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早期乳腺癌伴 1-3 个阳性淋巴结的女性术后放疗。

Post-mastectomy radiotherapy for women with early breast cancer and one to three positive lymph nodes.

机构信息

Breast Surgery, Lancashire Teaching Hospitals NHS Foundation Trust, Chorley, UK.

Breast Surgery, HEE East Midlands, Leicester, UK.

出版信息

Cochrane Database Syst Rev. 2023 Jun 16;6(6):CD014463. doi: 10.1002/14651858.CD014463.pub2.

Abstract

BACKGROUND

Continual improvement in adjuvant therapies has resulted in a better prognosis for women diagnosed with breast cancer. A surrogate marker used to detect the spread of disease after treatment of breast cancer is local and regional recurrence. The risk of local and regional recurrence after mastectomy increases with the number of axillary lymph nodes affected by cancer. There is a consensus to use radiotherapy as an adjuvant treatment after mastectomy (postmastectomy radiotherapy (PMRT)) in women diagnosed with breast cancer and found to have disease in four or more positive axillary lymph nodes. Despite data showing almost double the risk of local and regional recurrence in women treated with mastectomy and found to have one to three positive lymph nodes, there is a lack of international consensus on the use of PMRT in this group.

OBJECTIVES

To assess the effects of PMRT in women diagnosed with early breast cancer and found to have one to three positive axillary lymph nodes.

SEARCH METHODS

We searched the Cochrane Breast Cancer Group's Specialised Register, CENTRAL, MEDLINE, Embase, the World Health Organization (WHO) International Clinical Trials Registry Platform (ICTRP) and ClinicalTrials.gov up to 24 September 2021.

SELECTION CRITERIA

We included randomised controlled trials (RCTs). The inclusion criteria included women diagnosed with breast cancer treated with simple or modified radical mastectomy and axillary surgery (sentinel lymph node biopsy (SLNB) alone or those undergoing axillary lymph node clearance with or without prior SLNB). We included only women receiving PMRT using X-rays (electron and photon radiation), and we defined the radiotherapy dose to reflect what is currently being recommended (i.e. 40 Gray (Gy) to 50 Gy in 15 to 25/28 fractions in 3 to 5 weeks. The included studies did not administer any boost to the tumour bed. In this review, we excluded studies using neoadjuvant chemotherapy as a supportive treatment before surgery.

DATA COLLECTION AND ANALYSIS

We used Covidence to screen records. We collected data on tumour characteristics, adjuvant treatments and the outcomes of local and regional recurrence, overall survival, disease-free survival, time to progression, short- and long-term adverse events and quality of life. We reported on time-to-event outcome measures using the hazard ratio (HR) and subdistribution HR. We used Cochrane's risk of bias tool (RoB 1), and we presented overall certainty of the evidence using the GRADE approach.

MAIN RESULTS

The RCTs included in this review were subgroup analyses of original RCTs conducted in the 1980s to assess the effectiveness of PMRT. Hence, the type and duration of adjuvant systemic treatments used in the studies included in this review were suboptimal compared to the current standard of care. The review involved three RCTs with a total of 829 women diagnosed with breast cancer and low-volume axillary disease. Amongst the included studies, only a single study pertained to the modern-day radiotherapy practice. The results from this one study showed a reduction of local and regional recurrence (HR 0.20, 95% confidence interval (CI) 0.13 to 0.33, 1 study, 522 women; low-certainty evidence) and improvement in overall survival with PMRT (HR 0.76, 95% CI 0.60 to 0.97, 1 study, 522 women; moderate-certainty evidence). One of the other studies using radiotherapy techniques that do not reflect modern-day practice reported on disease-free survival in women with low-volume axillary disease (subdistribution HR 0.63, 95% CI 0.41 to 0.96, 1 study, 173 women). None of the included studies reported on PMRT side effects or quality-of-life outcome measures.

