Department of Surgery and Cancer Research Institute, Seoul National University College of Medicine, 28 Yongon-dong, Chongno-gu, Seoul 110-744, Korea.
Breast Cancer Res Treat. 2012 Aug;134(3):1133-40. doi: 10.1007/s10549-012-2145-y. Epub 2012 Jul 3.
Estrogen receptor (ER) expression status is an independent factor predicting response to neoadjuvant systemic treatment (NST). In the current study, we aimed to investigate the characteristics of NST response and benefits of extended NST cycles according to ER expression status. We investigated the outcomes of different durations of anthracycline-taxane-based NST in 377 operable breast cancer patients treated between Aug 2008 and June 2011. In 89 patients, the serial radiologic tumor response was assessed with either ultrasonography or computed tomography. Ninety-six patients (25.5 %) received extended cycles of anthracycline-taxane-based NST (6-8 cycles) and 281 patients (74.5 %) received 3-4 cycles of NST. Treatment with extended cycles of NST led to a significant increase in the pCR rate in ER-positive tumors only (2.1-11.7 %, p = 0.008 for ER-positive tumors and 20.0-19.4 %, p = 0.941 for ER-negative tumors). Serial assessment of radiologic tumor size during extended NST therapy revealed continuous shrinkage of ER-positive tumors during the chemotherapy cycles, while ER-negative tumors mainly achieved size reduction during the first 3-4 cycles with no significant additional tumor shrinkage during the extended cycles of NST. In this study, we report a distinct pattern of response to NST according to ER expression status in breast cancer. Our observation generates the hypothesis that the optimal duration of NST can be tailored to the molecular phenotypes of tumors.
雌激素受体(ER)表达状态是预测新辅助全身治疗(NST)反应的独立因素。在本研究中,我们旨在根据 ER 表达状态研究 NST 反应的特征和延长 NST 周期的获益。我们研究了 377 例可手术乳腺癌患者在 2008 年 8 月至 2011 年 6 月期间接受的不同持续时间蒽环类药物-紫杉烷类 NST 的结果。在 89 例患者中,采用超声或计算机断层扫描评估连续的影像学肿瘤反应。96 例患者(25.5%)接受了延长的蒽环类药物-紫杉烷类 NST 周期(6-8 个周期),281 例患者(74.5%)接受了 3-4 个 NST 周期。延长的 NST 周期治疗导致仅 ER 阳性肿瘤的 pCR 率显著增加(2.1-11.7%,p=0.008,ER 阳性肿瘤;20.0-19.4%,p=0.941,ER 阴性肿瘤)。在延长的 NST 治疗期间对影像学肿瘤大小的连续评估显示,ER 阳性肿瘤在化疗周期中持续缩小,而 ER 阴性肿瘤主要在前 3-4 个周期中实现了肿瘤缩小,在延长的 NST 周期中没有明显的额外肿瘤缩小。在这项研究中,我们根据乳腺癌的 ER 表达状态报告了对 NST 反应的明显模式。我们的观察结果提出了一个假设,即 NST 的最佳持续时间可以根据肿瘤的分子表型进行定制。