Long-term cardiovascular disease risk after anthracycline and trastuzumab treatments in US breast cancer survivors.

IF 9.9 1区 医学 Q1 ONCOLOGY JNCI Journal of the National Cancer Institute Pub Date : 2024-08-01 DOI:10.1093/jnci/djae107
Jacqueline B Vo, Cody Ramin, Lene H S Veiga, Carolyn Brandt, Rochelle E Curtis, Clara Bodelon, Ana Barac, Véronique L Roger, Heather Spencer Feigelson, Diana S M Buist, Erin J Aiello Bowles, Gretchen L Gierach, Amy Berrington de González
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Abstract

Background: Although breast cancer survivors are at risk for cardiovascular disease (CVD) from treatment late effects, evidence to inform long-term and age-specific cardiovascular surveillance recommendations is lacking.

Methods: We conducted a retrospective cohort study of 10 211 women diagnosed with first primary unilateral breast cancer in Kaiser Permanente Washington or Colorado (aged 20 years and older, survived ≥1 year). We estimated multivariable adjusted hazard ratios (HRs) for associations between initial chemotherapy regimen type (anthracycline and/or trastuzumab, other chemotherapies, no chemotherapy [referent]) and CVD risk, adjusted for patient characteristics, other treatments, and CVD risk factors. Cumulative incidence was calculated considering competing events.

Results: After 5.79 median years, 14.67% of women developed CVD (cardiomyopathy and/or heart failure [HF], ischemic heart disease, stroke). Women treated with anthracyclines and/or trastuzumab had a higher risk of CVD compared with no chemotherapy (adjusted HR = 1.53, 95% confidence interval [CI] = 1.31 to 1.79), persisting at least 5 years postdiagnosis (adjusted HR5-<10 years = 1.85, 95% CI = 1.44 to 2.39; adjusted HR≥10 years = 1.83, 95% CI = 1.34 to 2.49). Cardiomyopathy and/or HF risks were elevated among women treated with anthracyclines and/or trastuzumab compared with no chemotherapy, especially for those aged younger than 65 years (adjusted HR20-54years = 2.97, 95% CI = 1.72 to 5.12; adjusted HR55-64years = 2.21, 95% CI = 1.52 to 3.21), differing for older women (adjusted HR≥65 years = 1.32, 95% CI = 0.97 to 1.78), and at least 5 years postdiagnosis (adjusted HR5-<10years = 1.89, 95% CI = 1.35 to 2.64; adjusted HR≥10 years = 2.21, 95% CI = 1.52 to 3.20). Anthracyclines and/or trastuzumab receipt was associated with increased ischemic heart disease risks after 5 or more years (adjusted HR5-<10years = 1.51, 95% CI = 1.06 to 2.14; adjusted HR≥10 years = 1.86, 95% CI = 1.18 to 2.93) with no clear age effects, and stroke risk (adjusted HR = 1.33, 95% CI = 1.05 to 1.69), which did not vary by time or age. There was some evidence of long-term cardiomyopathy and/or HF and ischemic heart disease risks with other chemotherapies. Among women aged younger than 65 treated with anthracyclines and/or trastuzumab, up to 16% developed CVD by 10 years (20-54 years = 6.91%; 55-64 years = 16.00%), driven by cardiomyopathy and/or HF (20-54 years = 3.90%; 55-64 years = 9.78%).

Conclusions: We found increased long-term risks of cardiomyopathy and/or HF and ischemic heart disease among breast cancer survivors treated with anthracyclines and/or trastuzumab and increased cardiomyopathy and/or HF risk among women aged younger than 65 years.

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美国乳腺癌幸存者接受蒽环类和曲妥珠单抗治疗后的长期心血管疾病风险。
背景:尽管乳腺癌幸存者有可能因治疗晚期效应而罹患心血管疾病(CVD),但目前还缺乏相关证据来为长期和特定年龄的心血管监测建议提供依据:我们对华盛顿州或科罗拉多州凯撒医疗集团的 10211 名首次诊断为原发性单侧乳腺癌的女性(年龄在 20 岁以上,存活时间≥1 年)进行了一项回顾性队列研究。我们估算了初始化疗方案类型(蒽环类和/或曲妥珠单抗、其他化疗方案、无化疗方案 [参考])与心血管疾病风险之间的多变量调整危险比 (aHR),并对患者特征、其他治疗方法和心血管疾病风险因素进行了调整。计算累积发病率时考虑了竞争事件:中位数为5.79年后,14.67%的女性发生了心血管疾病(心肌病/心力衰竭(CM/HF)、缺血性心脏病(IHD)、中风)。与未接受化疗相比,接受蒽环类药物和/或曲妥珠单抗治疗的女性患心血管疾病的风险更高(aHR=1.53,95%CI=1.31-1.79),且在确诊后持续5年以上(aHR5-结论:我们发现,在接受蒽环类药物和/或曲妥珠单抗治疗的乳腺癌幸存者中,CM/HF 和 IHD 的长期风险增加,而在年龄超过 50 岁的女性中,CM/HF 风险增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
17.00
自引率
2.90%
发文量
203
审稿时长
4-8 weeks
期刊介绍: The Journal of the National Cancer Institute is a reputable publication that undergoes a peer-review process. It is available in both print (ISSN: 0027-8874) and online (ISSN: 1460-2105) formats, with 12 issues released annually. The journal's primary aim is to disseminate innovative and important discoveries in the field of cancer research, with specific emphasis on clinical, epidemiologic, behavioral, and health outcomes studies. Authors are encouraged to submit reviews, minireviews, and commentaries. The journal ensures that submitted manuscripts undergo a rigorous and expedited review to publish scientifically and medically significant findings in a timely manner.
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