Müller Volkmar, Witzel Isabell, Pantel Klaus, Krenkel Sylke, Lück Hans Joachim, Neumann Rainer, Keller Thomas, Dittmer Jürgen, Jänicke Fritz, Thomssen Christoph
Department of Gynecology, University Medical Center Hamburg-Eppendorf, Martinistrasse 52, 20246 Hamburg, Germany.
Anticancer Res. 2006 Mar-Apr;26(2B):1479-87.
A soluble fragment of the epidermal growth factor receptor (EGFR) extracellular domain (sEGFR) can be detected in the serum of cancer patients, but the role of sEGFR is still unclear.
Blood samples from patients receiving chemotherapy for metastatic breast cancer were collected before (n = 101) and after 3 courses of therapy (n=39). Levels of sEGFR and serum HER-2/neu extracellular domain (ECD) were determined by standardized ELISA.
A higher percentage of cancer patients (15%) showed sEGFR values below 45ng/mL compared with control subjects (3%, p<0.001). Patients with sEGFR levels below 45 ng/mL showed a trend towards shorter overall survival (median 11.7 versus 15.4 months, p=0.08), which was more pronounced in patients with estrogen receptor-positive primary tumors (median 9.6 versus 15.4 months, p=0.022) Patients with low sEGFR and elevated serum HER-2/neu ECD (>15 ng/mL) also showed a shorter overall survival than those with normal values for both parameters (7.1 versus 15.4 months, p=0.03). Again, this difference was higher in patients with estrogen receptor-positive tumors (4.6 versus 15.4 month, p<0.0001). During treatment, a decrease of sEGFR levels occurred in 74.4% of the patients (p=0.014).
Low sEGFR levels in patients with metastatic breast cancer are associated with a shorter overall survival, particularly in patients with estrogen receptor-positive tumors. Chemotherapy frequently induces a decrease of sEGFR. The combined, determination of sEGFR and serum HER-2/neu ECD also delivers relevant information. These findings suggest that the sEGFR status in metastatic breast cancer could be of clinical relevance.
在癌症患者血清中可检测到表皮生长因子受体(EGFR)胞外域的可溶性片段(sEGFR),但其作用仍不明确。
收集转移性乳腺癌化疗患者化疗前(n = 101)及3个疗程化疗后(n = 39)的血样。采用标准化酶联免疫吸附测定法(ELISA)测定sEGFR及血清HER-2/neu胞外域(ECD)水平。
与对照组(3%,p<0.001)相比,更高比例的癌症患者(15%)sEGFR值低于45ng/mL。sEGFR水平低于45 ng/mL的患者总体生存期有缩短趋势(中位生存期11.7个月对15.4个月,p = 0.08),在雌激素受体阳性原发性肿瘤患者中更明显(中位生存期9.6个月对15.4个月,p = 0.022)。sEGFR低且血清HER-2/neu ECD升高(>15 ng/mL)的患者总体生存期也短于两项参数均正常的患者(7.1个月对15.4个月,p = 0.03)。同样,这种差异在雌激素受体阳性肿瘤患者中更高(4.6个月对15.4个月,p<0.0001)。治疗期间,74.4%的患者sEGFR水平下降(p = 0.014)。
转移性乳腺癌患者sEGFR水平低与总体生存期缩短相关,尤其是雌激素受体阳性肿瘤患者。化疗常导致sEGFR下降。联合测定sEGFR和血清HER-2/neu ECD也能提供相关信息。这些发现提示转移性乳腺癌中sEGFR状态可能具有临床意义。