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[[Category:Bladder Cancer]]
[[Category:Bladder Cancer]]


== Pathology of Bladder Cancer ==
== Common Malignant Bladder Cancer Histology ==
*'''<span style="color:#ff0000">Urothelial carcinoma</span>'''
**'''Most common (90%) bladder cancer histology'''
*'''<span style="color:#ff0000">Non-urothelial carcinoma</span>'''
**'''See [[Non-Urothelial Bladder Cancer|Non-Urothelial Bladder Cancer Chapter]]'''
**'''<span style="color:#ff0000">Squamous cell carcinoma</span>'''
***'''Second most common bladder cancer histology'''
****2-5% of all bladder cancers
**'''<span style="color:#ff0000">Adenocarcinoma</span>'''
**'''<span style="color:#ff0000">Others</span>'''
***'''<span style="color:#ff0000">Small cell</span>'''
***'''<span style="color:#ff0000">Primary Signet Ring Cell Carcinoma</span>'''


* '''Histology'''
== Urothelial Carcinoma ==
** '''90% urothelial carcinoma'''
*** '''The term urothelial cancer is preferable to the term transitional cell cancer'''
** '''2-5% squamous cell carcinomas'''
*** More common in women, spinal-cord injury patients, chronic irritation (UTI, stones)
** '''Other variants'''
*** '''2% adenocarcinoma'''
**** '''Majority represent metastases from other primary adenocarcinomas such as colon, breast, or lung cancers.'''
***** Patients should undergo investigations of other sites (e.g. coloscopy)
**** '''Risk factors for primary bladder adenocarcinoma (4):'''
****# '''Nonfunctioning bladder'''
****# '''Obstruction'''
****# '''Chronic irritation'''
****# '''Bladder exstrophy'''
**** '''Patients who undergo bladder augmentation with bowel are at risk of bladder adenocarcinoma'''
***** Low incidence of malignancy following a bladder augmentation (approximately 1.5-2.5% of patients per decade)
***** '''Screening for bladder adenocarcinoma in patients with a previous augmentation is not recommended.'''
****** Current recommendation for follow-up in patients with previous bladder augmentation with bowel is for annual visits with renal and bladder ultrasound (rule-out stones or the development of hydronephrosis secondary to noncompliance with CIC), electrolytes (rule out metabolic abnormalities), creatinine, serum B12 (rule-out nutritional deficiencies), and urinalysis (assess for hematuria).
**** '''Urachal adenocarcinoma arises from the urachas'''
*** '''Small cell'''
**** '''Should be treated with initial chemotherapy followed by radiation or cystectomy as consolidation, if there is no metastatic disease§'''
**** '''Even small components of small cell histology within urothelial carcinoma should be managed as small cell'''
*** '''Primary Signet Ring Cell Carcinoma'''
**** Extremely rare, making up less than 1% of all epithelial bladder neoplasms
**** Can be of urachal origin and directly extend into the bladder.
**** Generally present as high-grade, high-stage tumors and have a uniformly poor prognosis.
***** In the majority of cases there are regional or distant metastases at the time of presentation, and the mean survival time is less than 20 months
**** Carcinoembryonic antigen (CEA) may be elevated
**** Primary treatment is radical cystectomy
**** Understaging is very common in signet ring cell carcinoma, with peritoneal studding common at the time of surgical exploration.
*** '''Urothelial carcinoma'''
**** '''Grading'''
***** '''Classified as low grade (LG) vs. high grade (HG)'''
****** 1973 World Health Organization defined 3 categories: grades 1, 2, and 3
******* Middle category was overreported
****** 2004, International Society of Urologic Pathologists updated classification to 3 categories:
******* Papillary urothelial neoplasm of low malignant potential (PUNLMP)
******* Low-grade
******* High-grade
****** 2016 reviewed system without major changes
****** With the 2004/2016 WHO/ISUP system, 30-40% of the former grade 2 lesions with bland cytological features were re-classified as LG, while the other 60-70% were re-classified as HG
****** '''TaLG lesions recur at a rate of 50-70% and