Quality of and compliance with colonoscopy in Lynch Syndrome surveillance: are we getting it right?

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Quality of and compliance with colonoscopy in Lynch Syndrome surveillance: are we getting it right? Hartery K 1, Sukha A 1, Thomas-Gibson S 1, Thomas H 1,2, Latchford A 1,2. 1 Wolfson Endoscopy Unit, St. Mark s Hospital, London, UK. 2 St.Mark s Polyposis Registry, St. Mark s Hospital, London, UK.

INTRODUCTION Colorectal surveillance is only surveillance protocol in Lynch Syndrome (LS) proven to be effective. 1,2 Data on colonoscopic KPIs in LS is sparse. 3,4 What do we know? Accelerated adenoma-colorectal cancer pathway 5 Difficult to visualise non-polypoid, R sided lesions 6 Interval? 1-2 year recommended. 7-9 1 Jarvinen et al Gastroenterology 2000 2 de Jong Gastroenterology 2006 3 Newton et al Colorectal Disease 2014 4 Haanstra et al Gastroenterology 2000 5 Edelstein CGH 2011 6 Rondagh Endoscopy 2013 7 Mecklin Gastroenterology 2007 8 Vasen Gastroenterology 2010 9 Engel CGH 2010

St. Mark s Family Polyposis Registry 355 LS pts % Colonoscopies Performed Wolfson Endoscopy Unit 66.1 79 90.8 96.1 149 attended endoscopy unit 2007-2018 2 2.11 2.25 2.5 Surveillance Interval (Time in yrs) 594 colonoscopies

PATIENT DEMOGRAPHICS N=149 Male n, % 47 (31.5) Gene positive or obligate carriers n,% MLH1 63 MSH2 51 MSH6 28 PMS2 7 EPCAM 0 CRC, prior to surveillance n, % 36 (24.2) Age at index colonoscopy median, range(yrs) 44.2 (21.7-84.9) Mean number of colonoscopies per patient, n 3.94

COLONOSCOPY KPIs N=594 Caecal intubation rate (CIR), % 97.4 Optimal bowel prep, % 92.5 Adenoma detection rate, % 18.6 Mean number per colonoscopy 1.88 Sedation use, median Midazolam use (mg) 1.25 (0-5) Fentanyl use (mg) 0 (0-100)

CRC on SURVEILLANCE N=9 Location, % Distal 33.3 Proximal 66.6 Duke s stage, % A 77.8 B 0 C 22.2 Median age at CRC, yrs (range) 57.7 (32.7-72.6) Gene MLH1 6 MSH2 3 Median interval from prev colonoscopy, yrs (range) 1.44 (0.12-2.09) Adenoma resected in CRC segment, % 55.6 Previous CRC, % 50

FINDINGS AFTER A NEGATIVE COLONOSCOPY... N= Interval after negative colonoscopy (y) *Advanced adenoma n, (%) Cancer n, (%) 356 median 1.55 (range 0.05-5.1) 14 (3.9) 2 (0.6) 275 2 8 (2.9) 1 (0.4) 105 1 3 (2.8) 1 (0.9) Negative colonoscopy = colonoscopy without polyps (adenomatous or SSL) *Advanced adenoma = one adenomatous polyp 10mm in diameter, villous component or high grade dysplasia

MANAGEMENT OF ADVANCED ADENOMAS Colon location Size, mm Villous comp HGD present Follow-up, yrs *Recurrence Recurrence histology HF 2 X 2.23 No AC 6 X 4.4 No Rectum 6 X X 0.25 Yes TVA with HGD DC 10 2.12 No Rectum 10 1.99 Yes TA with HGD SC 10 X Awaiting AC 10 4.4 No HF 10 2 No SF 10 3.11 No HF 10 2.3 No DC 10 X 3.3 No HGD= high grade dysplasia *Recurrence = further adenoma/adenocarcinoma occurring in same colonic segment

MANAGEMENT OF ADVANCED ADENOMAS Colon location Size, mm Villous comp HGD present Follow-up time, yrs *Recurrence Recurrence histology Caecal 13 X X 0.25 Yes Adenocarcinoma DC 15 1.84 No SC 15 No SC 15 3.63 No SC 20 X >8.00 No SC 25 0.5 No TC 25 1.02 No AC 40 1.73 No TC 40 X Not endo resectable No

CHROMOENDOSCOPY IN LS Chromoendoscopy WLE N= 61 533 PDR, % 41.0 31.3 Mean no of polyps/patient, n 0.98 0.53 ADR, % 18 18.9 Mean no of adenomas/patient, n 0.39 0.31 R sided adenomas, n(%) 19 (79) 88 (53)

CONCLUSION Despite good quality parameters, interval cancers still occurred Approximate 10-year rate of incidence CRC 8% Fortunately surveillance CRC were predominantly early (78% Dukes A) 95% of advanced adenomas were endoscopically resectable 15% recurrence rate