Evidence map›Paper›PMID 33242185›Full record

ArticleAmerican journal of clinical dermatology2021

Therapeutic Drug Monitoring in Patients with Suboptimal Response to Adalimumab for Hidradenitis Suppurativa: A Retrospective Case Series.

Tasnim Abdalla, Mark Mansour, Dorra Bouazzi, Michelle A Lowes, Gregor B E Jemec, Afsaneh Alavi

Abstract read
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In one paragraph

Article in American journal of clinical dermatology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 18% of its field
1 · What the graph read from it

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.

2 · The registry

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Observational
  2. Article
  3. New and Emerging Targeted Therapies for Hidradenitis Suppurativa.International journal of molecular sciences · 2022
    Review
  4. Review
  5. Article
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 5 institutions in 3 countries.

Tasnim AbdallaFaculty of Medicine, University of Toronto, Toronto, Canada.ORCID http://orcid.org/0000-0001-7033-4725
Mark MansourSchulich School of Medicine & Dentistry, Western University, London, Canada.ORCID http://orcid.org/0000-0002-1431-660X
Dorra BouazziDepartment of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0002-8969-7144
Michelle A LowesThe Rockefeller University, New York, NY, USA.ORCID http://orcid.org/0000-0003-4256-478X
Gregor B E JemecDepartment of Dermatology, Zealand University Hospital, Roskilde, Denmark.ORCID http://orcid.org/0000-0002-0712-2540
Afsaneh AlaviFaculty of Medicine, University of Toronto, Toronto, Canada. Alavi.Afsaneh@mayo.edu.ORCID http://orcid.org/0000-0003-1171-4917
University of Copenhagen · DKMayo Clinic · USRockefeller University · USUniversity of Toronto · CAWestern University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdalimumab, a tumor necrosis factor-α inhibitor, is a biologic used for the treatment of moderate-to-severe hidradenitis suppurativa (HS). It is well known that patients may experience loss of efficacy from its use in other conditions, and it is suggested that developing a strategy for therapeutic drug monitoring (TDM) may help secure optimal clinical outcomes.

objectivesWe sought to determine serum adalimumab concentrations and anti-adalimumab antibody (AAA) status in patients with moderate-to-severe HS.

methodsA retrospective case series of 38 patients with suboptimal response to adalimumab 40 mg weekly was conducted at a community dermatology clinic. Adalimumab serum trough levels, AAA status, and inflammatory biomarkers were collected. Blood was drawn on identification of suboptimal response (after a minimum of 12 weeks) and was collected once prior to receiving the next scheduled dose. Kruskal-Wallis and Chi-squared tests were used for data analysis.

resultsA total of 38 patients had a median adalimumab trough concentration of 8.76 (interquartile range [IQR] 1.3-12.5) µg/mL. The median duration of adalimumab therapy of all patients was 21 (IQR 12-24) months. AAAs were detected in nine patients (24%), and all had subtherapeutic serum concentrations (< 6 µg/mL). Patients who were AAA+ had a significantly lower median adalimumab concentration than those who were AAA- (0.02 µg/mL [range 0.02-0.81] vs. 10.14 [range 0.76-48.00]; p = 0.0006).

conclusionPatients with AAAs had significantly lower serum adalimumab levels. The current study suggests that TDM may identify underlying reasons for suboptimal response and detect patients who may benefit from dose optimization strategies.

Indexed as

AdalimumabAdultBiomarkersDose-Response Relationship, DrugDrug MonitoringFemaleHidradenitis SuppurativaHumansMaleRetrospective StudiesSeverity of Illness IndexTreatment OutcomeYoung AdultAdalimumabBiomarkers

Identifiers

PMID33242185
OpenAlexW3107149649

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.