Mocellin Simone, Pasquali Sandro
Meta-Analysis Unit, Department of Surgery,Oncology and Gastroenterology, University of Padova, Via Giustiniani 2, Padova, Veneto, 35128, Italy.
Cochrane Database Syst Rev. 2015 Feb 6;2015(2):CD009944. doi: 10.1002/14651858.CD009944.pub2.
Endoscopic ultrasound (EUS) is proposed as an accurate diagnostic device for the locoregional staging of gastric cancer, which is crucial to developing a correct therapeutic strategy and ultimately to providing patients with the best chance of cure. However, despite a number of studies addressing this issue, there is no consensus on the role of EUS in routine clinical practice.
To provide both a comprehensive overview and a quantitative analysis of the published data regarding the ability of EUS to preoperatively define the locoregional disease spread (i.e., primary tumor depth (T-stage) and regional lymph node status (N-stage)) in people with primary gastric carcinoma.
We performed a systematic search to identify articles that examined the diagnostic accuracy of EUS (the index test) in the evaluation of primary gastric cancer depth of invasion (T-stage, according to the AJCC/UICC TNM staging system categories T1, T2, T3 and T4) and regional lymph node status (N-stage, disease-free (N0) versus metastatic (N+)) using histopathology as the reference standard. To this end, we searched the following databases: the Cochrane Library (the Cochrane Central Register of Controlled Trials (CENTRAL)), MEDLINE, EMBASE, NIHR Prospero Register, MEDION, Aggressive Research Intelligence Facility (ARIF), ClinicalTrials.gov, Current Controlled Trials MetaRegister, and World Health Organization International Clinical Trials Registry Platform (WHO ICTRP), from 1988 to January 2015.
We included studies that met the following main inclusion criteria: 1) a minimum sample size of 10 patients with histologically-proven primary carcinoma of the stomach (target condition); 2) comparison of EUS (index test) with pathology evaluation (reference standard) in terms of primary tumor (T-stage) and regional lymph nodes (N-stage). We excluded reports with possible overlap with the selected studies.
For each study, two review authors extracted a standard set of data, using a dedicated data extraction form. We assessed data quality using a standard procedure according to the Quality Assessment of Diagnostic Accuracy Studies (QUADAS-2) criteria. We performed diagnostic accuracy meta-analysis using the hierarchical bivariate method.
We identified 66 articles (published between 1988 and 2012) that were eligible according to the inclusion criteria. We collected the data on 7747 patients with gastric cancer who were staged with EUS. Overall the quality of the included studies was good: in particular, only five studies presented a high risk of index test interpretation bias and two studies presented a high risk of selection bias.For primary tumor (T) stage, results were stratified according to the depth of invasion of the gastric wall. The meta-analysis of 50 studies (n = 4397) showed that the summary sensitivity and specificity of EUS in discriminating T1 to T2 (superficial) versus T3 to T4 (advanced) gastric carcinomas were 0.86 (95% confidence interval (CI) 0.81 to 0.90) and 0.90 (95% CI 0.87 to 0.93) respectively. For the diagnostic capacity of EUS to distinguish T1 (early gastric cancer, EGC) versus T2 (muscle-infiltrating) tumors, the meta-analysis of 46 studies (n = 2742) showed that the summary sensitivity and specificity were 0.85 (95% CI 0.78 to 0.91) and 0.90 (95% CI 0.85 to 0.93) respectively. When we addressed the capacity of EUS to distinguish between T1a (mucosal) versus T1b (submucosal) cancers the meta-analysis of 20 studies (n = 3321) showed that the summary sensitivity and specificity were 0.87 (95% CI 0.81 to 0.92) and 0.75 (95% CI 0.62 to 0.84) respectively. Finally, for the metastatic involvement of lymph nodes (N-stage), the meta-analysis of 44 studies (n = 3573) showed that the summary sensitivity and specificity were 0.83 (95% CI 0.79 to 0.87) and 0.67 (95% CI 0.61 to 0.72), respectively.Overall, as demonstrated also by the Bayesian nomograms, which enable readers to calculate post-test probabilities for any target condition prevalence, the EUS accuracy can be considered clinically useful to guide physicians in the locoregional staging of people with gastric cancer. However, it should be noted that between-study heterogeneity was not negligible: unfortunately, we could not identify any consistent source of the observed heterogeneity. Therefore, all accuracy measures reported in the present work and summarizing the available evidence should be interpreted cautiously. Moreover, we must emphasize that the analysis of positive and negative likelihood values revealed that EUS diagnostic performance cannot be considered optimal either for disease confirmation or for exclusion, especially for the ability of EUS to distinguish T1a (mucosal) versus T1b (submucosal) cancers and positive versus negative lymph node status.
