Value of α‐methylacyl‐CoA racemase immunochemistry for predicting neoplastic progression in Barrett's oesophagus. Issue 5 (5th September 2013)
- Record Type:
- Journal Article
- Title:
- Value of α‐methylacyl‐CoA racemase immunochemistry for predicting neoplastic progression in Barrett's oesophagus. Issue 5 (5th September 2013)
- Main Title:
- Value of α‐methylacyl‐CoA racemase immunochemistry for predicting neoplastic progression in Barrett's oesophagus
- Authors:
- Kastelein, Florine
Biermann, Katharina
Steyerberg, Ewout W
Verheij, Joanne
Kalisvaart, Marit
Looijenga, Leendert H J
Stoop, Hans A
Walter, Laurens
Kuipers, Ernst J
Spaander, Manon C W
Bruno, Marco J - Abstract:
- <abstract abstract-type="main" id="his12216-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="his12216-sec-0001" sec-type="section"> <title>Aim</title> <p>To investigate the value of α‐methylacyl‐CoA racemase (AMACR) immunohistochemistry for predicting neoplastic progression in Barrett's oesophagus (BO).</p> </sec> <sec id="his12216-sec-0002" sec-type="section"> <title>Methods and results</title> <p>We conducted a case–control study within a prospective cohort of 720 BO patients. Patients who developed high‐grade dysplasia or oesophageal adenocarcinoma were classified as cases, and patients without neoplastic progression as controls. AMACR expression was determined by immunohistochemistry in 12 127 biopsies from 635 patients, and was scored independently by two expert pathologists. Relative risks adjusted for age, gender, BO length and oesophagitis (RR<sup>a</sup>) were calculated in log‐linear models. During a median follow‐up of 6.6 years, 49 patients (8%) developed high‐grade dysplasia or oesophageal adenocarcinoma. Although mild AMACR expression was associated with a trend towards an increased risk of neoplastic progression (RR<sup>a</sup> 1.6, 95% CI 0.9–3.1), the risk was especially elevated with strong AMACR expression (RR<sup>a</sup> 4.8, 95% CI 1.9–12.6). The positive predictive value of strong AMACR expression was slightly higher than that of low‐grade dysplasia (22% versus 15%); the negative predictive value was slightly lower (91% versus<abstract abstract-type="main" id="his12216-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="his12216-sec-0001" sec-type="section"> <title>Aim</title> <p>To investigate the value of α‐methylacyl‐CoA racemase (AMACR) immunohistochemistry for predicting neoplastic progression in Barrett's oesophagus (BO).</p> </sec> <sec id="his12216-sec-0002" sec-type="section"> <title>Methods and results</title> <p>We conducted a case–control study within a prospective cohort of 720 BO patients. Patients who developed high‐grade dysplasia or oesophageal adenocarcinoma were classified as cases, and patients without neoplastic progression as controls. AMACR expression was determined by immunohistochemistry in 12 127 biopsies from 635 patients, and was scored independently by two expert pathologists. Relative risks adjusted for age, gender, BO length and oesophagitis (RR<sup>a</sup>) were calculated in log‐linear models. During a median follow‐up of 6.6 years, 49 patients (8%) developed high‐grade dysplasia or oesophageal adenocarcinoma. Although mild AMACR expression was associated with a trend towards an increased risk of neoplastic progression (RR<sup>a</sup> 1.6, 95% CI 0.9–3.1), the risk was especially elevated with strong AMACR expression (RR<sup>a</sup> 4.8, 95% CI 1.9–12.6). The positive predictive value of strong AMACR expression was slightly higher than that of low‐grade dysplasia (22% versus 15%); the negative predictive value was slightly lower (91% versus 93%).</p> </sec> <sec id="his12216-sec-0003" sec-type="section"> <title>Conclusions</title> <p>Strong AMACR expression is associated with an increased risk of neoplastic progression in BO. However, AMACR expression appears to be a less powerful predictor for neoplastic progression than low‐grade dysplasia.</p> </sec> </abstract> … (more)
- Is Part Of:
- Histopathology. Volume 63:Issue 5(2014)
- Journal:
- Histopathology
- Issue:
- Volume 63:Issue 5(2014)
- Issue Display:
- Volume 63, Issue 5 (2014)
- Year:
- 2014
- Volume:
- 63
- Issue:
- 5
- Issue Sort Value:
- 2014-0063-0005-0000
- Page Start:
- 630
- Page End:
- 639
- Publication Date:
- 2013-09-05
- Subjects:
- Histology, Pathological -- Periodicals
611.018 - Journal URLs:
- http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=his ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2559 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/his.12216 ↗
- Languages:
- English
- ISSNs:
- 0309-0167
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4316.027000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4237.xml