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采用 70 基因签名超低分类法限制绝经后乳腺癌患者的全身内分泌过度治疗。

Limiting systemic endocrine overtreatment in postmenopausal breast cancer patients with an ultralow classification of the 70-gene signature.

机构信息

Department of Molecular Pathology, Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX, Amsterdam, Netherlands.

Biometrics Department, Netherlands Cancer Institute, Amsterdam, Netherlands.

出版信息

Breast Cancer Res Treat. 2022 Jul;194(2):265-278. doi: 10.1007/s10549-022-06618-z. Epub 2022 May 19.

DOI:10.1007/s10549-022-06618-z
PMID:35587322
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9239940/
Abstract

PURPOSE

Guidelines recommend endocrine treatment for estrogen receptor-positive (ER+) breast cancers for up to 10 years. Earlier data suggest that the 70-gene signature (MammaPrint) has potential to select patients that have an excellent survival without chemotherapy and limited or no tamoxifen treatment. The aim was to validate the 70-gene signature ultralow-risk classification for endocrine therapy decision making.

METHODS

In the IKA trial, postmenopausal patients with non-metastatic breast cancer had been randomized between no or limited adjuvant tamoxifen treatment without receiving chemotherapy. For this secondary analysis, FFPE tumor material was obtained of ER+HER2- patients with 0-3 positive lymph nodes and tested for the 70-gene signature. Distant recurrence-free interval (DRFI) long-term follow-up data were collected. Kaplan-Meier curves were used to estimate DRFI, stratified by lymph node status, for the three predefined 70-gene signature risk groups.

RESULTS

A reliable 70-gene signature could be obtained for 135 patients. Of the node-negative and node-positive patients, respectively, 20% and 13% had an ultralow-risk classification. No DRFI events were observed for node-negative patients with an ultralow-risk score in the first 10 years. The 10-year DRFI was 90% and 66% in the low-risk (but not ultralow) and high-risk classified node-negative patients, respectively.

CONCLUSION

These survival analyses indicate that the postmenopausal node-negative ER+HER2- patients with an ultralow-risk 70-gene signature score have an excellent 10-year DRFI after surgery with a median of 1 year of endocrine treatment. This is in line with published results of the STO-3-randomized clinical trial and supports the concept that it is possible to reduce the duration of endocrine treatment in selected patients.

摘要

目的

指南建议对雌激素受体阳性(ER+)乳腺癌进行长达 10 年的内分泌治疗。早期数据表明,70 基因标志物(MammaPrint)具有选择无需化疗且接受有限或无他莫昔芬治疗即可获得良好生存的患者的潜力。目的是验证 70 基因标志物超低风险分类用于内分泌治疗决策。

方法

在 IKA 试验中,绝经后患有非转移性乳腺癌的患者被随机分为不接受或仅接受有限的辅助他莫昔芬治疗而不接受化疗。为此二次分析,获得了 0-3 个阳性淋巴结的 ER+HER2-患者的 FFPE 肿瘤标本,并进行了 70 基因标志物检测。收集了远处无复发生存期(DRFI)的长期随访数据。使用 Kaplan-Meier 曲线按淋巴结状态对三个预设的 70 基因标志物风险组进行分层,估计 DRFI。

结果

可获得 135 例患者的可靠 70 基因标志物。在淋巴结阴性和淋巴结阳性患者中,分别有 20%和 13%的患者为超低风险分类。在第一个 10 年内,淋巴结阴性且超低风险评分的患者未观察到 DRFI 事件。低风险(而非超低风险)和高风险分类的淋巴结阴性患者的 10 年 DRFI 分别为 90%和 66%。

结论

这些生存分析表明,绝经后淋巴结阴性 ER+HER2-且 70 基因标志物超低风险评分的患者在手术后接受中位数为 1 年的内分泌治疗后,10 年 DRFI 极好。这与 STO-3 随机临床试验的发表结果一致,并支持这样一种概念,即有可能减少选定患者内分泌治疗的持续时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84d6/9239940/30efde52345b/10549_2022_6618_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84d6/9239940/2ff7b864f32a/10549_2022_6618_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84d6/9239940/bbc70d22f0ed/10549_2022_6618_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84d6/9239940/39c4892c16d4/10549_2022_6618_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84d6/9239940/30efde52345b/10549_2022_6618_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84d6/9239940/2ff7b864f32a/10549_2022_6618_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84d6/9239940/bbc70d22f0ed/10549_2022_6618_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84d6/9239940/39c4892c16d4/10549_2022_6618_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84d6/9239940/30efde52345b/10549_2022_6618_Fig4_HTML.jpg

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