Köstler Wolfgang J, Schwab Barbara, Singer Christian F, Neumann Rainer, Rücklinger Ernst, Brodowicz Thomas, Tomek Sandra, Niedermayr Monika, Hejna Michael, Steger Günther G, Krainer Michael, Wiltschke Christoph, Zielinski Christoph C
Department of Medicine I, University Hospital of Vienna, Austria.
Clin Cancer Res. 2004 Mar 1;10(5):1618-24. doi: 10.1158/1078-0432.ccr-0385-3.
The present pilot study was performed to elucidate whether early changes in serum Her-2/neu extracellular domain (ECD) levels during trastuzumab-based treatment would predict the clinical course of disease in patients with metastatic breast cancer.
Sera from 55 patients with Her-2/neu-overexpressing metastatic breast cancer obtained immediately before each weekly administration of trastuzumab were analyzed by a serum Her-2/neu ELISA.
Whereas response rates were significantly higher in patients with elevated (>or=15 ng/ml) ECD levels before initiation of treatment (35% versus 7%, P = 0.045), progression-free and overall survival did not differ significantly between patients with normal and elevated ECD levels. In patients responding to treatment, ECD levels decreased significantly as early as from day 8 of treatment onwards (all P for weekly measurements versus baseline <0.001). In contrast, no significant change in ECD levels was observed in patients with progressive disease. Multiple logistic regression analyses identified kinetics of ECD levels as the only factor that allowed for the accurate prediction of response likelihood as early as from day 8 of trastuzumab-based treatment onwards (P = 0.020). In addition, determination of serial ECD levels allowed for the prediction of the risk for disease progression within the observed period as early as day 15 of treatment (P = 0.010).
Serial monitoring of the ECD may represent a valuable tool for early prediction of the probability of response and progression-free survival to trastuzumab-based treatment and is thus likely to contribute to an optimization of treatment and resource allocation.
进行本初步研究以阐明在基于曲妥珠单抗的治疗过程中血清Her-2/neu细胞外结构域(ECD)水平的早期变化是否可预测转移性乳腺癌患者的疾病临床进程。
采用血清Her-2/neu酶联免疫吸附测定法分析55例Her-2/neu过表达转移性乳腺癌患者在每次每周给予曲妥珠单抗之前即刻采集的血清。
治疗开始前ECD水平升高(≥15 ng/ml)的患者缓解率显著更高(35%对7%,P = 0.045),但ECD水平正常和升高的患者之间无进展生存期和总生存期无显著差异。在对治疗有反应的患者中,ECD水平早在治疗第8天起就显著下降(与基线相比,每周测量的所有P值均<0.001)。相比之下,疾病进展患者的ECD水平未观察到显著变化。多因素逻辑回归分析确定ECD水平的动力学是唯一能够早在基于曲妥珠单抗的治疗第8天起就准确预测反应可能性的因素(P = 0.020)。此外,连续测定ECD水平早在治疗第15天起就可预测观察期内疾病进展风险(P = 0.010)。
连续监测ECD可能是早期预测基于曲妥珠单抗治疗的反应概率和无进展生存期的有价值工具,因此可能有助于优化治疗和资源分配。