Cussenot O, Villette J M, Valeri A, Cariou G, Desgrandchamps F, Cortesse A, Meria P, Teillac P, Fiet J, Le Duc A
Departments of Urology, Hormone Biology, and Pathology, Hôpital Saint Louis, Paris, France.
J Urol. 1996 Apr;155(4):1340-3.
Approximately 50% of all malignant prostatic tumors contain neuroendocrine cells, which cannot be attributed to small cell prostatic carcinoma or carcinoid-like tumors, and which represent only 1 to 2% of all prostatic malignancies. Only limited data are available concerning the plasma levels of neuroendocrine markers in patients with prostatic tumors. Therefore, we determine the incidence of high plasma levels of neuroendocrine markers in patients with benign and malignant prostatic disease.
The presence of elevated plasma neuropeptide levels was investigated in 135 patients with prostatic carcinoma and 28 with benign prostatic hyperplasia. Plasma chromogranin A, neurone-specific enolase, substance P, calcitonin, somatostatin, neurotensin and bombesin levels were analyzed by immunoassays, and were compared to clinical and pathological stages of disease. Plasma prostatic acid phosphatase and prostate specific antigen levels were also determined. All patients were followed for at least 2 years after inclusion in the study.
Significantly elevated levels of chromogranin A were detected in 15% of patients with prostatic carcinoma before any treatment. During hormone resistant prostate cancer progression plasma chromogranin A and neuron-specific enolase levels were elevated in 55% and 30% of the patients, respectively. In patients with stage D3 disease survival curves were generated by the Kaplan-Meier method, and log rank analysis revealed a statistically significant difference between groups positive and negative for chromogranin A. Substance P and bombesin were also occasionally elevated in prostatic tumors. Determination of neuroendocrine differentiation by neuron-specific enolase or chromogranin A immunoassays was not helpful in the prediction of progressive localized prostatic carcinoma.
Future studies of plasma neuropeptide levels should confirm whether these parameters can be used as prognostic markers during late progression of prostatic carcinoma or for the selection of patients suitable for evaluation of new antineoplastic drugs to be active against neuroendocrine tumors.
所有恶性前列腺肿瘤中约50%含有神经内分泌细胞,这些细胞不能归因于小细胞前列腺癌或类癌样肿瘤,且仅占所有前列腺恶性肿瘤的1%至2%。关于前列腺肿瘤患者神经内分泌标志物血浆水平的资料有限。因此,我们测定了良性和恶性前列腺疾病患者血浆神经内分泌标志物高水平的发生率。
研究了135例前列腺癌患者和28例良性前列腺增生患者血浆神经肽水平升高的情况。通过免疫测定分析血浆嗜铬粒蛋白A、神经元特异性烯醇化酶、P物质、降钙素、生长抑素、神经降压素和蛙皮素水平,并与疾病的临床和病理分期进行比较。还测定了血浆前列腺酸性磷酸酶和前列腺特异性抗原水平。所有患者纳入研究后至少随访2年。
15%未经任何治疗的前列腺癌患者检测到嗜铬粒蛋白A水平显著升高。在激素抵抗性前列腺癌进展过程中,分别有55%和30%的患者血浆嗜铬粒蛋白A和神经元特异性烯醇化酶水平升高。对于D3期疾病患者,采用Kaplan-Meier法生成生存曲线,对数秩分析显示嗜铬粒蛋白A阳性和阴性组之间存在统计学显著差异。P物质和蛙皮素在前列腺肿瘤中也偶尔升高。通过神经元特异性烯醇化酶或嗜铬粒蛋白A免疫测定来确定神经内分泌分化,对预测局限性进展性前列腺癌并无帮助。
未来关于血浆神经肽水平的研究应证实这些参数是否可作为前列腺癌晚期进展的预后标志物,或用于选择适合评估对神经内分泌肿瘤有效的新型抗肿瘤药物的患者。