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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Smith, Rona M. Jones, Rachel B. Guerry, Mary-Jane Laurino, Simona Catapano, Fausta Chaudhry, Afzal Smith, Kenneth G. C. Jayne, David R. W. |
| Description | Country affiliation: United kingdom Author Affiliation: Smith RM ( Addenbrooke's Hospital, Cambridge, UK. ho0919@catholic.ac.kr) |
| Abstract | OBJECTIVE: Rituximab is effective induction therapy in refractory or relapsing antineutrophil cytoplasmic antibody-associated vasculitis (AAV). However, further relapse is common, and maintenance strategies are required. The aim of this study was to reduce relapse rates using a fixed-interval rituximab re-treatment protocol. METHODS: Retrospective, standardized collection of data from sequential patients receiving rituximab for refractory or relapsing AAV at a single center was studied. Group A patients (n = 28) received rituximab induction therapy (4 infusions of 375 mg/m(2) or 2 infusions 1 gm) and further rituximab at the time of subsequent relapse. Group B patients (n = 45) received routine rituximab re-treatment for 2 years: 2 doses of 1 gm each for remission induction, then 1 gm every 6 months (total of 6 gm). Group C patients (n = 19) comprised patients in group A who subsequently relapsed and began routine re-treatment for 2 years. RESULTS: Response (complete/partial remission) occurred in 26 of the 28 patients (93%) in group A, 43 of the 45 patients (96%) in group B, and 18 of the 19 patients (95%) in group C. At 2 years, relapses had occurred in 19 of 26 patients (73%) in group A, 5 of 43 (12%) in group B (P < 0.001), and 2 of 18 (11%) in group C (P < 0.001). At the last followup (median of 44 months), relapses had occurred in 85% of those in group A (22 of 26), 26% of those in group B (11 of 43; P < 0.001), and 56% of those in group C (10 of 18; P = 0.001). Glucocorticoid dosages were decreased and immunosuppression therapy was withdrawn in the majority of patients. Routine rituximab re-treatment was well tolerated, and no new safety issues were identified. CONCLUSION: Two-year, fixed-interval rituximab re-treatment was associated with a reduction in relapse rates during the re-treatment period and a more prolonged period of remission during subsequent followup. In the absence of biomarkers that accurately predict relapse, routine rituximab re-treatment may be an effective strategy for remission maintenance in patients with refractory and relapsing AAV. |
| File Format | HTM / HTML |
| ISSN | 00043591 |
| e-ISSN | 15290131 |
| Journal | Arthritis & Rheumatism |
| Issue Number | 11 |
| Volume Number | 64 |
| Language | English |
| Publisher | Wiley-Blackwell |
| Publisher Date | 2012-11-01 |
| Publisher Place | United States |
| Access Restriction | Subscribed |
| Subject Keyword | Immunologic Factors Research Support, Non-u.s. Gov't Glucocorticoids Immunoglobulin G Anti-neutrophil Cytoplasmic Antibody-associated Vasculitis Secondary Prevention Antibodies, Monoclonal, Murine-derived Blood Antibodies, Antineutrophil Cytoplasmic Immunology Dose-response Relationship, Drug Retrospective Studies Drug Therapy, Combination Prednisolone Adverse Effects Drug Therapy Rituximab Administration & Dosage Remission Induction Adolescent Discipline Rheumatic Diseases |
| Content Type | Text |
| Resource Type | Article |
| Subject | Immunology and Allergy Immunology Pharmacology (medical) Rheumatology |
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