Progression to cancer in patients with confirmed dysplasia compared to dysplasia downgraded to non-dysplastic metaplasia in Barrett's esophagus: a retrospective cohort study in Sweden

被引:2
作者
Elbe, Peter [1 ,2 ]
Ost, Ake [3 ]
Mellbom, Lennart [4 ]
Thorell, Anders [5 ,6 ]
Hakanson, Bengt [5 ,6 ]
Klevebro, Fredrik [1 ,2 ]
Lindblad, Mats [1 ,2 ]
机构
[1] Karolinska Univ Hosp, Dept Upper Digest Dis, Halsovagen 11, S-14186 Stockholm, Sweden
[2] Karolinska Inst, Dept Clin Sci Intervent & Technol, Div Surg, Stockholm, Sweden
[3] Synlab AB Taby, Stockholm, Sweden
[4] Karlskrona Hosp, Dept Pathol, KARLSKRONA, Sweden
[5] Karolinska Inst, Danderyds Hosp, Dept Clin Sci, Stockholm, Sweden
[6] Ersta Hosp, Dept Surg, Stockholm, Sweden
关键词
Adenocarcinoma; Barrett esophagus; Surveillance; LOW-GRADE DYSPLASIA; MANAGEMENT; SURVEILLANCE; DIAGNOSIS; GUIDELINE; SOCIETY;
D O I
10.5946/ce.2023.313
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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. Methods: 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. Results: 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). Conclusions: 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.
引用
收藏
页码:768 / 774
页数:7
相关论文
共 21 条
[1]  
Aaboud M, 2020, J HIGH ENERGY PHYS, DOI 10.1007/JHEP10(2020)048
[2]   Prevalence and risk factors for Barrett's esophagus in Taiwan [J].
Chen, Yan-Hua ;
Yu, Hsien-Chung ;
Lin, Kung-Hung ;
Lin, Huey-Shyan ;
Hsu, Ping-, I .
WORLD JOURNAL OF GASTROENTEROLOGY, 2019, 25 (25) :3231-3241
[3]   PROGRESS IN MEDICAL INFORMATION MANAGEMENT - SYSTEMATIZED NOMENCLATURE OF MEDICINE (SNOMED) [J].
COTE, RA ;
ROBBOY, S .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1980, 243 (08) :756-762
[4]   Systematic review of the published guidelines on Barrett's esophagus: should we stress the consensus or the differences? [J].
de Sa, Ines Marques ;
Pereira, Antonio Dias ;
Sharma, Prateek ;
Dinis-Ribeiro, Mario .
DISEASES OF THE ESOPHAGUS, 2021, 34 (05)
[5]   Barrett's oesophagus patients with low-grade dysplasia can be accurately risk-stratified after histological review by an expert pathology panel [J].
Duits, Lucas C. ;
Phoa, K. Nadine ;
Curvers, Wouter L. ;
ten Kate, Fiebo J. W. ;
Meijer, Gerrit A. ;
Seldenrijk, Cees A. ;
Offerhaus, G. Johan ;
Visser, Mike ;
Meijer, Sybren L. ;
Krishnadath, Kausilia K. ;
Tijssen, Jan G. P. ;
Mallant-Hent, Rosalie C. ;
Bergman, Jacques J. G. H. M. .
GUT, 2015, 64 (05) :700-706
[6]   Esophageal abnormalities and the risk for gastroesophageal cancers-a histopathology-register-based study in Sweden [J].
Ekheden, Isabella ;
Ludvigsson, Jonas F. ;
Yin, Li ;
Elbe, Peter ;
Ye, Weimin .
EUROPEAN JOURNAL OF EPIDEMIOLOGY, 2022, 37 (04) :401-411
[7]   British Society of Gastroenterology guidelines on the diagnosis and management of Barrett's oesophagus [J].
Fitzgerald, Rebecca C. ;
di Pietro, Massimiliano ;
Ragunath, Krish ;
Ang, Yeng ;
Kang, Jin-Yong ;
Watson, Peter ;
Trudgill, Nigel ;
Patel, Praful ;
Kaye, Philip V. ;
Sanders, Scott ;
O'Donovan, Maria ;
Bird-Lieberman, Elizabeth ;
Bhandari, Pradeep ;
Jankowski, Janusz A. ;
Attwood, Stephen ;
Parsons, Simon L. ;
Loft, Duncan ;
Lagergren, Jesper ;
Moayyedi, Paul ;
Lyratzopoulos, Georgios ;
de Caestecker, John .
GUT, 2014, 63 (01) :7-42
[8]   Risk stratification in Barrett's esophagus patients with diagnoses of indefinite for dysplasia: the definite silver bullet has not (yet) been found [J].
Frei, Nicola F. ;
Stachler, Matthew D. ;
Bergman, Jacques J. G. H. M. .
GASTROINTESTINAL ENDOSCOPY, 2020, 91 (01) :11-13
[9]   The utility of P53 immunohistochemistry in the diagnosis of Barrett's oesophagus with indefinite for dysplasia [J].
Januszewicz, Wladyslaw ;
Pilonis, Nastazja D. ;
Sawas, Tarek ;
Phillips, Richard ;
O'Donovan, Maria ;
Miremadi, Ahmad ;
Malhotra, Shalini ;
Tripathi, Monika ;
Blasko, Adrienn ;
Katzka, David A. ;
Fitzgerald, Rebecca C. ;
di Pietro, Massimiliano .
HISTOPATHOLOGY, 2022, 80 (07) :1081-1090
[10]   Impact of surveillance for Barrett's oesophagus on tumour stage and survival of patients with neoplastic progression [J].
Kastelein, F. ;
van Olphen, S. H. ;
Steyerberg, E. W. ;
Spaander, M. C. W. ;
Bruno, M. J. .
GUT, 2016, 65 (04) :548-554