progress in ≈5% of patients'''
****** '''T1HG lesions recur at a rate > 80% and progress in 50% of patients''' [different numbers than Chapter 93]
****** The variance in biologic behavior for LG versus HG lesions correlates with the known dual molecular lines of genetic development for these two pathways and supports the concept that HG and LG cancers may be considered as essentially different diseases; LG papillary tumors tend to exhibit relatively few chromosomal abnormalities compared to HG tumors
**** '''CIS'''
***** A flat, non'''-'''invasive urothelial carcinoma
***** '''HG''' '''by definition''' '''and is regarded as a precursor to the development of invasive HG cancer'''
****** '''Lesions interpreted as severe dysplasia or severe atypia are regarded as being the same entity as CIS'''
***** Rarely found in isolation; majority (90%) found in association with papillary or nodular bladder tumours
***** Considered a field disease, as it can affect multiple areas in the bladder, the upper urinary tract, and the urethra
***** Classified as
****** Primary: no previous history of bladder cancer (best prognosis)
****** Secondary: new lesion diagnosed during followup
**** Dysplasia
***** Good indication of urothelial instability and a marker of recurrence and progression in those with known urothelial cancer
**** '''PUNLMP: papillary urothelial neoplasm of low malignant potential'''
***** '''Essentially benign tumour with orderly cellular arrangement, minimal architectural abnormalities, and minimal nuclear atypia'''
***** '''Recurs within the bladder in 12-35% of patients'''
****** '''Post-operative treatment with mitomycin C is warranted'''
****** '''Follow-up is warranted'''
******* '''Usually the new tumours are of similar histology, but occasionally these subsequent lesions manifest as urothelial carcinoma'''
******* '''Should be followed similarly to low-grade tumors'''
***** '''Progression is rare (4%)'''
**** '''Histologic variants of urothelial cancer'''
***** 75% of urothelial carcinomas are classified as pure, while 25% have a secondary histological variant
***** Squamous
****** Most common (20-40%)
****** Urothelial with squamous differentiation outcomes similar to pure urothelial
***** Glandular
****** Second most common (20%)
****** Urothelial with glandular differentiation outcomes similar to pure urothelial
***** '''Sarcomatoid'''
****** '''Aggressive; consider upfront cystectomy'''
***** '''Plasmacytoid'''
****** '''Aggressive; consider upfront cystectomy'''
******* '''Usually manifests at an advanced stage'''
******* '''Respond very poorly''' '''to systemic chemotherapy'''
******* Median survival < 27 months from time of diagnosis
***** '''Micropapillary'''
****** '''Aggressive; consider upfront cystectomy'''
******* High (≈70%) progression rate from NMIBC to MIBC with a high subsequent metastatic rate despite treatment; usually manifests at an advanced stage
******* Cancer-specific survival <22% at 4 years despite aggressive chemotherapy and surgical resection in patients with locally advanced disea'''s'''se
****** '''The most effective treatment for all stages of micropapillary urothelial carcinoma is surgical resection.'''
******* '''Treatment with transurethral resection and BCG therapy is ineffective unless the tumor is completely resected'''
******* '''Neoadjuvant chemotherapy does not appear effective in micropapillary urothelial carcinoma, and may actually worsen survival by delaying therapy when compared with immediate cystectomy.'''
***** '''Nested'''
****** Rare
****** Associated with higher stage and nodal invasion
****** Oncological outcomes comparable to patients with pure urothelial carcinoma when matched by stage in both the NMIBC and MIBC setting
****** '''Can be confused with benign lesions, such as Von Brunn nests that are in the lamina propria, cystitis cystica, and inverted papillomas'''
***** '''Clear cell variant of urothelial carcinoma'''
****** '''Not associated with worse prognosis'''
***** '''Adenocarcinoma differentiation'''


