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临床治疗评分5(CTS5)在评估未经选择的非试验性早期雌激素受体阳性乳腺癌患者晚期复发风险中的临床有效性。

Clinical validity of clinical treatment score 5 (CTS5) for estimating risk of late recurrence in unselected, non-trial patients with early oestrogen receptor-positive breast cancer.

作者信息

Richman Juliet, Ring Alistair, Dowsett Mitch, Sestak Ivana

机构信息

Ralph Lauren Centre for Breast Cancer Research, Royal Marsden Hospital NHS Foundation Trust, London, UK.

Breast Unit, Royal Marsden Hospital NHS Foundation Trust, London, UK.

出版信息

Breast Cancer Res Treat. 2021 Feb;186(1):115-123. doi: 10.1007/s10549-020-06013-6. Epub 2020 Nov 21.

DOI:10.1007/s10549-020-06013-6
PMID:33222093
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7940308/
Abstract

PURPOSE

Clinical Treatment Score at 5 years (CTS5) is a prognostic tool to estimate distant recurrence (DR) risk after 5 years of endocrine therapy for postmenopausal women with oestrogen receptor-positive (ER-positive) breast cancer.

METHODS

The validity of CTS5 was tested in a retrospective cohort of patients diagnosed with early ER-positive breast cancer. The primary endpoint was DR in years 5-10. The primary analysis cohort consisted of postmenopausal women, with premenopausal women as a secondary analysis cohort. Cox regression models were used to determine the prognostic value of CTS5 and Kaplan-Meier curves were used with associated 10-year DR risks (%).

RESULTS

2428 women were included with a median follow-up of 13.4 years. The CTS5 was significantly prognostic in both postmenopausal (N = 1662, HR = 2.18 95% CI (1.78-2.67)) and premenopausal women (N = 766, HR = 1.84 95% CI (1.32-2.56)). The 10-year DR risks were 2.9% (1.9-4.5), 7.2% (5.3-9.9), and 12.9% (10.0-16.7) for low, intermediate and high risk in postmenopausal women and 3.8% (2.2-6.7), 6.9% (4.4-10.8), and 11.1% (7.4-16.5) in premenopausal women, respectively. The number of observed DRs was significantly greater than expected in those predicted to be at high risk by CTS5 but this discordance was lost when those receiving more than 60 months of endocrine therapy were excluded.

CONCLUSIONS

The CTS5 demonstrated clinical validity for predicting late DR within a large cohort of unselected postmenopausal patients but less so in premenopausal patients. Calibration of the CTS5 was good in patients who did not receive extended endocrine therapy. The CTS5 low-risk cohort has risk of DR so low as to not warrant extended endocrine therapy.

摘要

目的

5年临床治疗评分(CTS5)是一种预后工具,用于评估绝经后雌激素受体阳性(ER阳性)乳腺癌患者接受5年内分泌治疗后的远处复发(DR)风险。

方法

在一个诊断为早期ER阳性乳腺癌患者的回顾性队列中测试CTS5的有效性。主要终点是5至10年的远处复发。主要分析队列包括绝经后女性,绝经前女性作为次要分析队列。使用Cox回归模型确定CTS5的预后价值,并使用Kaplan-Meier曲线及相关的10年远处复发风险(%)。

结果

纳入2428名女性,中位随访时间为13.4年。CTS5在绝经后女性(N = 1662,HR = 2.18,95%CI(1.78 - 2.67))和绝经前女性(N = 766,HR = 1.84,95%CI(1.32 - 2.56))中均具有显著的预后价值。绝经后女性低、中、高风险组的10年远处复发风险分别为2.9%(1.9 - 4.5)、7.2%(5.3 - 9.9)和12.9%(10.0 - 16.7),绝经前女性分别为3.8%(2.2 - 6.7)、6.9%(4.4 - 10.8)和11.1%(7.4 - 16.5)。在CTS5预测为高风险的患者中,观察到的远处复发数量显著高于预期,但当排除接受超过60个月内分泌治疗的患者时,这种不一致性消失。

结论

CTS5在一大群未经选择的绝经后患者中显示出预测晚期远处复发的临床有效性,但在绝经前患者中效果较差。在未接受延长内分泌治疗的患者中,CTS5的校准良好。CTS5低风险组的远处复发风险极低,无需延长内分泌治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf1c/7940308/9f1a5f30dc5d/10549_2020_6013_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf1c/7940308/683b87115f81/10549_2020_6013_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf1c/7940308/3c47d268f17c/10549_2020_6013_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf1c/7940308/a63aaa44d6f9/10549_2020_6013_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf1c/7940308/9f1a5f30dc5d/10549_2020_6013_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf1c/7940308/683b87115f81/10549_2020_6013_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf1c/7940308/3c47d268f17c/10549_2020_6013_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf1c/7940308/a63aaa44d6f9/10549_2020_6013_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf1c/7940308/9f1a5f30dc5d/10549_2020_6013_Fig4_HTML.jpg

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