Evidence map›Paper›PMID 26712595›Full record

SynthesisInternal and emergency medicine2016

Risk of severe cardiotoxicity following treatment with trastuzumab: a meta-analysis of randomized and cohort studies of 29,000 women with breast cancer.

Stefania Mantarro, Marta Rossi, Martina Bonifazi, Roberto D'Amico, Corrado Blandizzi, Carlo La Vecchia, Eva Negri, Lorenzo Moja

Open access · greenAbstract readMeta-AnalysisReview
PubMed Publisher
In one paragraph

Synthesis in Internal and emergency medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 2 pooled it
4.9field-weighted citation impact, top 3% 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

48 citing papers in PubMed, 2 syntheses or guidelines pooled it, 93 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 5 institutions in 1 country.

Stefania MantarroDepartment of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Marta RossiDepartment of Epidemiology, IRCSS Institute for Pharmacological Research "Mario Negri", Milan, Italy.
Martina BonifaziDepartment of Epidemiology, IRCSS Institute for Pharmacological Research "Mario Negri", Milan, Italy.
Roberto D'AmicoItalian Cochrane Centre, University of Modena and Reggio Emilia, Modena, Italy.
Corrado BlandizziDepartment of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Carlo La VecchiaDepartment of Clinical Medicine and Community Health, University of Milan, Milan, Italy.
Eva NegriDepartment of Epidemiology, IRCSS Institute for Pharmacological Research "Mario Negri", Milan, Italy.
Lorenzo MojaDepartment of Biomedical Sciences for Public Health, University of Milan, Via Carlo Pascal 36, 20133, Milan, Italy. lorenzo.moja@unimi.it.
Mario Negri Institute for Pharmacological Research · ITUniversity of Milan · ITUniversity of Pisa · ITIstituto Ortopedico Galeazzi · ITUniversity of Modena and Reggio Emilia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Trastuzumab prolongs survival in women with HER2-positive breast cancer, but may increase the risk of heart disease. The occurrence of severe cardiotoxicity, however, is not defined in real-life settings. We performed a meta-analysis of clinical trials and cohort studies to estimate the frequency of cardiotoxicities following trastuzumab treatment. We searched MEDLINE, EMBASE, and the Cochrane Library (1996-January 2014). The primary outcome was the frequency of severe cardiotoxicities up to 3-years after trastuzumab initiation. Among 58 studies (29,598 patients), severe cardiotoxicity occurred in 3.00% (95% CI 2.41-3.64), 2.62% (95% CI 1.97-3.35), and 3.14% (95% CI 2.12-4.37) of overall, early (EBC) and metastatic (MBC) breast cancer patients, respectively. In EBC, the proportion increased from 2.40% at the first year to a plateau of approximately 3% after the second year. In MBC, the proportion increased from 3.00 to 3.68% when trastuzumab was used as first line or further lines of therapy, respectively. In EBC, cardiotoxicity occurred in 2.90% of patients treated with taxanes and anthracyclines compared to 0.92% in patients treated with taxanes without anthracyclines. The occurrence of cardiotoxicity varied according to age, increasing from 2.31% in individuals <50 years, to 3.46% in those 50-59 years, to 4.91% in those >60 years of age. Cardiotoxicity was higher in smokers (5.3%), dyslipidemic patients (3.9%), BMI ≥25 (6.5%), diabetes (6.2%), hypertension (5.5%), or positive history of cardiac disease (19.1%). RCTs consistently report lower cardiac toxicity rates than observational studies (EBC: 1.7 versus 3.2; MBC: 2.8 versus 4.4). Following trastuzumab initiation, approximately three in 100 patients develop severe cardiotoxicity after 2 years. Patients enrolled in cohort studies, who more closely reflect women treated for breast cancer in real-life settings compared to RCTs, are at higher risk of developing cardiac events.

Indexed as

Antineoplastic AgentsBreast NeoplasmsCardiotoxicityCardiovascular DiseasesFemaleHumansTrastuzumabAntineoplastic AgentsTrastuzumabCardiotoxicityEarly breast cancerHeart failureMeta-analysisMetastatic breast cancerTrastuzumab

Identifiers

PMID26712595
OpenAlexW2205841570

What OpenQuestion holds

Textmetadata
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.