Formica V, Wotherspoon A, Cunningham D, Norman A R, Sirohi B, Oates J, Chong G
Department of Medicine, Royal Marsden Hospital, London and Sutton, Surrey, UK.
Br J Cancer. 2007 Apr 23;96(8):1178-82. doi: 10.1038/sj.bjc.6603699. Epub 2007 Apr 3.
The World Health Organisation (WHO) classification (2000) is widely used to classify neuroendocrine carcinomas (NECs), yet its prognostic value needs to be confirmed. In this study, patients with metastatic NECs (n=119) were classified according to WHO guidelines into well differentiated and poorly differentiated (WDNECs and PDNECs). Histological differentiation based on WHO criteria had the highest impact on overall survival (OS) (PDNECs : WDNECs hazard ratio (HR)=4.02, P=0.02); however, PDNECs represented only a small percentage of patients (8%). In a WDNEC-restricted analysis, abnormal liver function tests (LFTs) and elevated urinary 5-hydroxyindoleacetic acid (u5HIAA) were independent prognostic factors for survival (HR=2.65, P=0.006 and HR=2.51, P=0.003, respectively) and were used to create a WDNEC-specific prognostic model (low risk=both normal, intermediate risk=one of them abnormal, high risk=both abnormal). Low-risk WDNECs had the most favourable prognosis (median OS, mOS 8.1 years), which was significantly better compared to both intermediate-risk and high-risk WDNECs (mOS 3.2 and 1.4 years, with P=0.01 and P<0.001, respectively). High-risk WDNECs displayed the shortest OS (1.3 years), which was similar to that of PDNECs (P=0.572). This analysis supports the prognostic value of WHO classification for metastatic NECs arising from the gastroenteropancreatic tract; however, risk stratification using readily available u5HIAA and LFTs may be necessary for the heterogeneous group of WDNECs.
世界卫生组织(WHO)2000年分类法被广泛用于神经内分泌癌(NEC)的分类,但其预后价值尚需证实。在本研究中,转移性NEC患者(n = 119)根据WHO指南分为高分化和低分化(WDNEC和PDNEC)。基于WHO标准的组织学分化对总生存期(OS)影响最大(PDNEC:WDNEC风险比(HR)= 4.02,P = 0.02);然而,PDNEC仅占患者的一小部分(8%)。在仅针对WDNEC的分析中,肝功能检查异常(LFT)和尿5-羟吲哚乙酸(u5HIAA)升高是生存的独立预后因素(HR分别为2.65,P = 0.006和HR = 2.51,P = 0.003),并用于创建WDNEC特异性预后模型(低风险=两者均正常,中风险=其中之一异常,高风险=两者均异常)。低风险WDNEC的预后最佳(中位OS,mOS 8.1年),与中风险和高风险WDNEC相比均显著更好(mOS分别为3.2年和1.4年,P分别为0.01和P < 0.001)。高风险WDNEC的OS最短(1.3年),与PDNEC相似(P = 0.572)。该分析支持WHO分类法对源自胃肠胰道的转移性NEC的预后价值;然而,对于异质性的WDNEC组,可能需要使用易于获得的u5HIAA和LFT进行风险分层。