AUTHORS' CONCLUSIONS: Based on one study, the use of PMRT in women diagnosed with breast cancer and low-volume axillary disease indicated a reduction in locoregional recurrence and an improvement in survival. There is a need for more research to be conducted using modern-day radiotherapy equipment and methods to support and supplement the review findings.

摘要

背景

辅助治疗的不断改进使得诊断为乳腺癌的女性预后更好。一种用于检测乳腺癌治疗后疾病扩散的替代标志物是局部和区域复发。乳腺癌根治术后局部和区域复发的风险随着受癌症影响的腋窝淋巴结数量的增加而增加。在诊断为乳腺癌且腋窝淋巴结有 4 个或更多阳性淋巴结的患者中,使用放射治疗作为辅助治疗(乳腺癌根治术后放射治疗(PMRT))已达成共识。

尽管数据显示,在腋窝淋巴结有 1 至 3 个阳性淋巴结的接受乳腺癌根治术的女性中,局部和区域复发的风险几乎增加了一倍,但在这一人群中使用 PMRT 的国际共识尚缺乏。

目的

评估 PMRT 在诊断为早期乳腺癌且腋窝淋巴结有 1 至 3 个阳性淋巴结的女性中的作用。

检索方法

我们检索了 Cochrane 乳腺癌组的专着登记处、CENTRAL、MEDLINE、Embase、世界卫生组织(WHO)国际临床试验注册平台(ICTRP)和 ClinicalTrials.gov,检索时间截至 2021 年 9 月 24 日。

选择标准

我们纳入了随机对照试验(RCT)。纳入标准包括接受单纯或改良根治性乳房切除术和腋窝手术(单独前哨淋巴结活检(SLNB)或接受腋窝淋巴结清扫术联合或不联合 SLNB)治疗的乳腺癌女性。我们仅纳入使用 X 射线(电子和光子辐射)进行 PMRT 的女性,并定义放射治疗剂量以反映目前的推荐剂量(即 15 至 25/28 分次 3 至 5 周内 40 至 50 Gy)。纳入的研究未对肿瘤床进行任何加量照射。在本综述中,我们排除了使用新辅助化疗作为手术前辅助治疗的研究。

数据收集和分析

我们使用 Covidence 筛选记录。我们收集了肿瘤特征、辅助治疗以及局部和区域复发、总生存、无病生存、进展时间、短期和长期不良事件以及生活质量的结局数据。我们使用风险比(HR)和亚分布 HR 报告时间事件结局指标。我们使用 Cochrane 的偏倚风险工具(RoB 1),并使用 GRADE 方法报告证据的总体确定性。

主要结果

本综述纳入的 RCT 是对 20 世纪 80 年代进行的评估 PMRT 有效性的原始 RCT 的亚组分析。因此,纳入研究中使用的辅助全身治疗的类型和持续时间与目前的护理标准相比并不理想。本综述涉及三项 RCT,共纳入 829 名诊断为乳腺癌且腋窝疾病低容量的女性。在纳入的研究中,只有一项研究涉及现代放射治疗实践。这项研究的结果显示,PMRT 可降低局部和区域复发(HR 0.20,95%置信区间(CI)0.13 至 0.33,1 项研究,522 名女性;低确定性证据)和改善总生存(HR 0.76,95% CI 0.60 至 0.97,1 项研究,522 名女性;中等确定性证据)。另一项使用不反映现代实践的放射治疗技术的研究报告了低容量腋窝疾病女性的无病生存情况(亚分布 HR 0.63,95% CI 0.41 至 0.96,1 项研究,173 名女性)。纳入的研究均未报告 PMRT 副作用或生活质量结局指标。

作者结论

基于一项研究,在诊断为乳腺癌且腋窝淋巴结低容量疾病的女性中使用 PMRT 可降低局部区域复发率并提高生存率。需要进行更多使用现代放射治疗设备和方法的研究,以支持和补充本综述的研究结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f211/10275354/c124f18e3d26/tCD014463-FIG-01.jpg

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