Evidence map›Paper›PMID 18183036›Full record

ArticleClinical pharmacology and therapeutics2008

Population pharmacokinetic model for docetaxel in patients with varying degrees of liver function: incorporating cytochrome P4503A activity measurements.

A C Hooker, A J Ten Tije, M A Carducci, J Weber, E Garrett-Mayer, H Gelderblom, W P McGuire, J Verweij, M O Karlsson, S D Baker

Open access · greenAbstract readComparative Study
In one paragraph

Article in Clinical pharmacology and therapeutics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
8.7field-weighted citation impact, top 3% 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

26 citing papers in PubMed, 54 citations in OpenAlex.

  1. Trial
  2. OATP1B1 polymorphism as a determinant of erythromycin disposition.Clinical pharmacology and therapeutics · 2012
    Trial
  3. Castration-dependent pharmacokinetics of docetaxel in patients with prostate cancer.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2010
    Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. The effects of advanced age and serum αBritish journal of clinical pharmacology · 2017
    Article
  11. Metabolism and excretion of novel pulmonary-targeting docetaxel liposome in rabbits.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2017
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Serum alanine transaminase total bilirubin concentrations predict CYP3A activity as measured by midazolam and 1'-hydroxylation.Medical science monitor : international medical journal of experimental and clinical research · 2015
    Article
  18. Review
  19. Article
  20. 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

10 authors at 6 institutions in 3 countries.

A C HookerDivision of Pharmacokinetics and Drug Therapy, Department of Pharmaceutical Biosciences, Uppsala University, Uppsala, Sweden.
A J Ten Tije
M A Carducci
J Weber
E Garrett-Mayer
H Gelderblom
W P McGuire
J Verweij
M O Karlsson
S D Baker
Sidney Kimmel Comprehensive Cancer Center · USErasmus MC · NLUppsala University · SEJohns Hopkins University · USLeiden University Medical Center · NLMedStar Franklin Square Medical Center · US

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
NCI NIH HHS P30 CA006973
6 · The paper itself

Abstract

The relationship between cytochrome P4503A4 (CYP3A4) activity and docetaxel clearance in patients with varying degrees of liver function (LF) was evaluated. Docetaxel 40, 50, or 75 mg/m(2) was administered to 85 patients with advanced cancer; 23 of 77 evaluable patients had abnormalities in LF tests. Baseline CYP3A activity was assessed using the erythromycin breath test (ERMBT). Pharmacokinetic studies and toxicity assessments were performed during cycle 1 of therapy and population modeling was performed using NONMEM. Docetaxel unbound clearance was lower (317 vs. 470 l/h) and more variable in patients with LF abnormalities compared to patients with normal LF. Covariates evaluated accounted for 83% of variability on clearance in patients with liver dysfunction, with CYP3A4 activity accounting for 47% of variation; covariates accounted for only 23% of variability in patients with normal LF. The clinical utility of the ERMBT may lie in identifying safe docetaxel doses for patients with LF abnormalities.

Indexed as

Models, BiologicalAdultAgedCytochrome P-450 CYP3ADocetaxelEnzyme ActivationFemaleHumansLiverLiver Function TestsMaleMiddle AgedProspective StudiesResearch DesignTaxoidsCytochrome P-450 CYP3ADocetaxelTaxoids

Identifiers

PMID18183036
PMCPMC3092481
OpenAlexW2107480117

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.