AUTHORS' CONCLUSIONS: By analyzing the data from the largest series ever considered, we found that the diagnostic accuracy of EUS might be considered clinically useful to guide physicians in the locoregional staging of people with gastric carcinoma. However, the heterogeneity of the results warrants special caution, as well as further investigation for the identification of factors influencing the outcome of this diagnostic tool. Moreover, physicians should be warned that EUS performance is lower in diagnosing superficial tumors (T1a versus T1b) and lymph node status (positive versus negative). Overall, we observed large heterogeneity and its source needs to be understood before any definitive conclusion can be drawn about the use of EUS can be proposed in routine clinical settings.
内镜超声检查(EUS)被认为是一种用于胃癌局部区域分期的准确诊断设备,这对于制定正确的治疗策略并最终为患者提供最佳治愈机会至关重要。然而,尽管有多项研究探讨了这一问题,但对于EUS在常规临床实践中的作用尚无共识。
对已发表的关于EUS术前确定原发性胃癌患者局部区域疾病扩散情况(即原发性肿瘤深度(T分期)和区域淋巴结状态(N分期))能力的数据进行全面综述和定量分析。
我们进行了系统检索,以识别使用组织病理学作为参考标准,研究EUS(指标试验)在评估原发性胃癌浸润深度(T分期,根据美国癌症联合委员会/国际抗癌联盟TNM分期系统分为T1、T2、T3和T4)和区域淋巴结状态(N分期,无病(N0)与转移(N+))方面诊断准确性的文章。为此,我们检索了以下数据库:Cochrane图书馆(Cochrane对照试验中心注册库(CENTRAL))、MEDLINE、EMBASE、NIHR Prospero注册库、MEDION、积极研究情报设施(ARIF)、ClinicalTrials.gov、当前对照试验元注册库以及世界卫生组织国际临床试验注册平台(WHO ICTRP),检索时间为1988年至2015年1月。
我们纳入了符合以下主要纳入标准的研究:1)至少10例经组织学证实为原发性胃癌(目标疾病)的患者样本量;2)在原发性肿瘤(T分期)和区域淋巴结(N分期)方面将EUS(指标试验)与病理评估(参考标准)进行比较。我们排除了与所选研究可能重叠的报告。
对于每项研究,两名综述作者使用专用数据提取表提取一组标准数据。我们根据诊断准确性研究质量评估(QUADAS-2)标准,采用标准程序评估数据质量。我们使用分层双变量方法进行诊断准确性荟萃分析。
我们识别出66篇(发表于1988年至2012年之间)符合纳入标准的文章。我们收集了7747例接受EUS分期的胃癌患者的数据。总体而言,纳入研究的质量良好:特别是,只有五项研究存在指标试验解释偏倚的高风险,两项研究存在选择偏倚的高风险。对于原发性肿瘤(T)分期,结果根据胃壁浸润深度进行分层。对50项研究(n = 4397)的荟萃分析表明,EUS区分T1至T2(浅表)与T3至T4(进展期)胃癌的汇总敏感性和特异性分别为0.86(95%置信区间(CI)0.81至0.90)和0.90(95%CI为0.87至0.93)。对于EUS区分T1(早期胃癌,EGC)与T2(肌层浸润)肿瘤的诊断能力,对46项研究(n = 2742)的荟萃分析表明,汇总敏感性和特异性分别为0.85(95%CI 0.78至0.91)和0.90(95%CI 0.85至0.93)。当我们探讨EUS区分T1a(黏膜)与T1b(黏膜下)癌的能力时,对20项研究(n = 3321)的荟萃分析表明,汇总敏感性和特异性分别为0.87(95%CI 0.81至0.92)和0.75(95%CI 0.62至0.84)。最后,对于淋巴结转移情况(N分期),对44项研究(n = 3573)的荟萃分析表明,汇总敏感性和特异性分别为0.83(95%CI 0.79至0.87)和0.67(95%CI 0.61至0.72)。总体而言,正如贝叶斯列线图所示,其使读者能够计算任何目标疾病患病率的检验后概率,EUS的准确性在临床上可被认为有助于指导医生对胃癌患者进行局部区域分期。然而,应注意的是,研究间的异质性不可忽视:不幸的是,我们无法确定观察到的异质性的任何一致来源。因此,本研究中报告的并总结现有证据的所有准确性测量结果都应谨慎解释。此外,我们必须强调,对阳性和阴性似然值的分析表明,无论是对于疾病确诊还是排除,EUS的诊断性能都不能被认为是最佳的,特别是对于EUS区分T1a(黏膜)与T1b(黏膜下)癌以及阳性与阴性淋巴结状态的能力。
通过分析有史以来最大系列的数据,我们发现EUS的诊断准确性在临床上可能有助于指导医生对胃癌患者进行局部区域分期。然而,结果的异质性需要特别谨慎,以及进一步研究以确定影响该诊断工具结果的因素。此外,应提醒医生,EUS在诊断浅表肿瘤(T1a与T1b)和淋巴结状态(阳性与阴性)方面的性能较低。总体而言,我们观察到很大的异质性,在能够就EUS在常规临床环境中的使用提出任何明确结论之前,需要了解其来源。