Evidence map›Paper›PMID 29904814›Full record

ReviewThe AAPS journal2018

Dashboards for Therapeutic Monoclonal Antibodies: Learning and Confirming.

Diane R Mould, Richard N Upton, Jessica Wojciechowski, Becky L Phan, Stacy Tse, Marla C Dubinsky

Open access · bronzeAbstract readReview
PubMed Publisher
In one paragraph

Review in The AAPS journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 19 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Observational
  6. Article
  7. Appropriate Therapeutic Drug Monitoring of Biologic Agents for Patients With Inflammatory Bowel Diseases.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2019
    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 2 countries.

Diane R MouldProjections Research Inc., 535 Springview Lane, Phoenixville, Pennsylvania, 19460, USA. drmould@pri-home.net.ORCID 0000-0002-8908-0136
Richard N UptonProjections Research Inc., 535 Springview Lane, Phoenixville, Pennsylvania, 19460, USA.
Jessica WojciechowskiPfizer, Inc., Groton, Connecticut, 06340, USA.
Becky L PhanIcahn School of Medicine at Mount Sinai, New York, New York, 10029, USA.
Stacy TseMount Sinai Hospital, New York, New York, 10029, USA.
Marla C DubinskyIcahn School of Medicine at Mount Sinai, New York, New York, 10029, USA.
Icahn School of Medicine at Mount Sinai · USMount Sinai Hospital · USPfizer (United States) · USSpringhouse · USUniversity of South Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammatory diseases (ID) are incurable, progressive diseases. Literature evidence cites increasing incidence of these diseases worldwide. When treatments with chemical immunosuppressive agents fail, patients are often treated with monoclonal antibodies (MAbs). However, MAb failure rates are generally high, with approximately half the patients being discontinued within 4 years, necessitating switching to another MAb. One potential cause of treatment failure is subtherapeutic exposure. Several studies demonstrated associations between trough MAb concentrations and clinical response, supporting the notion that improving drug exposure may result in improved outcomes. MAbs exhibit complex and highly variable pharmacokinetics in ID patients with numerous factors affecting clearance. Bayesian-guided dosing with dashboard systems is a new tool being investigated in the treatment of ID to reduce variability in exposure. Simulations suggest dashboards will be effective at maintaining patients at target troughs. However, when patients are dosed using doses or intervals outside those listed in prescribing information, there is concern that patients may have drug exposures beyond or below the ranges found to be safe and efficacious. This manuscript reviews the rationale behind dashboard development, evaluations of expected performance, and a simulated assessment of MAb exposure with dashboard-based dosing versus dosing based on the prescribing information. We introduce the concept of pharmacologic equivalence-if patients are dosed based on individual pharmacokinetics, the resulting exposure is consistent with exposures achieved using labeled dosing. We further show that dashboard-based dosing results in observed exposures that are generally contained within the range of exposures achieved with labeled dosing.

Indexed as

Models, BiologicalAntibodies, MonoclonalBayes TheoremBiological Variation, PopulationComputer SimulationDose-Response Relationship, DrugHumansImmunosuppressive AgentsInflammationTreatment FailureAntibodies, MonoclonalImmunosuppressive AgentsBayesdashboardIBDindividualized dosingmonoclonal antibodies

Identifiers

PMID29904814
OpenAlexW2807752300

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.