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T2N0 期食管癌临床分期准确性的系统评价和荟萃分析。

Accuracy of clinical staging for T2N0 oesophageal cancer: systematic review and meta-analysis.

机构信息

Division of Surgery and Interventional Science, University College London, London, UK.

Department of Gastroenterology, University College Hospital NHS Foundation Trust, London, UK.

出版信息

Dis Esophagus. 2021 Aug 10;34(8). doi: 10.1093/dote/doab002.

Abstract

Oesophageal cancer is the sixth commonest cause of overall cancer mortality. Clinical staging utilizes multiple imaging modalities to guide treatment and prognostication. T2N0 oesophageal cancer is a treatment threshold for neoadjuvant therapy. Data on accuracy of current clinical staging tests for this disease subgroup are conflicting. We performed a meta-analysis of all primary studies comparing clinical staging accuracy using multiple imaging modalities (index test) to histopathological staging following oesophagectomy (reference standard) in T2N0 oesophageal cancer. Patients that underwent neoadjuvant therapy were excluded. Electronic databases (MEDLINE, Embase, Cochrane Library) were searched up to September 2019. The primary outcome was diagnostic accuracy of combined T&N clinical staging. Publication date, first recruitment date, number of centers, sample size and geographical location main histological subtype were evaluated as potential sources of heterogeneity. The search strategy identified 1,199 studies. Twenty studies containing 5,213 patients met the inclusion criteria. Combined T&N staging accuracy was 19% (95% CI, 15-24); T staging accuracy was 29% (95% CI, 24-35); percentage of patients with T downstaging was 41% (95% CI, 33-50); percentage of patients with T upstaging was 28% (95% CI, 24-32) and percentage of patients with N upstaging was 34% (95% CI, 30-39). Significant sources of heterogeneity included the number of centers, sample size and study region. T2N0 oesophageal cancer staging remains inaccurate. A significant proportion of patients were downstaged (could have received endotherapy) or upstaged (should have received neoadjuvant chemotherapy). These findings were largely unchanged over the past two decades highlighting an urgent need for more accurate staging tests for this subgroup of patients.

摘要

食管癌是第六大常见的癌症死因。临床分期利用多种影像学方法来指导治疗和预后判断。T2N0 食管癌是新辅助治疗的治疗阈值。关于该疾病亚组目前临床分期检测准确性的数据存在争议。我们对所有比较使用多种影像学方法(试验)进行 T2N0 食管癌临床分期准确性与食管切除术后组织病理学分期(参考标准)的主要研究进行了荟萃分析。排除了接受新辅助治疗的患者。检索了电子数据库(MEDLINE、Embase、Cochrane 图书馆)截至 2019 年 9 月的数据。主要结局是联合 T&N 临床分期的诊断准确性。评估了出版日期、首次招募日期、中心数量、样本量和地理位置主要组织学亚型作为异质性的潜在来源。检索策略确定了 1199 项研究。20 项包含 5213 名患者的研究符合纳入标准。联合 T&N 分期准确性为 19%(95%CI,15-24);T 分期准确性为 29%(95%CI,24-35);T 降期患者比例为 41%(95%CI,33-50);T 升期患者比例为 28%(95%CI,24-32),N 升期患者比例为 34%(95%CI,30-39)。显著的异质性来源包括中心数量、样本量和研究区域。T2N0 食管癌分期仍然不准确。相当一部分患者降期(可接受内镜治疗)或升期(应接受新辅助化疗)。这些发现近二十年来基本没有变化,突显了迫切需要为这组患者开发更准确的分期检测方法。

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