Observational studyFrontiers in immunology2026
Longitudinal monitoring of adalimumab levels and anti-adalimumab antibodies in Chinese patients with ankylosing spondylitis: a prospective cohort study.
Observational study in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04875299 (Evaluation of the Optimal Concentration Range of Adalimumab for Ankylosing Spondylitis in a Prospective Observational Study), which is not on this map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Evaluation of the Optimal Concentration Range of Adalimumab for Ankylosing Spondylitis in a Prospective Observational Study
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
14 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Objective: This study aimed to clarify the association between longitudinal adalimumab concentrations, anti-adalimumab antibodies (AAA) levels, and clinical response in Chinese patients with ankylosing spondylitis (AS). Methods: A prospective multi-center, observational cohort study of AS patients receiving adalimumab therapy was conducted. Disease activity was assessed with the AS Disease Activity Score (ASDAS), and clinical responders were defined based on ASDAS improvement together with C-reactive protein normalization. Adalimumab concentrations were measured using a validated sandwich immunoassay. Measurement of AAA levels was performed with a laboratory-developed immunoassay system integrating electrochemiluminescence technology with specific immunomagnetic separation, with result reported as signal-to-noise ratio (S/N). Results: A total of 140 patients receiving adalimumab monotherapy were included. The median follow-up period was 169 days, and 711 plasma samples were available for adalimumab concentrations and AAA levels measurements. Seven patients had pre-existing AAA, and 120 (90.2%) of the remaining 133 patients tested positive for AAA during follow-up. A total of 48 patients were excluded from the exposure-response relationship dataset owing to pre-existing AAA (n=7), lack of active disease (n=26), incomplete follow-up (n=8), and prolonged dosing intervals (n=7). Among the remaining 92 patients, a total of 58 (63%) achieved clinical response. Adalimumab concentrations were higher, and AAA levels were significantly lower, in responders compared with non-responders at multiple time points. Exposure-response relationship models also revealed a steady-state adalimumab concentration target of 5.1 μg/mL and a week-4 concentration target of 3.3 μg/mL, corresponding to an 80% probability of clinical response. Thirty-six of 92 patients (39.1%) exhibited AAA-S/N values exceeding the putative clinically meaningful threshold (AAA-S/N=10). Patients in the high-AAA group (AAA-S/N≥10) had lower drug levels (median: 1.5 μg/mL vs. 6.9 μg/mL, Conclusions: Our results demonstrate that longitudinal profiles of adalimumab concentrations and AAA levels show a strong association with clinical responses in this Chinese AS cohort, which may inform therapeutic drug monitoring-guided adalimumab treatment strategies that remain to be further validated. Trial registration: ClinicalTrials.gov (NCT04875299).
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.