Related Experiment Video
Updated: Jan 2, 2026

07:25
In Vitro Methods for Comparing Target Binding and CDC Induction Between Therapeutic Antibodies: Applications in Biosimilarity Analysis
Published on: May 4, 2017
18.2K
The prompt use of rituximab could decrease adverse effects in patient with pemphigus vulgaris: A preliminary
Paolo G Arduino1, Roberto Broccoletti1, Mario Carbone1
1Department of Surgical Sciences, CIR-Dental School, University of Turin, Italy.
Summary
Early use of rituximab (RTX) in pemphigus vulgaris (PV) significantly reduces adverse effects compared to standard corticosteroid therapy. This approach offers a safer treatment option, minimizing side effects for patients with oral PV.
Area of Science:
- Dermatology
- Immunology
Background:
- Systemic corticosteroids are standard for pemphigus vulgaris (PV) but cause frequent adverse effects.
- Rituximab (RTX) is typically a second-line treatment for PV after other therapies fail.
- Early RTX administration may mitigate treatment-related adverse events.
Purpose of the Study:
- To evaluate the efficacy and safety of early rituximab (RTX) as a first-line treatment for pemphigus vulgaris (PV).
- To compare adverse effects in patients receiving early RTX versus traditional corticosteroid therapy.
Main Methods:
- A single-center study involving patients with predominantly oral PV.
- Treatment consisted of systemic corticosteroids and prompt intravenous RTX (1000 mg, two weeks apart).
- Clinical response and adverse effects were monitored for 24 months and compared to a historical control group.
Main Results:
- The study included 11 patients, compared to 98 in the control group.
- Complete clinical remission averaged 3.2 months; all study patients achieved remission without medication.
- Early RTX use reduced the likelihood of adverse effects by 94% (P = .001), with only 27.3% experiencing side effects.
Conclusions:
- This study presents the first report on RTX as a first-line therapy for oral PV.
- The proposed RTX regimen significantly minimizes adverse effects compared to corticosteroid-centered treatments.
- Further validation through multi-center randomized controlled trials is warranted.

