- Colorectal cancer is second commonest cancer causing death in the UK
- 20,000 new cases per year in UK - 40% rectal and 60% colonic
- 3% patients present with more than one tumour (=synchronous tumours)
- A previous colonic neoplasm increases the risk of a second tumour (=metachronous tumour)
- Some cases are hereditary
- Most related to environmental factors - dietary red fat and animal fat
Adenoma - carcinoma sequence
- Of all adenomas - 70% tubular, 10% villous and 20% tubulovillous
- Most cancers believed to arise within pre-existing adenomas
- Risk of cancer greatest in villous adenoma
- Series of mutations results in epithelial changes from normality, through dysplasia to invasion
- Important genes - APC, DCC, k-ras, p53.
Clinical presentation
- Right-sided lesions present with
- Iron deficiency anaemia due occult GI Blood loss
- Weight loss
- Right iliac fossa mass
- Left-sided lesions present with
- Abdominal pain
- Alteration in bowel habit
- Rectal bleeding
- 40% of cancers present as a surgical emergency with either obstruction or perforation
- Emergency presentation is associated with a poorer outcome

Picture supplied by Mr N P J Cripps, Consultant Colorectal Surgeon, Chichester, United Kingdom

Picture provided by Mr David Anderson, St John's Hospital, Livingston, Scotland
Investigation
- In elective cases diagnosis can be confirmed by a combination of:
- Rigid sigmoidoscopy
- Flexible sigmoidoscopy
- Colonoscopy
- Double contrast barium enema
- In patients presenting with large bowel obstruction single contrast enema (after rigid sigmoidoscopy) is the
investigation of choice


Surgical options
- Any surgical resection requires 5 cm proximal and 2 cm distal clearance for colonic lesions
- 1 cm distal clearance of rectal lesions adequate if mesorectum resected
- Radial margin should be histopathologically free of tumour if possible
- Lymph node resection should be performed to the origin of the feeding vessel
- En Bloc resection of adherent tumours should be performed
- The value of a 'no-touch' techniques remains unproven
- Depending on site of lesion surgical options are:
- Caecum, ascending colon, hepatic flexure – Right hemicolectomy
- Transverse colon – Extended right hemicolectomy
- Splenic flexure, descending colon – Left hemicolectomy
- Sigmoid colon – High anterior resection
- Upper rectum – Anterior resection
- Consider defunctioning loop ileostomy is anastomosis <12 cm from anal margin
- Lower rectum – Abdomino-perineal resection
- Small lower rectal cancers may be resectable by transanal microsurgery
- Laparoscopic surgery is unproven
- Early studies raised concerns about port site recurrence
- Recent studies suggest equivalent overall and disease-free survival
Surgery for upper rectal cancers
- Risk of local recurrence reduced by performing total mesorectal excision (TME)
- Pelvic peritoneum and lateral ligaments divides
- Plane between visceral (rectum, mesorectum) and somatic structures dissected

- Middle rectal vessels divided laterally
- Rectal stump washed out with cytocidal fluid (water, Betadine) from below.

Picture provided by Prof Ian Bradford, Prince of Wales Hospital, Shatin, Hong Kong
Dukes Classification
- Developed by Cuthbert Duke in 1932 for rectal cancers
- Dukes staging of colorectal cancer

