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蒽环类药物相关心脏毒性与同源重组缺陷(HRD)突变特征的乳腺癌患者。

Anthracycline-related cardiotoxicity in patients with breast cancer harboring mutational signature of homologous recombination deficiency (HRD).

机构信息

Department of Surgical, Oncological and Oral Sciences, Section of Medical Oncology, University of Palermo, Palermo.

Division of Cardiology, University Hospital Paolo Giaccone, Palermo; Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties (PROMISE) "G. D'Alessandro", University of Palermo, Palermo.

出版信息

ESMO Open. 2024 Jan;9(1):102196. doi: 10.1016/j.esmoop.2023.102196. Epub 2023 Dec 19.

Abstract

BACKGROUND

The BRCA proteins play a key role in the homologous recombination (HR) pathway. Beyond BRCA1/2, other genes are involved in the HR repair (HRR). Due to the prominent role in the cellular repair process, pathogenic or likely pathogenic variants (PV/LPVs) in HRR genes may cause inadequate DNA damage repair in cardiomyocytes.

PATIENTS AND METHODS

This was a multicenter, hospital-based, retrospective cohort study to investigate the heart toxicity from anthracycline-containing regimens (ACRs) in the adjuvant setting of breast cancer (BC) patients carrying germline BRCA PV/LPVs and no-BRCA HRR pathway genes. The left ventricular ejection fraction (LVEF) was assessed using cardiac ultrasound before starting ACR therapy and at subsequent time points according to clinical indications.

RESULTS

Five hundred and three BC patients were included in the study. We predefined three groups: (i) BRCA cohort; (ii) no-BRCA cohort; (iii) variant of uncertain significance (VUS)/wild-type (WT) cohort. When baseline (T0) and post-ACR (T1) LVEFs between the three cohorts were compared, pre-treatment LVEF values were not different (BRCA1/2 versus HRR-no-BRCA versus VUS/WT cohort). Notably, during monitoring (T1, median 3.4 months), patients carrying BRCA or HRR no-BRCA germline pathogenic or likely pathogenic variants showed a statistically significant reduction of LVEF compared to baseline (T0). To assess the relevance of HRR on the results, we included the analysis of the subgroup of 20 BC patients carrying PV/LPVs in other genes not involved in HRR, such as mismatch repair genes (MUTYH, PMS2, MSH6). Unlike HRR genes, no significant differences in T0-T1 were found in this subgroup of patients.

CONCLUSION

Our data suggest that deleterious variants in HRR genes, leading to impaired HR, could increase the sensitivity of cardiomyocytes to ACR in early BC patients. In this subgroup of patients, other measurements, such as the global longitudinal strain, and a more in-depth assessment of risk factors may be proposed in the future to optimize cardiovascular risk management and improve long-term survival.

摘要

背景

BRCA 蛋白在同源重组(HR)途径中发挥关键作用。除 BRCA1/2 外,其他基因也参与 HR 修复(HRR)。由于在细胞修复过程中起重要作用,HRR 基因中的致病变异或可能致病变异(PV/LPVs)可能导致心肌细胞中 DNA 损伤修复不足。

患者和方法

这是一项多中心、基于医院的回顾性队列研究,旨在调查携带胚系 BRCA PV/LPVs 且无 BRCA HRR 通路基因的乳腺癌(BC)患者辅助接受含蒽环类药物方案(ACRs)治疗时的心脏毒性。在开始 ACR 治疗前和根据临床指征随后的时间点使用心脏超声评估左心室射血分数(LVEF)。

结果

本研究共纳入 503 例 BC 患者。我们预先定义了三组:(i)BRCA 组;(ii)非 BRCA 组;(iii)意义不明变异(VUS)/野生型(WT)组。当比较三组之间的基线(T0)和 ACR 后(T1)LVEF 时,治疗前 LVEF 值无差异(BRCA1/2 与 HRR-非 BRCA 与 VUS/WT 组)。值得注意的是,在监测期间(T1,中位数 3.4 个月),携带 BRCA 或 HRR 非 BRCA 种系致病性或可能致病性变异的患者与基线(T0)相比,LVEF 有统计学意义的下降。为了评估 HRR 对结果的相关性,我们纳入了 20 例携带不参与 HRR 的其他基因(错配修复基因 MUTYH、PMS2、MSH6)中 PV/LPVs 的 BC 患者亚组的分析。与 HRR 基因不同,该亚组患者在 T0-T1 期间无显著差异。

结论

我们的数据表明,HRR 基因中的有害变异导致 HR 受损,可能增加早期 BC 患者对 ACR 的敏感性。在该亚组患者中,未来可能会提出其他测量方法,如整体纵向应变,以及更深入的危险因素评估,以优化心血管风险管理并提高长期生存率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50a1/10837774/1f820e0a63e7/ga1.jpg

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