== TNM Staging (AJCC 8th edition§) ==
* '''<span style="color:#ff0000">Accounts for 90% of all bladder cancers</span>'''


* '''pTstage'''
* '''The term "urothelial cancer" is preferable to the term transitional cell cancer'''
** '''pTX: tumour cannot be assessed'''
=== Grading ===
** '''pT0: no evidence of tumour'''
* '''<span style="color:#ff0000">Classified as low grade (LG) vs. high grade (HG)</span>'''
** '''pTa: non-invasive (confined to epithelial mucosa) papillary carcinoma'''
** 1973 World Health Organization defined 3 categories: grades 1, 2, and 3
** '''pTis: carcinoma in-situ'''
*** Middle category was overreported
** '''pT1: invades lamina propria''' (subepithelial connective tissue)
** 2004, International Society of Urologic Pathologists updated classification to 3 categories:
*** Subdivision into pT1a vs. pT1b has been proposed with some studies suggesting that deep lamina propria invasion carries a substantially more serious prognosis. However, the value of substaging has not been validated in other studies
*** Papillary urothelial neoplasm of low malignant potential (PUNLMP)
** '''pT2'''
*** Low-grade
*** '''pT2a: invades superficial muscularis propria'''
*** High-grade
*** '''pT2b: invades deep muscularis propria'''
** 2016 reviewed system without major changes
** '''pT3'''
** With the 2004/2016 WHO/ISUP system, 30-40% of the former grade 2 lesions with bland cytological features were re-classified as LG, while the other 60-70% were re-classified as HG
*** '''pT3a: invades perivesical fat microscopically'''
** '''TaLG lesions recur at a rate of 50-70% and progress in ≈5% of patients'''
*** '''pT3b: invades perivesical fat macroscopically'''
** '''T1HG lesions recur at a rate > 80% and progress in 50% of patients''' [different numbers than Chapter 93]
** '''pT4'''
** The variance in biologic behavior for LG versus HG lesions correlates with the known dual molecular lines of genetic development for these two pathways and supports the concept that HG and LG cancers may be considered as essentially different diseases; LG papillary tumors tend to exhibit relatively few chromosomal abnormalities compared to HG tumors
*** '''pT4a: invades prostatic stroma, seminal vesicles, uterus, or vagina'''
**** '''Extension of the tumor into the prostatic urethra WITHOUT stromal invasion is currently classified under the prostatic urethral cancer staging and does not carry an adverse prognosis for patients with known bladder cancer'''
*** '''pT4b: invades pelvic/abdominal wall'''
** Prognostic value of T2 and T3 substaging has been widely debated and reported
* '''Nstage'''
** '''Nx: lymph nodes cannot be assessed'''
** '''N0: no lymph node metastasis'''
** '''N1: single regional lymph node in the true pelvis'''
*** '''True pelvis lymph nodes (5)'''
***# '''Perivesical'''
***# '''Obturator'''
***# '''Internal iliac (hypogastric)'''
***# '''External iliac'''
***# '''Presacral lymph nodes'''
** '''N2: multiple regional lymph node metastases in the true pelvic'''
** '''N3: lymph node metastasis to the common iliac lymph nodes'''
* '''Mstage'''
** '''M0: no distant metastasis'''
** '''M1: distant metastasis'''


* '''Pathologically, organ-confined bladder cancer is considered to be pT2bN0M0 or less at the time of cystectomy'''
=== CIS ===
* A flat, non-invasive urothelial carcinoma
* '''HG by definition and is regarded as a precursor to the development of invasive HG cancer'''
** '''<span style="color:#ff0000">Lesions interpreted as severe dysplasia or severe atypia are regarded as being the same entity as CIS</span>'''
* Rarely found in isolation; majority (90%) found in association with papillary or nodular bladder tumours
* Considered a field disease, as it can affect multiple areas in the bladder, the upper urinary tract, and the urethra
* Classified as
** Primary: no previous history of bladder cancer (best prognosis)
** Secondary: new lesion diagnosed during follow-up


INSERT FIGURE
=== Dysplasia ===
* Good indication of urothelial instability and a marker of recurrence and progression in those with known urothelial cancer
 
=== Papillary urothelial neoplasm of low malignant potential ===
* Also known as PUNMLP
*'''<span style="color:#ff0000">Essentially benign tumour</span> with orderly cellular arrangement, minimal architectural abnormalities, and minimal nuclear atypia'''
* '''<span style="color:#ff0000">Recurs within the bladder in 12-35% of patients</span>'''
** '''Post-operative treatment with mitomycin C is warranted'''
** '''<span style="color:#ff0000">Follow-up is warranted</span>'''
*** '''Usually the new tumours are of similar histology, but occasionally these subsequent lesions manifest as urothelial carcinoma'''
*** '''<span style="color:#ff0000">Should be followed similarly to low-grade tumors</span>'''
* '''<span style="color:#ff0000">Progression is rare (4%)</span>'''
 
