) is the most common type of pemphigus. Corticosteroids, a standard first-line treatment for PV, have significant side-effects. Although their effects are unproven, adjuvant corticosteroid-sparing agents are routinely used to minimize steroid exposure and corticosteroid-related side-effects. There is evidence that the anti-CD20 antibody rituximab is effective in the treatment of patients with severe recalcitrant pemphigus and in patients with newly diagnosed pemphigus. What does this study add? This study provides a more detailed analysis of patients with PV enrolled in an investigator-initiated trial. Rituximab plus prednisone had a steroid-sparing effect and more patients achieved complete remission off prednisone. Fewer patients experienced grade 3 or grade 4 steroid-related adverse events than those on prednisone alone. This collaboration between academia and industry, utilizing independent post hoc analyses, led to regulatory authority approvals of rituximab in moderate-to-severe PV.

SUBMITTER: Chen DM 

PROVIDER: S-EPMC7317434 | biostudies-literature | 2020 May

REPOSITORIES: biostudies-literature

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Rituximab is an effective treatment in patients with pemphigus vulgaris and demonstrates a steroid-sparing effect.

Chen D M DM   Odueyungbo A A   Csinady E E   Gearhart L L   Lehane P P   Cheu M M   Maho-Vaillant M M   Prost-Squarcioni C C   Hebert V V   Houivet E E   Calbo S S   Caillot F F   Golinski M L ML   Labeille B B   Picard-Dahan C C   Paul C C   Richard M A MA   Bouaziz J D JD   Duvert-Lehembre S S   Bernard P P   Caux F F   Alexandre M M   Ingen-Housz-Oro S S   Vabres P P   Delaporte E E   Quereux G G   Dupuy A A   Debarbieux S S   Avenel-Audran M M   D'Incan M M   Bedane C C   Bénéton N N   Jullien D D   Dupin N N   Misery L L   Machet L L   Beylot-Barry M M   Dereure O O   Sassolas B B   Benichou J J   Musette P P   Joly P P  

The British journal of dermatology 20191128 5


<h4>Background</h4>Corticosteroids (CS) with or without adjuvant immunosuppressant agents are standard treatment for pemphigus vulgaris (PV). The efficacy of adjuvant therapies in minimizing steroid-related adverse events (AEs) is unproven.<h4>Objectives</h4>To utilize data collected in a French investigator-initiated, phase III, open-label, randomized controlled trial to demonstrate the efficacy and safety of rituximab and seek approval for its use in PV.<h4>Methods</h4>This was an independentl  ...[more]

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