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浸润性导管乳腺癌伴或不伴导管原位癌成分的 21 基因复发评分的综合分析。

Comprehensive analysis of the 21-gene recurrence score in invasive ductal breast carcinoma with or without ductal carcinoma in situ component.

机构信息

Department of General Surgery, Comprehensive Breast Health Center, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Br J Cancer. 2021 Mar;124(5):975-981. doi: 10.1038/s41416-020-01212-w. Epub 2020 Dec 17.

Abstract

BACKGROUND

Invasive ductal carcinoma (IDC) is often accompanied by ductal carcinoma in situ (DCIS). Whether the DCIS component affects the 21-gene recurrence score (RS) is unclear.

METHODS

Consecutive ER-positive, HER2-negative, N0-1 patients with RS results were included. Patients were divided into pure IDC and IDC with DCIS (IDC/DCIS) groups. The RS, the expression of its 16 cancer genes and prognosis were compared between IDC and IDC/DCIS patients.

RESULTS

A total of 1458 patients were enrolled, 320 of whom had concomitant DCIS. DCIS component was independently associated with lower RS (P = 0.038). IDC/DCIS patients more often had a low-risk RS (P = 0.018) or intermediate-risk RS (P = 0.024). Regarding individual genes in the RS panel, Ki67, CCNB1 and MYBL2 in the proliferation group and MMP11 and CTSL2 in the invasion group were significantly lower among IDC/DCIS patients than pure IDC patients. Among IDC/DCIS patients, lower RS was independently correlated with a higher DCIS proportion and lower DCIS grade. Within a median follow-up of 31 months, the DCIS component in IDC did not significantly influence prognosis.

CONCLUSIONS

IDC with DCIS component is associated with a lower 21-gene RS, possibly due to lower expression of proliferation and invasion genes. DCIS proportion and grade independently influenced the 21-gene RS in IDC/DCIS patients. Due to the relatively short follow-up period and low recurrence rate, the impact of the DCIS component in IDC on prognosis needs further evaluation.

摘要

背景

浸润性导管癌(IDC)常伴有导管原位癌(DCIS)。DCIS 成分是否影响 21 基因复发评分(RS)尚不清楚。

方法

纳入连续的 ER 阳性、HER2 阴性、N0-1 且有 RS 结果的患者。患者分为单纯 IDC 组和 IDC 合并 DCIS(IDC/DCIS)组。比较 IDC 和 IDC/DCIS 患者的 RS、其 16 个癌症基因的表达和预后。

结果

共纳入 1458 例患者,其中 320 例伴有 DCIS。DCIS 成分与较低的 RS 独立相关(P=0.038)。IDC/DCIS 患者更常具有低风险 RS(P=0.018)或中风险 RS(P=0.024)。在 RS 面板中的个别基因方面,增殖组的 Ki67、CCNB1 和 MYBL2 以及侵袭组的 MMP11 和 CTSL2 在 IDC/DCIS 患者中显著低于单纯 IDC 患者。在 IDC/DCIS 患者中,较低的 RS 与较高的 DCIS 比例和较低的 DCIS 分级独立相关。在中位数为 31 个月的随访中,IDC 中的 DCIS 成分并未显著影响预后。

结论

IDC 合并 DCIS 成分与较低的 21 基因 RS 相关,可能是由于增殖和侵袭基因表达较低。DCIS 比例和分级独立影响 IDC/DCIS 患者的 21 基因 RS。由于随访时间相对较短且复发率较低,IDC 中 DCIS 成分对预后的影响需要进一步评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a738/7921681/67c447c5f57a/41416_2020_1212_Fig1_HTML.jpg

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