Evidence map›Paper›PMID 39110914›Full record

Observational studyRevista medica del Instituto Mexicano del Seguro Social2024

[Cardiotoxicity from anti-HER-2 therapies in patients with HER-2 positive breast cancer].

Natalia Camejo-Martínez, Cecilia Castillo-Leska, Valeria Rodríguez-Saenz, Guadalupe Herrera-Álvarez, Dahiana Amarillo-Hernández, María Carolina Dörner-Cabrera, Gabriel Krygier-Waltier

Abstract readEnglish AbstractObservational Study
In one paragraph

Observational study in Revista medica del Instituto Mexicano del Seguro Social, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Natalia Camejo-MartínezUniversidad de la República, Facultad de Medicina, Servicio de Oncología Clínica. Montevideo, Uruguay.ORCID 0000-0002-8684-0291
Cecilia Castillo-LeskaUniversidad de la República, Facultad de Medicina, Servicio de Oncología Clínica. Montevideo, Uruguay.ORCID 0000-0002-0417-0512
Valeria Rodríguez-SaenzUniversidad de la República, Facultad de Medicina, Servicio de Oncología Clínica. Montevideo, Uruguay.ORCID 0000-0001-8333-2438
Guadalupe Herrera-ÁlvarezUniversidad de la República, Facultad de Medicina, Departamento de Métodos Cuantitativos. Montevideo, Uruguay.ORCID 0000-0001-6888-2343
Dahiana Amarillo-HernándezUniversidad de la República, Facultad de Medicina, Servicio de Oncología Clínica. Montevideo, Uruguay.ORCID 0000-0002-8615-8639
María Carolina Dörner-CabreraHospital Departamental de Soriano "Zoilo A. Chelle", Unidad Ejecutora 30. Mercedes, Soriano, Uruguay.ORCID 0000-0003-3758-2545
Gabriel Krygier-WaltierUniversidad de la República, Facultad de Medicina, Servicio de Oncología Clínica. Montevideo, Uruguay.ORCID 0000-0002-0518-1854

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: HER-2 positive (+) breast cancer (BC) accounts for 20-25% of BC, it is more aggressive, and it has a lower survival rate. Since the approval of trastuzumab in 1998, other HER-2-targeted therapies such as pertuzumab and trastuzumab emtansine (TDM1) have been introduced, improving patient survival. However, cardiotoxicity is an adverse effect of these treatments. Objective: To estimate the incidence of cardiotoxicity with trastuzumab, trastuzumab/pertuzumab, and TDM1 in women with HER-2 + BC treated over a 6-year period at the Hospital de Clínicas and the Hospital Departamental de Soriano. Material and methods: Observational, descriptive, and retrospective study which included patients with HER-2 + BC treated with trastuzumab, trastuzumab/pertuzumab, or TDM1. Results: 81 patients were included, with a cardiotoxicity incidence of 23.4%. Cardiotoxicity was determined by a > 10% decrease in left ventricular ejection fraction (LVEF) (57.9%) and a LVEF < 50% evident during treatment (42.1%). Only 1 patient presented symptomatic heart failure. 63.1% of those who discontinued treatment due to cardiotoxicity managed to resume it. No relationship was evident between cardiovascular history or the administration regimen and the development of cardiotoxicity. Conclusion: The study showed a cardiotoxicity incidence similar to the international one. Most did not present cardiac toxicity, and if they did, it was asymptomatic and reversible.

Indexed as

Ado-Trastuzumab EmtansineAntibodies, Monoclonal, HumanizedBreast NeoplasmsCardiotoxicityErb-b2 Receptor Tyrosine KinasesTrastuzumabAdultAgedAntineoplastic Agents, ImmunologicalFemaleHumansIncidenceMaytansineMiddle AgedRetrospective StudiesAdo-Trastuzumab EmtansineAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesMaytansinepertuzumabTrastuzumabBreast NeoplasmsCardiotoxicityc erbB 2 ProteinUruguay

Identifiers

PMID39110914
PMCPMC12101866

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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.