Evidence map›Paper›PMID 39434019›Full record

ArticleBMC nephrology2024

A low-dose pemetrexed-cisplatin combination regimen induces significant nephrotoxicity in mice.

Samson A Iwhiwhu, Ravi Kumar, Abdul H Khan, Jeremiah M Afolabi, Jada D Williams, Julia E de la Cruz, Adebowale Adebiyi

Abstract read
In one paragraph

Article in BMC nephrology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

7 authors.

Samson A IwhiwhuDepartment of Physiology, University of Tennessee Health Science Center, Memphis, TN, USA.
Ravi KumarDepartment of Physiology, University of Tennessee Health Science Center, Memphis, TN, USA.
Abdul H KhanDepartment of Physiology, University of Tennessee Health Science Center, Memphis, TN, USA.
Jeremiah M AfolabiDepartment of Physiology, University of Tennessee Health Science Center, Memphis, TN, USA.
Jada D WilliamsDepartment of Physiology, University of Tennessee Health Science Center, Memphis, TN, USA.
Julia E de la CruzDepartment of Physiology, University of Tennessee Health Science Center, Memphis, TN, USA.
Adebowale AdebiyiDepartment of Physiology, University of Tennessee Health Science Center, Memphis, TN, USA. a.adebiyi@health.missouri.edu.

Funding

Control of microvascular function by ion channelsR01HL151735 · NHLBI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI ADEBIYI, ADEBOWALE · 2020 to 2023
$2.0M
Vanderbilt University Cardiovascular Medicine Training ProgramT32HL170965 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Ravi Shah, Quinn Stanton Wells · 2024 to 2026
$1.2M
NHLBI NIH HHS R01 HL151735NHLBI NIH HHS R01HL151735NHLBI NIH HHS T32 HL170965
6 · The paper itself

Abstract

backgroundPemetrexed is combined with cisplatin to treat cancer. Whether pemetrexed-cisplatin combination chemotherapy exacerbates cisplatin nephrotoxicity is unclear. Here, we investigated kidney injury in mice administered a non-lethal low-dose regimen of pemetrexed or cisplatin alone and compared it with a pemetrexed-cisplatin combination.

methodsMice were randomly divided into four groups and administered intraperitoneally the experimental drugs solubilized in captisol (sulfobutylether β-cyclodextrin). Group 1 received captisol, Group 2 pemetrexed (10 mg/kg), Group 3 cisplatin (1 mg/kg), and Group 4 pemetrexed (10 mg/kg) plus cisplatin (1 mg/kg). The mice were treated every other day for two weeks, three times per week. Glomerular filtration rate (GFR) was determined on the third day after the last treatment, followed by a necropsy.

resultsWhereas the relative kidney weight was comparable in the control vs. pemetrexed or cisplatin alone group, it was significantly increased in the combination group. Mice treated with cisplatin and pemetrexed-cisplatin combination exhibited reduced GFR. The pemetrexed-cisplatin combination caused significant increases in the plasma or urinary levels of kidney injury biomarkers, renal lipid peroxidation, and nitrosative stress compared with pemetrexed or cisplatin alone. Histopathology revealed that pemetrexed or cisplatin alone had minimal effects on the kidneys. By contrast, the pemetrexed-cisplatin combination caused tubular degeneration, dilatation, and granular casts. Live-cell imaging showed that the pemetrexed-cisplatin combination caused more severe apoptosis of primary renal epithelial cells than individual concentrations.

conclusionsThese findings suggest that combining pemetrexed and cisplatin causes oxidative kidney damage at individual doses that do not cause significant nephrotoxicity. Hence, the renal function of patients undergoing treatment with the pemetrexed-cisplatin combination needs extensive monitoring.

Indexed as

CisplatinPemetrexedAnimalsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsGlomerular Filtration RateKidneyKidney DiseasesMaleMiceAntineoplastic AgentsCisplatinPemetrexedCisplatinCombination chemotherapyNephrotoxicityPemetrexed

Identifiers

PMID39434019
PMCPMC11494951

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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.