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淋巴结阳性乳腺癌的流式细胞术:癌症与白血病B组方案8869

Flow cytometry in node-positive breast cancer: cancer and leukemia group B protocol 8869.

作者信息

Kute T E, Quadri Y, Muss H, Zbieranski N, Cirrincione C, Berry D A, Barcos M, Thor A P, Liu E, Koerner F

机构信息

Bowman Gray School of Medicine, Winston-Salem, North Carolina, USA.

出版信息

Cytometry. 1995 Dec 15;22(4):297-306. doi: 10.1002/cyto.990220406.

Abstract

This report describes a companion flow cytometry study (Cancer and Leukemia Group B (CALGB)--8869) using tumors derived from patients enrolled in a large randomized clinical trial (CALGB-8541) performed on 1,572 patients with early stage, node-positive breast cancer. The CALGB initiated an adjuvant breast cancer trial in 1985 to determine if dose intensification (dose of drug per unit time) of chemotherapy was related to relapse-free and overall survival. Patients were randomized by pretreatment clinical variables to one of three different dosage regimens of chemotherapy. Using a tumor enrichment procedure, 442 paraffin-embedded blocks were analyzed by flow cytometry, and S-phase fraction (SPF) was analyzed by three different methods. Ploidy analysis was performed using standard procedures. Tissue from 90% of the patients was suitable for ploidy analysis, whereas only 68% could be assessed for SPF. With a median follow-up time of 80 months, our results show that ploidy status had no clinical utility, whereas high SPF predicted poorer overall survival. The rectangular fit model for SPF was more predictive of outcome than both the area fit model and a computer fit model (modfit) for SPF. In univariate analysis, patients with a low SPF (< 10%) had a better prognosis than those patients with a high SPF (> 10%), but they responded equally well to the different treatment regimens. Patients with high SPF (> 10%) had longer relapse-free and overall survival to high dose chemotherapy compared to low or standard dose chemotherapy. Multivariate analysis indicated that treatment intensity as well as the number of positive nodes, tumor size, steroid receptor status, and c-erb B-2 expression were significant in predicting overall and disease-free survival. The multivariate analysis, however, revealed that SPF was significant in predicting overall but not disease-free survival, but there was no longer any relationship among SPF, dose intensity, and outcome.

摘要

本报告描述了一项配套的流式细胞术研究(癌症与白血病B组(CALGB)-8869),该研究使用了来自参加一项大型随机临床试验(CALGB-8541)的患者的肿瘤,该试验针对1572例早期、淋巴结阳性乳腺癌患者进行。CALGB于1985年启动了一项辅助性乳腺癌试验,以确定化疗的剂量强化(单位时间内的药物剂量)是否与无复发生存率和总生存率相关。患者根据预处理临床变量被随机分配到三种不同化疗剂量方案中的一种。使用肿瘤富集程序,对442个石蜡包埋块进行了流式细胞术分析,并通过三种不同方法分析了S期分数(SPF)。使用标准程序进行倍性分析。90%患者的组织适合进行倍性分析,而只有68%的组织可用于评估SPF。中位随访时间为80个月,我们的结果表明倍性状态无临床实用价值,而高SPF预示总生存率较差。SPF的矩形拟合模型比SPF的面积拟合模型和计算机拟合模型(modfit)更能预测预后。在单变量分析中,低SPF(<10%)的患者预后优于高SPF(>10%)的患者,但他们对不同治疗方案的反应相同。与低剂量或标准剂量化疗相比,高SPF(>10%)的患者接受高剂量化疗后的无复发生存期和总生存期更长。多变量分析表明,治疗强度以及阳性淋巴结数量、肿瘤大小、类固醇受体状态和c-erb B-2表达在预测总生存期和无病生存期方面具有显著性。然而,多变量分析显示,SPF在预测总生存期方面具有显著性,但在预测无病生存期方面不具有显著性,而且SPF、剂量强度和预后之间不再存在任何关系。

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