Bowel Cancer Screening
NHS programme offering faecal immunochemical testing (FIT) every 2 years to adults aged 56-74. Screening reduces CRC mortality by ~25%. Positive FIT (≥120 μg Hb/g) triggers diagnostic colonoscopy.
Key Facts
NHS Bowel Cancer Screening Programme (BCSP): FIT every 2 years for ages 56-74 (being extended to 50-74); self-completion home test kit FIT (faecal immunochemical test): quantitative test for human haemoglobin in stool; replaced guaiac FOBt in 2019; more sensitive and specific; single sample Screening threshold: ≥120 μg Hb/g faeces (positive rate ~2-3%); diagnostic threshold in symptomatic patients: ≥10 μg Hb/g (NICE NG12/DG30) Screening colonoscopy findings: ~40% have adenomas; ~10% have cancer; screen-detected cancers are earlier stage (>70% Dukes A/B vs ~50% in symptomatic) CRC mortality reduction: ~25% in those who participate in screening (UK Flexible Sigmoidoscopy trial, FIT-based screening RCTs) Bowel scope screening (one-off flexible sigmoidoscopy at age 55): being phased out in favour of FIT-only programme
Overview
Key Facts
Bowel cancer screening aims to detect colorectal cancer at an earlier, more treatable stage and to prevent CRC by detecting and removing premalignant adenomatous polyps. The NHS BCSP is one of the most established cancer screening programmes in the UK.
Epidemiology
CRC screening is offered because: CRC is common (~42,900 cases/year), has a long premalignant phase (adenoma-carcinoma sequence ~10 years), effective screening tests exist, and early detection dramatically improves survival (stage I 5-year survival >90% vs stage IV ~10%). Uptake of bowel cancer screening in England is approximately 65-70% — lower in men, younger age groups, and deprived populations.
Aetiology
Screening is offered to the average-risk population. Higher-risk groups have separate surveillance pathways:
- Family history: first-degree relative with CRC <50 or 2+ first-degree relatives → earlier/more frequent colonoscopy
- Lynch syndrome: colonoscopy every 2 years from age 25
- FAP: annual sigmoidoscopy/colonoscopy from age 12-14
- IBD: surveillance colonoscopy from 8 years after onset of extensive colitis
Pathophysiology
Screening exploits the biology of the adenoma-carcinoma sequence:
- Adenomas take ~10 years to progress to cancer — screening interval of 2 years provides multiple opportunities for detection
- Adenomas and cancers bleed intermittently — FIT detects haemoglobin in stool
- Polypectomy at screening colonoscopy interrupts the adenoma-carcinoma sequence, preventing cancer development
- Earlier stage detection at screening → better prognosis and less intensive treatment needed
Clinical Presentation
Screening Pathway
- Invitation: automatic letter with FIT kit sent to home address; ages 56-74 every 2 years
- FIT completion: collect small stool sample at home; return by post
- Results: within 2 weeks; normal (<120 μg Hb/g) — routine recall in 2 years; abnormal (≥120 μg Hb/g) — invitation for screening colonoscopy
- Specialist screening practitioner (SSP) consultation: pre-colonoscopy assessment
Screening Colonoscopy Outcomes
- No abnormality: return to routine screening
- Adenomatous polyps: polypectomy + enter surveillance programme
- Cancer detected: staging and MDT referral
- Incomplete colonoscopy: CT colonography offered
Red Flags (Outside Screening)
- Symptomatic patients should NOT wait for screening — investigate per NICE NG12
- FIT can be used as a triage tool in symptomatic patients (threshold ≥10 μg Hb/g — NICE DG30)
- Screening is for asymptomatic average-risk population only
Differential Diagnosis
| FIT Result | Possible Cause | Next Step |
|---|---|---|
| Positive (≥120 screening; ≥10 symptomatic) | CRC, adenoma, IBD, diverticular bleeding, haemorrhoids | Colonoscopy |
| Negative (<120 screening) | No significant bleeding source; note: FIT is not 100% sensitive | Routine screening recall in 2 years |
| Repeated positive, normal colonoscopy | Upper GI source, small bowel pathology | Consider OGD, capsule endoscopy |
Diagnosis / Investigation
Bedside
- FIT (faecal immunochemical test): quantitative measurement of human haemoglobin; specific to lower GI bleeding (unlike guaiac which detected any haem)
