Evidence map›Paper›PMID 26975454›Full record

ArticleWiener klinische Wochenschrift2016

Crizotinib-induced toxicity in an experimental rat model.

Ozge Gumusay, Guldal Esendagli-Yilmaz, Aytug Uner, Bulent Cetin, Suleyman Buyukberber, Mustafa Benekli, Mustafa N Ilhan, Ugur Coskun, Ozlem Gulbahar, Ahmet Ozet

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In one paragraph

Article in Wiener klinische Wochenschrift, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Renal Injury during Long-Term Crizotinib Therapy.International journal of molecular sciences · 2018
    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

10 authors at 3 institutions in 1 country.

Ozge GumusayDivision of Medical Oncology, Department of Internal Medicine, Faculty of Medicine, Gaziosmanpasa University, 60250, Tokat, Turkey. ozgebostankolu@hotmail.com.
Guldal Esendagli-YilmazDepartment of Medical Pathology, Faculty of Medicine, Gazi University, Ankara, Turkey.
Aytug UnerDepartment of Internal Medicine, Division of Medical Oncology, Faculty of Medicine, Gazi University, Ankara, Turkey.
Bulent CetinDepartment of Internal Medicine, Division of Medical Oncology, Cumhuriyet University Sivas, Sivas, Turkey.
Suleyman BuyukberberDepartment of Internal Medicine, Division of Medical Oncology, Faculty of Medicine, Gazi University, Ankara, Turkey.
Mustafa BenekliDepartment of Internal Medicine, Division of Medical Oncology, Faculty of Medicine, Gazi University, Ankara, Turkey.
Mustafa N IlhanDepartment of Public Health, Faculty of Medicine, Gazi University, Ankara, Turkey.
Ugur CoskunDepartment of Internal Medicine, Division of Medical Oncology, Faculty of Medicine, Gazi University, Ankara, Turkey.
Ozlem GulbaharDepartment of Biochemistry, Faculty of Medicine, Gazi University, Ankara, Turkey.
Ahmet OzetDepartment of Internal Medicine, Division of Medical Oncology, Faculty of Medicine, Gazi University, Ankara, Turkey.
Gazi University · TRSivas Cumhuriyet Üniversitesi · TRTokat Gaziosmanpaşa Üniversitesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimThe aim of the present study was to evaluate the effect of crizotinib on visceral organs in an experimental rat model.

methodsEighteen Wistar albino rats were divided into three groups: experimental toxicity was induced with crizotinib (10 mg/kg) administered for 28 days (Group 1), 42 days (Group 2) orally by gavage. Control group received only distilled water. Rats in Group 1 and Group 2 were sacrificed after the collection of blood and tissue samples on the 28th and 42nd days, respectively.

resultsSubjects in Group 1 and Group 2 had abnormal histology mainly in lung and liver. There were intraalveolar hemorrhage in lungs; mild portal inflammation, perivenular focal and confluent necrosis in liver; inflammatory reaction in renal pelvis and periureteral areas, and focal pancreatitis in pancreas.

conclusionThis study is the first to evaluate the histopathological features of toxicity of crizotinib in a rat model.

Indexed as

Disease Models, AnimalAdministration, OralAnimalsAntineoplastic AgentsCrizotinibDose-Response Relationship, DrugMaleOrgan SpecificityPyrazolesPyridinesRatsRats, WistarTreatment OutcomeVisceraAntineoplastic AgentsCrizotinibPyrazolesPyridinesCrizotinibPulmonary intraalveolar hemorrhageRatToxicity

Identifiers

PMID26975454
OpenAlexW2302107892

What OpenQuestion holds

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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.