Evidence map›Paper›PMID 34944899›Full record

ArticleCancers2021

Developing a Nationwide Infrastructure for Therapeutic Drug Monitoring of Targeted Oral Anticancer Drugs: The ON-TARGET Study Protocol.

Anna M Mc Laughlin, Eduard Schmulenson, Olga Teplytska, Sebastian Zimmermann, Patrick Opitz, Stefanie L Groenland, Alwin D R Huitema, Neeltje Steeghs, Lothar Müller, Stefan Fuxius and 10 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. 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

20 authors at 11 institutions in 3 countries.

Anna M Mc LaughlinDepartment of Clinical Pharmacy and Biochemistry, Institute of Pharmacy, Freie Universität Berlin, 12169 Berlin, Germany.ORCID 0000-0002-5936-1877
Eduard SchmulensonDepartment of Clinical Pharmacy, Institute of Pharmacy, University of Bonn, 53121 Bonn, Germany.
Olga TeplytskaDepartment of Clinical Pharmacy, Institute of Pharmacy, University of Bonn, 53121 Bonn, Germany.
Sebastian ZimmermannInstitute of Pharmacy and Food Chemistry, Julius-Maximilians-Universität Würzburg, 97074 Würzburg, Germany.ORCID 0000-0002-6282-297X
Patrick OpitzDepartment of Pharmaceutical and Medical Chemistry, Clinical Pharmacy, University of Muenster, 48149 Muenster, Germany.
Stefanie L GroenlandThe Netherlands Cancer Institute, Department of Clinical Pharmacology, Division of Medical Oncology, 1066 CX Amsterdam, The Netherlands.
Alwin D R HuitemaThe Netherlands Cancer Institute, Department of Pharmacy & Pharmacology, 1066 CX Amsterdam, The Netherlands.
Neeltje SteeghsThe Netherlands Cancer Institute, Department of Clinical Pharmacology, Division of Medical Oncology, 1066 CX Amsterdam, The Netherlands.ORCID 0000-0003-2989-2279
Lothar MüllerOnkologie UnterEms, 26789 Leer, Germany.ORCID 0000-0001-9252-4650
Stefan FuxiusOnkologische Schwerpunktpraxis Heidelberg, 69115 Heidelberg, Germany.
Gerald IllerhausKlinik für Hämatologie, Onkologie, und Palliativmedizin, Klinikum Stuttgart, 70174 Stuttgart, Germany.
Markus JoergerCantonal Hospital St. Gallen, Department of Medical Oncology & Hematology, CH-9000 St. Gallen, Switzerland.ORCID 0000-0001-6602-6287
Frank MayerPraxis und Tagesklinik, Prof. Dr. Helmut Oettle und Prof. Dr. Dr. Frank Mayer, 88045 Friedrichshafen, Germany.
Uwe FuhrDepartment I of Pharmacology, Faculty of Medicine and University Hospital Cologne, Center for Pharmacology, University of Cologne, 50923 Cologne, Germany.ORCID 0000-0001-7087-5871
Stefan HoldenriederGerman Heart Center Munich, Technical University Munich, Institute of Laboratory Medicine, 80636 Munich, Germany.
Georg HempelDepartment of Pharmaceutical and Medical Chemistry, Clinical Pharmacy, University of Muenster, 48149 Muenster, Germany.ORCID 0000-0002-5790-6423
Oliver Scherf-ClavelInstitute of Pharmacy and Food Chemistry, Julius-Maximilians-Universität Würzburg, 97074 Würzburg, Germany.ORCID 0000-0002-1967-9231
Ulrich JaehdeDepartment of Clinical Pharmacy, Institute of Pharmacy, University of Bonn, 53121 Bonn, Germany.
Charlotte KloftDepartment of Clinical Pharmacy and Biochemistry, Institute of Pharmacy, Freie Universität Berlin, 12169 Berlin, Germany.
For The On-Target Study Consortium
University of Bonn · DEFreie Universität Berlin · DEPraxis für Hämatologie und Onkologie · DEThe Netherlands Cancer Institute · NLUniversity of Münster · DEUniversity of Würzburg · DEDeutsches Herzzentrum München · DEKlinikum Stuttgart · DEUniversity of Cologne · DEUniversity of St.Gallen · CHUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exposure-efficacy and/or exposure-toxicity relationships have been identified for up to 80% of oral anticancer drugs (OADs). Usually, OADs are administered at fixed doses despite their high interindividual pharmacokinetic variability resulting in large differences in drug exposure. Consequently, a substantial proportion of patients receive a suboptimal dose. Therapeutic Drug Monitoring (TDM), i.e., dosing based on measured drug concentrations, may be used to improve treatment outcomes. The prospective, multicenter, non-interventional ON-TARGET study (DRKS00025325) aims to investigate the potential of routine TDM to reduce adverse drug reactions in renal cell carcinoma patients receiving axitinib or cabozantinib. Furthermore, the feasibility of using volumetric absorptive microsampling (VAMS), a minimally invasive and easy to handle blood sampling technique, for sample collection is examined. During routine visits, blood samples are collected and sent to bioanalytical laboratories. Venous and VAMS blood samples are collected in the first study phase to facilitate home-based capillary blood sampling in the second study phase. Within one week, the drug plasma concentrations are measured, interpreted, and reported back to the physician. Patients report their drug intake and toxicity using PRO-CTCAE-based questionnaires in dedicated diaries. Ultimately, the ON-TARGET study aims to develop a nationwide infrastructure for TDM for oral anticancer drugs.

Indexed as

oral anticancer drugsrenal cell carcinomatherapeutic drug monitoringvolumetric absorptive microsampling

Identifiers

PMID34944899
PMCPMC8699239
OpenAlexW4200145210

What OpenQuestion holds

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Read underepoch 390

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.