Radiation Oncology/Bladder/Overview
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Bladder Cancer Overview
Epidemiology
[edit | edit source]- 5th most common cancer in U.S., incidence ~71 thousand cases (2009), with ~14 thousand deaths
- Increasing incidence, +20% over 20 years
- Male:female = 3:1
- Peak in 50's - 70's
- ~4% incidence of synchronous upper urothelial lesion (ureters or renal pelvis)
- 70% are superficial, 25% muscle invasive, 5% metastatic at presentation.
- Two separate behaviors driven by separate molecular alterations
- Superficial (Ta, Tis, T1): commonly recur, but progression to muscle invasion is rare (10-20%) and prognosis is good
- Muscle-invasive (T2-T4): poor prognosis, 80% mortality within 2 years if untreated
Risk factors
[edit | edit source]- Genetic abnormalities
- Please see below in Pathology
- Chemical exposure
- Tobacco - increases risk 2-3x
- Aromatic amines, aniline dyes, and nitrites and nitrates (e.g. leather industry workers)
- Cyclophosphamide
- Chronic irritation - increases risk for squamous cell tumors
- Indwelling catheters
- Schistosoma haematobium
- Pelvic RT
Screening
[edit | edit source]- No good screening test
- Screening for microhematuria
- In normal population, microhematuria present in 4%-20%
- In patients with microhematuria, bladder cancer in 1%-5%
- Yield low (0.005%-0.2%), and patients typically have superficial disease
- Cytology 40-60% sensitivity, but ~90% specificity
Clinical Presentation
[edit | edit source]- Painless gross hematuria
- Unexplained irritative voiding and frequency
- Advanced cases pelvic pain, ureteral obstruction, hydronephrosis
Work Up
[edit | edit source]- Cytology
- Cystoscopy
- Renal/ureter CT scan
- TURBT - determines clinical staging
- Urethral biopsies should be considered for patients at high risk for involvement (recurrent cancer, bladder neck involvement, vaginal extension in women)
- Bimanual examination to evaluate extravesical extension
- If muscle-invasive disease on TURBT, need systemic staging
Anatomy
[edit | edit source]- Hollow, muscular organ
- Located in deep pelvis, but it is a true intra-abdominal organ that can project above the umbilicus
- Several segments
- Apex: ends as fibrous cord (derivative of urachus) connecting the bladder to the umbilicus
- Superior surface/Dome: only part of bladder covered by peritoneum
- Base: Posterior, separated from rectum by vas deferens/seminal vesicles in men and uterus/vagina in women
- Inferior and lateral surfaces: separated from pubic bone by retropubic space
- Bladder neck: inferior-most portion, above prostate in men and urethra in women. Fixed in place during distention
- Ureters: enter bladder superior and lateral to seminal vesicles
- Bladder mucosas is lined with transitional epithelium
- Lymphatic drainage
- Anterior and posterior: internal illiac and common illiac
- Trigone: external illiac
Pathology
[edit | edit source]- Transitional cell carcinoma (TCC) in 93%, squamous cell in 5% in US (higher in countries with Schistosoma), adenoCA, small cell
- Tumors of mixed histology (with squamous or adeno components) are frequent, and are classified (and behave) as TCC
- Molecular alterations:
- Superficial: deletions of chromosome 9, mutation of FGF receptor (FGFR3), mutation of PIK3CA kinase, mutation of Ras
- Muscle-invasive: multiple genetic abnormalities, including EGFR (overexpressed 10-50%; 19% on RTOG trials), p53 and Rb inactivation, and CDKN2A
- To demonstrate muscle invasion (T2+), muscularis propria must be present in the slide, though fragmentary nature of TURBT makes estimate of true depth of invasion difficult
Spread
[edit | edit source]- Lymph nodes
- Overall LN+ ~20%
- pT1 ~5%
- pT2-T3a ~30%
- pT3b-T4 50%-60%
- Distant spread ~8%
- It has been estimated that as many as 50% of muscle-invasive patients may already have occult metastatic disease, accounting for the high rate of metastatic failure after local treatment