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年轻是印戒样前列腺癌患者生存不良的独立预测因素。

Younger age is an independent predictor for poor survival in patients with signet ring prostate carcinoma.

作者信息

Wang Jue, Wang Fen Wei, Hemstreet George P

机构信息

Department of Internal Medicine, Section of Oncology-Hematology, University of Nebraska Medical Center, Omaha, NE 68198-7680, USA.

出版信息

Prostate Cancer. 2011;2011:216169. doi: 10.1155/2011/216169. Epub 2010 Jul 20.

DOI:10.1155/2011/216169
PMID:22110982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3216005/
Abstract

Objective. The aim of this study was to examine the epidemiology, natural history, treatment pattern, and predictors of long-term survival of signet ring prostate carcinoma (SRPC) patients based on the analysis of the national Surveillance, Epidemiology, and End Results (SEER) database. Methods & Results. Between 1980 and 2004, a total of 93 patients with pathologically confirmed SRPC were identified. The mean age was 70 ± 11 years old. 82.8% of the patients had poorly or undifferentiated histology grade. 13.9% patients presented with metastatic disease. The 1-, 3-, and 5-year cancer-specific survival rates were 94.6%, 89.6%, and 83.8%, respectively. Using multivariate Cox proportional hazard model, younger age (40-50 versus age >70 yrs, P = .01), advanced tumor stage (distant versus local/regional, P = .02), and earlier diagnosis year (before 1995 versus after 1995, P = .01) were predictors of worse cancer specific survival. Conclusions. Despite more aggressive cancer therapy, younger SRPC patients had a worse cancer specific survival. This information could be useful when counseling these patients and emphasizes the need for new strategies and molecular-based therapeutic approaches for younger patients with SRPC.

摘要

目的。本研究旨在通过对国家监测、流行病学和最终结果(SEER)数据库的分析,探讨印戒细胞前列腺癌(SRPC)患者的流行病学、自然史、治疗模式以及长期生存的预测因素。方法与结果。在1980年至2004年期间,共识别出93例经病理证实的SRPC患者。平均年龄为70±11岁。82.8%的患者组织学分级为低分化或未分化。13.9%的患者出现转移性疾病。1年、3年和5年的癌症特异性生存率分别为94.6%、89.6%和83.8%。使用多变量Cox比例风险模型,较年轻的年龄(40 - 50岁与>70岁,P = 0.01)、晚期肿瘤分期(远处转移与局部/区域,P = 0.02)以及较早的诊断年份(1995年之前与1995年之后,P = 0.01)是癌症特异性生存较差的预测因素。结论。尽管癌症治疗更积极,但年轻的SRPC患者癌症特异性生存更差。这些信息在为这些患者提供咨询时可能有用,并强调需要为年轻的SRPC患者制定新的策略和基于分子的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76e6/3216005/aff66d16be2a/PC2011-216169.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76e6/3216005/aff66d16be2a/PC2011-216169.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76e6/3216005/aff66d16be2a/PC2011-216169.001.jpg

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