Evidence map›Paper›PMID 32825359›Full record

ArticlePharmaceutics2020

Influence of Probenecid on the Pharmacokinetics and Pharmacodynamics of Sorafenib.

Koen G A M Hussaarts, Leni van Doorn, Karel Eechoute, Jeffrey Damman, Qiang Fu, Nadia van Doorn, Eric D Eisenmann, Alice A Gibson, Esther Oomen-de Hoop, Peter de Bruijn and 7 more

Open access · goldAbstract 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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 14 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

17 authors at 3 institutions in 2 countries.

Koen G A M HussaartsDepartment of Medical Oncology, Erasmus MC Cancer Institute, 3015 CE Rotterdam, The Netherlands.ORCID 0000-0002-4234-865X
Leni van DoornDepartment of Medical Oncology, Erasmus MC Cancer Institute, 3015 CE Rotterdam, The Netherlands.ORCID 0000-0002-2494-4482
Karel EechouteDepartment of Medical Oncology, Erasmus MC Cancer Institute, 3015 CE Rotterdam, The Netherlands.
Jeffrey DammanDepartment of Pathology, Erasmus MC, 3015 CE Rotterdam, The Netherlands.
Qiang FuDivision of Pharmaceutics & Pharmaceutical Chemistry, College of Pharmacy & Comprehensive Cancer Center, Ohio State University, Columbus, OH 43210, USA.
Nadia van DoornDepartment of Medical Oncology, Erasmus MC Cancer Institute, 3015 CE Rotterdam, The Netherlands.
Eric D EisenmannDivision of Pharmaceutics & Pharmaceutical Chemistry, College of Pharmacy & Comprehensive Cancer Center, Ohio State University, Columbus, OH 43210, USA.ORCID 0000-0003-1176-675X
Alice A GibsonDivision of Pharmaceutics & Pharmaceutical Chemistry, College of Pharmacy & Comprehensive Cancer Center, Ohio State University, Columbus, OH 43210, USA.
Esther Oomen-de HoopDepartment of Medical Oncology, Erasmus MC Cancer Institute, 3015 CE Rotterdam, The Netherlands.
Peter de BruijnDepartment of Medical Oncology, Erasmus MC Cancer Institute, 3015 CE Rotterdam, The Netherlands.
Sharyn D BakerDivision of Pharmaceutics & Pharmaceutical Chemistry, College of Pharmacy & Comprehensive Cancer Center, Ohio State University, Columbus, OH 43210, USA.
Stijn L W KoolenDepartment of Medical Oncology, Erasmus MC Cancer Institute, 3015 CE Rotterdam, The Netherlands.
Teun van GelderDepartment of Hospital Pharmacy, Erasmus MC, 3015 CE Rotterdam, The Netherlands.
Roelof W F van LeeuwenDepartment of Medical Oncology, Erasmus MC Cancer Institute, 3015 CE Rotterdam, The Netherlands.
Ron H J MathijssenDepartment of Medical Oncology, Erasmus MC Cancer Institute, 3015 CE Rotterdam, The Netherlands.
Alex SparreboomDivision of Pharmaceutics & Pharmaceutical Chemistry, College of Pharmacy & Comprehensive Cancer Center, Ohio State University, Columbus, OH 43210, USA.
Sander BinsDepartment of Medical Oncology, Erasmus MC Cancer Institute, 3015 CE Rotterdam, The Netherlands.
Erasmus MC Cancer Institute · NLThe Ohio State University · USErasmus MC · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prior studies have demonstrated an organic anion transporter 6 (OAT6)-mediated accumulation of sorafenib in keratinocytes. The OAT6 inhibitor probenecid decreases sorafenib uptake in skin and might, therefore, decrease sorafenib-induced cutaneous adverse events. Here, the influence of probenecid on sorafenib pharmacokinetics and toxicity was investigated. Pharmacokinetic sampling was performed in 16 patients on steady-state sorafenib treatment at days 1 and 15 of the study. Patients received sorafenib (200-800 mg daily) in combination with probenecid (500 mg two times daily (b.i.d.)) on days 2-15. This study was designed to determine bioequivalence with geometric mean Area under the curve from zero to twelve hours (AUC

Indexed as

hand-foot skin reaction (HFSR)OAT6pharmacokineticsprobenecidsorafenib

Identifiers

PMID32825359
PMCPMC7559746
OpenAlexW3058294323

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.