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Eur J Cancer. 2019 Sep;118:131-141. doi: 10.1016/j.ejca.2019.06.014. Epub 2019 Jul 19.
2
Tailoring Adjuvant Endocrine Therapy for Premenopausal Breast Cancer.绝经前乳腺癌的辅助内分泌治疗。
N Engl J Med. 2018 Jul 12;379(2):122-137. doi: 10.1056/NEJMoa1803164. Epub 2018 Jun 4.
3
Adjuvant Endocrine Therapy for Women With Hormone Receptor-Positive Breast Cancer: American Society of Clinical Oncology Clinical Practice Guideline Update on Ovarian Suppression.激素受体阳性乳腺癌女性的辅助内分泌治疗:美国临床肿瘤学会临床实践指南关于卵巢抑制的更新。
J Clin Oncol. 2016 May 10;34(14):1689-701. doi: 10.1200/JCO.2015.65.9573. Epub 2016 Feb 16.
4
Twelve-Month Estrogen Levels in Premenopausal Women With Hormone Receptor-Positive Breast Cancer Receiving Adjuvant Triptorelin Plus Exemestane or Tamoxifen in the Suppression of Ovarian Function Trial (SOFT): The SOFT-EST Substudy.激素受体阳性乳腺癌绝经前女性在卵巢功能抑制试验(SOFT)中接受辅助性曲普瑞林加依西美坦或他莫昔芬治疗时的12个月雌激素水平:SOFT-EST子研究
J Clin Oncol. 2016 May 10;34(14):1584-93. doi: 10.1200/JCO.2015.61.2259. Epub 2016 Jan 4.
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Predictors of recovery of ovarian function during aromatase inhibitor therapy.芳香化酶抑制剂治疗期间卵巢功能恢复的预测因素。
Ann Oncol. 2013 Aug;24(8):2011-6. doi: 10.1093/annonc/mdt149. Epub 2013 Apr 23.
6
Incidence and predictors of ovarian function recovery (OFR) in breast cancer (BC) patients with chemotherapy-induced amenorrhea (CIA) who switched from tamoxifen to exemestane.化疗诱导闭经(CIA)的乳腺癌(BC)患者从他莫昔芬转为依西美坦后卵巢功能恢复(OFR)的发生率和预测因素。
Ann Oncol. 2013 Mar;24(3):674-9. doi: 10.1093/annonc/mds464. Epub 2012 Oct 28.
7
Endocrine effects of adjuvant letrozole + triptorelin compared with tamoxifen + triptorelin in premenopausal patients with early breast cancer.与他莫昔芬 + 曲普瑞林相比,来曲唑 + 曲普瑞林辅助治疗对绝经前早期乳腺癌患者的内分泌影响。
J Clin Oncol. 2008 Jan 10;26(2):264-70. doi: 10.1200/JCO.2007.13.5319. Epub 2007 Dec 17.
8
Use of luteinising-hormone-releasing hormone agonists as adjuvant treatment in premenopausal patients with hormone-receptor-positive breast cancer: a meta-analysis of individual patient data from randomised adjuvant trials.促黄体生成素释放激素激动剂在激素受体阳性绝经前乳腺癌患者中作为辅助治疗的应用:来自随机辅助试验的个体患者数据的荟萃分析
Lancet. 2007 May 19;369(9574):1711-23. doi: 10.1016/S0140-6736(07)60778-8.
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Adjuvant aromatase inhibitors for early breast cancer after chemotherapy-induced amenorrhoea: caution and suggested guidelines.化疗所致闭经后早期乳腺癌的辅助芳香化酶抑制剂:注意事项及建议指南
J Clin Oncol. 2006 Jun 1;24(16):2444-7. doi: 10.1200/JCO.2005.05.3694.
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Endogenous sex hormones and breast cancer in postmenopausal women: reanalysis of nine prospective studies.绝经后女性体内的内源性性激素与乳腺癌:九项前瞻性研究的重新分析
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评估接受卵巢抑制治疗的绝经前雌激素受体阳性乳腺癌患者的卵巢逃逸。

Measuring Ovarian Escape in Premenopausal Estrogen Receptor-Positive Breast Cancer Patients on Ovarian Suppression Therapy.

