Division of Oncology and Hematology, Istituto Clinico Humanitas, Via Manzoni 56, Rozzano, 20089 Milano, Italy.
Breast. 2013 Aug;22(4):419-24. doi: 10.1016/j.breast.2013.03.013. Epub 2013 May 3.
We investigated in a single institution series of 124 women with operable breast cancer whether tumor clinicopathological features could predict the 70-gene signature (Mammaprint, MP) results, and whether MP results could help to make decisions for the use of chemotherapy (CT) in patients (pts) with ER positive breast cancer beyond recommendations of international guidelines.
Among the 68 ER/PgR positive, HER2 negative tumors, Ki-67 ≥ 20% was the only significant predictor of a high risk-MP among standard clinicopathological features. In candidates for endocrine therapy with undetermined benefit from CT according to international guidelines, MP results would have led to different treatment decisions in 13/46 (28%) and in 20/68 (29%) pts according to NCCN and St. Gallen recommendations, respectively.
Ki-67 independently predicted high risk-MP in ER/PgR positive, HER2 negative tumors. MP results would have led to discordant treatment recommendations in about 30% of cases, generally increasing indication rate for CT. The results of large randomized trials are warranted in order to understand whether we should rely on multigene assays rather than on standard clinicopathological features for treatment decisions.
我们在一家机构中对 124 名可手术治疗的乳腺癌女性进行了研究,以确定肿瘤临床病理特征是否可以预测 70 基因特征(Mammaprint,MP)结果,以及 MP 结果是否有助于为国际指南推荐之外的 ER 阳性乳腺癌患者使用化疗(CT)做出决策。
在 68 例 ER/PgR 阳性、HER2 阴性肿瘤中,Ki-67≥20%是标准临床病理特征中唯一可预测高风险-MP 的因素。对于国际指南中根据内分泌治疗的不确定获益而被列入候选的患者,根据 NCCN 和 St. Gallen 指南,MP 结果将导致分别在 13/46(28%)和 20/68(29%)例患者中做出不同的治疗决策。
Ki-67 可独立预测 ER/PgR 阳性、HER2 阴性肿瘤的高风险-MP。MP 结果将导致约 30%的病例中出现治疗建议不一致的情况,通常会增加 CT 的指征率。需要进行大规模随机试验,以了解我们是否应该依赖多基因检测而不是标准临床病理特征来做出治疗决策。