Gallbladder cancer
Appearance
Epidemiology
[edit | edit source]- Generally occurs 50-70yo
- High incidence in:
- Bolivia
- Chile
- India
- Pakistan
- Poland
- Rare in Western countries (1.13 per 100,000)
- F:M 2:1
- Found in approximately 1% of cholecystectomy specimens
- Porcelain gallbladder - 2-3% have cancer
- This is probably reflective of long-term inflammation
Risk factors
[edit | edit source]- Gallstones present in 70-90%
- Large stones (>3cm) seem to give a ten-fold increase in risk compared to small stones
- Type of stone not important
- Females
- Older age
- Obesity
- Chronic cholecystitis
- Occupational carcinogen exposure
- Poor diet
- Chronic salmonella infection
- Biliary cysts
- Aberrant PBDJ (long common channel)
- Choledochal cysts
- PSC
- Medications
- Methyldopa
- Isoniazid
Pathophysiology
[edit | edit source]- Generally adenocarcinoma (90%), with some squamous or adenosquamous type
- Subtypes:
- Infiltrative - most common - spread in sub-serosal plane (same plane dissected during cholecystectomy)
- Nodular - tend to grow as a more circumscribed mass and can invade the liver
- Papillary - better prognosis - tend to be limited to GB wall at time of diagnosis
- Combined
- Subtypes:
- Two proposed pathways:
- Chronic inflammation leading to mucosal transformation (most likely)
- Aberrant PBDJ with pancreatic juice reflux
- There is some suggestion of an adenoma-carcinoma sequence, as carcinomas are often adjacent to carcinomas-in-situ or severe dysplasia, but no known increased risk from small polyps <10mm
- Location
- 60% fundus
- 30% body
- 10% neck
- The GB wall is thin, with only a narrow lamina propria, and is only a single muscular layer with no serosal covering between it and the liver, so early liver invasion is common
- Spreads via lymphatics, blood and via local invasion into peritoneal cavity or along surgical tract wounds
- First draining nodal basin includes the cystic and peri-choledochal nodes, then to the retro-portal and pancreaticoduodenal nodes, and then the coeliac, superior mesenteric, and finally aortocaval nodes (so full staging may require a Kocher manoeuvre
- High propensity to spread to peritoneum, causing carcinomatosis
- Can also directly extend into porta hepatis structures
- Common metastatic locations:
- Noncontiguous liver mets (91%)
- Lung (32%)
- Brain (5%)
Presentation
[edit | edit source]- Frequently asymptomatic, since most cancers form in body/neck
- Symptoms are a good prognostic indicator, since it means they present earlier
- Can present with symptoms of acute or chronic cholecystitis
- Constitutional symptoms
- Specific situations:
- Pre-operative workup for biliary symptoms
- Cancer can cause similar symptoms to biliary colic
- Incidental imaging finding
- Any GB mass, or polyp > 1cm, or presence of porcelain GB, should raise suspicion
- DDx of GB mass
- Benign:
- Cholesterolosis
- Cholesterol polyps
- Adenomyomatosis
- Intracholecystic papillary-tubular neoplasms (ICPN/inflammatory polyps and adenomas)
- Malignant
- GB cancer
- Mets
- Benign:
- Intra-operatively
- Do not need to immediately convert to open - best to abort operation and refer to HPB surgeon
- Post-operatively on histopathology
- Early GB cancer may be difficult to differentiate from chronic cholecystitis
- Post-operatively on histopathology
Workup
[edit | edit source]- USS as initial evaluation
- MRCP is better at differentiating benign from malignant lesions, and looking for invasion
- CT C/A/P indications:
- Suspected GB cancer pre-op
- Post-op if intra-op impression of >T1a stage
- CEA - >4ng/mL is 93% sp for GB cancer but only 50% sensitive
- CA19-9 >20units/mL is 79.4% sp / 79.2% se
- Imaging review for liver involvement, biliary extension, vascular involvement, ascites, and/or mets
- PTC/ERCP has low yield
- FDG-PET: 86% of GB cancer is avid, however there is a low overall sensitivity for detecting mets, and rarely changes management
- Utility increased among patients without a prior cholecystectomy, or patients with suspicious nodal disease on CT, or consider when looking for distant mets while deciding whether to operate
- Avoid percutaneous biopsy - tends to seed biopsy tracts
Staging
[edit | edit source]- If T2/3/4 disease is present, >50% chance of regional lymphatic mets
- Mostly diagnosed at a late stage
- 35% nodal disease and 40% metastases
- Gallbladder cancer TNM staging AJCC UICC 8th edition - to follow
Management
[edit | edit source]- Principles
- Resection is the only chance for cure
- Based on TNM stage
- T1a disease:
- Cholecystectomy is sufficient
- Out of 706 patients, only 1.8% had LN mets, and only 1.1% died from disease
- Carefully verify negative margins, especially cystic duct
- If GB wall margin is involved, liver resection will be necessary
- If cystic duct margin is involved, CHD and extra-hepatic CBD excision with Roux-en-Y reconstruction, but no staging workup or nodal dissection necessary
- T1b disease:
- Need complete staging workup
- Traditionally, simple cholecystectomy, but now aggressive resection is favoured, especially in setting of high-risk histopathological factors (perineural, lymphatic or vascular invasion)
- Higher rate of LN mets than T1a (10.9%) and up to 13% have residual disease at re-excision
- Offer re-excision with radical/extended cholecystectomy
- T2a disease:
- May not need to re-resect because rate of liver involvement is obviously lower, although this is partly controversial, and UTD still recommends re-resection as for T2b
- T2b disease:
- 10.4% have hepatic disease
- 31% have N1 LN involvement
- Strong indication for definitive extended re-excision - extend 5-year survival from 20% to >80%
- Radical cholecystectomy
- Advanced tumours (T3):
- Radical resection may be potentially curative in some patients, although outcomes are poor
- Start with staging laparoscopy - peritoneal or hepatic metastases preclude an operation
- Everything aimed at getting complete resection - no role for debulking if R0 cannot be obtained
- Likely to be considered for adjuvant chemotherapy
- T4
- UTD states that attempts at resection are likely futile. Could still be considered.
- Choice of re-resection procedure
- 2cm rim of liver tissue vs anatomic IVb/V resection - similar recurrence rate, as long as negative margins are obtained, but the anatomic resection has a lower complication rate
- Either way, remove lymph nodes from cystic triangle, hepatoduodenal ligament and porta hepatis
- May require resection of CBD margin, in which case reconstruction will be needed
- Consider port site resection although probably not
- Unresectable or metastatic disease
- Chemotherapy and radiotherapy have not shown survival benefits
- Jaundiced patient with advanced unresectable disease should have PTC or ERCP drainage
- Biliary bypass is generally difficult because of advanced disease in porta hepatis
- Neurolysis of coeliac plexus can help with pain
- Can get GOO from local extension of tumour, which can be managed by an endoscopic duodenal stent
- Portal lymphadenectomy
- Indicated in T2-T4 tumours
- Most surgeons resect cystic, periportal, and hepatic artery nodes
- Guidelines suggest that you need six nodes to be considered node negative
- Port site resection
- Not associated with improved overall or disease-free survival
- Absolute contraindications to surgery:
- Medical comorbidities preventing surgery
- Distant mets including liver, peritoneum
- Involvement of N2 lymph nodes (coeliac, peripancreatic, peri-duodenal, or SMA
- Malignant ascites
- Significant involvement of hepatoduodenal ligament
- Encasement of major vasculature
Five year survival rate
[edit | edit source]- Stage I: 40%
- II: 12%
- III: 5%
- IV: 1%, median survival 13 months