Quek Marcus L, Daneshmand Siamak, Rodrigo Sonali, Cai Jie, Dorff Tanya B, Groshen Susan, Skinner Donald G, Lieskovsky Gary, Pinski Jacek
Department of Urology, Loyola University Stritch School of Medicine, Maywood, Illinois, USA.
Urology. 2006 Jun;67(6):1247-52. doi: 10.1016/j.urology.2005.12.009. Epub 2006 May 12.
To evaluate the expression of chromogranin A, a marker for neuroendocrine (NE) differentiation, in patients with lymph node-positive prostate cancer to determine its prognostic significance. NE cells are involved in cellular growth and differentiation in both normal and pathologic conditions of the prostate.
We reviewed the data of 140 patients with lymph node-positive prostate adenocarcinoma treated with radical prostatectomy and pelvic lymphadenectomy. The median follow-up was 10.9 years (range 0.8 to 19.7). Immunohistochemical staining for chromogranin A was evaluated in areas of benign epithelium, primary prostate cancer, and lymph node metastasis. The association between chromogranin A expression and the clinical and pathologic factors (preoperative serum prostate-specific antigen and prostatectomy Gleason score and stage) and clinical outcomes, including overall and recurrence-free survival, was evaluated.
Staining was positive in 86% of benign areas, 61% of primary cancer specimens, and 12% of lymph node deposits. The preoperative serum prostate-specific antigen level and pathologic stage and grade of the primary tumor did not show any statistically significant correlation with NE staining in any of the areas. Only NE expression in the primary tumor was associated with clinical recurrence, with a 10-year recurrence-free survival rate for those with less than 5% staining of 67% compared with 35% for those with 5% staining or greater (P = 0.03). Furthermore, after adjusting for age, greater NE expression in the primary tumor (relative risk 2.15, P = 0.02) and lymph node deposit (relative risk 2.03, P = 0.03) was associated with poorer overall survival.
NE expression in the primary tumor and lymph node metastasis of patients with node-positive prostate cancer may provide additional prognostic stratification.
评估嗜铬粒蛋白A(一种神经内分泌(NE)分化标志物)在淋巴结阳性前列腺癌患者中的表达,以确定其预后意义。NE细胞参与前列腺正常和病理状态下的细胞生长与分化。
我们回顾了140例接受根治性前列腺切除术和盆腔淋巴结清扫术的淋巴结阳性前列腺腺癌患者的数据。中位随访时间为10.9年(范围0.8至19.7年)。对良性上皮、原发性前列腺癌和淋巴结转移区域进行嗜铬粒蛋白A的免疫组织化学染色评估。评估嗜铬粒蛋白A表达与临床和病理因素(术前血清前列腺特异性抗原、前列腺切除术后Gleason评分和分期)以及临床结局(包括总生存期和无复发生存期)之间的关联。
86%的良性区域、61%的原发性癌标本和12%的淋巴结转移灶染色呈阳性。术前血清前列腺特异性抗原水平以及原发性肿瘤的病理分期和分级在任何区域均与NE染色无统计学显著相关性。仅原发性肿瘤中的NE表达与临床复发相关,染色低于5%的患者10年无复发生存率为67%,而染色为5%或更高的患者为35%(P = 0.03)。此外,在调整年龄后,原发性肿瘤(相对风险2.15,P = 0.02)和淋巴结转移灶(相对风险2.03,P = 0.03)中较高的NE表达与较差的总生存期相关。
淋巴结阳性前列腺癌患者原发性肿瘤和淋巴结转移中的NE表达可能提供额外的预后分层。