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新辅助治疗后非pCR乳腺癌标本中的激素受体和HER2状态转换

Hormone Receptor and HER2 Status Switch in Non-pCR Breast Cancer Specimens after Neoadjuvant Therapy.

作者信息

Dimpfl Moritz, Mayr Doris, Schmoeckel Elisa, Degenhardt Tom, Eggersmann Tanja K, Harbeck Nadia, Wuerstlein Rachel

机构信息

aDepartment of Obstetrics and Gynecology, Breast Center and CCC Munich, LMU University Hospital, Munich, Germany.

bInstitute of Pathology and CCC Munich, Ludwig-Maximilian-University, Munich, Germany.

出版信息

Breast Care (Basel). 2022 Oct;17(5):501-507. doi: 10.1159/000524698. Epub 2022 Apr 27.

Abstract

INTRODUCTION

This project aimed to identify the frequency of a switch of hormone receptor (HR) and/or HER2 status after neoadjuvant chemotherapy (NAC) for early breast cancer.

METHODS

Tumor samples from patients without pathological complete response (non-pCR) were evaluated. Pathological complete response (pCR) was defined as no invasive tumor in breast and lymph nodes (ypT0/is ypN0). HR and HER2 status determined before NAC was compared with the corresponding receptor status determined in the surgical specimen after NAC.

RESULTS

245 consecutive patients with primary invasive breast cancer, treated with NAC with/without targeted therapy between January 1, 2016 and December 31, 2019, at the LMU Breast Center, Munich, Germany, were identified. In 128 patients (52%), surgery revealed non-pCR after completed NAC. In 35 cases (27%), a switch of either HR and/or HER2 status between the initial biopsy and the surgical specimen was detected. Twenty cases had a switch in HR status, while 15 cases had a switch in HER2 status.

CONCLUSION

In a substantial number (27%) of non-pCR cases, a switch in biomarker status after completed neoadjuvant treatment was detected. These results are consistent with prior evidence. Yet, routine reevaluation of HR and HER2 status is not recommended in guidelines so far. Future research needs to address the impact of HR and HER2 status switch on therapy adaptation and on subsequent patient outcome. Particularly, in view of the recent therapy advances, it will be critical to evaluate whether individualization of treatment concepts based on the biology of the non-pCR specimens is preferable to the initial therapy concept based on the pathology at primary diagnosis.

摘要

引言

本项目旨在确定早期乳腺癌新辅助化疗(NAC)后激素受体(HR)和/或HER2状态转换的频率。

方法

对未达到病理完全缓解(非pCR)患者的肿瘤样本进行评估。病理完全缓解(pCR)定义为乳腺和淋巴结无浸润性肿瘤(ypT0/is ypN0)。将NAC前确定的HR和HER2状态与NAC后手术标本中确定的相应受体状态进行比较。

结果

确定了2016年1月1日至2019年12月31日期间在德国慕尼黑LMU乳腺中心接受NAC联合/不联合靶向治疗的245例原发性浸润性乳腺癌连续患者。128例患者(52%)在完成NAC后手术显示为非pCR。在35例(27%)患者中,检测到初始活检和手术标本之间HR和/或HER2状态的转换。20例患者HR状态发生转换,15例患者HER2状态发生转换。

结论

在相当数量(27%)的非pCR病例中,检测到新辅助治疗完成后生物标志物状态的转换。这些结果与先前的证据一致。然而,目前指南中不建议常规重新评估HR和HER2状态。未来的研究需要解决HR和HER2状态转换对治疗调整和后续患者结局的影响。特别是,鉴于最近的治疗进展,评估基于非pCR标本生物学特性的治疗方案个体化是否优于基于初诊病理的初始治疗方案至关重要。

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