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Colon Cancer (Colorectal Cancer) — Causes, Staging & Treatment Guide — Symptoms, Causes & Treatment | MyMedicPlus

Updated: 2026-07-06
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Quick Facts

Type
Malignant gastrointestinal cancer
Specialist
Colorectal Surgeon / Medical Oncologist / Gastroenterologist
Key Treatment
Surgical resection, adjuvant FOLFOX chemotherapy (Stage III), FOLFIRI + bevacizumab/cetuximab (metastatic), immunotherapy (MSI-H)
Prevalence
1.9 million new cases annually; 3rd most common cancer; 5-year survival 65% overall (Stage I: 90%; Stage IV: 14%)

Overview: Colon Cancer

Colorectal cancer (CRC) includes cancers of the colon and rectum. It is the 3rd most common cancer and 2nd leading cause of cancer death globally, with 1.9 million new cases and 935,000 deaths annually. Over 90% of CRCs develop from adenomatous polyps (adenomas) — benign growths on the colon lining that can transform into cancer over 10-15 years. This adenoma-carcinoma sequence makes CRC highly preventable through colonoscopic polypectomy. CRC staging by TNM classification (Stages I-IV) is the most important prognostic factor: Stage I 5-year survival 90%; Stage II 80%; Stage III 60%; Stage IV 14%. The adenoma-carcinoma sequence — the step-by-step molecular and histological transformation of a benign adenomatous polyp into invasive colorectal carcinoma over 10-15 years — provides a uniquely long window for prevention through colonoscopic polypectomy, making colorectal cancer one of the most preventable major cancers when organised population screening is effectively implemented.

Causes & Risk Factors

Modifiable risk factors: low dietary fibre (under 15g/day), high red and processed meat consumption, obesity, physical inactivity, smoking, excess alcohol, Type 2 diabetes, and chronic inflammation (IBD — ulcerative colitis and Crohn's disease). Non-modifiable risk factors: age over 50 (incidence doubles every 10 years), personal or family history of CRC or adenomatous polyps, inflammatory bowel disease, and hereditary syndromes. Lynch syndrome (mismatch repair gene mutations — MLH1, MSH2, MSH6, PMS2) accounts for 3-5% of CRC — associated with early-onset cancer (age 40-45) and other cancers (endometrial, ovarian, gastric, urinary). Familial adenomatous polyposis (FAP — APC gene mutation) causes thousands of polyps and near 100% CRC risk if untreated.

Symptoms & Signs

Early CRC is often asymptomatic — detected on screening colonoscopy. Symptoms of more advanced disease: rectal bleeding (bright red blood with stools or dark altered blood), change in bowel habit (diarrhoea, constipation, narrowing of stools — persistent over 4 weeks), abdominal pain or cramping, sensation of incomplete bowel emptying (tenesmus), unexplained weight loss, iron deficiency anaemia (from chronic slow bleeding — a common presentation of right-sided colon cancer), and abdominal mass. Complications of advanced disease: bowel obstruction (usually left-sided tumours), bowel perforation (causing peritonitis), and fistula formation. Any rectal bleeding or persistent change in bowel habit in adults over 40 warrants investigation.

How It Is Diagnosed

Colonoscopy is the gold standard diagnostic test — allows direct visualisation and biopsy of the entire colon and rectum. Flexible sigmoidoscopy examines only the left colon and rectum. CT colonography (virtual colonoscopy) is an alternative for those unable to tolerate colonoscopy. Biopsy provides histological diagnosis. Staging CT chest/abdomen/pelvis assesses regional lymph nodes and distant metastases (liver and lung — most common). MRI pelvis for rectal cancer (definitive local staging for surgical planning). CEA (carcinoembryonic antigen) tumour marker — elevated in 60% of CRC; useful for monitoring treatment response and recurrence. Molecular testing: MSI (microsatellite instability) status — MSI-H predicts immunotherapy response (pembrolizumab) and is found in 15-20% of CRC. RAS/BRAF mutation testing — guides anti-EGFR therapy (cetuximab/panitumumab only effective in RAS wild-type).

Treatment Options

Stage I: endoscopic polypectomy or colectomy — surgery curative in over 90%. Stage II: colectomy (right or left hemicolectomy or sigmoid resection based on location); adjuvant chemotherapy for high-risk features (bowel perforation, T4 tumour, inadequate node sampling). Stage III: colectomy + adjuvant FOLFOX chemotherapy (oxaliplatin + fluorouracil + leucovorin) for 6 months — reduces recurrence by 25-30%. Stage IV (metastatic): FOLFOX or FOLFIRI (irinotecan + fluorouracil + leucovorin) plus biologics: bevacizumab (anti-VEGF — for most patients) or cetuximab/panitumumab (anti-EGFR — only for RAS wild-type tumours). Trifluridine-tipiracil (Lonsurf) or regorafenib for refractory disease. Pembrolizumab is highly effective for MSI-H/dMMR CRC — first-line for MSI-H metastatic CRC. Liver metastases: hepatic resection is potentially curative in 20-30%; combined with systemic therapy and interventional procedures (ablation, SIRT).

Complications If Untreated

Untreated CRC progresses from local invasion to regional lymph node metastasis to distant (Stage IV) disease — most commonly to the liver, lung, peritoneum, and ovaries. Bowel obstruction from untreated large tumours causes severe abdominal distension, vomiting, and is a surgical emergency. Bowel perforation causes life-threatening peritonitis and sepsis. Chronic bleeding causes severe iron deficiency anaemia. Peritoneal carcinomatosis (seeding of cancer throughout the abdominal cavity) causes intractable ascites and bowel obstruction. Screening colonoscopy and polypectomy are highly effective at preventing CRC — removing adenomas before they transform into cancer. An estimated 90% of CRC is preventable or detectable at an early curable stage with regular screening.

