Effectiveness of two different doses of rituximab for the treatment of rheumatoid arthritis in an international cohort : data from the CERERRA collaboration

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http://hdl.handle.net/10138/164978

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Chatzidionysiou , K , Lie , E , Nasonov , E , Lukina , G , Hetland , M L , Tarp , U , Ancuta , I , Pavelka , K , Nordstrom , D C , Gabay , C , Canhao , H , Tomsic , M , van Riel , P L C M , Gomez-Reino , J , Kvien , T K , van Vollenhoven , R F & Rheumatic Dis Portuguese Register 2016 , ' Effectiveness of two different doses of rituximab for the treatment of rheumatoid arthritis in an international cohort : data from the CERERRA collaboration ' , Arthritis research & therapy , vol. 18 , 50 . https://doi.org/10.1186/s13075-016-0951-z

Julkaisun nimi: Effectiveness of two different doses of rituximab for the treatment of rheumatoid arthritis in an international cohort : data from the CERERRA collaboration
Tekijä: Chatzidionysiou, Katerina; Lie, Elisabeth; Nasonov, Evgeny; Lukina, Galina; Hetland, Merete Lund; Tarp, Ulrik; Ancuta, Ioan; Pavelka, Karel; Nordstrom, Dan C.; Gabay, Cem; Canhao, Helene; Tomsic, Matija; van Riel, Piet L. C. M.; Gomez-Reino, Juan; Kvien, Tore K.; van Vollenhoven, Ronald F.; Rheumatic Dis Portuguese Register
Tekijän organisaatio: Clinicum
Department of Medicine
Päiväys: 2016-02-16
Kieli: eng
Sivumäärä: 6
Kuuluu julkaisusarjaan: Arthritis research & therapy
ISSN: 1478-6354
DOI-tunniste: https://doi.org/10.1186/s13075-016-0951-z
URI: http://hdl.handle.net/10138/164978
Tiivistelmä: Background: The approved dose of rituximab (RTX) in rheumatoid arthritis is 1000 mg x 2, but some data have suggested similar clinical efficacy with 500 mg x 2. The purpose of this study was to compare the effectiveness of the regular and low doses given as first treatment course. Methods: Twelve European registries participating in the CERERRA collaboration (The European Collaborative Registries for the Evaluation of Rituximab in Rheumatoid Arthritis) submitted anonymized datasets with demographic, efficacy and treatment data for patients who had started RTX. Treatment effectiveness was assessed by DAS28 reductions and EULAR responses after 6 months. Results: Data on RTX dose were available for 2,873 patients, of whom 2,625 (91.4 %) and 248 (8.6 %) received 1000 mg x 2 and 500 mg x 2, respectively. Patients treated with 500 mg x 2 were significantly older, had longer disease duration, higher number of prior DMARDs, but lower number of prior biologics and lower baseline DAS28 than those treated with 1000 mg x 2. Fewer patients in the low-dose group received concomitant DMARDs but more frequently received concomitant corticosteroids. Both doses led to significant clinical improvements at 6 months. DAS28 reductions at 6 months were comparable in the 2 dose regimens [mean DeltaDAS28 +/- SD -2.0 +/- 1.3 (high dose) vs. -1.7 +/- 1.4 (low dose), p = 0.23 adjusted for baseline differences]. Similar percentages of patients achieved EULAR good response in the two dose groups, 18.4 % vs. 17.3 %, respectively (p = 0.36). Conclusions: In this large observational cohort initial treatment with RTX at 500 mg x 2 and 1000 mg x 2 led to comparable clinical outcomes at 6 months.
Avainsanat: Rituximab
Rheumatoid arthritis
Observational
MONOCLONAL-ANTIBODY
PLUS METHOTREXATE
CONTROLLED-TRIAL
JOINT DAMAGE
DOUBLE-BLIND
EFFICACY
SAFETY
DEPLETION
THERAPY
INHIBITION
3121 General medicine, internal medicine and other clinical medicine
Vertaisarvioitu: Kyllä
Pääsyrajoitteet: openAccess
Rinnakkaistallennettu versio: publishedVersion


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