- Advantages over guaiac FOBt: single sample, no dietary restrictions, automated analysis, quantitative result, higher sensitivity for CRC (~95% vs ~60%)
Bloods
- FBC: iron deficiency anaemia (in symptomatic patients)
- CEA: not used for screening — used for monitoring after treatment
Imaging
- CT colonography: alternative if colonoscopy incomplete, contraindicated, or patient preference; detects polyps >6 mm with >90% sensitivity
Special Tests
- Colonoscopy: gold standard investigation following positive FIT; allows biopsy and polypectomy
- Flexible sigmoidoscopy: previously used in bowel scope screening (one-off at age 55); being phased out
- Capsule endoscopy: for complete colonic assessment if colonoscopy not possible (emerging role)
- ctDNA (circulating tumour DNA): emerging blood-based screening technology under investigation (e.g. multi-cancer early detection tests)
Management
Non-pharmacological
- Population-level screening: FIT every 2 years, ages 56-74 (extending to 50-74)
- Informed choice: screening information leaflet with invitation; consent required
- Quality assurance: BCSP has rigorous QA standards for colonoscopy (caecal intubation rate >95%, adenoma detection rate >25%, polyp retrieval rate >90%)
- Address health inequalities: targeted interventions to improve uptake in underserved populations (GP endorsement, text reminders, translated materials)
Pharmacological
- Aspirin chemoprevention: evidence of CRC risk reduction (~20% with regular aspirin use); not currently recommended as primary prevention for average-risk population but considered in Lynch syndrome (CaPP2 trial — aspirin 600 mg/day reduced CRC in Lynch syndrome)
Surgical/Interventional
- Polypectomy: at screening colonoscopy — curative for adenomas
- Surgery: if screen-detected cancer (see CRC management)
- Post-polypectomy surveillance: per BSG guideline based on risk stratification
Referral Criteria
- Positive screening FIT → automatic referral to screening centre for colonoscopy
- Symptomatic patients with FIT ≥10 → 2WW referral per NICE NG12
- High-risk family history → genetics/high-risk surveillance programme
- Lynch syndrome → 2-yearly colonoscopy from age 25
Prognosis
Bowel cancer screening reduces CRC mortality by approximately 25% in participants. The UK Flexible Sigmoidoscopy Trial showed 30% reduction in CRC incidence and 35% reduction in CRC mortality with one-off sigmoidoscopy at 55. Screen-detected cancers have significantly better stage distribution: >70% Dukes A/B vs ~50% in symptomatic presentation. 5-year survival for screen-detected CRC is approximately 75-80% vs ~55% overall. National uptake of ~65-70% means significant numbers are not benefiting — improving uptake is a key public health priority.
Other Relevant Information
NHS BCSP Key Parameters
| Parameter | Detail |
|---|---|
| Test | FIT (faecal immunochemical test) |
| Age range | 56-74 (extending to 50-74) |
| Frequency | Every 2 years |
| Positive threshold | ≥120 μg Hb/g faeces |
| Positivity rate | ~2-3% |
| Uptake | ~65-70% |
| Cancer detection rate | ~10% of positive screens |
| Adenoma detection rate | ~40% of positive screens |
| PPV for cancer | ~10% |
| PPV for adenoma | ~40% |
High-Risk Surveillance Pathways
| Risk Group | Surveillance |
|---|---|
| 1 FDR with CRC <50, or 2 FDRs any age | Colonoscopy at 55 (or 10 years before youngest case) |
| Lynch syndrome | 2-yearly colonoscopy from age 25 |
| FAP | Annual sigmoidoscopy/colonoscopy from 12-14; consider colectomy |
| MUTYH-associated polyposis | 2-yearly colonoscopy from 18-20 |
| IBD (extensive colitis >8 years) | Surveillance colonoscopy per BSG guideline |
Wilson & Jungner Screening Criteria Applied to CRC
| Criterion | Application |
|---|---|
| Important health problem | ✓ 3rd most common cancer, 2nd cause of cancer death |
| Recognised latent/early stage | ✓ Adenoma-carcinoma sequence (~10 years) |
| Suitable test | ✓ FIT — sensitive, specific, acceptable |
| Treatment for early stage | ✓ Polypectomy, curative surgery |
| Better prognosis if detected early | ✓ Stage I >90% vs Stage IV ~10% 5-year survival |