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Record W2587162403 · doi:10.1093/ecco-jcc/jjx002.532

P407 Prospective evaluation of clinical efficacy and safety of golimumab in biologic experienced and naïve patients with moderate to severe ulcerative colitis: experience from a tertiary referral centre

2017· article· en· W2587162403 on OpenAlexaboutno aff
Beatrice Orlandini, Gabriele Dragoni, Siro Bagnoli, S. Deiana, Giuseppe Macrí, Francesca Rogai

Bibliographic record

VenueJournal of Crohn s and Colitis · 2017
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicInflammatory Bowel Disease
Canadian institutionsnot available
Fundersnot available
KeywordsGolimumabUlcerative colitisMedicineTertiary referral centreInternal medicineReferralProspective cohort studyFamily medicineInfliximab

Abstract

fetched live from OpenAlex

Background: Golimumab is a fully human monoclonal antibody to TNFα approved for the treatment of patients with moderate to severe ulcerative colitis (UC) with inadequate response or intolerance to corticosteroids or immunosuppressive therapy. The aim of this study is to evaluate the efficacy and tolerability profile of golimumab in both biologic naïve (BN) and biologic experienced (BE) patients. Methods: Data were prospectively collected from a cohort of UC patients treated with golimumab from March 2015 to November 2016 at our Centre. Descriptive analyses were obtained from two patient cohorts, namely patients who were naive to anti-TNFα therapies (BN) and patients who have already failed biologic treatment with infliximab or adalimumab (BE) or both. Patients received golimumab 200 mg subcutaneously at week 0, 100 mg sc. at week 2, then 50 mg or 100 mg sc. every 4 weeks depending on body weight. The primary outcomes of interest were clinical response to treatment and rate of adverse events (AE). Results: Overall, 27 patients were enrolled. Of these, 11 (41%) were BN and 16 (59%) BE. Baseline patient characteristics and main results are shown in Table 1. The majority of patients received >5 cycles of systemic steroids before starting golimumab (91% and 82% in the BN and BE groups, respectively). According to the Montreal classification of disease extension, most patients were E2 (55% in BN group, 25% in BE group) or E3 (45% and 75% of the BN and BE groups, respectively). Endoscopic disease activity was scored as Mayo 3 in 82% and 80% for BN and BE patients, respectively. Median (range) duration of golimumab therapy was 3 (1–6) months in the BN group and 3 (1–16) months in the BE group. In 3 (27%) patients in the BN group and 4 (25%) in the BE group AEs were recorded, most of which were skin/genito-urinary infections. Of note, two cases of basal cell carcinoma were registered. The overall remission rate was 45% and 25% in the BN and BE patients, respectively. The main cause of golimumab discontinuation was lack or loss of clinical response (specifically in 71% of BN patients and 92% of BE patients). Among unresponder patients, proctocolectomy was performed in 3 cases. Table 1 Conclusions: In our cohort, clinical remission was obtained in almost half of BN patients but only one quarter of BE patients, with a similar rate of AEs. However, treatment duration was highly variable in our series. Although our findings need to be confirmed in larger series, golimumab therapy seems to achieve better disease control in the biologic naïve setting.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.002
metaresearch head score (Gemma)0.003
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Non-randomized trial · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.009

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0020.003
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0010.000
Open science0.0000.001
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0020.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.022
GPT teacher head0.323
Teacher spread0.301 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designNon-randomized trial
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations1
Published2017
Admission routes1
Has abstractyes

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