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在基因组检测时代,使用腋窝超声引导乳腺癌管理。

Use of axillary ultrasound to guide breast cancer management in the genomic assay era.

机构信息

Breast Department, KK Women's and Children's Hospital, Singapore.

Duke-NUS Medical School, Singapore.

出版信息

Breast Dis. 2024;43(1):19-23. doi: 10.3233/BD-230032.

Abstract

INTRODUCTION

Chemotherapy is conventionally offered to non-stage IV breast cancer patients with metastatic nodes. However, the RxPONDER trial showed that chemotherapy can be omitted in selected patients with 1-3 metastatic nodes if the 21-gene assay recurrence score is ≤25. We aimed to investigate if axillary ultrasound can identify this group of patients with limited nodal burden so that they can undergo upfront surgery followed by gene assay testing, to potentially avoid chemotherapy.

METHODS

T1-3, node positive, hormone receptor-positive and HER2-negative breast cancer patients ≥50 years old with axillary lymph node dissection (ALND) were reviewed from 2 centres. Patients with neoadjuvant chemotherapy and bilateral cancers were excluded. Number of ultrasound-detected abnormal axillary nodes, demographic and histological parameters were correlated with the number of metastatic nodes found on ALND.

RESULTS

138 patients were included, 59 (42.8%) and 79 (57.2%) patients had 1-3 and >3 metastatic nodes on ALND respectively. On logistic regression and ROC analysis, the number of ultrasound-detected abnormal nodes was significant (p < 0.001) for predicting limited nodal burden (ROC AUC = 0.7135). Probabilities of <4 metastatic nodes with ultrasound cut-offs of 5, 6 and 8 abnormal nodes were 0.057, 0.026 and 0.005 respectively, with 100% specificity.

CONCLUSION

A cut-off of ≤5 ultrasound-detected abnormal nodes can distinguish between patients with limited versus high nodal burden, with high specificity. Hence, incorporating the number of abnormal ultrasound-detected nodes into clinical practice may prove useful in guiding between upfront surgery and gene assay testing or neoadjuvant chemotherapy in this group of patients.

摘要

介绍

化疗通常用于转移性淋巴结非 IV 期乳腺癌患者。然而,RxPONDER 试验表明,如果 21 基因检测复发评分≤25,对于 1-3 个转移性淋巴结的选定患者可以省略化疗。我们旨在研究腋窝超声是否可以识别这组淋巴结受累有限的患者,以便他们可以接受 upfront 手术,然后进行基因检测,以潜在地避免化疗。

方法

回顾了来自 2 个中心的 T1-3、淋巴结阳性、激素受体阳性和 HER2 阴性的年龄≥50 岁的乳腺癌患者,这些患者接受了腋窝淋巴结清扫术(ALND)。排除了接受新辅助化疗和双侧癌症的患者。腋窝超声检测到的异常淋巴结数量、人口统计学和组织学参数与 ALND 中发现的转移性淋巴结数量相关。

结果

共纳入 138 例患者,59 例(42.8%)和 79 例(57.2%)患者在 ALND 上分别有 1-3 个和>3 个转移性淋巴结。在逻辑回归和 ROC 分析中,超声检测到的异常淋巴结数量对预测有限的淋巴结受累具有显著意义(p<0.001)(ROC AUC = 0.7135)。超声截止值为 5、6 和 8 个异常淋巴结时,预测<4 个转移性淋巴结的概率分别为 0.057、0.026 和 0.005,特异性均为 100%。

结论

超声检测到的异常淋巴结数量≤5 个可以区分局限性和高淋巴结受累患者,具有较高的特异性。因此,将异常超声检测到的淋巴结数量纳入临床实践可能有助于指导这组患者进行 upfront 手术与基因检测或新辅助化疗之间的选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc63/10977404/3c244afd1a74/bd-43-bd230032-g001.jpg

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