The CREST Trial. Funded by Cancer Research UK and developed by the National Cancer Research Institute

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The CREST Trial A randomised phase III study of stenting as a bridge to surgery in obstructing colorectal cancer. Results of the UK ColoRectal Endoscopic Stenting Trial (CREST). Funded by Cancer Research UK and developed by the National Cancer Research Institute

Current acute oncological problem NBOCA audit report 2015 Emergency admission with colorectal cancer remains at a stubborn 21 % of all cases. Over 5,000 cases per year 16 per cent of patients having major surgery had an urgent or emergency procedure 90 day mortality 13.3% for patients having emergency surgery 2% for elective surgery

Rationale of CREST Converting emergency into elective surgery Pre-operative correction of fluid and electrolyte balance Reduction of diaphragmatic splinting and pain with improvement in respiratory function Treatment of medical co-morbid disease Accurate pre-operative staging Referral to a specialist colorectal surgeon Major surgery may be avoided for patients with: Rapidly progressive cancer Unstable comorbid disease

Stenting needs to be properly evaluated in a randomised controlled trial addressing two key questions: * Is there a worthwhile net benefit (in reduced operative mortality and morbidity, reduced stoma formation and better quality of life adjusted survival) from endoluminal stenting for patients presenting with an obstructing colonic cancer? * If a benefit exists, is this identifiable in patients undergoing attempted curative treatment, palliative treatment, or both?

Self-expandable metal stents for obstructing colonic and extracolonic cancer: European Society of Gastrointestinal Endoscopy (ESGE) Clinical Guideline - Endoscopy 2014; 46: 990 1002 SEMS placement is recommended as the preferred treatment for palliation of malignant colonic obstruction (strong recommendation, high quality evidence). SEMS placement as a bridge to elective surgery is not recommended as a standard treatment of symptomatic left-sided malignant colonic obstruction (strong recommendation, high quality evidence). For patients with potentially curable disease, stent placement may be considered in those who have an increased risk of postoperative mortality (weak recommendation, low quality evidence).

CREST Primary Objectives A phase III, multi-center randomised controlled trial to determine if endoluminal stenting for obstructing colonic cancers can result in: Reduced perioperative morbidity as assessed by length of hospital stay Reduced 30-day mortality

CREST Secondary outcome measures Stenting completion and complication rate Presence and duration of a stoma/anastomosis rate 6-month survival Proportion disease-free at 3 years Quality of life Perioperative morbidity

The CREST Trial Design Emergency Surgery Obstructing colorectal cancer R Target recruitment : 400 Insertion of endoluminal stent Trial recruitment ended: 31 st December 2014 Failed stenting Successful decompression Palliative care Elective surgery

CREST Eligibility Criteria Left-sided colorectal cancer Radiological evidence of obstruction Patient fit for surgery No evidence of peritonitis and/or perforation Patient able and willing to give written informed consent Patients stratified by palliative or potentially curative

CReST Recruitment 70% acceptance Recruitment ended: 31 st December 2014 Revised Target recruitment: 400 Actual recruitment: 245

Compliance with Randomised Treatment Allocation Randomised N=245 Allocated stent N=123 Allocated emergency surgery N=122 Palliative N=10 Potentially curative N=113 Palliative N=9 Potentially curative N=113 Stent Attempted N=10 (3 of which were non-cancer patients) Stent not Attempted N=0 Stent Attempted N=113 Stent not Attempted N=1 Resectional surgery N=4 Stoma formation only N=3 Crossover to palliative stent N=1 Patient withdrawal N=1 Resectional surgery N=75 Stoma formation only N=24 NON-CANCER PATIENTS Resectional surgery N=9 Stoma formation only N=2 No surgery N=3

CREST Patient Demographics Gender: Male Mean Age: (sd) Stenting (N=123) Surgery (N=122) 72 (59%) 77 (63%) 69.9 (12.2) 34-94 69.1 (11.2) 36-89 range Age group: <50 50-59 60-69 70+ 7 (6%) 17 (14%) 30 (24%) 69 (56%) 7 (6%) 15 (12%) 38 (31%) 62 (51%)

CREST Patient Baseline Data Transverse Colon Splenic Flexure Descending Colon Sigmoid Rectosigmoid Rectum ASA Grade P1 P2 Stenting (N=123) 4 (3%) 7 (6%) 28 (23%) 68 (55%) 15 (12%) 1 (1%) 24 (20%) 78 (63%) 21 (17%) Surgery (N=122) 3 (2%) 7 (6%) 30 (25%) 67 (55%) 14 (11%) 1 (1%) 27 (22%) 75 (62%) 20 (16%) P3

CREST Patient Baseline Data - Stratification Stenting (N=123) Surgery (N=122) Palliative 10 (8%) 9 (7%) Potentially curative 113 (92%) 113 (93%) Likelihood of cure: Probably not Probably yes Uncertain (possibly yes) 3 (3%) 78 (69%) 32 (28%) 6 (5%) 72 (64%) 35 (31%)

Does stenting reduce length of stay and 30-day mortality? Days in hospital (curative patients with complete 1 year data) N Median (IQR) Deaths within 30 days of randomisation Time to death for these patients (days from randomisation to death) Median (IQR) Stenting Surgery 86 14.5 (9, 24) 92 13.5 (9.5, 22.5) 5 6 7 (6, 15) 5 (3, 9)

