Evidence map›Paper›PMID 34390437›Full record

ArticleInternational urology and nephrology2022

Evaluation of acute and chronic nephrotoxicity in patients received cisplatin-based chemotherapy: has anything changed over time?

Şule Çelik Kamacı, Gülay Koçak, Aylia Yeşilova, Şener Cihan

Abstract read
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In one paragraph

Article in International urology and nephrology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Platinum accumulation in chemotherapy: toxicity mechanisms, challenges, and mitigation strategies.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2026
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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

4 authors at 1 institution in 2 countries.

Şule Çelik KamacıDepartment of Internal Medicine, Okmeydani Training and Research Hospital, University of Health Sciences, İstanbul, Turkey.
Gülay KoçakDepartment of Nephrology, University of Health Sciences, Okmeydani Training and Research Hospital, Anka sokak, Mashattan blokları, B3 blok, no 59, Maslak, Sarıyer, İstanbul, Turkey. gulaykad@hotmail.com.ORCID http://orcid.org/0000-0002-3633-9546
Aylia YeşilovaDepartment of Internal Medicine, Okmeydani Training and Research Hospital, University of Health Sciences, İstanbul, Turkey.
Şener CihanDepartment of Medical Oncology, University of Health Sciences, Okmeydani Training and Research Hospital, İstanbul, Turkey.
Sağlık Bilimleri Üniversitesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe aim of this study was to determine the frequency and the risk factors of acute and chronic nephrotoxicity in patients who received cisplatin due to malignancy. MATERIALS AND

methodsMedical records of all patients who received cisplatin-based chemotherapy regimen between January 2013 and July 2019 were retrospectively evaluated. The data of 203 patients who met the study criteria were examined. The patients were evaluated for acute nephrotoxicity at 48 h and late nephrotoxicity at 3rd month after first course of cisplatin. Early and late nephrotoxicity were defined by NCI CTCAE Version 4.0 criteria.

resultsThe mean age of the study patients was 56.44 ± 12.69 years, 78.8% were males and 21.2% were females. It is revealed that the incidence of cisplatin-induced acute nephrotoxicity was 9.2% and chronic nephrotoxicity was 37.9%. While the development of acute nephrotoxicity was associated with female gender, history of diabetes mellitus, history of ischemic heart disease and use of antiplatelet drug, the development of chronic nephrotoxicity was associated with older age, female gender and using of diuretics. High serum creatinine, urea and low eGFR value before treatment were found to be associated with both early and late nephrotoxicity (p < 0.05). There was no statistically significant relationship between acute or chronic nephrotoxicity and cumulative dose of cisplatin, hydration or intravenous magnesium supplementation.

conclusionHigh initial serum creatinine value and low initial eGFR are the most important determinants of both early and late nephrotoxicity.

Indexed as

Antineoplastic AgentsNeoplasmsAdultAgedCisplatinCreatinineFemaleHumansMaleMiddle AgedRetrospective StudiesAntineoplastic AgentsCisplatinCreatinineCisplatinCisplatin-induced acute nephrotoxicityCisplatin-induced chronic nephrotoxicity

Identifiers

PMID34390437
OpenAlexW3188750606

What OpenQuestion holds

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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.