Suppr超能文献

从 ER+ 乳腺癌的新辅助内分泌治疗试验中吸取精准肿瘤学的经验教训。

Lessons in precision oncology from neoadjuvant endocrine therapy trials in ER+ breast cancer.

机构信息

Lester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX, USA.

出版信息

Breast. 2017 Aug;34 Suppl 1(Suppl 1):S104-S107. doi: 10.1016/j.breast.2017.06.039. Epub 2017 Jun 30.

Abstract

For post-menopausal women with clinical stage II/III estrogen receptor positive (ER+) breast cancer neoadjuvant endocrine therapy (NET) is an under-utilized and low-toxicity alternative to chemotherapy for increasing breast conservation rates. Individual responses to endocrine therapy can also be used to tailor systemic treatment. The Preoperative Endocrine Prognostic Index (PEPI) was developed to identify patients at low risk of relapse after NET so that adjuvant chemotherapy can safely be avoided. In a recent validation study, patients with pathological stage 1 or 2A breast cancers with a Ki67 value of 2.7% or less in the surgical specimen (PEPI = 0) after 16-18 weeks of aromatase inhibitor therapy had a 97% disease free survival after 5.5 years of median follow up. Two approaches are currently underway to extend the PEPI model. The first is to determine whether fulvestrant increases the PEPI-0 rate versus anastrozole, as this would increase the number of patients who could be safely managed without adjuvant chemotherapy. The second is to develop new approaches for tumors that exhibit endocrine therapy resistance identified during NET. Preliminary studies demonstrate that tumors that exhibit AI resistant proliferation in the neoadjuvant setting is often sensitive to palbociclib, a CDK4/6 inhibitor. Serial Ki67 monitoring before surgery is therefore logical approach to tailored use of adjuvant CDK4/6i adjuvant treatment. Finally serial sampling of the tumor inherent in the PEPI approach facilitates the identification of new therapeutic targets, mechanisms of resistance and monitoring of tumor evolution in response to AI therapy.

摘要

对于临床 II/III 期雌激素受体阳性(ER+)乳腺癌的绝经后妇女,新辅助内分泌治疗(NET)是一种增加保乳率的低毒性替代化疗的方法。内分泌治疗的个体反应也可用于定制全身治疗。术前内分泌预后指数(PEPI)旨在识别 NET 后复发风险低的患者,以便安全避免辅助化疗。在最近的一项验证研究中,在接受芳香化酶抑制剂治疗 16-18 周后,手术标本中 Ki67 值为 2.7%或更低(PEPI=0)的病理分期 1 或 2A 乳腺癌患者,在中位随访 5.5 年后无疾病生存 97%。目前有两种方法可扩展 PEPI 模型。第一种方法是确定氟维司群是否比阿那曲唑增加 PEPI-0 率,因为这将增加无需辅助化疗即可安全管理的患者数量。第二种方法是开发针对 NET 期间出现内分泌治疗耐药的肿瘤的新方法。初步研究表明,在新辅助治疗中表现出 AI 耐药增殖的肿瘤通常对 CDK4/6 抑制剂 palbociclib 敏感。因此,在手术前进行连续 Ki67 监测是针对辅助 CDK4/6i 辅助治疗进行个体化使用的合理方法。最后,PEPI 方法中肿瘤固有样本的连续采样有助于确定新的治疗靶点、耐药机制和监测肿瘤对 AI 治疗的反应。

相似文献

1
Lessons in precision oncology from neoadjuvant endocrine therapy trials in ER+ breast cancer.
Breast. 2017 Aug;34 Suppl 1(Suppl 1):S104-S107. doi: 10.1016/j.breast.2017.06.039. Epub 2017 Jun 30.
3
Outcome prediction for estrogen receptor-positive breast cancer based on postneoadjuvant endocrine therapy tumor characteristics.
J Natl Cancer Inst. 2008 Oct 1;100(19):1380-8. doi: 10.1093/jnci/djn309. Epub 2008 Sep 23.
7
The Growing Role of CDK4/6 Inhibitors in Treating Hormone Receptor-Positive Advanced Breast Cancer.
Curr Treat Options Oncol. 2017 Jan;18(1):6. doi: 10.1007/s11864-017-0443-7.

引用本文的文献

1
Dalpiciclib plus aromatase inhibitor versus neoadjuvant chemotherapy for ER-positive, HER2-negative breast cancer.
Front Oncol. 2025 Apr 30;15:1566146. doi: 10.3389/fonc.2025.1566146. eCollection 2025.
2
PKMYT1 Is a Marker of Treatment Response and a Therapeutic Target for CDK4/6 Inhibitor-Resistance in ER+ Breast Cancer.
Mol Cancer Ther. 2024 Oct 1;23(10):1494-1510. doi: 10.1158/1535-7163.MCT-23-0564.
3
Breast cancer gene expression signatures: development and clinical significance-a narrative review.
Transl Breast Cancer Res. 2022 Oct 27;4:7. doi: 10.21037/tbcr-22-39. eCollection 2023.
4
Neoadjuvant endocrine therapy in ER-positive breast cancer: evolution, indication, and tailored treatment strategy.
Ther Adv Med Oncol. 2023 Sep 29;15:17588359231200457. doi: 10.1177/17588359231200457. eCollection 2023.
8
The Present and Future of Neoadjuvant Endocrine Therapy for Breast Cancer Treatment.
Cancers (Basel). 2021 May 21;13(11):2538. doi: 10.3390/cancers13112538.
9
Mismatch repair deficiency predicts response to HER2 blockade in HER2-negative breast cancer.
Nat Commun. 2021 May 19;12(1):2940. doi: 10.1038/s41467-021-23271-0.

本文引用的文献

6
Whole-genome analysis informs breast cancer response to aromatase inhibition.
Nature. 2012 Jun 10;486(7403):353-60. doi: 10.1038/nature11143.
8
9
Outcome prediction for estrogen receptor-positive breast cancer based on postneoadjuvant endocrine therapy tumor characteristics.
J Natl Cancer Inst. 2008 Oct 1;100(19):1380-8. doi: 10.1093/jnci/djn309. Epub 2008 Sep 23.
10

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验