Broët P, Spyratos F, Romain S, Quillien V, Daver A, Ricolleau G, Rallet A, Toulas C, Asselain B
Département de Biostatistiques, Institut Curie, Paris, France.
Br J Cancer. 1999 May;80(3-4):536-45. doi: 10.1038/sj.bjc.6690389.
The purpose of this retrospective multicentre study was to assess the prognostic value of urokinase plasminogen activator (uPA) and p53 levels in a large series of primary breast cancer, using an automatic quantitative luminometric method. Samples of 1245 operable breast tumours were collected from seven French institutions and patients were followed for a median of 75 months. The median uPA and p53 levels assayed in cytosols by means of the immunoluminometric technique (LIA) were 0.31 and 0.20 ng mg(-1) of protein respectively. In univariate analysis, high levels of uPA and p53 were associated with shorter disease-specific survival, disease-free interval, and distant recurrence-free interval. The 5-year survival rates were 95.5% among patients with uPA values below the 20th percentile, and 77.5% in those with values above the 80th percentile. The 5-year survival rates were 91.0% in patients with p53 values below the 20th percentile, and 77.6% in those with values above the 80th percentile. In multivariate analysis, the risk of disease-related death increased with uPA levels after adjustment for tumour size, histological grade, lymph node involvement, and estrogen receptor status. A high level of uPA was also related to a shorter disease-free interval and distant recurrence-free interval. In node-negative patients, a high level of uPA remained strongly related to the three outcomes. When adjusted for other prognostic factors, p53 was no longer significantly related to the outcomes. Given its rapidity and simple application to routinely prepared cytosols, this LIA may be useful for evaluating the prognostic impact of uPA in primary breast cancer, particularly in node-negative patients. According to our results, the prognostic value of p53 accumulation is limited when uPA is included in multivariate analysis.
这项回顾性多中心研究的目的是,采用自动定量发光法评估大量原发性乳腺癌中尿激酶型纤溶酶原激活剂(uPA)和p53水平的预后价值。从法国七家机构收集了1245例可手术乳腺癌肿瘤样本,对患者进行了中位时间为75个月的随访。通过免疫发光技术(LIA)在细胞溶质中检测到的uPA和p53水平中位数分别为0.31和0.20 ng mg(-1)蛋白质。单因素分析中,uPA和p53水平高与疾病特异性生存期、无病间期和远处无复发生存期较短相关。uPA值低于第20百分位数的患者5年生存率为95.5%,而值高于第80百分位数的患者为77.5%。p53值低于第20百分位数的患者5年生存率为91.0%,而值高于第80百分位数的患者为77.6%。多因素分析中,在调整肿瘤大小、组织学分级、淋巴结受累情况和雌激素受体状态后,疾病相关死亡风险随uPA水平升高而增加。uPA水平高还与较短的无病间期和远处无复发生存期相关。在淋巴结阴性患者中,uPA水平高仍与这三个结局密切相关。在调整其他预后因素后,p53与结局不再显著相关。鉴于该LIA快速且易于应用于常规制备的细胞溶质,可能有助于评估uPA在原发性乳腺癌中的预后影响,尤其是在淋巴结阴性患者中。根据我们的结果,当uPA纳入多因素分析时,p53积累的预后价值有限。