Therapeutic response to leflunomide in combo therapy and monotherapy is associated to serum teriflunomide (A77 1726) levels.
Nicte S Fajardo-RobledoHeriberto Jacobo-CuevasPerez-Guerrero Edsaul EmilioEsther Guadalupe Corona-SánchezSaldaña-Cruz Ana MiriamElba M Romero-TejedaNorma Alejandra Rodriguez-JimenezSylvia Elena Totsuka-SuttoRocío Ivette López-RoaPonce-Guarneros Juan ManuelMiriam Fabiola Alcaraz-LopezSergio Cerpa-CruzJosé Francisco Munoz-ValleErnesto German Cardona MuñozGonzalez-Lopez LauraJorge Ivan Gamez-Navanull nullPublished in: Scientific reports (2022)
There is a significant rate of therapeutic failure in rheumatoid arthritis (RA) patients treated with leflunomide (LEF). This study investigates the utility values of teriflunomide levels (A77 1726) in identifying RA patients who remained with moderate or severe disease activity after the treatment with LEF. In this cross-sectional study, we compared: (a) RA patients who achieved a DAS28-ESR ≤ 3.2, and (b) RA patients who maintained a DAS28-ESR > 3.2 after treatment. ROC curves determined the cut-off of A77 1726 with the better performance to identify patients achieving a DAS28-ESR ≤ 3.2. Of the 115 patients treated with LEF, 69 (60%) remained with moderate/severe disease activity and 46 (40%) achieved low disease activity/remission. Higher A77 1726 levels showed a negative correlation with DAS28-ESR (r = - 0.42, p < 0.001) and other parameters of disease activity. We obtained the following utility values with the cut-off of A77 1726 > 10 µg/mL to identify RA patients who achieved a DAS28-ESR ≤ 3.2: sensitivity of 91.31%; specificity of 73.91%; positive predictive value of 70.00%; and negative predictive value of 92.73%. Serum A77 1726 discriminated between RA patients who remained with moderate/severe disease activity despite the treatment with LEF both as monotherapy and LEF as combo therapy.
Keyphrases
- disease activity
- rheumatoid arthritis
- systemic lupus erythematosus
- ankylosing spondylitis
- rheumatoid arthritis patients
- estrogen receptor
- juvenile idiopathic arthritis
- combination therapy
- high intensity
- interstitial lung disease
- early onset
- ejection fraction
- newly diagnosed
- stem cells
- clinical trial
- prognostic factors
- mesenchymal stem cells
- chronic kidney disease
- replacement therapy
- patient reported outcomes
- bone marrow
- randomized controlled trial
- structural basis