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Colonoscopy; Surveillance Indications
SR Brown Colorectal Surgeon Sheffield Teaching Hospitals
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Colorectal cancer screening in high risk groups
Gut 2002;51(Suppl V)
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Screening vs Surveillance
Asymptomatic population Surveillance Previous symptoms/high risk
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High risk groups Previous colorectal cancer Acromegaly
Ureterosigmoidostomy Hereditary and Familial bowel cancer IBD Previous polyps
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Aims To discuss salient aspects of guidelines
To highlight recent developments in colonoscopic surveillance
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Colorectal cancer surveillance
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Colorectal cancer surveillance; aims
Detect recurrence Diagnose and treat metachronous neoplasia Evaluate anastomosis
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Colorectal cancer surveillance
‘Incidence metachronous tumours 5-10%’ Metachronous cancers approx. 2% Cochrane review 1.3% (18/1342) Metachronous adenomas 22% (425/1923)
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Colorectal cancer surveillance
Synchronous/‘early’ metachronous cancers 4% 0.6% ‘missed’ due to incomplete colon exam
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Familial cancer surveillance
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Familial Cancer Summary
Family group Screening procedure Age at initial screen Screening procedure and interval 2 FDR with CRC Colonoscopy At 1st consult or age years (whichever later) If initial clear repeat at age 55 1 FDR<45 yr with CRC
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Lifetime risk of colorectal cancer
Risk Group Risk (of dying) General population 1:50 Any family history 1:17 One affected relative <45 years 1:10 Two affected relatives 1:6 Houlston et al. 1970
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Familial Cancer Summary
Family group Screening procedure Age at initial screen Screening procedure and interval 2 FDR with CRC Colonoscopy At 1st consult or age years (whichever later) If initial clear repeat at age 55 1 FDR<45 yr with CRC
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Chances of preventing death with screening colonoscopy 35 year old with FDR<45 years
1 in 25,000 people aged develop colorectal cancer per year Relative risk = 5 Risk of cancer = 1 in 5000 in per year Assume asymptomatic cancer dwell time of 3 years Chance of detecting cancer 1 in 1660
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Familial Cancer Summary
Family group Screening procedure Age at initial screen Screening procedure and interval 2 FDR with CRC Colonoscopy At 1st consult or age years (whichever later) If initial clear repeat at age 55 1 FDR<45 yr with CRC
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Chances of preventing death with screening colonoscopy 55 year old with FDR<45 years
1 in 1,630 people aged develop colorectal cancer per year Relative risk = 3 Risk of cancer = 1 in 543 per year Assume asymptomatic cancer dwell time of 3 years Chance of detecting cancer 1 in 181
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Hereditary cancer surveillance
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Hereditary Cancer Summary
Family group Screening procedure Age at initial screen Screening procedure and interval FAP Genetic testing Flexi sig+OGD Puberty Flexi sig yearly Colectomy if +ve HNPCC Colonoscopy +/- OGD 25 yrs or 5 yrs before earliest CRC in family 2 yearly colonoscopy and OGD Juvenile polyposis Peutz-Jegher Genetic testing Colonoscopy + OGD
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IBD surveillance
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IBD Summary Disease group Screening procedure Age at initial screen
Screening procedure and interval UC or Crohn’s coloitis Colonoscopy+ biopsies every 10cm After 8 years for pan colitis, 15 years for left sided colitis 3 yrly 2nd decade, 2yrly 3rd decade, yrly thereafter UC + PSC Colonoscopy At diagnosis PSC Annually
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Controversies ? Survival advantage (Cochrane review 2004)
No clear evidence May allow earlier detection of cancer ?lead-time bias
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Controversies Ongoing inflammation increases risk
Dysplasia as a marker for cancer Reliability Detection Histological interpretation
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Controversies;detection
Pan-chromoscopy and targeted biopsy (Rutter 2004) Back-to-back colonoscopy Conventional then dye-spray Conventional no dysplasia in 2904 random biopsies Targeted 157 biopsies 7 patients with dysplasia
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Ileo-anal pouch surveillance
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Pouch cancer 15 case reports 10 residual rectal mucosa
5 ??pouch mucosa All pre-existing dysplasia 8 had cancer in original resection 9 had mucosectomy
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Surveillance recommendations
Pouchoscopy 1st year then 2-3 yearly Increased surveillance (yearly) if Pre-existing dysplasia/cancer PSC Mucosectomy if high risk
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Polyp surveillance
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Summary Read guidelines!!
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