scholarly journals SAT0184 Therapeutic drug monitoring on rheumatoid arthritis patients with reduced doses of intravenous tocilizumab

Author(s):  
V Ruiz-Esquide ◽  
C Bastida ◽  
M Pascal ◽  
J Yagüe ◽  
D Soy ◽  
...  
2017 ◽  
Vol 39 (4) ◽  
pp. 364-369 ◽  
Author(s):  
Frédéric Medina ◽  
Chamaida Plasencia ◽  
Philippe Goupille ◽  
David Ternant ◽  
Alejandro Balsa ◽  
...  

2017 ◽  
Vol 83 (5) ◽  
pp. 962-975 ◽  
Author(s):  
Carla Bastida ◽  
Virginia Ruíz ◽  
Mariona Pascal ◽  
Jordi Yagüe ◽  
Raimon Sanmartí ◽  
...  

2016 ◽  
Vol 75 (9) ◽  
pp. 1693-1696 ◽  
Author(s):  
M Begoña Ruiz-Argüello ◽  
Ainara Maguregui ◽  
Ainhoa Ruiz del Agua ◽  
Dora Pascual-Salcedo ◽  
Ana Martínez-Feito ◽  
...  

ObjectivesThe aim of this study was to determine whether antibodies to infliximab (IFX) in Remicade-treated patients cross-react with the biosimilar CT-P13.Methods250 consecutive patients with rheumatic diseases under Remicade and 77 controls were retrospectively selected for the study. Anti-IFX antibodies at drug through levels were measured in parallel with three different bridging ELISA assays: Promonitor-ANTI-IFX kit, which uses Remicade to detect antibodies, and two more assays that use either Inflectra or Remsima with the same format. Correlation and association between each assay was studied.Results50.4% of patients were tested positive with Promonitor-ANTI-IFX. All were antibodies to IFX (ATI)-positive when either Inflectra or Remsima assays were used. In all comparisons positive and negative percentage agreements were 100%, and correlation coefficients were ≥0.995. No differences between rheumatoid arthritis and spondyloarthritis, or between concomitant immunosuppressives, were observed.ConclusionsAnti-IFX antibodies of Remicade-treated patients cross-react with either Inflectra or Remsima. Although additional epitopes may be present in the biosimilar, results suggest that epitopes influencing the immune response to IFX are also present in the biosimilar. Antibody-positive patients treated with Remicade should not be switched to the biosimilar, since antibodies will interact with the new drug and potentially lead to loss of response. This finding supports the utility for therapeutic drug monitoring before a switching strategy is considered.


2018 ◽  
Vol 30 (3) ◽  
pp. 266-275 ◽  
Author(s):  
Alfons A. den Broeder ◽  
Noortje van Herwaarden ◽  
Bart J.F. van den Bemt

2020 ◽  
Vol 14 (4) ◽  
pp. 60-64
Author(s):  
G. I. Gridneva ◽  
Yu. V. Muravyev ◽  
N. V. Baimeeva ◽  
V. S. Sygyrta ◽  
S. I. Glukhova ◽  
...  

Objective: to assess the time course of changes in the concentration of methotrexate (MTX) and its main metabolites in the red blood cells (RBC) and mononuclear cells (MNC) of patients with rheumatoid arthritis (RA), by taking into account individual characteristics (age, statin therapy, and smoking).Patients and methods. The investigation enrolled 33 MTX-treated patients (mean age 53.2±11.7 years) with RA, who underwent therapeutic drug monitoring to measure the RBC and MNC concentrations of free MTX and MTX polyglutamates (MTXPGs) with 2, 3, and 4 glutamate residues (MTXPG 2–4) in using tandem chromatomass spectrometry after 4, 12, and 24 weeks of therapy.Results and discussion. Following 12 weeks, the concentration of MTXPG4 in the MNC was higher in patients taking statins, while that of MTX and MTXPG2 in the RBC were significantly lower than in smokers. At 24 weeks, older patients were observed to have a higher MTX level and a lower MTXPG4 concentration in the RBC.Conclusion. After 24 weeks of therapy, the RBC concentration of MTPG4 was lower and that of MTX was higher in older patients than in others, which confirms data on a slower MTX metabolism in the elderly. The use of statins is likely to have a positive impact on the accumulation of MTXPG. There is a statistically significantly lower RBC concentration of MTXPG in at 12 weeks of therapy.


2016 ◽  
Vol 75 (Suppl 2) ◽  
pp. 1012.1-1012
Author(s):  
M.J. l'Ami ◽  
A.F. Marsman ◽  
C.L. Krieckaert ◽  
J. Ruwaard ◽  
E.L. Kneepkens ◽  
...  

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