Department of Surgery, Cancer Centre Amsterdam, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
West of Scotland Pancreatic Unit, Glasgow Royal Infirmary, University of Glasgow, Glasgow, UK.
Br J Surg. 2019 Mar;106(4):342-354. doi: 10.1002/bjs.11111. Epub 2019 Feb 13.
As more therapeutic options for pancreatic cancer are becoming available, there is a need to improve outcome prediction to support shared decision-making. A systematic evaluation of prediction models in resectable pancreatic cancer is lacking.
This systematic review followed the CHARMS and PRISMA guidelines. PubMed, Embase and Cochrane Library databases were searched up to 11 October 2017. Studies reporting development or validation of models predicting survival in resectable pancreatic cancer were included. Models without performance measures, reviews, abstracts or more than 10 per cent of patients not undergoing resection in postoperative models were excluded. Studies were appraised critically.
After screening 4403 studies, 22 (44 319 patients) were included. There were 19 model development/update studies and three validation studies, altogether concerning 21 individual models. Two studies were deemed at low risk of bias. Eight models were developed for the preoperative setting and 13 for the postoperative setting. Most frequently included parameters were differentiation grade (11 of 21 models), nodal status (8 of 21) and serum albumin (7 of 21). Treatment-related variables were included in three models. The C-statistic/area under the curve values ranged from 0·57 to 0·90. Based on study design, validation methods and the availability of web-based calculators, two models were identified as the most promising.
Although a large number of prediction models for resectable pancreatic cancer have been reported, most are at high risk of bias and have not been validated externally. This overview of prognostic factors provided practical recommendations that could help in designing easily applicable prediction models to support shared decision-making.
随着越来越多的胰腺癌治疗选择的出现,需要提高预后预测能力,以支持共同决策。目前缺乏对可切除性胰腺癌预测模型的系统评价。
本系统评价遵循 CHARMS 和 PRISMA 指南。检索了 PubMed、Embase 和 Cochrane Library 数据库,检索日期截至 2017 年 10 月 11 日。纳入了报道用于预测可切除性胰腺癌生存模型的开发或验证的研究。排除了未报告性能测量指标、综述、摘要或术后模型中超过 10%的患者未接受切除术的模型,以及仅有 10 名以下患者的研究。对研究进行了严格评估。
经过筛选 4403 篇研究,最终纳入 22 项研究(44319 名患者)。其中 19 项为模型开发/更新研究,3 项为验证研究,共涉及 21 个独立模型。有 2 项研究被认为存在低偏倚风险。8 个模型用于术前评估,13 个用于术后评估。最常纳入的参数包括分化程度(21 个模型中的 11 个)、淋巴结状态(21 个模型中的 8 个)和血清白蛋白(21 个模型中的 7 个)。有 3 个模型纳入了治疗相关变量。C 统计量/曲线下面积范围为 0.57 至 0.90。根据研究设计、验证方法以及是否有在线计算器,确定了两个最有前途的模型。
尽管已经报道了大量用于可切除性胰腺癌的预测模型,但大多数模型存在较高的偏倚风险,并且尚未进行外部验证。本综述对预后因素的分析提供了实用的建议,有助于设计易于应用的预测模型,以支持共同决策。