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.
BMC Cancer. 2018 May 4;18(1):526. doi: 10.1186/s12885-018-4331-8.
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).
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).
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).
After adjustment for clinical covariates, the 21-gene RS result is a significant prognostic factor in N+/HR+ patients receiving adjuvant chemoendocrine therapy.
Not applicable.
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)。
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。
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)。
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。
不适用。