Evidence map›Paper›PMID 30740760›Full record

ArticleBritish journal of clinical pharmacology2019

Cabozantinib-related cardiotoxicity: a prospective analysis in a real-world cohort of metastatic renal cell carcinoma patients.

Roberto Iacovelli, Chiara Ciccarese, Giuseppe Fornarini, Francesco Massari, Davide Bimbatti, Claudia Mosillo, Sara Elena Rebuzzi, Vincenzo Di Nunno, Massimiliano Grassi, Emanuela Fantinel and 2 more

Abstract readMulticenter Study
In one paragraph

Article in British journal of clinical pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Cardiotoxicity induced by traditional chemotherapy: mechanisms and mitigation strategies.Apoptosis : an international journal on programmed cell death · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Roberto IacovelliDepartment of Medical Oncology, Azienda Ospedaliera Universitaria Integrata (AOUI), Verona, Italy.ORCID 0000-0002-1750-2117
Chiara CiccareseDepartment of Medical Oncology, Azienda Ospedaliera Universitaria Integrata (AOUI), Verona, Italy.
Giuseppe FornariniDepartment of Medical Oncology, IRCCS Azienda Ospedaliera Universitaria San Martino-Istituto Nazionale per la Ricerca sul Cancro, Genova, Italy.
Francesco MassariDepartment of Medical Oncology, Sant'Orsola-Malpighi Hospital, Bologna, Italy.
Davide BimbattiDepartment of Medical Oncology, Azienda Ospedaliera Universitaria Integrata (AOUI), Verona, Italy.
Claudia MosilloDepartment of Medical Oncology, Azienda Ospedaliera Universitaria Integrata (AOUI), Verona, Italy.
Sara Elena RebuzziDepartment of Medical Oncology, IRCCS Azienda Ospedaliera Universitaria San Martino-Istituto Nazionale per la Ricerca sul Cancro, Genova, Italy.
Vincenzo Di NunnoDepartment of Medical Oncology, Sant'Orsola-Malpighi Hospital, Bologna, Italy.
Massimiliano GrassiDepartment of Medical Oncology, IRCCS Azienda Ospedaliera Universitaria San Martino-Istituto Nazionale per la Ricerca sul Cancro, Genova, Italy.
Emanuela FantinelDepartment of Medical Oncology, Azienda Ospedaliera Universitaria Integrata (AOUI), Verona, Italy.
Andrea ArdizzoniDepartment of Medical Oncology, Sant'Orsola-Malpighi Hospital, Bologna, Italy.
Giampaolo TortoraDepartment of Medical Oncology, Azienda Ospedaliera Universitaria Integrata (AOUI), Verona, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsData regarding the cardiac toxicity of cabozantinib lacks. The aim of our study was to assess the risk of cabozantinib-related cardiotoxicity in mRCC patients.

methodsWe performed a multicentre prospective study on mRCC patients treated with cabozantinib between October 2016 and November 2017. Transthoracic echocardiogram and plasma biomarkers assay were assessed at baseline, 3 and 6 months after cabozantinib initiation.

resultsThe study population included 22 mRCC patients. At baseline, 9.1% had a reduced left ventricular ejection fraction (LVEF), but none had a left ventricular systolic dysfunction. Patients with baseline reduced LVEF did not show further significant LVEF modification after 3 months. After 6 months, only 1 had an LVEF decline >10% compared to baseline, resulting in LV systolic dysfunction. At baseline, 64.7% and 27.3% of patients had elevated precursor brain natriuretic peptide (proBNP) and high-sensitivity troponin I (hsTnI), respectively. Among patients with basal normal proBNP and hsTnI, none had elevated values at 3 and 6 months. No correlation was found between basal elevated proBNP and basal reduced LVEF (P = .29), and between elevated proBNP and reduced LVEF after 6 months (P = .37). Similarly, we found no correlations between elevated hsTnI and reduced LVEF or elevated proBNP at baseline (P = .47; P = .38), at 3 (P = .059; P = .45) and after 6 months (P = .72; P = 1.0).

conclusionsThis prospective study revealed a modest risk of developing left ventricular systolic dysfunction related to cabozantinib. A lack of correlation between elevated cardiac biomarkers and reduced LVEF at different time-points was detected. Assessments of the cardiac function should be reserved at the occurrence of clinical symptoms.

Indexed as

AgedAnilidesAntineoplastic AgentsBiomarkersCarcinoma, Renal CellCardiotoxicityFemaleHumansIncidenceItalyKidney NeoplasmsMaleNatriuretic Peptide, BrainProspective StudiesProtein Kinase InhibitorsPyridinesAnilidesAntineoplastic AgentsBiomarkerscabozantinibNatriuretic Peptide, BrainProtein Kinase InhibitorsPyridinesTroponin Icabozantinibcardiotoxicityhigh-sensitivity troponin Imetastatic renal cell carcinomaprecursor brain natriuretic peptide

Identifiers

PMID30740760
PMCPMC6533423

What OpenQuestion holds

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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.