David W Dodington, Stefano Serra, Tim Bracey, Runjan Chetty, Klaudia M Nowak
{"title":"新辅助治疗后食管腺癌的神经内分泌分化和血清素表达:与临床病理特征和预后的相关性。","authors":"David W Dodington, Stefano Serra, Tim Bracey, Runjan Chetty, Klaudia M Nowak","doi":"10.1111/his.15364","DOIUrl":null,"url":null,"abstract":"<p><strong>Aims: </strong>Oesophageal adenocarcinoma (EAC) is a glandular or mucinous epithelial malignancy that can show immunohistochemical evidence of neuroendocrine differentiation (NED) and express the hormone serotonin. The objective of this study was to correlate the presence of NED and serotonin with clinicopathological characteristics and patient outcome after neoadjuvant chemoradiation.</p><p><strong>Methods and results: </strong>A retrospective cohort of patients treated between 2002 and 2021 was established and included 218 oesophagectomy specimens with residual tumour. Representative full-face sections of tumour were stained for synaptophysin, chromogranin-A and serotonin by immunohistochemistry, and staining results were correlated with disease-free survival (DFS) and overall survival (OS). In total, 129 (59%) tumours showed evidence of NED, defined as immunohistochemical expression of synaptophysin or chromogranin-A, while 40 (18%) showed evidence of NED and expressed serotonin. Patients with neuroendocrine-positive tumours had significantly shorter median OS compared to those with neuroendocrine-negative tumours (22.5 versus 48.8 months, P = 0.006), but similar median DFS (13.3 versus 17.8 months, P = 0.34). Using Cox regression, the association between NED and OS was significant in univariate [hazard ratio (HR) = 1.68, 95% confidence interval (CI) = 1.16-2.45] and multivariate (HR = 1.65, 95% CI = 1.08-2.52) analysis. Patients with serotonin-expressing tumours had similar median OS (21.7 versus 25.9 months, P = 0.24) and DFS (7.3 versus 15.6 months, P = 0.12) compared to those with NED but lacking serotonin. Using Cox regression, serotonin expression was associated with reduced OS in univariate (HR = 1.62, 95% CI = 1.06-2.47) but not multivariate (HR = 1.03, 95% CI = 0.64-1.65) analysis.</p><p><strong>Conclusions: </strong>Our findings support NED as independent predictor of OS in EAC after neoadjuvant chemoradiation. While a subset of tumours with NED expressed serotonin, this did not provide additional prognostic information.</p>","PeriodicalId":13219,"journal":{"name":"Histopathology","volume":" ","pages":""},"PeriodicalIF":3.9000,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Neuroendocrine differentiation and serotonin expression in oesophageal adenocarcinomas after neoadjuvant therapy: correlation with clinicopathological features and outcome.\",\"authors\":\"David W Dodington, Stefano Serra, Tim Bracey, Runjan Chetty, Klaudia M Nowak\",\"doi\":\"10.1111/his.15364\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Aims: </strong>Oesophageal adenocarcinoma (EAC) is a glandular or mucinous epithelial malignancy that can show immunohistochemical evidence of neuroendocrine differentiation (NED) and express the hormone serotonin. The objective of this study was to correlate the presence of NED and serotonin with clinicopathological characteristics and patient outcome after neoadjuvant chemoradiation.</p><p><strong>Methods and results: </strong>A retrospective cohort of patients treated between 2002 and 2021 was established and included 218 oesophagectomy specimens with residual tumour. Representative full-face sections of tumour were stained for synaptophysin, chromogranin-A and serotonin by immunohistochemistry, and staining results were correlated with disease-free survival (DFS) and overall survival (OS). In total, 129 (59%) tumours showed evidence of NED, defined as immunohistochemical expression of synaptophysin or chromogranin-A, while 40 (18%) showed evidence of NED and expressed serotonin. Patients with neuroendocrine-positive tumours had significantly shorter median OS compared to those with neuroendocrine-negative tumours (22.5 versus 48.8 months, P = 0.006), but similar median DFS (13.3 versus 17.8 months, P = 0.34). Using Cox regression, the association between NED and OS was significant in univariate [hazard ratio (HR) = 1.68, 95% confidence interval (CI) = 1.16-2.45] and multivariate (HR = 1.65, 95% CI = 1.08-2.52) analysis. Patients with serotonin-expressing tumours had similar median OS (21.7 versus 25.9 months, P = 0.24) and DFS (7.3 versus 15.6 months, P = 0.12) compared to those with NED but lacking serotonin. Using Cox regression, serotonin expression was associated with reduced OS in univariate (HR = 1.62, 95% CI = 1.06-2.47) but not multivariate (HR = 1.03, 95% CI = 0.64-1.65) analysis.