Bewick M, Chadderton T, Conlon M, Lafrenie R, Morris D, Stewart D, Glück S
Northeastern Ontario Regional Cancer Centre, Sudbury, Ontario, Canada.
Bone Marrow Transplant. 1999 Aug;24(4):377-84. doi: 10.1038/sj.bmt.1701907.
C-erbB-2/HER-2 (designated HER-2) is overexpressed in both primary and metastatic breast cancer and predicts poor prognosis. We investigated the expression of HER-2 in patients with metastatic breast cancer undergoing high-dose chemotherapy (HDCT) with autologous blood stem cell (ABSC) support and correlated the presence (positive) or absence (negative) of HER-2 overexpression in these patients with response to treatment, progression-free survival (PFS) and overall survival (OS). The level of HER-2 expression was analyzed in 57 patients with metastatic breast cancer undergoing HDCT with ABSC support. Plasma from peripheral blood was taken at three different time points during the course of treatment and was analyzed using an enzyme immunoassay (EIA) to detect circulating levels of the extracellular portion of HER-2. HER-2 levels were elevated (>0.2 U/mg protein) in 27/57 (47.4%) patients at one or more time points during treatment. The level of HER-2 varied during the course of treatment. Following induction chemotherapy (ICT), five patients who were negative initially, showed overexpression of HER-2. Three patients overexpressed HER-2 only after HDCT/ABSC. Response to treatment was similar in patients independent of plasma HER-2 levels. Overexpression of HER-2 was associated with a significantly shorter PFS (P = 0.004, log rank) and OS (P = 0.003, log rank) after HDCT/ABSC. HER-2 overexpression, patient age, estrogen receptor status, progesterone receptor status, and previous hormone treatment were assessed by univariate and multivariate analysis. Univariate analysis determined that only HER-2 overexpression correlated significantly with decreases in progression free survival (P = 0.005, Cox regression). Decreased overall survival correlated significantly with HER-2 overexpression (P = 0.004) and decreased expression of both estrogen receptor (P = 0.032) and progesterone receptor (P = 0.039). In multivariate analysis of these variables, only HER-2 expression levels proved to be of independent statistical significance in predicting outcome for both PFS (P = 0.007) and OS (P = 0.002). These results suggest that overexpression of HER-2, measured by EIA in plasma may predict a shorter PFS and OS in patients with metastatic breast cancer treated with HDCT and ABSC support.
C-erbB-2/HER-2(命名为HER-2)在原发性和转移性乳腺癌中均呈过表达,且提示预后不良。我们研究了接受高剂量化疗(HDCT)并伴有自体血干细胞(ABSC)支持的转移性乳腺癌患者中HER-2的表达情况,并将这些患者中HER-2过表达的存在(阳性)或不存在(阴性)与治疗反应、无进展生存期(PFS)和总生存期(OS)相关联。分析了57例接受HDCT并伴有ABSC支持的转移性乳腺癌患者的HER-2表达水平。在治疗过程中的三个不同时间点采集外周血血浆,并使用酶免疫测定法(EIA)进行分析,以检测HER-2细胞外部分的循环水平。在治疗期间的一个或多个时间点,27/57(47.4%)的患者HER-2水平升高(>0.2 U/mg蛋白)。HER-2水平在治疗过程中有所变化。诱导化疗(ICT)后,最初为阴性的5例患者出现了HER-2过表达。3例患者仅在HDCT/ABSC后HER-2过表达。无论血浆HER-2水平如何,患者的治疗反应相似。HDCT/ABSC后,HER-2过表达与显著缩短的PFS(P = 0.004,对数秩检验)和OS(P = 0.003,对数秩检验)相关。通过单因素和多因素分析评估HER-2过表达、患者年龄、雌激素受体状态、孕激素受体状态和既往激素治疗情况。单因素分析确定,只有HER-2过表达与无进展生存期的缩短显著相关(P = 0.005,Cox回归)。总生存期的缩短与HER-2过表达(P = 0.004)以及雌激素受体(P = 0.032)和孕激素受体表达的降低(P = 0.039)显著相关。在对这些变量的多因素分析中,只有HER-2表达水平在预测PFS(P = 0.007)和OS(P = 0.002)的结果方面具有独立的统计学意义。这些结果表明,通过EIA检测血浆中HER-2的过表达可能预示着接受HDCT和ABSC支持治疗的转移性乳腺癌患者的PFS和OS较短。