Department of Breast Surgery, St Vincent's University Hospital, Dublin, Ireland.
Br J Surg. 2021 Jan 27;108(1):24-31. doi: 10.1093/bjs/znaa048.
A recurrence score based on a 21-gene expression assay predicts the benefit of adjuvant chemotherapy in oestrogen receptor (ER)-positive, human epidermal growth factor receptor 2 (HER2)-negative breast cancer. This systematic review aimed to determine whether the 21-gene expression assay performed on core biopsy at diagnosis predicted pathological complete response (pCR) to neoadjuvant chemotherapy.
The study was performed according to PRISMA guidelines. Relevant databases were searched to identify studies assessing the value of the 21-gene expression assay recurrence score in predicting response to neoadjuvant chemotherapy in patients with breast cancer. The Newcastle-Ottawa Scale was used to assess the quality of the studies. Results are reported as risk ratio (RR) with 95 per cent confidence interval using the Cochrane-Mantel-Haenszel method for meta-analysis. Sensitivity analyses were carried out where appropriate.
Seven studies involving 1744 patients reported the correlation between pretreatment recurrence score and pCR. Of these, 777 patients (44.6 per cent) had a high recurrence score and 967 (55.4 per cent) a low-intermediate score. A pCR was achieved in 94 patients (5.4 per cent). The pCR rate was significantly higher in the group with a high recurrence score than in the group with a low-intermediate score (10.9 versus 1.1 per cent; RR 4.47, 95 per cent c.i. 2.76 to 7.21; P < 0.001). A significant risk difference was observed between the two groups (risk difference 0.10, 0.04 to 0.15; P = 0.001).
A high recurrence score is associated with higher pCR rates and a low-intermediate recurrence score may indicate chemoresistance. Routine assessment of recurrence score by the 21-gene expression assay on core biopsy might be of value when considering neoadjuvant chemotherapy in patients with ER-positive, HER2-negative breast cancer.
基于 21 基因表达检测的复发评分可预测雌激素受体(ER)阳性、人表皮生长因子受体 2(HER2)阴性乳腺癌患者接受辅助化疗的获益。本系统评价旨在确定诊断时核心活检的 21 基因表达检测是否可预测新辅助化疗的病理完全缓解(pCR)。
本研究按照 PRISMA 指南进行。检索相关数据库,以确定评估 21 基因表达检测复发评分在预测乳腺癌患者新辅助化疗反应中的价值的研究。使用纽卡斯尔-渥太华量表评估研究质量。使用 Cochrane-Mantel-Haenszel 方法进行荟萃分析,结果以风险比(RR)和 95%置信区间报告。在适当的情况下进行敏感性分析。
有 7 项研究纳入了 1744 例患者,报道了治疗前复发评分与 pCR 的相关性。其中,777 例(44.6%)患者复发评分高,967 例(55.4%)患者评分低-中度。104 例(5.4%)患者获得 pCR。高复发评分组的 pCR 率显著高于低-中度评分组(10.9%比 1.1%;RR 4.47,95%置信区间 2.76 至 7.21;P<0.001)。两组间存在显著的风险差异(风险差 0.10,0.04 至 0.15;P=0.001)。
高复发评分与较高的 pCR 率相关,低-中度复发评分可能提示化疗耐药。对于 ER 阳性、HER2 阴性乳腺癌患者,在考虑新辅助化疗时,核心活检 21 基因表达检测的复发评分常规评估可能具有价值。