Epidemiology
2nd most common. It most commonly affects males aged between 50 and 80 years of age. Those who are current, or previous (within 20 years), smokers have a 2-5 fold increased risk of the disease.
Pathology
- Histology (cell type)
- Transitional cell carcinoma TCC (>90% of cases) NB most have papillary pattern
- Squamous cell carcinoma SCC ( 1-7%)
- Adenocarcinoma (2%)
- Morphology (appearance)
- Papillary (70%) (better prognosis as less muscle invasion)
- Sessile or mixed (20% worse prognosis)
- Nodular
Papillary TCC is the most common histopathological diagnosis
Risk factors:
- Risk factors for transitional cell carcinoma of the bladder:
- Smoking
- Exposure to aniline dyes in the printing and textile industry: examples are 2-naphthylamine and benzidine
- Rubber manufacture
- Cyclophosphamide
- Risk factors for squamous cell carcinoma of the bladder:
- Schistosomiasis
- Calmette-Guérin (BCG) treatment
- Smoking
Presentation
- Gross painless haematuria (in 85% of patients)
- Haematuria can be microscopic (typically seen in females)
- Symptoms of bladder irritation- dysuria, frequency and urgency
TNM Staging
Stage | Description |
---|---|
T0 | No evidence of tumour |
Ta | Non invasive papillary carcinoma |
T1 | Tumour invades sub epithelial connective tissue |
T2a | Tumor invades superficial muscularis propria (inner half) |
T2b | Tumor invades deep muscularis propria (outer half) |
T3 | Tumour extends to perivesical fat |
T4 | Tumor invades any of the following: prostatic stroma, seminal vesicles, uterus, vagina |
T4a | Invasion of uterus, prostate or bowel |
T4b | Invasion of pelvic sidewall or abdominal wall |
N0 | No nodal disease |
N1 | Single regional lymph node metastasis in the true pelvis (hypogastric, obturator, external iliac, or presacral lymph node) |
N2 | Multiple regional lymph node metastasis in the true pelvis (hypogastric, obturator, external iliac, or presacral lymph node metastasis) |
N3 | Lymph node metastasis to the common iliac lymph nodes |
M0 | No distant metastasis |
M1 | Distant disease |
Staging
- Most will undergo a cystoscopy and biopsies or TURBT, this provides histological diagnosis and information relating to depth of invasion.
- Local spread by MRI
- Distant disease by CT scanning.
- Nodes of uncertain significance by PET CT
Main prognostic groups
- Low-grade proliferative lesions that develop into non-muscle invasive tumours (~80%)
- Highly proliferative invasive tumours with a propensity to metastasise (high risk also of recurrence and progression)
- Carcinoma in situ- which can penetrate the lamina propria and eventually progress
Management
- Tis/Ta/T1 (non-muscle invasive)
- TURBT
- Intravesical BCG
- Chemo with mitomycin, epirubicin, and gencitabine
- T2-3 (muscle invasive)
- Radical cystectomy is gold standard (better than radiotherapy)
- Orthotopic reconstruction of the bladder using ileum is an option if baldder neck not involved
- Neo-adjuvant and adjuvant chemo with M-VAC (MTX, VinB, Dox, Cis)
- T4 (organ invasive)
- Palliative chemo/radiotherapy
- Long term catheter
Follow up cystoscopy
- Low risk non-muscle invasive bladder cancer: @ 3 months and 12 months after diagnosis
- Intermediate risk non-muscle invasive: @ 3, 9, 18 months and once a year thereafter
- High risk non-muslce invasive: @ 3 months for 2 years, 6 monthly for 2 years and once a year thereafter