机构信息

Department of Medicine, Houston Methodist Hospital, Houston, Texas, USA.

Department of Hematology and Medical Oncology, Houston Methodist Cancer Center, Houston, Texas, USA.

出版信息

Oncologist. 2021 Jun;26(6):e936-e942. doi: 10.1002/onco.13722. Epub 2021 Mar 11.

DOI:10.1002/onco.13722
PMID:33594769
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8176991/
Abstract

PURPOSE

This study evaluated the proportion of premenopausal women who experience persistent ovarian escape (OE) while receiving ovarian suppression (OS) therapy for estrogen receptor-positive (ER+) breast cancer treatment. The study also examined clinical factors that may predispose to higher risk of persistent OE.

MATERIALS AND METHODS

This was a retrospective, "real-world" study to evaluate premenopausal women receiving adjuvant endocrine OS therapy. The primary objective was to measure the percentage of persistent OE within the first 3 months of OS injections (using either leuprolide or goserelin). The secondary objective was to associate baseline clinical data (age, body mass index [BMI], and previous chemotherapy) with the probability of OE.

RESULTS

Of the 46 patients included in this analysis, 11 (23.9%) women did not achieve OS within 3 months. Three women (6.5%) remained in OE at 12 months. Older age (odds ratio, 0.86; confidence interval, 0.76-0.98, p = .024) was associated with lower chance of developing OE. BMI, previous chemotherapy, and drug used (tamoxifen versus aromatase inhibitor) did not correlate with the likelihood of OE in this patient cohort.

CONCLUSION

Among the premenopausal women who did not attain complete ovarian suppression, young age was a significant risk factor for likelihood of OE. Although the clinical relevance of this finding is not yet known, it should prompt further studies to determine whether inadequate OS is associated with higher recurrence risk for patients with ER+ breast cancer.

IMPLICATIONS FOR PRACTICE

Because up to a quarter of premenopausal women do not attain adequate ovarian suppression within the first 3 months of gonadotropin-releasing hormone (GnRH) agonist therapy, bloodwork should be checked to ascertain hormone levels prior to starting aromatase inhibitor therapy, and at regular intervals, for these women.

摘要

目的

本研究评估了接受雌激素受体阳性(ER+)乳腺癌治疗的卵巢抑制(OS)治疗的绝经前妇女中持续卵巢逃逸(OE)的比例。该研究还检查了可能导致更高风险持续 OE 的临床因素。

材料和方法

这是一项回顾性的“真实世界”研究,评估了接受辅助内分泌 OS 治疗的绝经前妇女。主要目的是测量 OS 注射后前 3 个月内持续 OE 的百分比(使用亮丙瑞林或戈舍瑞林)。次要目的是将基线临床数据(年龄、体重指数[BMI]和既往化疗)与 OE 发生的概率相关联。

结果

在这项分析中,46 名患者中有 11 名(23.9%)女性在 3 个月内未达到 OS。3 名女性(6.5%)在 12 个月时仍处于 OE 状态。年龄较大(优势比,0.86;置信区间,0.76-0.98,p =.024)与 OE 发生的可能性较低相关。BMI、既往化疗和所用药物(他莫昔芬与芳香化酶抑制剂)在该患者队列中与 OE 的可能性无关。

结论

在未能达到完全卵巢抑制的绝经前妇女中,年轻是 OE 发生可能性的显著危险因素。尽管这一发现的临床意义尚不清楚,但它应该促使进一步的研究,以确定 ER+乳腺癌患者的 OS 不足是否与更高的复发风险相关。

实践意义

由于多达四分之一的绝经前妇女在 GnRH 激动剂治疗的前 3 个月内未能达到足够的卵巢抑制,因此应在开始芳香化酶抑制剂治疗前以及定期检查这些妇女的激素水平。