Evidence map›Paper›PMID 28399109›Full record

ArticleBritish journal of cancer2017

Tyrosine kinase-targeting drugs-associated heart failure.

N Gronich, I Lavi, O Barnett-Griness, W Saliba, D R Abernethy, G Rennert

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 37 citations in OpenAlex.

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  10. Cardio-Oncology: Mechanisms, Drug Combinations, and Reverse Cardio-Oncology.International journal of molecular sciences · 2022
    Review
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  19. Cardiotoxicity of Novel Targeted Chemotherapeutic Agents.Current treatment options in cardiovascular medicine · 2018
    Review
  20. A Review of Matched-pairs Feature Selection Methods for Gene Expression Data Analysis.Computational and structural biotechnology journal · 2018
    Review
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

6 authors at 3 institutions in 2 countries.

N GronichDepartment of Community Medicine and Epidemiology, Lady Davis Carmel Medical Center, and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, 7 Michal Street, Haifa 3436212, Israel.
I LaviDepartment of Community Medicine and Epidemiology, Lady Davis Carmel Medical Center, and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, 7 Michal Street, Haifa 3436212, Israel.
O Barnett-GrinessDepartment of Community Medicine and Epidemiology, Lady Davis Carmel Medical Center, and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, 7 Michal Street, Haifa 3436212, Israel.
W SalibaDepartment of Community Medicine and Epidemiology, Lady Davis Carmel Medical Center, and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, 7 Michal Street, Haifa 3436212, Israel.
D R AbernethyDrug Safety Group, Office of Clinical Pharmacology, US Food and Drug Administration, 10903 New Hampshire Avenue, Silver Spring, MD 20993, USA.
G RennertDepartment of Community Medicine and Epidemiology, Lady Davis Carmel Medical Center, and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, 7 Michal Street, Haifa 3436212, Israel.
Technion – Israel Institute of Technology · ILClalit Health Services · ILUnited States Food and Drug Administration · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe impact of cancer therapies on cardiac disease in the general adult cancer survivor population is largely unknown. Our objective was to evaluate which tyrosine kinase-targeting drugs are associated with greater risk for new-onset heart failure (HF).

methodsA nested case-control analysis was conducted within a cohort of 27 992 patients of Clalit Health Services, newly treated with a tyrosine kinase-targeting, and/or chemotherapeutic drug, for a malignant disease, between 1 January 2005 and 31 December 2012. Each new case of HF was matched to up to 30 controls from the cohort on calendar year of cohort entry, age, gender, and duration of follow-up. Main outcome measure was odds ratio (OR) with 95% confidence interval (CI) of new-onset HF.

resultsThere were 936 incident cases of HF during 71 742 person-years of follow-up. Trastuzumab (OR 1.90, 95% CI 1.46-2.49), cetuximab (OR 1.72, 1.10-2.69), panitumumab (OR 3.01, 1.02-8.85), and sunitinib (OR 3.39, 1.78-6.47) were associated with increased HF risk. Comorbidity independently associated with higher risk in a multivariable conditional regression model was diabetes mellitus, hypertension, chronic renal failure, ischaemic heart disease, valvular heart disease, arrhythmia, and smoking.

conclusionsTrastuzumab, cetuximab, panitumumab, and sunitinib are associated with increased risk for new-onset HF.

Indexed as

AgedAged, 80 and overAntibodies, MonoclonalAntineoplastic AgentsCase-Control StudiesCetuximabCohort StudiesHeart FailureHumansIncidenceIndolesIsraelMiddle AgedNeoplasmsOdds RatioPanitumumabAntibodies, MonoclonalAntineoplastic AgentsCetuximabIndolesPanitumumabProtein Kinase InhibitorsPyrrolesSunitinibTrastuzumab

Identifiers

PMID28399109
PMCPMC5482733
OpenAlexW2605940892

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.