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Extended endoscopic mucosal resection does not reduce recurrence compared with standard endoscopic mucosal resection of large laterally spreading colorectal lesions - 20/04/17

Doi : 10.1016/j.gie.2016.05.015 
Farzan F. Bahin, MBBS (Hons), MPhil, FRACP 1, 2, ∗, Maria Pellise, MD, PhD 1, ∗, Stephen J. Williams, MBBS, FRACP, MD 1, Michael J. Bourke, MBBS, FRACP 1, 2, ⁎
1 Department of Gastroenterology and Hepatology, Westmead Hospital, Westmead, NSW, Australia 
2 Faculty of Medicine, University of Sydney, Sydney, NSW, Australia 

∗Reprint requests: Professor Michael J. Bourke, Director of Endoscopy, Westmead Hospital Department of Gastroenterology and Hepatology, c/o Suite 106a, 151-155 Hawkesbury Road, Westmead, Sydney, NSW 2145, Australia.Director of EndoscopyWestmead Hospital Department of Gastroenterology and Hepatologyc/o Suite 106a, 151-155 Hawkesbury Road, WestmeadSydneyNSW 2145Australia

Abstract

Background and Aims

Effective interventions to prevent residual and/or recurrent adenoma (RRA) after EMR of large sessile and laterally spreading colorectal lesions (LSL) are yet to be determined. RRA may occur due to inconspicuous adenoma at the EMR margin. We aimed to determine the efficacy and safety of extended EMR (X-EMR) compared with standard EMR (S-EMR).

Methods

A single-center post hoc analysis of LSL ≥20 mm referred for treatment was performed. S-EMR was the standard sequential inject and resect method including a 1-mm to 2-mm margin of normal mucosa around the lesion. With X-EMR, at least a 5-mm margin of normal mucosa was excised. Patient and lesion characteristics and procedural outcomes were recorded. The primary endpoint was RRA at first surveillance colonoscopy at 4 months.

Results

Between January 2009 and May 2011, 471 lesions (mean size, 37.9 mm) in 424 patients were resected by S-EMR, and between January 2012 and December 2013, 448 lesions (mean size, 39.1 mm) in 396 patients were resected by X-EMR. Resection was successful in 92.3% and 92.6% of referred lesions in the S-EMR and X-EMR groups, respectively (P = .978). X-EMR was independently associated with a higher risk of intraprocedural bleeding (IPB) (odds ratio, 3.1; 95% confidence interval [CI], 2.0-5.0; P < .001) but not other adverse events. RRA was present in 39 of 333 patients (11.7%) and 30 of 296 patients (10.1%) in the S-EMR and X-EMR groups, respectively (P = .15). X-EMR was not related to recurrence (hazard ratio, 0.8; 95% CI, 0.5-1.3; P = .399).

Conclusions

X-EMR does not reduce RRA and increases the risk of IPB compared with S-EMR. Alternative methods for the prevention of RRA are required.

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Abbreviations : CI, ESD, HGD, IPB, LGD, LSL, RRA, SC1, SD, S-EMR, SMIC, SSA/P, X-EMR


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 DISCLOSURE: All authors disclosed no financial relationships relevant to this publication.
 Dr Farzan Bahin was supported by a grant from the National Health and Medical Research Council of Australia (NHMRC). There was no influence from the NHMRC on study design or conduct, data collection and management, analysis, interpretation, preparation, and review or approval of the manuscript.
 If you would like to chat with an author of this article, you may contact Dr Bourke at [email protected].


© 2016  American Society for Gastrointestinal Endoscopy. Pubblicato da Elsevier Masson SAS. Tutti i diritti riservati.
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