Peyrat J P, Vanlemmens L, Fournier J, Huet G, Révillion F, Bonneterre J
Laboratoire d'Oncologie Moléculaire Humaine, Centre Oscar Lambret, Lille, France.
Clin Cancer Res. 1998 Jan;4(1):189-96.
We measured the levels of p53 and urokinase-type plasminogen activator (uPA) in 634 tumor tissues from 634 different node-negative primary breast cancer patients who underwent locoregional surgery in the Center Oscar Lambret between July 1989 and September 1994. p53 and uPA were assayed using commercially available kits in cytosols prepared for estradiol receptor (ER) and progesterone receptor (PgR) assays. The optimum clinical thresholds were chosen for prognostic studies: 4 ng/ml for p53 and 0.5 ng/ml for uPA. p53 was elevated in 13.7% of the tumors, and uPA was elevated in 27.5% of the tumors; they were negatively related (chi 2 test) to ER and PgR and positively related to histoprognostic grading (HPG) and tumor diameter. uPA was negatively correlated to ER and PgR, and p53 and uPA were positively correlated to each other (P = 0.0001; Spearman test). In the prognostic studies, the 316 patients who did not receive adjuvant chemotherapy were included to avoid treatment interference; this number corresponds to all of the patients operated on between 1989 and 1992. The mean duration of follow-up of living patients was 4 years. In overall survival studies, Cox univariate analyses demonstrated a prognostic value of p53 (P = 0.011; risk ratio, 1.59), uPA (P = 0.038; risk ratio, 2.32), PgR, HPG, and tumor diameter. In Cox multivariate analyses, only HPG had a statistically significant prognostic value. In relapse-free survival studies, univariate analyses demonstrated prognostic values of uPA (P = 0.0011) and of age, and both parameters retained their prognostic value in multivariate analyses (uPA: P = 0.0004). This study demonstrates not only that p53 and uPA have prognostic value but also that these two parameters are linked to other classical clinical, histological, or biological prognostic parameters, as well as to each other. Moreover, because uPA is of prognostic value in multivariate relapse-free survival studies, uPA is an important prognostic factor in node-negative breast cancer patients.
我们检测了1989年7月至1994年9月期间在奥斯卡·兰布雷特中心接受局部区域手术的634例不同的淋巴结阴性原发性乳腺癌患者的634份肿瘤组织中的p53和尿激酶型纤溶酶原激活剂(uPA)水平。使用市售试剂盒在为雌二醇受体(ER)和孕酮受体(PgR)检测制备的细胞溶胶中检测p53和uPA。为预后研究选择了最佳临床阈值:p53为4 ng/ml,uPA为0.5 ng/ml。13.7%的肿瘤中p53升高,27.5%的肿瘤中uPA升高;它们与ER和PgR呈负相关(卡方检验),与组织预后分级(HPG)和肿瘤直径呈正相关。uPA与ER和PgR呈负相关,p53和uPA相互呈正相关(P = 0.0001;Spearman检验)。在预后研究中,纳入了316例未接受辅助化疗的患者以避免治疗干扰;这个数字对应于1989年至1992年期间所有接受手术的患者。存活患者的平均随访时间为4年。在总生存研究中,Cox单因素分析显示p53(P = 0.011;风险比,1.59)、uPA(P = 0.038;风险比,2.32)、PgR、HPG和肿瘤直径具有预后价值。在Cox多因素分析中,只有HPG具有统计学显著的预后价值。在无复发生存研究中,单因素分析显示uPA(P = 0.0011)和年龄具有预后价值,并且这两个参数在多因素分析中均保留其预后价值(uPA:P = 0.0004)。这项研究不仅表明p53和uPA具有预后价值,而且这两个参数与其他经典的临床、组织学或生物学预后参数相关,并且相互关联。此外,由于uPA在多因素无复发生存研究中具有预后价值,uPA是淋巴结阴性乳腺癌患者的一个重要预后因素。