=== Histologic variants of urothelial cancer ===
* '''75% of urothelial carcinomas are classified as pure, while 25% have a secondary histological variant'''
* Squamous
** Most common (20-40%)
** Urothelial with squamous differentiation outcomes similar to pure urothelial
* Glandular
** Second most common (20%)
** Urothelial with glandular differentiation outcomes similar to pure urothelial
* '''<span style="color:#ff0000">Sarcomatoid</span>'''
** '''<span style="color:#ff0000">Aggressive</span>; consider upfront cystectomy'''
* '''<span style="color:#ff0000">Plasmacytoid</span>'''
** '''<span style="color:#ff0000">Aggressive; consider upfront cystectomy'''
*** '''Usually manifests at an advanced stage</span>'''
*** '''Respond very poorly''' '''to systemic chemotherapy'''
*** Median survival < 27 months from time of diagnosis
* '''<span style="color:#ff0000">Micropapillary</span>'''
** '''<span style="color:#ff0000">Aggressive</span>; consider upfront cystectomy'''
*** High (≈70%) progression rate from NMIBC to MIBC with a high subsequent metastatic rate despite treatment; usually manifests at an advanced stage
*** Cancer-specific survival <22% at 4 years despite aggressive chemotherapy and surgical resection in patients with locally advanced disease'''
** '''<span style="color:#ff0000">The most effective treatment for all stages of micropapillary urothelial carcinoma is surgical resection.</span>'''
*** '''Treatment with transurethral resection and BCG therapy is ineffective unless the tumor is completely resected'''
*** '''<span style="color:#ff0000">Neoadjuvant chemotherapy does not appear effective in micropapillary urothelial carcinoma, and may actually worsen survival by delaying therapy when compared with immediate cystectomy.</span>'''
* '''<span style="color:#ff0000">Nested</span>'''
** Rare
** Associated with higher stage and nodal invasion
** Oncological outcomes comparable to patients with pure urothelial carcinoma when matched by stage in both the NMIBC and MIBC setting
** '''Can be confused with benign lesions, such as Von Brunn nests that are in the lamina propria, cystitis cystica, and inverted papillomas'''
* '''<span style="color:#ff0000">Clear cell variant of urothelial carcinoma</span>'''
** '''<span style="color:#ff0000">Not associated with worse prognosis</span>'''
* '''Adenocarcinoma differentiation'''


== Questions ==
== Questions ==


# Which patients are at risk of bladder adenocarcinoma?
#  
# Which variant histologies are considered aggressive?
# What is the pT staging of bladder cancer?


== Answers ==
== Answers ==


# Which patients are at risk of bladder adenocarcinoma?
#  
#* Patients with nonfunctioning bladder, obstruction, chronic irritation, or bladder exstrophy
# Which variant histologies are considered aggressive?
#* Micropapillary, nested, plasmacytoid, sarcomatoid
# What is the pT staging of bladder cancer?
#* pTstage
#* pTX: tumour cannot be assessed
#* pT0: no evidence of tumour
#* pTa: non-invasive (confined to epithelial mucosa) papillary carcinoma
#* pTis: carcinoma in-situ
#* pT1: invades lamina propria (subepithelial connective tissue)
#* pT2
#** pT2a: invades superficial muscularis propria
#** pT2b: invades deep muscularis propria
#* pT3
#** pT3a: invades perivesical fat microscopically
#** pT3b: invades perivesical fat macroscopically
#* pT4
#** pT4a: invades prostatic stroma, seminal vesicles, uterus, or vagina
#** pT4b: invades pelvic/abdominal wall


== Next Chapter: Diagnosis and Evaluation ==
== Next Chapter: [[Bladder Cancer: TNM Staging|TNM Staging]] ==


== References ==
== References ==
Line 172: Line 101:
* Wein AJ, Kavoussi LR, Partin AW, Peters CA (eds): CAMPBELL-WALSH UROLOGY, ed 11. Philadelphia, Elsevier, 2015, chap 92
* Wein AJ, Kavoussi LR, Partin AW, Peters CA (eds): CAMPBELL-WALSH UROLOGY, ed 11. Philadelphia, Elsevier, 2015, chap 92
* Bhindi, Bimal, et al. "Canadian Urological Association guideline on the management of non-muscle invasive bladder cancer." ''Canadian Urological Association Journal'' 15.8 (2021).
* Bhindi, Bimal, et al. "Canadian Urological Association guideline on the management of non-muscle invasive bladder cancer." ''Canadian Urological Association Journal'' 15.8 (2021).
*Flaig, Thomas W., et al. "Bladder cancer, version 2.2022, NCCN clinical practice guidelines in oncology."

Latest revision as of 19:10, 17 March 2024


Common Malignant Bladder Cancer Histology[edit | edit source]

  • Urothelial carcinoma
    • Most common (90%) bladder cancer histology
  • Non-urothelial carcinoma
    • See Non-Urothelial Bladder Cancer Chapter
    • Squamous cell carcinoma
      • Second most common bladder cancer histology
        • 2-5% of all bladder cancers
    • Adenocarcinoma
    • Others
      • Small cell
      • Primary Signet Ring Cell Carcinoma

Urothelial Carcinoma[edit | edit source]

  • Accounts for 90% of all bladder cancers
  • The term "urothelial cancer" is preferable to the term transitional cell cancer

Grading[edit | edit source]

