R.C. Grant , K. Duan , R. Jackson , W. Greenhalf , E. Costello-Goldring , P. Ghaneh , C. Halloran , D. Palmer , T. Hackert , M. Büchler , S. Hutchinson , S. Ramotar , A. Dodd , J. Wilson , F. Notta , G. O’Kane , J. Knox , J. Neoptolemos , S. Gallinger , S.E. Fischer
{"title":"胰腺癌手术切除后GATA6免疫组化与预后:来自ESPAC-4试验的结果","authors":"R.C. Grant , K. Duan , R. Jackson , W. Greenhalf , E. Costello-Goldring , P. Ghaneh , C. Halloran , D. Palmer , T. Hackert , M. Büchler , S. Hutchinson , S. Ramotar , A. Dodd , J. Wilson , F. Notta , G. O’Kane , J. Knox , J. Neoptolemos , S. Gallinger , S.E. Fischer","doi":"10.1016/j.esmogo.2025.100138","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>No prognostic biomarker is currently used in clinical management of patients with surgically resected pancreatic cancer other than CA-19-9. In this study, we tested the prognostic value of GATA6 measured with immunohistochemistry and digital assistance.</div></div><div><h3>Patients and methods</h3><div>One hundred and ninety-three patients with resected pancreatic ductal adenocarcinoma from the ESPAC-4 trial of adjuvant gemcitabine and capecitabine were included. Two pathologists independently assessed GATA6 protein expression by immunohistochemistry in tissue microarray cores, manually and with digital assistance. Overall survival was compared across GATA6 levels using multivariate Cox proportional hazard regressions, with exploratory analyses evaluating recurrence-free survival and differential treatment effects.</div></div><div><h3>Results</h3><div>Interobserver concordance improved with digitally assisted scoring (kappa 0.72 versus 0.25, <em>P</em> < 0.001). Median overall survival was 24.3 months [95% confidence interval (CI) 19.2-32.1 months] with low GATA6 expression versus 35.2 months (95% CI 29.9-53.0 months) with high GATA6 expression (adjusted hazard ratio 1.60, 95% CI 1.08-2.38, <em>P =</em> 0.02). Similar results were observed for recurrence-free survival (adjusted hazard ratio 1.45, 95% CI 0.99-2.14, <em>P =</em> 0.06). GATA6 expression was not associated with differential treatment effects.</div></div><div><h3>Conclusions</h3><div>GATA6 expression measured by immunohistochemistry with digital assistance was a prognostic biomarker among people with pancreatic adenocarcinoma treated with surgical resection and adjuvant chemotherapy.</div></div>","PeriodicalId":100490,"journal":{"name":"ESMO Gastrointestinal Oncology","volume":"8 ","pages":"Article 100138"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"GATA6 immunohistochemistry and prognosis after surgical resection of pancreatic adenocarcinoma: results from the ESPAC-4 trial\",\"authors\":\"R.C. Grant , K. Duan , R. Jackson , W. Greenhalf , E. Costello-Goldring , P. Ghaneh , C. Halloran , D. Palmer , T. Hackert , M. Büchler , S. Hutchinson , S. Ramotar , A. Dodd , J. Wilson , F. Notta , G. O’Kane , J. Knox , J. Neoptolemos , S. Gallinger , S.E. Fischer\",\"doi\":\"10.1016/j.esmogo.2025.100138\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>No prognostic biomarker is currently used in clinical management of patients with surgically resected pancreatic cancer other than CA-19-9. In this study, we tested the prognostic value of GATA6 measured with immunohistochemistry and digital assistance.</div></div><div><h3>Patients and methods</h3><div>One hundred and ninety-three patients with resected pancreatic ductal adenocarcinoma from the ESPAC-4 trial of adjuvant gemcitabine and capecitabine were included. Two pathologists independently assessed GATA6 protein expression by immunohistochemistry in tissue microarray cores, manually and with digital assistance. Overall survival was compared across GATA6 levels using multivariate Cox proportional hazard regressions, with exploratory analyses evaluating recurrence-free survival and differential treatment effects.