Evidence map›Paper›PMID 29691991›Full record

Observational studyClinical and translational science2018

Predicting Acute Renal Injury in Cancer Patients Receiving Cisplatin Using Urinary Neutrophil Gelatinase-Associated Lipocalin and Cystatin C.

Michael J Jelinek, Sang Mee Lee, Alicia Wyche Okpareke, Claudia Wing, Jay L Koyner, Patrick T Murray, Walter M Stadler, Peter H O' Donnell

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Clinical and translational science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 31% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 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 2 countries.

Michael J JelinekDepartment of Medicine/Section of Hematology/Oncology, University of Chicago, Chicago, Illinois, USA.ORCID 0000-0003-4959-2222
Sang Mee LeeDepartment of Health Sciences, University of Chicago, Chicago, Illinois, USA.ORCID 0000-0002-2144-3869
Alicia Wyche OkparekeDepartment of Medicine/Section of Hematology/Oncology, University of Chicago, Chicago, Illinois, USA.
Claudia WingDepartment of Medicine/Section of Hematology/Oncology, University of Chicago, Chicago, Illinois, USA.ORCID 0000-0002-8243-5598
Jay L KoynerDepartment of Medicine/Section of Nephrology, University of Chicago, Chicago, Illinois, USA.
Patrick T MurraySchool of Medicine, University College Dublin, Dublin, Ireland.
Walter M StadlerDepartment of Medicine/Section of Hematology/Oncology, University of Chicago, Chicago, Illinois, USA.
Peter H O' DonnellDepartment of Medicine/Section of Hematology/Oncology, University of Chicago, Chicago, Illinois, USA.
University of Illinois Chicago · USChicago Department of Public Health · USUniversity College Dublin · IE

Funding

Developing an Oncology Workforce for the 21st Century - Renewal 01K12CA139160 · NCI · UNIVERSITY OF CHICAGO · PI OLOPADE, OLUFUNMILAYO F., SMITH, SONALI · 2010 to 2024
$10.6M
NCI NIH HHS K12 CA139160
6 · The paper itself

Abstract

Acute kidney injury (AKI) limits cisplatin use. We tested whether urine cystatin C (uCyC) and neutrophil gelatinase-associated lipocalin (uNGAL) can preidentify patients at risk for AKI. Patients initiating cisplatin-based chemotherapy were prospectively enrolled. uNGAL/uCyC were measured pre/post-cisplatin administration and compared with serum creatinine (sCr). AKI was defined as sCr increase ≥50% or ≥0.3 mg/dL above baseline. In all, 102 patients were enrolled; 95 provided evaluable data. Twenty-five patients developed AKI. Median baseline and pre-cisplatin uNGAL levels were significantly higher in AKI patients. Although immediate changes in uNGAL/uCyC 2 h after cisplatin were not detectable, post-cisplatin peak values over the course of therapy were markedly and significantly elevated in AKI patients. In multivariate modeling with age, baseline glomerular filtration rate, and histology, maximum uCyC was a significant independent AKI predictor. These findings suggest pre-cisplatin uNGAL and peak uCyC levels can identify patients with increased AKI risk, potentially allowing for tailored modification of cisplatin-based treatment regimens.

Indexed as

Acute Kidney InjuryAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsBiomarkersCisplatinCystatin CFemaleGlomerular Filtration RateHumansLipocalin-2MaleMiddle AgedNeoplasmsPrognosisBiomarkersCisplatinCystatin CLCN2 protein, humanLipocalin-2

Identifiers

PMID29691991
PMCPMC6039203
OpenAlexW2802369568

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.