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基因谱分析对 ER 阳性、T1-2 期绝经后乳腺癌辅助治疗推荐的影响:基因谱分析能否消除前哨淋巴结活检的需要?

The Impact of Genomic Profiling on Adjuvant Therapy Recommendation in Postmenopausal Women with ER-Positive, T1-2 Breast Cancer: Can Genomic Profiling Eliminate the Need for Sentinel Lymph Node Biopsy?

机构信息

Rebecca Fortney Breast Center, Anne Arundel Medical Center, Annapolis, MD.

Maryland Oncology Hematology, Annapolis Division, Annapolis, MD.

出版信息

Clin Breast Cancer. 2021 Dec;21(6):e731-e737. doi: 10.1016/j.clbc.2021.02.011. Epub 2021 Mar 4.


DOI:10.1016/j.clbc.2021.02.011
PMID:34006481
Abstract

INTRODUCTION: With the advent of genomic assays, sentinel lymph node biopsy (SLNB) may be less impactful in determining adjuvant breast cancer therapy. We evaluated the influence of SLNB on adjuvant therapy recommendation when the Oncotype DX recurrence score (RS) is known. METHODS: We reviewed postmenopausal women with ER-positive/HER2-negative, pT1-2 breast cancers with non-suspicious axillary ultrasound treated with SLNB at the time of cancer resection, from 2011 to 2015. For each case, the recommended adjuvant therapy based on the actual SLNB was compared with recommendations if SLNB had been omitted (presumed negative). RESULTS: Surgical nodal status was N0 in 184 patients (84.8%), Nmi-N1 in 29 patients (13.4%), and N2-3 in 4 patients (1.8%). SLNB resulted in a recommendation for axillary lymph node dissection in 4.1% (n = 9). Axillary surgery resulted in a change in radiation recommendation (nodal radiation considered or recommended) in 15.2% (n = 33). Of the 147 patients with known RS, 95 patients had RS > 18, 29 had RS 18-25, and 23 had RS < 25. When chemotherapy was only recommended for RS > 25, or N2-3 disease, SLNB changed the recommendation to have chemotherapy in one patient (0.7%), and the recommendation of which chemotherapy regimen (second- vs. third-generation) in an additional 5 patients. CONCLUSION: SLNB changed the recommendation for/against chemotherapy, or the chemotherapy regiment recommended, in 4.8% of postmenopausal women with early-stage, ER-positive/HER2-negative breast cancer, and sonographically negative axilla when using RS > 25 or N2-3 disease as an indication for chemotherapy. Preoperative genomic profiling can guide de-escalation of axillary surgery.

摘要

简介:随着基因组分析的出现,前哨淋巴结活检(SLNB)在确定辅助乳腺癌治疗方面的作用可能降低。当已知 Oncotype DX 复发评分(RS)时,我们评估了 SLNB 对辅助治疗建议的影响。

方法:我们回顾了 2011 年至 2015 年间,在癌症切除时接受 SLNB 的绝经后 ER 阳性/HER2 阴性、pT1-2 乳腺癌且腋窝超声无可疑表现的女性患者。对于每例患者,根据实际 SLNB 推荐的辅助治疗与如果省略 SLNB(假定为阴性)的推荐进行了比较。

结果:184 例患者(84.8%)的手术淋巴结状态为 N0,29 例患者(13.4%)为 Nmi-N1,4 例患者(1.8%)为 N2-3。SLNB 导致 4.1%(n=9)的患者需要进行腋窝淋巴结清扫。腋窝手术导致 15.2%(n=33)的患者改变了放疗建议(考虑或推荐淋巴结放疗)。在已知 RS 的 147 例患者中,95 例患者的 RS > 18,29 例患者的 RS 18-25,23 例患者的 RS < 25。当仅建议 RS > 25 或 N2-3 疾病的患者使用化疗时,SLNB 改变了 1 例患者(0.7%)的治疗建议,还改变了另外 5 例患者的化疗方案(第二代与第三代)建议。

结论:在使用 RS > 25 或 N2-3 疾病作为化疗指征的情况下,SLNB 改变了 4.8%的早期 ER 阳性/HER2 阴性乳腺癌且超声阴性腋窝的绝经后女性对/不对化疗、或化疗方案推荐的建议。术前基因组分析可指导腋窝手术的简化。

相似文献

[1]
The Impact of Genomic Profiling on Adjuvant Therapy Recommendation in Postmenopausal Women with ER-Positive, T1-2 Breast Cancer: Can Genomic Profiling Eliminate the Need for Sentinel Lymph Node Biopsy?

Clin Breast Cancer. 2021-12

[2]
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Ann Surg Oncol. 2022-10

[3]
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[4]
Neoadjuvant chemotherapy and timing of sentinel lymph node biopsy in different molecular subtypes of breast cancer with clinically negative axilla.

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[5]
Cost-effectiveness analyses demonstrate that observation is superior to sentinel lymph node biopsy for postmenopausal women with HR + breast cancer and negative axillary ultrasound.

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[6]
How Often Does Neoadjuvant Chemotherapy Avoid Axillary Dissection in Patients With Histologically Confirmed Nodal Metastases? Results of a Prospective Study.

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[7]
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[8]
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[9]
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Breast Cancer Res Treat. 2024-1

[10]
Can We Forgo Sentinel Lymph Node Biopsy in Women Aged ≥ 50 Years with Early-Stage Hormone-Receptor-Positive HER2-Negative Special Histologic Subtype Breast Cancer?

Ann Surg Oncol. 2023-2

引用本文的文献

[1]
Sentinel lymph node-related lncRNA typing affects breast cancer prognosis and treatment response through the immune cell microenvironment.

Medicine (Baltimore). 2025-2-7

[2]
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