Stenting Completion and Immediate Complication Rate N = 123 Stent relieved the obstruction 98 (82%) Endoscopic + fluoroscopic Fluoroscopic only Endoscopic only Immediate complications None Haemorrhage Respiratory depression Migration Perforation Hypotension Other 91 3 4 92 - - 4 1-2 Immediate complications defined as those within 24 hours from stent insertion. Stent technique only shown for those patients who stent was said to relieve the obstruction

Stenting Intermediate and Late Complication Rates Stent relieved the obstruction Yes No Ineligible for stenting Stent not deployed Missing CRF Intermediate (24 hours 7 days after stenting) None Migration Haemorrhage Perforation Recurrent obstruction Other Late (7 28 days after stenting) None Haemorrhage Perforation Ongoing obstruction Any degree of sensation Other N = 123 98 16 4 4 1 85 2 0 2 4 7 78 0 3 3 10 3 Intermediate other complications: Small bowel ileus retention - suprapubic catheter. pneumonia (n=1) Pt suffered cardiac arrest (n=1) Infection (n=2) Febrile illness (n=1) Pyrexia (n=1) Respiratory depression (n=1) Late Other complications: Eating difficulties (n=1) Infection / fluid collection (n=1) Abdominal pain (n=1)

Stent related perforations N=6 5 resulted in an urgent surgery 1 stenting only 1 mechanical ventilation No post-operative deaths

Does stenting reduce stoma rates? Stenting (N = 123) Emergency surgery (N = 122) No surgery 24 3 P-value Patients who have had surgery Has the procedure resulted in a stoma? End Loop Unknown 99 119 46 / 99 (46%) 28 18-82 / 119 (69%) 48 33 1 0.001

CReST Reasons patients did not have surgery Stent (N=24) Indication changed from potentially curative to palliative post stenting 12 Palliative at randomisation 8 Died post stenting prior to elective surgery (D=3, D=7) 2 Patient declined surgery 2 Surgery (N=3) Non-cancer patient 1 Crossover to stent + palliative chemo post stent (PI believed pt ineligible post rand.) 1 Patient withdrawal from trial prior to randomised intervention 1

6-Month Survival Rates Stenting All deaths <1 month 1-6 months 6months 1 yr 1-2 yrs 2-3 yrs 3-4 yrs 4-5 yrs All deaths (cancer patients only) Deaths within 6 months Deaths within 6 months (cancer patients, bridge to surgery) (N = 123) Emergency Surgery (N = 122) 59 / 123 5 11 16 15 7 2 3 58 / 120 47 / 122 6 11 7 11 10 1 1 47 / 109 16 17 15/110 12/100

Severity of Surgical Complications (Clavien-Dindo Classification) Patients with Clavien Dindo classificatio n CD 3+ 22 (46%) Stenting Surgery P-value 48 45 27 (60%) 0.20

Summary Recruitment feasible in the emergency setting 5% will not have CRC Combined endoscopic fluoroscopic technique had good success rates & low complication rates across multiple hospital sites

Conclusions SEMS as a bridge to surgery Clinical success rate 80% Mortality and LoS unaffected Stoma rates significantly reduced Cancer specific survival not worse Reasonable alternative to emergency surgery

With special thanks to Bradford Royal Infirmary Leeds QE, Bham MRI Mid Yorks Addenbrookes Nevill Hall Royal Cornwall Frenchay & Southmead Durham Russell's Hall Queen's, Romford Royal Berkshire Hospital Derriford Raigmore North Tees Derby Royal John Radcliffe Queens Medical Centre James Paget Western General St Mark's Scarborough QE, Gateshead (closed) Princess of Wales Leighton (closed) Leicester Gartnavel Yeovil Salford Darent Valley North Devon Ulster Hospital Royal Sussex County Hospital Royal Bolton Northern General Musgrove Park Hospital Ipswich Imperial College Healthcare NHS Warwick Hospital Scunthorpe Royal Devon & Exeter Royal Albert Edward (closed) Queen Alexandra Hospital (closed) King's College Hospital Glasgow Royal Infirmary 2 2 2 2 2 1 22 1 1 0 11 0 0 0 5 3 44 2 33 6 77 7 10 1112 14 23 21 19 20 0 2 4 6 8 10 12 14 16 18 20 22 24 26 28 30 32 34 33

Learning Objectives for obstructing colorectal cancer Rates of urgent presentation of CRC Morbidity and mortality Current guidance on stenting in emergency setting Clinical success rate and complications of stenting Effect on stoma rates Effect on cancer survival

With thanks to Bradford Royal Infirmary, Leeds, QE, Bham MRI, Frenchay & Southmead, Addenbrookes, Nevill Hall Durham, Cornwall, Mid Yorks, Scarborough, Western General, St Mark's Raigmore, Leicester, Princess of Wales, Russell's Hall, Royal Bolton, Imperial College Queen's, Romford, Ipswich, Royal Sussex, Musgrove Park Gartnavel, Derriford, Leighton, QE, Gateshead, Frimley Park, Salford, Darent valley, Yeovil John Radcliffe, North Devon, Northern General North Tees, Derby Royal, James Pagett Royal Albert Edward, Royal Devon & Exeter, Salisbury District Hospital Glasgow Royal Infirmary, Warwick Hospital, Ulster Hospital Queens Medical Centre, Queen Alexandra Hospital North Manchester, Harrogate, King's College Hospital