Tandon A K, Clark G M, Chamness G C, Chirgwin J M, McGuire W L
Department of Medicine, University of Texas Health Science Center, San Antonio 78284-7884.
N Engl J Med. 1990 Feb 1;322(5):297-302. doi: 10.1056/NEJM199002013220504.
We investigated the possibility that cathepsin D, an estrogen-induced lysosomal protease, might have value as a prognostic factor in breast cancer by studying frozen tissue specimens from 397 patients. We measured the 34-kd mature form of the enzyme by Western blot assay and densitometry. Among 199 patients with node-negative disease, but not among 198 with node-positive disease, high levels of cathepsin D proved to be a significant predictor of reduced disease-free survival (median follow-up, 64 months), either as a continuous variable (log cathepsin D; P = 0.018) or as a dichotomous variable with an optimized cutoff point (P = 0.0001). Results were similar for overall survival (P = 0.009 and 0.0001, respectively). Relating the level of cathepsin D to other prognostic factors in the patients with node-negative disease, we found an association with aneuploidy but none with estrogen or progesterone receptors, tumor size, or the age of the patient. In multivariate analyses, a high level of cathepsin D was the most important independent factor in predicting shorter disease-free and overall survival in patients with node-negative disease. As compared with the risk in women with low levels of cathepsin D, the relative risk of tumor recurrence was 2.6 (95 percent confidence interval, 1.6 to 4.4) and the relative risk of death was 3.9 (95 percent confidence interval, 2.1 to 7.3) among those with high levels of cathepsin D. For disease-free survival, cathepsin D status was predictive of outcome primarily among those with aneuploid tumors; the actuarial five-year recurrence rates of aneuploid tumors were 60 percent among women with high levels of cathepsin D and 29 percent among those with low levels, as compared with 22 percent for all diploid tumors. We conclude that cathepsin D may be an independent predictor of early recurrence and death in node-negative breast cancer.
我们通过研究397例患者的冷冻组织标本,探讨了雌激素诱导的溶酶体蛋白酶组织蛋白酶D作为乳腺癌预后因素的可能性。我们采用蛋白质印迹分析和光密度测定法测量了该酶34-kd的成熟形式。在199例淋巴结阴性疾病患者中,组织蛋白酶D水平高被证明是无病生存期缩短的重要预测指标(中位随访时间64个月),无论是作为连续变量(组织蛋白酶D对数;P = 0.018)还是作为具有最佳临界点的二分变量(P = 0.0001)。总生存期的结果相似(分别为P = 0.009和0.0001)。将淋巴结阴性疾病患者的组织蛋白酶D水平与其他预后因素相关联,我们发现其与非整倍体有关,但与雌激素或孕激素受体、肿瘤大小或患者年龄无关。在多变量分析中,组织蛋白酶D水平高是预测淋巴结阴性疾病患者无病生存期和总生存期较短的最重要独立因素。与组织蛋白酶D水平低的女性相比,组织蛋白酶D水平高的女性肿瘤复发的相对风险为2.6(95%置信区间,1.6至4.4),死亡的相对风险为3.9(95%置信区间,2.1至7.3)。对于无病生存期,组织蛋白酶D状态主要在非整倍体肿瘤患者中预测预后;组织蛋白酶D水平高的女性非整倍体肿瘤的精算五年复发率为60%,水平低的为29%,而所有二倍体肿瘤的这一比例为22%。我们得出结论,组织蛋白酶D可能是淋巴结阴性乳腺癌早期复发和死亡的独立预测指标。