Prevention & Lifestyle Management

CRC screening is highly effective at reducing mortality: NHS Bowel Cancer Screening (UK) — faecal immunochemical test (FIT) every 2 years from age 50-74; FIT-positive results lead to colonoscopy. USA: colonoscopy every 10 years from age 45 (or FIT annually). Lynch syndrome patients: colonoscopy every 1-2 years from age 20-25. Dietary prevention: increase dietary fibre (at least 30g/day from whole grains, legumes, vegetables, fruit); reduce red and processed meat; maintain a healthy weight; exercise regularly (150-300 minutes/week of moderate activity reduces CRC risk by 15-25%). Stop smoking. Limit alcohol. Aspirin (75-150 mg daily) reduces CRC risk in people at elevated risk — discuss with GP, as benefits must be weighed against GI bleeding risk.

When to See a Doctor — Warning Symptoms

See your GP urgently for: rectal bleeding (blood in or on stools) that is not explained by haemorrhoids, especially if dark or mixed with stool; persistent change in bowel habit lasting more than 4 weeks (looser stools, increased frequency, or alternating constipation and diarrhoea); unexplained iron deficiency anaemia — which may indicate occult bowel bleeding from a right-sided tumour (causing tiredness, breathlessness, pale skin); unintentional weight loss with abdominal pain or change in bowel habit; a palpable abdominal or rectal mass. NICE recommends urgent 2-week-wait (2WW) referral for colorectal cancer if aged 40 or above with rectal bleeding plus change in bowel habit; aged 50 or above with unexplained rectal bleeding or change in bowel habit; or any age with unexplained iron deficiency anaemia, positive FIT test, or low rectal mass. Attend Emergency Department for: complete bowel obstruction — severe abdominal distension, inability to open bowels or pass wind, vomiting; bowel perforation — sudden severe abdominal pain with peritonism (rigid abdomen). Complete your NHS bowel cancer screening test when invited — FIT testing from age 50 saves lives.

Frequently Asked Questions

Screening colonoscopy recommendations vary by country and risk level. Average risk: USA guidelines recommend starting colonoscopy at age 45 (American Cancer Society) or 50 (US Preventive Services Task Force). UK offers FIT (stool blood test) every 2 years from ages 50-74; positive results lead to colonoscopy. High risk individuals should start earlier: personal history of CRC or adenomatous polyps — colonoscopy 1-3 years after resection; first-degree relative with CRC diagnosed under 60 — colonoscopy at age 40 or 10 years before the relative's diagnosis; Lynch syndrome — colonoscopy every 1-2 years from age 20-25; FAP — annual sigmoidoscopy from age 12 until colectomy. Discuss your individual risk with your GP.
Lynch syndrome (hereditary non-polyposis colorectal cancer/HNPCC) is caused by inherited mutations in DNA mismatch repair (MMR) genes (MLH1, MSH2, MSH6, PMS2). It is the most common hereditary CRC syndrome, accounting for 3-5% of all CRC. Lifetime CRC risk in Lynch syndrome is 40-80% (depending on the gene involved and sex). But Lynch syndrome does NOT mean cancer is inevitable — intensive surveillance (colonoscopy every 1-2 years from age 20-25), aspirin chemoprevention (CAPP2 trial: 600 mg daily for 2 years reduces Lynch CRC risk by 60%), and prophylactic surgery (total colectomy in selected high-risk patients) can prevent or detect cancer at an early curable stage. Cascade genetic testing of family members is essential once a mutation is identified.
Microsatellite instability (MSI) reflects dysfunction in the DNA mismatch repair (MMR) system — resulting in accumulation of mutations in microsatellite regions of DNA. MSI-high (MSI-H) or mismatch repair-deficient (dMMR) tumours occur in 15-20% of all CRC and 90% of Lynch syndrome CRC. MSI status is critical for treatment decisions: MSI-H/dMMR metastatic CRC responds dramatically to immune checkpoint inhibitors (pembrolizumab — anti-PD1) — KEYNOTE-177 trial showed pembrolizumab as first-line therapy doubled progression-free survival compared to chemotherapy. Conversely, MSI-H Stage II CRC does not benefit from adjuvant 5-FU-based chemotherapy (and may be harmed). MSI testing is now recommended for all CRC at diagnosis.
Whether a colostomy or ileostomy is needed depends on the location of the cancer, its stage, and individual patient factors. Right-sided colon cancers: right hemicolectomy typically restores bowel continuity with no stoma. Left-sided colon cancers: left hemicolectomy usually restores continuity. Rectal cancers: low-lying rectal tumours may require abdominoperineal resection (APR) — permanent colostomy — when the tumour is too close to the anal sphincter; however, neoadjuvant chemoradiotherapy can often shrink the tumour and allow sphincter-saving surgery (anterior resection with anastomosis). A temporary loop ileostomy is commonly used to protect a bowel anastomosis and is usually reversed after 3 months. Surgical advances including robotic surgery and neoadjuvant treatment have significantly reduced permanent stoma rates in rectal cancer surgery.

References

  1. GLOBOCAN 2022 — Colorectal Cancer Global Statistics
  2. National Comprehensive Cancer Network (NCCN) — Colon and Rectal Cancer Guidelines, 2024
  3. André T et al. — Pembrolizumab in Microsatellite-Instability-High Advanced Colorectal Cancer (KEYNOTE-177), NEJM, 2020
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Last updated: 2026-07-06

Important: This information is for educational purposes only and does not constitute medical advice. Always consult a qualified healthcare provider for diagnosis and treatment.

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