紫杉烷-蒽环类和紫杉烷单用治疗对乳腺癌患者心功能的影响——一项回顾性队列研究。

IF 3.2 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Árpád Kézdi, Emese Szelke, Magdolna Dank, Dorottya Mühl, Gyöngyvér Szentmártoni, Gergely Szabó, Dominic Joseph Fogarasi, István Takács, Viktor J Horváth, Ádám G Tabák
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引用次数: 0

摘要

导读:心脏毒性、蒽环类药物为基础的治疗在选定的乳腺癌患者中具有很高的价值。我们的目的是描述蒽环类药物加紫杉烷和单紫杉烷化疗对乳腺癌妇女超声心动图参数的影响。方法:回顾性分析Semmelweis大学内科和肿瘤科心脏病门诊2018-2021年治疗乳腺癌的68名女性(18岁)的数据。基线时收集心血管病史,每次就诊时完成经胸超声心动图。此外,我们还审查了电子病历,以获取其他相关医疗信息。测量的超声心动图参数根据第一次治疗后的时间分为5个时期(0-14天,然后每半年和545天以上)。通过线性混合模型分析随访期间射血分数和舒张功能相关指标的变化轨迹。结果:蒽环类药物加紫杉烷组平均年龄为52.7±14.1岁,单紫杉烷组平均年龄为55.2±13.1岁。蒽环类药物的平均剂量相当于240 mg/m2的阿霉素。总体既往心血管负担较低。只有蒽环类药物加紫杉烷组有统计学意义的变化:射血分数从基线时的65.5±3.1%轻度下降到181-365天时的62.1±3.2% (p = 0.007),减速时间从15-180天时的227.9±33.9 msec轻度下降到197.4±29.4 msec (p = 0.028)。这两种下降都只是暂时的,并且在随访期间的值接近基线值(p = NS vs.基线)。其他影响射血分数的重要因素是年龄和高血压。结论:我们的研究证实了单紫杉烷和蒽环类联合紫杉烷化疗对心功能的总体安全性,因为我们发现单紫杉烷治疗与超声心动图参数没有变化,而蒽环类联合紫杉烷化疗与射血分数的暂时降低和临床不显著的减速时间相关,随访1.5年。我们的研究受限于其回顾性的性质和较少的参与者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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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来源期刊
Cardio-oncology
Cardio-oncology Medicine-Cardiology and Cardiovascular Medicine
CiteScore
5.00
自引率
3.00%
发文量
17
审稿时长
7 weeks
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