</div></div><div><h3>Results</h3><div>Interobserver concordance improved with digitally assisted scoring (kappa 0.72 versus 0.25, <em>P</em> < 0.001). Median overall survival was 24.3 months [95% confidence interval (CI) 19.2-32.1 months] with low GATA6 expression versus 35.2 months (95% CI 29.9-53.0 months) with high GATA6 expression (adjusted hazard ratio 1.60, 95% CI 1.08-2.38, <em>P =</em> 0.02). Similar results were observed for recurrence-free survival (adjusted hazard ratio 1.45, 95% CI 0.99-2.14, <em>P =</em> 0.06). GATA6 expression was not associated with differential treatment effects.</div></div><div><h3>Conclusions</h3><div>GATA6 expression measured by immunohistochemistry with digital assistance was a prognostic biomarker among people with pancreatic adenocarcinoma treated with surgical resection and adjuvant chemotherapy.</div></div>\",\"PeriodicalId\":100490,\"journal\":{\"name\":\"ESMO Gastrointestinal Oncology\",\"volume\":\"8 \",\"pages\":\"Article 100138\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-03-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ESMO Gastrointestinal Oncology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S294981982500007X\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ESMO Gastrointestinal Oncology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S294981982500007X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
背景:除CA-19-9外,目前没有预后生物标志物用于手术切除胰腺癌患者的临床管理。在这项研究中,我们测试了免疫组织化学和数字辅助检测的GATA6的预后价值。患者和方法:在辅助治疗吉西他滨和卡培他滨的ESPAC-4试验中,纳入了193例胰腺导管腺癌切除术患者。两名病理学家通过免疫组织化学方法在组织微阵列核心中独立评估GATA6蛋白表达,手工和数字辅助。采用多变量Cox比例风险回归比较不同GATA6水平患者的总生存率,并通过探索性分析评估无复发生存率和差异治疗效果。结果数字辅助评分改善了观察者间的一致性(kappa 0.72 vs 0.25, P <;0.001)。GATA6低表达组的中位总生存期为24.3个月[95%可信区间(CI) 19.2-32.1个月],而GATA6高表达组的中位总生存期为35.2个月(95% CI 29.9-53.0个月)(校正风险比1.60,95% CI 1.08-2.38, P = 0.02)。无复发生存率观察到类似的结果(校正风险比1.45,95% CI 0.99-2.14, P = 0.06)。GATA6的表达与差异处理效果无关。结论数字辅助下免疫组化检测的gata6表达是胰腺腺癌手术切除和辅助化疗患者预后的生物标志物。
GATA6 immunohistochemistry and prognosis after surgical resection of pancreatic adenocarcinoma: results from the ESPAC-4 trial
Background
No prognostic biomarker is currently used in clinical management of patients with surgically resected pancreatic cancer other than CA-19-9. In this study, we tested the prognostic value of GATA6 measured with immunohistochemistry and digital assistance.
Patients and methods
One hundred and ninety-three patients with resected pancreatic ductal adenocarcinoma from the ESPAC-4 trial of adjuvant gemcitabine and capecitabine were included. Two pathologists independently assessed GATA6 protein expression by immunohistochemistry in tissue microarray cores, manually and with digital assistance. Overall survival was compared across GATA6 levels using multivariate Cox proportional hazard regressions, with exploratory analyses evaluating recurrence-free survival and differential treatment effects.
Results
Interobserver concordance improved with digitally assisted scoring (kappa 0.72 versus 0.25, P < 0.001). Median overall survival was 24.3 months [95% confidence interval (CI) 19.2-32.1 months] with low GATA6 expression versus 35.2 months (95% CI 29.9-53.0 months) with high GATA6 expression (adjusted hazard ratio 1.60, 95% CI 1.08-2.38, P = 0.02). Similar results were observed for recurrence-free survival (adjusted hazard ratio 1.45, 95% CI 0.99-2.14, P = 0.06). GATA6 expression was not associated with differential treatment effects.
Conclusions
GATA6 expression measured by immunohistochemistry with digital assistance was a prognostic biomarker among people with pancreatic adenocarcinoma treated with surgical resection and adjuvant chemotherapy.