Effects of taxane-anthracycline and taxane only treatment on cardiac function in breast cancer—a retrospective cohort study

Abstract Introduction Cardiotoxic, anthracycline-based therapies have high value in selected patients with breast cancer. We aimed to describe the effect of anthracycline plus taxane and single taxane chemotherapies on echocardiographic parameters in women with breast cancer. Methods We retrospectiv...

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Main Authors: Árpád Kézdi, Emese Szelke, Magdolna Dank, Dorottya Mühl, Gyöngyvér Szentmártoni, Gergely Szabó, Dominic Joseph Fogarasi, István Takács, Viktor J Horváth, Ádám G Tabák
Format: Article
Language:English
Published: BMC 2025-04-01
Series:Cardio-Oncology
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Online Access:https://doi.org/10.1186/s40959-025-00335-4
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author Árpád Kézdi
Emese Szelke
Magdolna Dank
Dorottya Mühl
Gyöngyvér Szentmártoni
Gergely Szabó
Dominic Joseph Fogarasi
István Takács
Viktor J Horváth
Ádám G Tabák
author_facet Árpád Kézdi
Emese Szelke
Magdolna Dank
Dorottya Mühl
Gyöngyvér Szentmártoni
Gergely Szabó
Dominic Joseph Fogarasi
István Takács
Viktor J Horváth
Ádám G Tabák
author_sort Árpád Kézdi
collection DOAJ
description Abstract Introduction Cardiotoxic, anthracycline-based therapies have high value in selected patients with breast cancer. We aimed to describe the effect of anthracycline plus taxane and single taxane chemotherapies on echocardiographic parameters in women with breast cancer. Methods We retrospectively analysed data of 68 women (> 18 years old) treated for breast cancer in 2018–2021 in the Cardiology Outpatient Clinic of Semmelweis University, Department of Internal Medicine and Oncology. Cardiovascular medical history was collected at baseline and transthoracic echocardiography was completed at each visit. Also, we reviewed electronic medical records for other relevant medical information. Measured echocardiography parameters were assigned to five periods (0–14 days, then every half year and beyond day 545) based on the time since the first treatment. Trajectories of ejection fraction and diastolic function associated markers over the follow-up periods were analysed by linear mixed models. Results Mean age of the anthracycline plus taxane group was 52.7 ± 14.1 years, of the single taxane group 55.2 ± 13.1 years. The mean anthracycline dose was equivalent to 240 mg/m2 of doxorubicin. Overall pre-existing cardiovascular burden was low. Statistically significant changes were found only in the anthracycline plus taxane group: ejection fraction decreased mildly from 65.5 ± 3.1% at baseline to 62.1 ± 3.2% at 181–365 days (p = 0.007) while deceleration time decreased mildly from 227.9 ± 33.9 msec to 197.4 ± 29.4 msec at 15–180 days (p = 0.028). Both drops were only temporary and values neared baseline values over follow-up (p = NS vs. baseline). Other important determinants of ejection fraction were age and hypertension among the investigated risk factors. Conclusion Our study confirms the overall safety on cardiac function of both single taxane and anthracycline plus taxane chemotherapy, as we found no changes in echocardiographic parameters associated with single taxane therapy, while anthracycline plus taxane chemotherapy was associated with a temporary and clinically insignificant reduction of ejection fraction and deceleration time over 1.5 years of follow-up. Our study is limited by its retrospective nature and the low number of participants.
