Charpin C, Garcia S, Bonnier P, Martini F, Andrac L, Horschowski N, Lavaut M N, Allasia C
Department of Pathology, Faculté de Médecine Timone, Institut Fédératif de Recherche en Cancérologie et Immunologie de Marseille, France.
J Clin Oncol. 1998 Jun;16(6):2025-31. doi: 10.1200/JCO.1998.16.6.2025.
bcl-2 protein is detectable in human cancers and may be involved in the response to antineoplastic drugs or endocrine therapy in breast carcinomas. In a previous study, we had developed optimal technical conditions for bcl-2 immunodetection. The aim of the present report was to determine the prognostic significance of bcl-2 expression in breast carinomas by the use of a similar immunocytochemical procedure.
bcl-2 immunocytochemical assays were performed on frozen sections by automated immunoperoxidase technique (Ventana) and computer-assisted analysis of digitized colored microscopic images (SAMBA) in a series of 170 breast carcinomas. The results of automated quantitative immunocytochemical assays were correlated with patient follow-up (120 months).
Intense bcl-2 immunocytochemical expression in tumors (cutpoint, 15%) significantly correlated with longer disease-free survival and longer recurrence-free survival in the entire cohort of patients (P = .028 and P = .035, respectively) and also in node-negative subgroups of patients (P = .028 and P = .01; Kaplan-Meier long-rank test; NCSS 6.0.1 software). But bcl-2 immunostained surfaces (cutpoint, 15%) did not correlate with overall survival. In multivariate analysis (proportional hazards regression, Cox model), bcl-2 prognostic significance in terms of disease-free survival was only independent of the tumor size and grade and histoprognostic index (Nottingham prognostic index [NPI]).
bcl-2 immunohistochemical expression is a significant indicator of favorable outcome only in terms of disease-free and local recurrence-free survival. However, bcl-2 expression in tumors is an independent weakly prognostic indicator in breast carcinomas. bcl-2 immunodetection assessed in optimal technical conditions (frozen samples, automation, quantitative analysis, scatter diagram cutoffs) may have some limited practical clinical relevance for the management of patients with breast carcinomas.
bcl-2蛋白在人类癌症中可检测到,可能参与乳腺癌对抗肿瘤药物或内分泌治疗的反应。在先前的一项研究中,我们已开发出用于bcl-2免疫检测的最佳技术条件。本报告的目的是通过使用类似的免疫细胞化学方法来确定bcl-2表达在乳腺癌中的预后意义。
采用自动免疫过氧化物酶技术(Ventana)和数字化彩色显微图像计算机辅助分析(SAMBA),对170例乳腺癌的冰冻切片进行bcl-2免疫细胞化学检测。自动定量免疫细胞化学检测结果与患者随访情况(120个月)相关。
肿瘤中强烈的bcl-2免疫细胞化学表达(切点为15%)与整个患者队列中更长的无病生存期和更长的无复发生存期显著相关(分别为P = 0.028和P = 0.035),在淋巴结阴性患者亚组中也是如此(P = 0.028和P = 0.01;Kaplan-Meier长秩检验;NCSS 6.0.1软件)。但bcl-2免疫染色面积(切点为15%)与总生存期无关。在多变量分析(比例风险回归,Cox模型)中,bcl-2在无病生存期方面的预后意义仅独立于肿瘤大小、分级和组织预后指数(诺丁汉预后指数[NPI])。
bcl-2免疫组化表达仅在无病生存期和局部无复发生存期方面是良好预后的重要指标。然而,肿瘤中的bcl-2表达在乳腺癌中是一个独立的弱预后指标。在最佳技术条件下(冰冻样本、自动化、定量分析、散点图切点)评估的bcl-2免疫检测对于乳腺癌患者的管理可能具有一些有限的实际临床意义。