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Therapeutic thresholds for golimumab serum concentrations during induction and maintenance therapy in ulcerative colitis: results from the GO‐LEVEL study
Author(s) -
Samaan Mark A.,
Cunningham Georgina,
Tamilarasan Aravind Gokul,
Beltran Luisa,
Pavlidis Polychronis,
Ray Shuvra,
Mawdsley Joel,
Anderson Simon H.,
Sanderson Jeremy D.,
Arkir Zehra,
Irving Peter M.
Publication year - 2020
Publication title -
alimentary pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.308
H-Index - 177
eISSN - 1365-2036
pISSN - 0269-2813
DOI - 10.1111/apt.15808
Subject(s) - golimumab , medicine , ulcerative colitis , calprotectin , gastroenterology , cohort , area under the curve , maintenance therapy , prospective cohort study , receiver operating characteristic , inflammatory bowel disease , disease , chemotherapy , infliximab
Summary Background Significant associations between serum golimumab concentrations and favourable outcomes have been observed during both induction and maintenance therapy in ulcerative colitis (UC). However, data regarding optimal therapeutic serum golimumab concentration thresholds are limited. Aims To identify optimal serum golimumab concentration thresholds during induction and maintenance treatment with golimumab. Methods GO‐LEVEL was an open label, phase IV study that included a prospective cohort of UC patients commencing golimumab, as well as a cross‐sectional cohort receiving maintenance treatment. Patients commencing induction for active UC (defined as a simple clinical colitis activity index [SCCAI] >5 in addition to a raised faecal calprotectin [FC] >59μg/g or, raised C‐reactive protein [CRP] [>5mg/L] or, Mayo endoscopic disease activity 2 or 3) were evaluated at weeks 6, 10 and 14. Patients receiving maintenance therapy were recruited either at the point of flare or during remission. Combined clinical‐biochemical remission was defined as SCCAI ≤2 and FC <250μg/g. Serum golimumab concentrations were measured using a commercially available ELISA (LISATRACKER, Theradiag). Results Thirty‐nine patients were included in the induction cohort, of whom 15 (38%) achieved combined clinical‐biochemical remission at week 6. The median serum golimumab concentration of those in combined clinical‐biochemical remission was significantly higher than those who were not (5.0 vs 3.1 μg/mL, respectively, P = 0.03). Receiver operating characteristic (ROC) curve analysis demonstrated 3.8 μg/mL as the optimal threshold (sensitivity 0.71, specificity 0.65, area under curve [AUC] 0.72, positive predictive value [PPV] 0.59 and negative predictive value [NPV] 0.79). Sixty‐three patients were included in the maintenance cohort; 31 (49%) were in combined remission, 32 (51%) were not. The median serum golimumab concentration of those in combined remission was significantly higher (2.9 vs 2.1 μg/mL, respectively, P = 0.01). ROC curve analysis demonstrated 2.4 μg/mL as the optimal threshold (sensitivity 0.68, specificity 0.66, AUC 0.68, PPV 0.65 and NPV 0.66). Conclusions GO‐LEVEL (NCT03124121) offers further evidence regarding golimumab's exposure‐response relationship. Clinicians may consider using therapeutic drug monitoring to optimise golimumab dosing aiming to achieve our suggested therapeutic thresholds of 3.8 μg/mL at week 6 and 2.4 μg/mL during maintenance.