Sparano Joseph A, Goldstein Lori J, Childs Barrett H, Shak Steven, Brassard Diana, Badve Sunil, Baehner Frederick L, Bugarini Roberto, Rowley Steve, Perez Edith, Shulman Lawrence N, Martino Silvana, Davidson Nancy E, Sledge George W, Gray Robert
Authors' Affiliations: Eastern Cooperative Oncology Group, Brookline, Massachusetts; Sanofi-Aventis, Bridgewater, New Jersey; Genomic Health, Inc., Redwood City, California; North Central Cancer Treatment Group, Rochester, Minnesota; Cancer and Leukemia Group B, Chicago, Illinois; and Southwest Oncology Group, Ann Arbor, Michigan.
Clin Cancer Res. 2009 Dec 15;15(24):7693-7700. doi: 10.1158/1078-0432.CCR-09-1450.
To perform an exploratory analysis of the relationship between gene expression and recurrence in operable hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-normal breast cancer patients treated with adjuvant doxorubicin-containing chemotherapy. EXPERIMENTAL DESIGN: RNA was extracted from archived tumor samples derived from 378 patients with stage I to III HR-positive, HER2-normal breast cancer and analyzed by reverse transcription-PCR for a panel of 374 genes, including the 21-gene recurrence score (RS). Patients were randomized to receive adjuvant doxorubicin plus cyclophosphamide or docetaxel in trial E2197, with no difference in recurrence seen in the treatment arms. All available recurrent cases were selected plus a nonrecurrent cohort. Cox proportional hazard models were used to identify relationships between gene expression and recurrence. RESULTS: TOP2A expression exhibited the strongest association with increased recurrence risk (P = 0.01), and was significantly associated with recurrence (P = 0.008) in a multivariate analysis adjusted for clinicopathologic features. Elevated TOP2A expression above the median was associated with a 2.6-fold increase (95% confidence interval, 1.3-5.2; P = 0.008) in risk of recurrence if the RS was <18, and a 2.0-fold increase (95% confidence interval, 1.2-3.2, P = 0.003) if there was an intermediate RS of 18 to 30. CONCLUSIONS: In patients with HR-positive, HER2-normal breast cancer, a population known to have a low incidence of TOP2A gene alterations thought to be predictive of anthracycline benefit, there is a range of TOP2A RNA expression that is strongly associated with recurrence after adjuvant anthracyclines, which provides information complementary to RS, indicating that it merits further evaluation as a prognostic and predictive marker. (Clin Cancer Res 2009;15(24):7693-700).
对接受含阿霉素辅助化疗的可手术激素受体(HR)阳性、人表皮生长因子受体2(HER2)阴性乳腺癌患者的基因表达与复发之间的关系进行探索性分析。实验设计:从378例Ⅰ至Ⅲ期HR阳性、HER2阴性乳腺癌患者的存档肿瘤样本中提取RNA,并通过逆转录聚合酶链反应分析一组374个基因,包括21基因复发评分(RS)。在试验E2197中,患者被随机分配接受阿霉素加环磷酰胺或多西他赛辅助治疗,各治疗组的复发率无差异。选取所有可用的复发病例以及一个无复发病例队列。采用Cox比例风险模型确定基因表达与复发之间的关系。结果:TOP2A表达与复发风险增加的关联最为显著(P = 0.01),在针对临床病理特征进行调整的多变量分析中与复发显著相关(P = 0.008)。如果RS<18,TOP2A表达高于中位数与复发风险增加2.6倍相关(95%置信区间,1.3 - 5.2;P = 0.008);如果RS为18至30,则与复发风险增加2.0倍相关(95%置信区间,1.2 - 3.2,P = 0.003)。结论:在HR阳性、HER2阴性乳腺癌患者中,这一群体被认为TOP2A基因改变发生率低,而TOP2A基因改变被认为可预测蒽环类药物的获益情况,存在一定范围的TOP2A RNA表达与蒽环类药物辅助治疗后的复发密切相关,这提供了与RS互补的信息,表明其作为预后和预测标志物值得进一步评估。(《临床癌症研究》2009年;15(24):7693 - 700)