Evidence map›Paper›PMID 36057542›Full record

ArticleVeterinary and comparative oncology2023

Fractionated oral dosing and its effect on cyclophosphamide pharmacokinetics in dogs with high-grade multicentric lymphoma.

Sridhar Veluvolu, Jennifer L Willcox, Katherine A Skorupski, Sami Al-Nadaf, Robert Rebhun, Luke Wittenburg

Open access · hybridAbstract read
In one paragraph

Article in Veterinary and comparative oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

0 citing papers in PubMed, 16 citations in OpenAlex.

No citing paper in PubMed yet.

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

6 authors at 2 institutions in 1 country.

Sridhar VeluvoluWilliam R Pritchard Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California-Davis, Davis, California, USA.
Jennifer L WillcoxWilliam R Pritchard Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California-Davis, Davis, California, USA.ORCID https://orcid.org/0000-0003-2107-6226
Katherine A SkorupskiWilliam R Pritchard Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California-Davis, Davis, California, USA.ORCID https://orcid.org/0000-0003-0324-445X
Sami Al-NadafWilliam R Pritchard Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California-Davis, Davis, California, USA.ORCID https://orcid.org/0000-0002-9348-2293
Robert RebhunWilliam R Pritchard Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California-Davis, Davis, California, USA.ORCID https://orcid.org/0000-0002-8047-3494
Luke WittenburgDepartment of Surgical and Radiological Sciences, School of Veterinary Medicine, University of California-Davis, Davis, California, USA.ORCID https://orcid.org/0000-0002-5543-0724
Veterinary Medical Teaching Hospital · USUniversity of California, Davis · US

Funding

Defining the role of core binding factor protein interactions in osteosarcomaK01OD026526 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI WITTENBURG, LUKE A. · 2018 to 2022
$675k
Davis Center for Companion Animal Health, University of CaliforniaNational Institutes of Health 5K01OD026526NIH HHS 5K01OD026526NIH HHS K01 OD026526
6 · The paper itself

Abstract

Cyclophosphamide (CP) is an alkylating agent commonly included in multi-drug treatment protocols for canine cancer. As a prodrug, CP requires hepatic metabolism for activation to the intermediate compound 4-hydroxycyclophosphamide (4-OHCP) which then spontaneously forms alkylating phosphoramide mustard. CP is frequently administered in a fractionated manner, with the total dose given over multiple days. CP is reported to cause auto-induction of metabolism in humans, with faster CP clearance and relatively increased 4-OHCP formation following fractionated versus bolus dosing, however canine pharmacokinetic studies of CP dose fractionation are lacking. The study objective was to evaluate the pharmacokinetics of fractionated oral CP dosing at a dose of 200-250 mg/m

Indexed as

Dog DiseasesLymphoma, Non-HodgkinNeoplasmsAnimalsArea Under CurveCyclophosphamideDogsHumansCyclophosphamidecanine lymphomachemotherapycyclophosphamidefractionated dosingpharmacokinetics

Identifiers

PMID36057542
PMCPMC9928601
OpenAlexW4294714332

What OpenQuestion holds

Textmetadata
LicenceTDM
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.