Müller Volkmar, Witzel Isabell, Lück Hans Joachim, Köhler Günter, von Minckwitz Gunther, Möbus Volker, Sattler Daniel, Wilczak Waldemar, Löning Thomas, Jänicke Fritz, Pantel Klaus, Thomssen Christoph
Department of Gynecology, University Hospital Hamburg-Eppendorf, Germany.
Breast Cancer Res Treat. 2004 Jul;86(1):9-18. doi: 10.1023/B:BREA.0000032919.83803.48.
The extracellular domain of the HER-2/neu -receptor (ECD) is shed from the receptor protein and can be detected in serum. However, the clinical implication of HER-2/neu ECD measurement must be further evaluated.
In patients with metastatic breast cancer participating in a trial on first-line chemotherapy, the association of serum HER-2/neu ECD with progression-free interval, survival, and response was studied. Blood samples of patients receiving epirubicin and either cyclophosphamide (EC) or paclitaxel (ET) were collected before (n = 103) and in addition, after three courses of therapy (n = 46).
HER-2/neu ECD levels correlate with HER-2/neu overexpression of corresponding primary tumors determined by immunohistochemistry (antibody CB11, p = 0.018) with an optimized cut-off at 15 ng/mL. Elevated serum levels of HER-2/neu ECD before chemotherapy were correlated with shorter overall survival (p = 0.0097), but not with reduced progression-free survival and response to chemotherapy. In subgroup analyses, patients with elevated pretherapeutic HER-2/neu ECD levels treated with EC showed shorter overall survival (p = 0.0092); no difference was seen in the ET group. With regard to progression-free survival, patients with elevated HER-2/neu ECD levels tended to benefit from ET (p = 0.0341), in patients with low levels no difference was observed between EC and ET. A decrease of HER-2/neu ECD levels after three courses of therapy was associated with response to therapy (p = 0.006).
In our group of metastatic breast cancer patients, elevated HER-2/neu ECD levels are associated with decreased overall survival. With regard to progression-free survival, particularly patients with high HER-2/neu ECD levels seem to benefit from taxane-containing chemotherapy.
HER-2/neu受体的细胞外结构域(ECD)会从受体蛋白上脱落,并可在血清中检测到。然而,HER-2/neu ECD检测的临床意义仍需进一步评估。
在参与一线化疗试验的转移性乳腺癌患者中,研究血清HER-2/neu ECD与无进展生存期、总生存期及反应的相关性。收集接受表柔比星联合环磷酰胺(EC)或紫杉醇(ET)治疗患者的血样,治疗前(n = 103)以及另外在三个疗程治疗后(n = 46)采集。
HER-2/neu ECD水平与通过免疫组织化学(抗体CB11)测定的相应原发性肿瘤的HER-2/neu过表达相关(p = 0.018),优化的临界值为15 ng/mL。化疗前血清HER-2/neu ECD水平升高与总生存期缩短相关(p = 0.0097),但与无进展生存期缩短及化疗反应无关。在亚组分析中,接受EC治疗且治疗前HER-2/neu ECD水平升高的患者总生存期较短(p = 0.0092);ET组未见差异。关于无进展生存期,HER-2/neu ECD水平升高的患者倾向于从ET治疗中获益(p = 0.0341),水平较低的患者中,EC和ET之间未观察到差异。三个疗程治疗后HER-2/neu ECD水平下降与治疗反应相关(p = 0.006)。
在我们的转移性乳腺癌患者组中,HER-2/neu ECD水平升高与总生存期降低相关。关于无进展生存期,尤其是HER-2/neu ECD水平高的患者似乎从含紫杉烷的化疗中获益。