</p><p><strong>Conclusions: </strong>Our findings support NED as independent predictor of OS in EAC after neoadjuvant chemoradiation. 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引用次数: 0
摘要
目的:食管腺癌(EAC)是一种腺性或粘液性上皮恶性肿瘤,可显示神经内分泌分化(NED)的免疫组化证据,并表达5-羟色胺激素。本研究的目的是将NED和5-羟色胺的存在与新辅助化疗后的临床病理特征和患者预后相关联:建立了2002年至2021年间接受治疗的患者回顾性队列,其中包括218例有残余肿瘤的食管切除术标本。用免疫组化方法对具有代表性的全切面肿瘤切片进行突触素、嗜铬粒蛋白-A和5-羟色胺染色,并将染色结果与无病生存期(DFS)和总生存期(OS)相关联。共有129例(59%)肿瘤显示有NED证据,即免疫组化表达突触素或嗜铬粒蛋白-A,40例(18%)肿瘤显示有NED证据并表达血清素。与神经内分泌阴性肿瘤患者相比,神经内分泌阳性肿瘤患者的中位OS明显缩短(22.5个月对48.8个月,P = 0.006),但中位DFS相似(13.3个月对17.8个月,P = 0.34)。使用Cox回归法进行单变量[危险比(HR)=1.68,95%置信区间(CI)=1.16-2.45]和多变量(HR=1.65,95%CI=1.08-2.52)分析,NED与OS之间的关系显著。与NED但缺乏血清素的患者相比,血清素表达肿瘤患者的中位OS(21.7个月对25.9个月,P = 0.24)和DFS(7.3个月对15.6个月,P = 0.12)相似。通过Cox回归分析,血清素的表达与单变量(HR = 1.62,95% CI = 1.06-2.47)但非多变量(HR = 1.03,95% CI = 0.64-1.65)分析中的OS降低相关:我们的研究结果表明,NED是预测EAC新辅助化疗后OS的独立指标。虽然有一部分NED肿瘤表达血清素,但这并不能提供额外的预后信息。
Neuroendocrine differentiation and serotonin expression in oesophageal adenocarcinomas after neoadjuvant therapy: correlation with clinicopathological features and outcome.
Aims: Oesophageal adenocarcinoma (EAC) is a glandular or mucinous epithelial malignancy that can show immunohistochemical evidence of neuroendocrine differentiation (NED) and express the hormone serotonin. The objective of this study was to correlate the presence of NED and serotonin with clinicopathological characteristics and patient outcome after neoadjuvant chemoradiation.
Methods and results: A retrospective cohort of patients treated between 2002 and 2021 was established and included 218 oesophagectomy specimens with residual tumour. Representative full-face sections of tumour were stained for synaptophysin, chromogranin-A and serotonin by immunohistochemistry, and staining results were correlated with disease-free survival (DFS) and overall survival (OS). In total, 129 (59%) tumours showed evidence of NED, defined as immunohistochemical expression of synaptophysin or chromogranin-A, while 40 (18%) showed evidence of NED and expressed serotonin. Patients with neuroendocrine-positive tumours had significantly shorter median OS compared to those with neuroendocrine-negative tumours (22.5 versus 48.8 months, P = 0.006), but similar median DFS (13.3 versus 17.8 months, P = 0.34). Using Cox regression, the association between NED and OS was significant in univariate [hazard ratio (HR) = 1.68, 95% confidence interval (CI) = 1.16-2.45] and multivariate (HR = 1.65, 95% CI = 1.08-2.52) analysis. Patients with serotonin-expressing tumours had similar median OS (21.7 versus 25.9 months, P = 0.24) and DFS (7.3 versus 15.6 months, P = 0.12) compared to those with NED but lacking serotonin. Using Cox regression, serotonin expression was associated with reduced OS in univariate (HR = 1.62, 95% CI = 1.06-2.47) but not multivariate (HR = 1.03, 95% CI = 0.64-1.65) analysis.
Conclusions: Our findings support NED as independent predictor of OS in EAC after neoadjuvant chemoradiation. While a subset of tumours with NED expressed serotonin, this did not provide additional prognostic information.
期刊介绍:
Histopathology is an international journal intended to be of practical value to surgical and diagnostic histopathologists, and to investigators of human disease who employ histopathological methods. Our primary purpose is to publish advances in pathology, in particular those applicable to clinical practice and contributing to the better understanding of human disease.