Elbe Peter, Öst Åke, Mellbom Lennart, Thorell Anders, Håkanson Bengt, Klevebro Fredrik, Lindblad Mats
Department of Upper Digestive Diseases, Karolinska University Hospital, Stockholm, Sweden.
Division of Surgery, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.
Clin Endosc. 2024 Nov;57(6):768-774. doi: 10.5946/ce.2023.313. Epub 2024 Nov 25.
BACKGROUND/AIMS: This study aimed to clarify the risk of progression in patients with non-dysplastic Barrett's esophagus (NDBE) and patients with confirmed low-grade dysplasia (LGD) and indefinite for dysplasia (IND) after an expert pathologist review of patients with BE with suspected dysplasia in a prospective cohort.
Patients with Barrett's esophagus diagnosed with dysplasia at Ersta Hospital in Stockholm from 1998 to 2012 were included. The first dysplastic specimen in all patients was re-evaluated by two expert pathologists and classified as NDBE, LGD, IND, or cancer, including high-grade dysplasia. The incidence rates (IRs) and IR ratios were calculated with 95% confidence intervals.
Of 423 patients with Barrett's esophagus with dysplasia, 266 (62.9%) were re-classified as NDBE, 83 (19.6%) had LGD, 71 (16.8%) had IND, and 3 (0.7%) patients had cancer. During the follow-up, 34 (8%) patients developed cancer, most of them within five years, while others progressed after up to 25 years of surveillance. IRs for cancer among patients with NDBE was 0.41%/year compared to 1.84%/year for LGD (p<0.001) and 1.43%/year for IND (p=0.008).
Long-term risk of progression to cancer did not differ between patients with confirmed LGD and IND. These findings suggest that patients with IND should undergo similar management as patients with LGD.
背景/目的:本研究旨在通过对前瞻性队列中疑似发育异常的巴雷特食管(BE)患者进行专家病理学家复查,阐明非发育异常性巴雷特食管(NDBE)患者、确诊为低级别发育异常(LGD)和发育异常不明确(IND)的患者的病情进展风险。
纳入1998年至2012年在斯德哥尔摩厄斯塔医院被诊断为发育异常的巴雷特食管患者。所有患者的首个发育异常标本由两名专家病理学家重新评估,并分类为NDBE、LGD、IND或癌症,包括高级别发育异常。计算发病率(IRs)和IR比率,并给出95%置信区间。
在423例有发育异常的巴雷特食管患者中,266例(62.9%)被重新分类为NDBE,83例(19.6%)为LGD,71例(16.8%)为IND,3例(0.7%)为癌症。在随访期间,34例(8%)患者发生癌症,其中大多数在五年内,其他患者在长达25年的监测后病情进展。NDBE患者的癌症发病率为每年0.41%,而LGD患者为每年1.84%(p<0.001),IND患者为每年1.43%(p=0.008)。
确诊的LGD和IND患者进展为癌症的长期风险无差异。这些发现表明,IND患者应接受与LGD患者相似的管理。