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21 基因复发评分检测可预测接受辅助序贯蒽环类和多西紫杉醇或蒽环类化疗治疗的淋巴结阳性、激素受体阳性乳腺癌患者的远处复发(PACS-01 试验)。

The 21-gene Recurrence Score® assay predicts distant recurrence in lymph node-positive, hormone receptor-positive, breast cancer patients treated with adjuvant sequential epirubicin- and docetaxel-based or epirubicin-based chemotherapy (PACS-01 trial).

机构信息

Department of Biopathology, Centre Jean Perrin and EA 4677 ERTICa, Université d'Auvergne, 58 rue Montalembert, 63000, Clermont-Ferrand, France.

Department of Biostatistics, Institut Claudius Régaud, Institut Universitaire du Cancer Toulouse-Oncopole, Toulouse, France.

出版信息

BMC Cancer. 2018 May 4;18(1):526. doi: 10.1186/s12885-018-4331-8.

Abstract

BACKGROUND

The 21-gene Recurrence Score (RS) result predicts outcome and chemotherapy benefit in node-negative and node-positive (N+), estrogen receptor-positive (ER+) patients treated with endocrine therapy. The purpose of this study was to evaluate the prognostic impact of RS results in N+, hormone receptor-positive (HR+) patients treated with adjuvant chemotherapy (6 cycles of FEC100 vs. 3 cycles of FEC100 followed by 3 cycles of docetaxel 100 mg/m) plus endocrine therapy (ET) in the PACS-01 trial (J Clin Oncol 2006;24:5664-5671).

METHODS

The current study included 530 HR+/N+ patients from the PACS-01 parent trial for whom specimens were available. The primary objective was to evaluate the relationship between the RS result and distant recurrence (DR).

RESULTS

There were 209 (39.4%) patients with low RS (< 18), 159 (30%) with intermediate RS (18-30) and 162 (30.6%) with high RS (≥ 31). The continuous RS result was associated with DR (hazard ratio = 4.14; 95% confidence interval: 2.67-6.43; p <  0.001), adjusting for treatment. In multivariable analysis, the RS result remained a significant predictor of DR (p <  0.001) after adjustment for number of positive nodes, tumor size, tumor grade, Ki-67 (immunohistochemical status), and chemotherapy regimen. There was no statistically significant interaction between RS result and treatment in predicting DR (p = 0.79).

CONCLUSIONS

After adjustment for clinical covariates, the 21-gene RS result is a significant prognostic factor in N+/HR+ patients receiving adjuvant chemoendocrine therapy.

TRIAL REGISTRATION

Not applicable.

摘要

背景

21 基因复发评分(RS)结果可预测内分泌治疗的淋巴结阴性和阳性(N+)、雌激素受体阳性(ER+)患者的预后和化疗获益。本研究的目的是评估 RS 结果在接受辅助化疗(6 个周期 FEC100 与 3 个周期 FEC100 序贯 3 个周期多西他赛 100mg/m2)联合内分泌治疗(ET)的 N+、激素受体阳性(HR+)患者中的预后影响,该研究在 PACS-01 试验中进行(J Clin Oncol 2006;24:5664-5671)。

方法

本研究纳入了 PACS-01 试验的 530 例 HR+/N+患者,这些患者的标本均可用。主要目的是评估 RS 结果与远处复发(DR)之间的关系。

结果

209 例(39.4%)患者 RS 低(<18),159 例(30%)患者 RS 中(18-30),162 例(30.6%)患者 RS 高(≥31)。连续 RS 结果与 DR 相关(风险比=4.14;95%置信区间:2.67-6.43;p<0.001),调整了治疗因素。多变量分析显示,调整阳性淋巴结数、肿瘤大小、肿瘤分级、Ki-67(免疫组化状态)和化疗方案后,RS 结果仍然是 DR 的显著预测因子(p<0.001)。RS 结果与治疗在预测 DR 方面无统计学显著交互作用(p=0.79)。

结论

在调整临床协变量后,21 基因 RS 结果是接受辅助化疗内分泌治疗的 N+/HR+患者的一个显著预后因素。

试验注册

不适用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1165/5936023/34887266d42f/12885_2018_4331_Fig1_HTML.jpg

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