Evidence map›Paper›PMID 31732882›Full record

ArticlePharmaceutical research2019

Exposure to Docetaxel in the Elderly Patient Population: a Population Pharmacokinetic Study.

Marie-Rose B S Crombag, Thomas P C Dorlo, Ellen van der Pan, Anoek van Straten, Andries M Bergman, Nielka P van Erp, Jos H Beijnen, Alwin D R Huitema

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Pharmaceutical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

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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 at 3 institutions in 1 country.

Marie-Rose B S CrombagDepartment of Pharmacy & Pharmacology, Antoni van Leeuwenhoek - Netherlands Cancer Institute, Plesmanlaan 121, 1066, CX, Amsterdam, the Netherlands. m.crombag@nki.nl.ORCID https://orcid.org/0000-0002-2241-252X
Thomas P C DorloDepartment of Pharmacy & Pharmacology, Antoni van Leeuwenhoek - Netherlands Cancer Institute, Plesmanlaan 121, 1066, CX, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0003-3076-8435
Ellen van der PanDivision of Pharmacology, Netherlands Cancer Institute, Amsterdam, the Netherlands.
Anoek van StratenDivision of Pharmacology, Netherlands Cancer Institute, Amsterdam, the Netherlands.
Andries M BergmanDivision of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0001-5223-2549
Nielka P van ErpDepartment of Pharmacy and Radboud Institute of Health Sciences, Radboud University Medical Center, Nijmegen, the Netherlands.ORCID https://orcid.org/0000-0003-1553-178X
Jos H BeijnenDepartment of Pharmacy & Pharmacology, Antoni van Leeuwenhoek - Netherlands Cancer Institute, Plesmanlaan 121, 1066, CX, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0003-0118-561X
Alwin D R HuitemaDepartment of Pharmacy & Pharmacology, Antoni van Leeuwenhoek - Netherlands Cancer Institute, Plesmanlaan 121, 1066, CX, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0003-1939-4639
The Netherlands Cancer Institute · NLUtrecht University · NLRadboud University Nijmegen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDocetaxel is commonly used in elderly patients, who are frequently diagnosed with prostate cancer. Although previous studies revealed no clinically relevant impact of older age on docetaxel pharmacokinetics (PK), this may be masked by indication. Metastatic castration-resistant prostate cancer (mCRPC) patients were reported to have approximately two-times lower systemic exposure compared to patients with other solid tumors. This study assessed the impact of older age on docetaxel PK, also considering the effect of indication on docetaxel PK.

methodsProspectively collected docetaxel PK data from patients aged ≥70 was pooled with PK data from an earlier published multicenter study. A 3-compartment population PK model, including multiple covariates, was used to describe docetaxel plasma concentration-time data. We added the effect of prostate cancer (mCRPC and metastatic hormone-sensitive prostate cancer (mHSPC)) on clearance to this model. Hereafter, we evaluated the additional impact of older age on docetaxel clearance, using a significance threshold of p < 0.005.

resultsDocetaxel plasma concentration-time data from 157 patients were analyzed. Median age in the total cohort was 67 years (range 31-87), with 49% of the total cohort aged ≥70. The impact of age on docetaxel clearance was statistically significant (p < 0.005). For a typical patient, a 10-year and 20-year increase of age led to a reduction in clearance of 17% and 34%, respectively.

conclusionIn this cohort study, age significantly and independently affected docetaxel clearance, showing lower docetaxel clearance in elderly patients. In our cohort, mCRPC and mHSPC patients both had higher clearance than patients with other solid tumors.

Indexed as

AdultAgedAged, 80 and overAge FactorsAntineoplastic AgentsCohort StudiesDocetaxelDose-Response Relationship, DrugFemaleHumansMaleMiddle AgedNeoplasmsTreatment OutcomeAntineoplastic AgentsDocetaxeldocetaxelolder agepharmacokineticsprostate cancer

Identifiers

PMID31732882
OpenAlexW2983918542

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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.