Kurosumi Masafumi, Tabei Toshio, Sano Muneaki, Honma Kenichi, Yanagita Yasuhiro, Yamamoto Naohito, Inoue Kenichi, Sato Nobuaki, Kimura Morihiko
Department of Pathology, Saitama Cancer Center, Saitama 362-0806, Japan.
Mol Med Rep. 2008 Jan-Feb;1(1):71-5.
The purpose of this study was to assess the efficacy and predictive biomarkers of combination docetaxel-trastuzumab in a neoadjuvant setting by means of a phase II trial. Women with histologically-confirmed advanced invasive breast cancer whose tumours overexpressed HER-2 received 4 cycles of docetaxel (70 mg/m2 every 3 weeks) and trastuzumab (4 mg/kg loading dose, 2 mg/kg weekly thereafter). Twenty-one patients were enrolled, and all completed 4 cycles of treatment. Two patients were later found to be inoperable, and neither pathological nor clinical response was assessed. The pathological complete response rate was 21% (4/19; 95% CI, 6-46%) and the overall clinical response rate 89% (17/19; 95% CI, 67-99%). The relationship between the expression of biomarkers (HER-2, c-MYC, BRCA1 and Ki-67) and pathological response was assessed. The results suggested the possibility that tumours showing a high signal ratio of HER-2/CEP17 or c-MYC/CEP17 might be more sensitive to this combination therapy. Based on these results, it can be speculated that approximately 30% pCR might be obtained in cases with a high signal ratio of HER2/CEP17 or c-MYC/CEP17. Further trials are needed.
本研究的目的是通过一项II期试验评估多西他赛联合曲妥珠单抗在新辅助治疗中的疗效及预测生物标志物。组织学确诊为晚期浸润性乳腺癌且肿瘤过表达HER-2的女性患者接受4个周期的多西他赛(每3周70mg/m²)和曲妥珠单抗(4mg/kg负荷剂量,此后每周2mg/kg)治疗。入组21例患者,均完成4个周期治疗。后来发现2例患者无法手术,未评估病理及临床反应。病理完全缓解率为21%(4/19;95%CI,6-46%),总体临床缓解率为89%(17/19;95%CI,67-99%)。评估了生物标志物(HER-2、c-MYC、BRCA1和Ki-67)表达与病理反应之间的关系。结果提示,HER-2/CEP17或c-MYC/CEP17信号比高的肿瘤可能对这种联合治疗更敏感。基于这些结果,可以推测HER2/CEP17或c-MYC/CEP17信号比高的病例可能获得约30%的病理完全缓解。需要进一步试验。