Evidence map›Paper›PMID 39495473›Full record

ArticleIrish journal of medical science2025

Evaluation of early cardiotoxicity in HER2-positive breast cancer patients receiving radiotherapy and concurrent trastuzumab.

Dicle Aslan, Sadik Ozoner, Mevlude Inanc, Oguz Galip Yildiz, Mehmet Tugrul Inanc

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Article in Irish journal of medical science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Dicle AslanDepartment of Radiation Oncology, Erciyes University, Faculty of Medicine, 38140, Kayseri, Türkiye. dicleaslan@erciyes.edu.tr.ORCID http://orcid.org/0000-0002-3716-3925
Sadik OzonerDepartment of Radiation Oncology, Mugla Education and Research Hospital, Mugla, Türkiye.
Mevlude InancDepartment of Medical Oncology, Erciyes University, Faculty of Medicine, Kayseri, Türkiye.
Oguz Galip YildizDepartment of Radiation Oncology, Erciyes University, Faculty of Medicine, 38140, Kayseri, Türkiye.
Mehmet Tugrul InancDepartment of Cardiology, Erciyes University, Faculty of Medicine, Kayseri, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOverexpression of human epidermal growth factor receptor 2 (HER-2) is associated with aggressive disease in breast cancer. Trastuzumab and radiotherapy are standard treatments for patients with HER-2 + breast cancer, but they may increase the risk of cardiotoxicity.

aimThis study aimed to assess early cardiotoxicity in patients receiving radiotherapy (RT) and concurrent trastuzumab.

methodThe study included 116 patients with HER-2 + breast cancer who received concurrent treatment with trastuzumab and RT (52 right-side; 64 left-side). Five left ventricular ejection fraction (LVEF) measurements were performed: one before treatment and four subsequent measurements taken at three-month intervals. LVEF was also assessed before (preRT-EF) and after (postRT-EF) radiotherapy.

resultsThe baseline LVEF was 62.27 ± 5.5%, while the 12-month LVEF was 59.8 ± 5.8% (p < 0.05). In subgroups, post-RT LVEF values ​​were significantly lower than pre-RT LVEF values (p < 0.05). No significant difference was found between the reduction in LVEF for patients receiving 50 Gy and 60 Gy doses. Moreover, the contribution of regional lymph node irradiation to the decrease in LVEF could not be demonstrated. A positive correlation was found between the total trastuzumab dose and the decrease in LVEF from preRT to postRT. Additionally, a positive correlation was observed between the total taxane dose and the reduction in LVEF from baseline to 9 months, both in the overall group and in the left breast cancer group.

conclusionIn our study,it was found that not only trastuzumab but also taxane-based agents could be cardiotoxic. However, no connection was found between RT doses and the decrease in LVEF.

Indexed as

Antineoplastic Agents, ImmunologicalBreast NeoplasmsCardiotoxicityErb-b2 Receptor Tyrosine KinasesTrastuzumabAdultAgedFemaleHumansMiddle AgedStroke VolumeVentricular Function, LeftAntineoplastic Agents, ImmunologicalERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesTrastuzumabBreast cancerCardiotoxicityRadiotherapyTrastuzumab

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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.