Evidence map›Paper›PMID 32989831›Full record

ArticleJournal of clinical pharmacology2021

Tucatinib Inhibits Renal Transporters OCT2 and MATE Without Impacting Renal Function in Healthy Subjects.

Ariel R Topletz-Erickson, Anthony J Lee, JoAl G Mayor, Evelyn L Rustia, Layth I Abdulrasool, Amanda L Wise, Ben Dailey, Sharon DeChenne, Luke N Walker, Stephen C Alley and 1 more

Open access · hybridAbstract readClinical Trial, Phase I
In one paragraph

Article in Journal of clinical pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Trial
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Ten tips for an onco-nephrology clinic.Clinical kidney journal · 2025
    Review
  11. Article
  12. Brief Report: Tyrosine Kinase Inhibitors for Lung Cancers That Inhibit MATE-1 Can Lead to "False" Decreases in Renal Function.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2024
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

11 authors at 2 institutions in 1 country.

Ariel R Topletz-EricksonClinical Pharmacology, Seattle Genetics, Bothell, Washington, USA.
Anthony J LeeDMPK, Seattle Genetics, Bothell, Washington, USA.
JoAl G MayorDevelopment, Seattle Genetics, Bothell, Washington, USA.
Evelyn L RustiaDevelopment, Seattle Genetics, Bothell, Washington, USA.
Layth I AbdulrasoolDevelopment, Seattle Genetics, Bothell, Washington, USA.
Amanda L WisePRA Health Sciences, Lenexa, Kansas, USA.
Ben DaileyPRA Health Sciences, Lenexa, Kansas, USA.
Sharon DeChenneAlturas Analytics, Inc., Moscow, Idaho, USA.
Luke N WalkerDevelopment, Seattle Genetics, Bothell, Washington, USA.
Stephen C AlleyTranslational Sciences, Seattle Genetics, Bothell, Washington, USA.
Christopher J EndresClinical Pharmacology, Seattle Genetics, Bothell, Washington, USA.
Seagen (United States) · USPRA Health Sciences · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tucatinib is a potent tyrosine kinase inhibitor selective for human epidermal growth factor receptor 2 (HER2) approved by the US Food and Drug Administration for the treatment of HER2-positive metastatic breast cancer and in development for other HER2-positive solid tumors. Modest, reversible serum creatinine (SCr) elevations have been observed in tucatinib clinical trials. SCr is conveyed by the renal drug transporters organic cation transporter 2 (OCT2) and multidrug and toxin extrusion protein 1 (MATE1) and 2-K (MATE2-K) and can increase in the presence of inhibitors of these transporters. In vitro, tucatinib inhibited OCT2-, MATE1-, and MATE2-K-mediated transport of metformin, with IC

Indexed as

AdolescentAdultAgedAnimalsAntineoplastic AgentsBiological TransportCreatinineCross-Over StudiesDogsErb-b2 Receptor Tyrosine KinasesFemaleGlomerular Filtration RateHealthy VolunteersHEK293 CellsHumansInhibitory Concentration 50Antineoplastic AgentsCreatinineERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesMetforminOrganic Cation Transporter 2Organic Cation Transport ProteinsOxazolesPyridinesQuinazolinesSLC47A1 protein, humantucatinibMATEmetforminOCT2pharmacokineticsrenal functiontucatinib

Identifiers

PMID32989831
PMCPMC7984390
OpenAlexW3091730840

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.