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spelling doaj-art-ff29f2010f7b4bf3a24b0181ca5ea6282025-08-20T03:06:50ZengBMCCardio-Oncology2057-38042025-04-0111111310.1186/s40959-025-00335-4Effects of taxane-anthracycline and taxane only treatment on cardiac function in breast cancer—a retrospective cohort studyÁrpád Kézdi0Emese Szelke1Magdolna Dank2Dorottya Mühl3Gyöngyvér Szentmártoni4Gergely Szabó5Dominic Joseph Fogarasi6István Takács7Viktor J Horváth8Ádám G Tabák9Department of Internal Medicine and Oncology, Semmelweis UniversityDepartment of Internal Medicine and Oncology, Semmelweis UniversityDepartment of Internal Medicine and Oncology, Semmelweis UniversityDepartment of Internal Medicine and Oncology, Semmelweis UniversityDepartment of Internal Medicine and Oncology, Semmelweis UniversityDepartment of Internal Medicine and Oncology, Semmelweis UniversityDepartment of Internal Medicine and Oncology, Semmelweis UniversityDepartment of Internal Medicine and Oncology, Semmelweis UniversityDepartment of Internal Medicine and Oncology, Semmelweis UniversityDepartment of Internal Medicine and Oncology, Semmelweis UniversityAbstract Introduction Cardiotoxic, anthracycline-based therapies have high value in selected patients with breast cancer. We aimed to describe the effect of anthracycline plus taxane and single taxane chemotherapies on echocardiographic parameters in women with breast cancer. Methods We retrospectively analysed data of 68 women (> 18 years old) treated for breast cancer in 2018–2021 in the Cardiology Outpatient Clinic of Semmelweis University, Department of Internal Medicine and Oncology. Cardiovascular medical history was collected at baseline and transthoracic echocardiography was completed at each visit. Also, we reviewed electronic medical records for other relevant medical information. Measured echocardiography parameters were assigned to five periods (0–14 days, then every half year and beyond day 545) based on the time since the first treatment. Trajectories of ejection fraction and diastolic function associated markers over the follow-up periods were analysed by linear mixed models. Results Mean age of the anthracycline plus taxane group was 52.7 ± 14.1 years, of the single taxane group 55.2 ± 13.1 years. The mean anthracycline dose was equivalent to 240 mg/m2 of doxorubicin. Overall pre-existing cardiovascular burden was low. Statistically significant changes were found only in the anthracycline plus taxane group: ejection fraction decreased mildly from 65.5 ± 3.1% at baseline to 62.1 ± 3.2% at 181–365 days (p = 0.007) while deceleration time decreased mildly from 227.9 ± 33.9 msec to 197.4 ± 29.4 msec at 15–180 days (p = 0.028). Both drops were only temporary and values neared baseline values over follow-up (p = NS vs. baseline). Other important determinants of ejection fraction were age and hypertension among the investigated risk factors. Conclusion Our study confirms the overall safety on cardiac function of both single taxane and anthracycline plus taxane chemotherapy, as we found no changes in echocardiographic parameters associated with single taxane therapy, while anthracycline plus taxane chemotherapy was associated with a temporary and clinically insignificant reduction of ejection fraction and deceleration time over 1.5 years of follow-up. Our study is limited by its retrospective nature and the low number of participants.https://doi.org/10.1186/s40959-025-00335-4Breast cancerCardiotoxicityAnthracyclineTaxaneEchocardiography
spellingShingle Árpád Kézdi
Emese Szelke
Magdolna Dank
Dorottya Mühl
Gyöngyvér Szentmártoni
Gergely Szabó
Dominic Joseph Fogarasi
István Takács
Viktor J Horváth
Ádám G Tabák
Effects of taxane-anthracycline and taxane only treatment on cardiac function in breast cancer—a retrospective cohort study
Cardio-Oncology
Breast cancer
Cardiotoxicity
Anthracycline
Taxane
Echocardiography
title Effects of taxane-anthracycline and taxane only treatment on cardiac function in breast cancer—a retrospective cohort study
title_full Effects of taxane-anthracycline and taxane only treatment on cardiac function in breast cancer—a retrospective cohort study
title_fullStr Effects of taxane-anthracycline and taxane only treatment on cardiac function in breast cancer—a retrospective cohort study
title_full_unstemmed Effects of taxane-anthracycline and taxane only treatment on cardiac function in breast cancer—a retrospective cohort study
title_short Effects of taxane-anthracycline and taxane only treatment on cardiac function in breast cancer—a retrospective cohort study
title_sort effects of taxane anthracycline and taxane only treatment on cardiac function in breast cancer a retrospective cohort study
topic Breast cancer
Cardiotoxicity
Anthracycline
Taxane
Echocardiography
url https://doi.org/10.1186/s40959-025-00335-4
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