  • Classified as low grade (LG) vs. high grade (HG)
    • 1973 World Health Organization defined 3 categories: grades 1, 2, and 3
      • Middle category was overreported
    • 2004, International Society of Urologic Pathologists updated classification to 3 categories:
      • Papillary urothelial neoplasm of low malignant potential (PUNLMP)
      • Low-grade
      • High-grade
    • 2016 reviewed system without major changes
    • With the 2004/2016 WHO/ISUP system, 30-40% of the former grade 2 lesions with bland cytological features were re-classified as LG, while the other 60-70% were re-classified as HG
    • TaLG lesions recur at a rate of 50-70% and progress in ≈5% of patients
    • T1HG lesions recur at a rate > 80% and progress in 50% of patients [different numbers than Chapter 93]
    • The variance in biologic behavior for LG versus HG lesions correlates with the known dual molecular lines of genetic development for these two pathways and supports the concept that HG and LG cancers may be considered as essentially different diseases; LG papillary tumors tend to exhibit relatively few chromosomal abnormalities compared to HG tumors

CIS[edit | edit source]

  • A flat, non-invasive urothelial carcinoma
  • HG by definition and is regarded as a precursor to the development of invasive HG cancer
    • Lesions interpreted as severe dysplasia or severe atypia are regarded as being the same entity as CIS
  • Rarely found in isolation; majority (90%) found in association with papillary or nodular bladder tumours
  • Considered a field disease, as it can affect multiple areas in the bladder, the upper urinary tract, and the urethra
  • Classified as
    • Primary: no previous history of bladder cancer (best prognosis)
    • Secondary: new lesion diagnosed during follow-up

Dysplasia[edit | edit source]

  • Good indication of urothelial instability and a marker of recurrence and progression in those with known urothelial cancer

Papillary urothelial neoplasm of low malignant potential[edit | edit source]

  • Also known as PUNMLP
  • Essentially benign tumour with orderly cellular arrangement, minimal architectural abnormalities, and minimal nuclear atypia
  • Recurs within the bladder in 12-35% of patients
    • Post-operative treatment with mitomycin C is warranted
    • Follow-up is warranted
      • Usually the new tumours are of similar histology, but occasionally these subsequent lesions manifest as urothelial carcinoma
      • Should be followed similarly to low-grade tumors
  • Progression is rare (4%)

Histologic variants of urothelial cancer[edit | edit source]

  • 75% of urothelial carcinomas are classified as pure, while 25% have a secondary histological variant
  • Squamous
    • Most common (20-40%)
    • Urothelial with squamous differentiation outcomes similar to pure urothelial
  • Glandular
    • Second most common (20%)
    • Urothelial with glandular differentiation outcomes similar to pure urothelial
  • Sarcomatoid
    • Aggressive; consider upfront cystectomy
  • Plasmacytoid
    • Aggressive; consider upfront cystectomy
      • Usually manifests at an advanced stage
      • Respond very poorly to systemic chemotherapy
      • Median survival < 27 months from time of diagnosis
  • Micropapillary
    • Aggressive; consider upfront cystectomy
      • High (≈70%) progression rate from NMIBC to MIBC with a high subsequent metastatic rate despite treatment; usually manifests at an advanced stage
      • Cancer-specific survival <22% at 4 years despite aggressive chemotherapy and surgical resection in patients with locally advanced disease
    • The most effective treatment for all stages of micropapillary urothelial carcinoma is surgical resection.
      • Treatment with transurethral resection and BCG therapy is ineffective unless the tumor is completely resected
      • Neoadjuvant chemotherapy does not appear effective in micropapillary urothelial carcinoma, and may actually worsen survival by delaying therapy when compared with immediate cystectomy.
  • Nested
    • Rare
    • Associated with higher stage and nodal invasion
    • Oncological outcomes comparable to patients with pure urothelial carcinoma when matched by stage in both the NMIBC and MIBC setting
    • Can be confused with benign lesions, such as Von Brunn nests that are in the lamina propria, cystitis cystica, and inverted papillomas
  • Clear cell variant of urothelial carcinoma
    • Not associated with worse prognosis
  • Adenocarcinoma differentiation

Questions[edit | edit source]

Answers[edit | edit source]

Next Chapter: TNM Staging[edit | edit source]

References[edit | edit source]

  • Wein AJ, Kavoussi LR, Partin AW, Peters CA (eds): CAMPBELL-WALSH UROLOGY, ed 11. Philadelphia, Elsevier, 2015, chap 92
  • Bhindi, Bimal, et al. "Canadian Urological Association guideline on the management of non-muscle invasive bladder cancer." Canadian Urological Association Journal 15.8 (2021).
  • Flaig, Thomas W., et al. "Bladder cancer, version 2.2022, NCCN clinical practice guidelines in oncology."
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