- Stage A - Tumour confined to the mucosa
- Stage B - Tumour infiltrating through muscle
- Stage C - Lymph node metastases present
- Five year survival - 90%, 70% and 30% for Stages A, B and C respectively
Adjuvant radiotherapy
- In patients with rectal cancer 50% undergoing curative resection develop local recurrence
- Median survival with local recurrence is less than one year
- Risk factors for local recurrence include:
- Local extent of tumour
- Nodal involvement
- Circumferential margin status
- Risk of local recurrence can be reduced by radiotherapy
- Can be given either preoperatively or postoperatively
- Preoperative radiotherapy given as short course immediately prior to surgery
- Reduces local recurrence
- Increases time to recurrence
- Improves 5-year survival
- Combination chemotherapy and radiotherapy may produce better outcome
Adjuvant chemotherapy
- Improves survival in Duke's C tumours
- Not required in Duke's A tumours which already have a good prognosis
- Role in Duke's B tumours remains to be defined
- Currently being investigated in the QUASAR (Quick and Simple and Reliable) trial
- Results of QUASAR study to date have shown
- 5FU and folinic acid is effective as adjuvant therapy
- High dose folinic acid rescue confers no additional benefit
- The use of levimasole confers no additional benefit
Colorectal cancer screening
- Screening for colorectal cancer can be divided into two categories
- Screening of high risk groups
- Population screening
Screening of high risk groups
- This includes
- Patients with family history
- Sporadic adenomatous polyps
- Inflammatory bowel disease
- Definition of the high risk group is difficult
- High risk patients should undergo colonoscopy at approximately 50 years
- Patients with family history of FAP or HNPCC should undergo genetic testing
- If mutation present should undergo intensive colonoscopic screening from adolescence
Population screening
- The role of screening is currently being investigated by either
- Faecal occult blood testing
- Colonoscopy
- Nottingham study has recruited over 150,000 patients
- 75,250 underwent biennial FOB testing
- Resulted in 1774 colonoscopies
- Seven complications occurred requiring operations in 6 patients
- No difference identified in stage of presentation in screened group
- Survival in screened group was significantly improved
Bibliography
Baigre R J, Berry A R. Management of advanced rectal cancer.
Br J Surg 1994; 81: 343-352.
Banerjee A K. Local excision of rectal cancers. Br
J Surg 1995; 82: 1165-1173.
Camma C, Giunta M, Fiorica
F, Pagliaro L, Craxi A,
Cottone M. Preoperative radiotherapy for resectable rectal
cancer. JAMA 2000; 284: 1008-1015.
Colorectal Cancer Collaborative Group. Adjuvant radiotherapy for rectal cancer: a systematic
overview of 8507 patients from 22 randomised trials. Lancet 2001; 358: 1291-1304.
Heald R J, Karanja N D. The
management of colorectal cancer. Curr Surg Pract 1993; 5: 195-201.
Huang A, Hindle K S, Tsavellas G. Colorectal cancer surveillance post surgery. Hosp
Med 2001: 62: 490-491.
Leslie A, Steele R J C. Management of colorectal cancer. Postgrad Med J 2002;
78: 473-478.
Leung K L, Kwok S P Y, Lam S C W. Laparoscopic resection of rectosigmoid carcinoma:
prospective randomised trial. Lancet 2004; 363: 1187-1192.
MacFarlane J K, Ryall R D H,
Heald R J. Mesorectal excision for rectal cancer.
Lancet 1993; 341:
457-460.
McArdle C S, Hole D J. Emergency presentation of colorectal cancer is associated with poor 5-year
survival. Br J Surg 2004; 91: 605-609.
Myint A S, Carter P, Hershman
M J. Improving outcome in rectal cancer.
Hosp Med 2000; 61:
706-710.
Nicholls R J, Hall C. Treatment of non-disseminated cancer of the
lower rectum. Br J Surg
1996: 83: 15-8.
Nelson H, Petrelli N, Carlin A et al. Guidelines 200 for colon and rectal cancer
surgery. J Natl Cancer Inst 2001; 93: 583-596.
Quasar Collaborative Group. Comparison of flurouracil with additional levimasole, higher-dose folinic
acid or both as adjuvant therapy for colorectal cancer: a randomised trial. Lancet 2000;
355: 1588-1596.
Rayter Z et al. Adjuvant
chemotherapy for colorectal cancer. Ann R Coll Surg 1995; 77: 81-84.
Renehan A G, Egger M, Saunders M P, O'Dwyer S T. Impact on survival of intensive follow
up after curative resection for colorectal cancer: systematic review and meta-analysis of randomised trials.
Br J Med 2002; 324: 1-8.
Robinson M H, Hardcastle J D, Moss S M et al. The risks of screening: data from
the Nottingham randomised controlled trial of faecal occult blood screening for colorectal cancer. Gut 1999;
45: 588-592.
Sagar P M. Surgical management of locally recurrent rectal cancer.
Br J Surg 1996; 83:
293-304.
Steele R J C. Anterior resection with total mesorectal excision.
J R Coll Surg Ed 1999; 44:
40-45. |