浸润性乳腺癌HER2≥4.0和<6.0:21基因表达试验和mamaprint Plus BluePrint检测的风险分类和分子分型

IF 3.3 4区 医学 Q2 ONCOLOGY
Qianming Bai, Hong Lv, Longlong Bao, Yu Yang, Xin Zhang, Heng Chang, Tian Xue, Min Ren, Xiaoli Zhu, Xiaoyan Zhou, Wentao Yang
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引用次数: 0

摘要

目的:探讨HER2≥4.0的浸润性乳腺癌的HER2状态及临床病理特征。方法:选取40例HER2≥4.0的乳腺癌患者。两组均以浸润性癌(NOS)为主,组织学分级为ⅱ级,HR+, Ki-67≥20%,HER2 2+,复发风险高,但a组患者较年轻,淋巴结转移较多。令人惊讶的是,两组HR+乳腺癌均为光型,HR-均为基底型或未知,所有病例的HER2指数均为毫无疑问,A组乳腺癌一直被诊断为HER2扩增,更有可能是HER2阴性,并且从抗HER2新辅助化疗中获益较少。在评估HER2 FISH时,应将A组乳腺癌与经典HER2阳性乳腺癌区分开来,并将更大的A组患者纳入进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Invasive Breast Cancer with HER2 ≥4.0 and <6.0: Risk Classification and Molecular Typing by a 21-Gene Expression Assay and MammaPrint Plus BluePrint Testing.

Invasive Breast Cancer with HER2 ≥4.0 and <6.0: Risk Classification and Molecular Typing by a 21-Gene Expression Assay and MammaPrint Plus BluePrint Testing.

Invasive Breast Cancer with HER2 ≥4.0 and <6.0: Risk Classification and Molecular Typing by a 21-Gene Expression Assay and MammaPrint Plus BluePrint Testing.

Invasive Breast Cancer with HER2 ≥4.0 and <6.0: Risk Classification and Molecular Typing by a 21-Gene Expression Assay and MammaPrint Plus BluePrint Testing.

Purpose: To investigate the HER2 status and clinicopathological features in invasive breast cancer with HER2 ≥4.0 and <6.0, which has always been controversial.

Methods: Forty breast cancer cases with HER2 ≥4.0 and <6.0 by fluorescence in situ hybridization (FISH) were collected and classified into two groups based on the HRE2/CEP17 ratio (Group A: ≥2.0, n=22; Group B: <2.0, n=18). Clinicopathological characteristics, HER2 status, risk classification, and molecular typing were further analyzed and compared by 21-Gene expression assay and MammaPrint plus BluePrint test.

Results: The majority of cases in both groups were invasive carcinoma (NOS), with histological grade II, HR+, Ki-67 ≥20%, HER2 2+, and a high risk of recurrence, although younger patients and lymph node metastases were more common in Group A. Surprisingly, all HR+ breast cancers in both groups were classified as luminal-type, HR- cases were all basal-type or unknown, and the index of HER2 in all cases was <0.000 using the BluePrint test, which indicated that HER2 status should be negative. Furthermore, the level of HER2 mRNA expression in all cases of both groups was <10.7, which was defined as HER2 negative by the 21-Gene expression assay. In addition, 10 patients of Group A received anti-HER2 neoadjuvant therapy; only one patient with HR- achieved Grade 5 based on the Miller-Payne system, whereas none of the patients achieved pathological complete response (pCR) based on the Residual Cancer Burden system.

Conclusion: Group A breast cancer, which has always been unquestionably diagnosed as HER2 amplification, was more likely to be HER2 negative and derived less benefit from anti-HER2 neoadjuvant chemotherapy. Group A breast cancer should be distinguished from classical HER2-positive breast cancers when assessing HER2 FISH, and a larger cohort of Group A patients should be included in further studies.

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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
40
审稿时长
16 weeks
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