Evidence map›Paper›PMID 32366029›Full record

ArticlePharmaceutics2020

Automated Real-Time Tumor Pharmacokinetic Profiling in 3D Models: A Novel Approach for Personalized Medicine.

Jan F Joseph, Leonie Gronbach, Jill García-Miller, Leticia M Cruz, Bernhard Wuest, Ulrich Keilholz, Christian Zoschke, Maria K Parr

Abstract read
In one paragraph

Article in Pharmaceutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
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

8 authors.

Jan F JosephFreie Universität Berlin, Core Facility BioSupraMol, 14195 Berlin, Germany.
Leonie GronbachFreie Universität Berlin, Institute of Pharmacy (Pharmacology & Toxicology), 14195 Berlin, Germany.ORCID 0000-0003-2008-3184
Jill García-MillerFreie Universität Berlin, Institute of Pharmacy (Pharmacology & Toxicology), 14195 Berlin, Germany.
Leticia M CruzFreie Universität Berlin, Institute of Pharmacy (Pharmacology & Toxicology), 14195 Berlin, Germany.
Bernhard WuestAgilent Technologies GmbH, 76337 Waldbronn, Germany, bernhard_wuest@agilent.com.ORCID 0000-0002-1597-9130
Ulrich KeilholzCharité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health, Comprehensive Cancer Center, 10117 Berlin, Germany Ulrich.Keilholz@charite.de.
Christian ZoschkeFreie Universität Berlin, Institute of Pharmacy (Pharmacology & Toxicology), 14195 Berlin, Germany.ORCID 0000-0003-2535-3606
Maria K ParrFreie Universität Berlin, Institute of Pharmacy (Pharmaceutical and Medicinal Chemistry), 14195 Berlin, Germany.ORCID 0000-0001-7407-8300

Funding

Freie Universität Berlin Focus Area Disease in Human Aging, "DynAge"
6 · The paper itself

Abstract

Cancer treatment often lacks individual dose adaptation, contributing to insufficient efficacy and severe side effects. Thus, personalized approaches are highly desired. Although various analytical techniques are established to determine drug levels in preclinical models, they are limited in the automated real-time acquisition of pharmacokinetic profiles. Therefore, an online UHPLC-MS/MS system for quantitation of drug concentrations within 3D tumor oral mucosa models was generated. The integration of sampling ports into the 3D tumor models and their culture inside the autosampler allowed for real-time pharmacokinetic profiling without additional sample preparation. Docetaxel quantitation was validated according to EMA guidelines. The tumor models recapitulated the morphology of head-and-neck cancer and the dose-dependent tumor reduction following docetaxel treatment. The administration of four different docetaxel concentrations resulted in comparable courses of concentration versus time curves for 96 h. In conclusion, this proof-of-concept study demonstrated the feasibility of real-time monitoring of drug levels in 3D tumor models without any sample preparation. The inclusion of patient-derived tumor cells into our models may further optimize the pharmacotherapy of cancer patients by efficiently delivering personalized data of the target tissue.

Indexed as

automatizationdrug absorptiondrug dosinghead-and-neck cancerpharmacokineticsreal-time measurementstaxanestissue engineeringUHPLC-MS/MS

Identifiers

PMID32366029
PMCPMC7284432

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Registered trials

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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.