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Penile cancer overview

Penile cancer is rare – 1 in 100 000 in USA/Europe.

More common in South America, SE Asia and parts of Africa.

Incidence increases with age – from 50 – 60s onwards.

More common in regions with high rates HPV. Vaccination expected to reduce risk.

 

Risk factors

  • Circumcision in childhood reduces risk
  • Phimosis increases risk > 10 x
  • Chronic penile inflammation (balanoposthitis, BXO)
  • Sporalene / ultraviolet A phototherapy (for psoriasis)
  • Smoking
  • HPV infection
  • Rural areas, low socioeconomic status and unmarried status
  • Multiple sexual partners and early age of first intercourse (presumably related to HPV)

 

Neonatal circumcision definite reduces the incidence of penile cancer, but adult circumcision does not appear to reduce risk.

Pre-malignant lesions like CIS are also associated with progression to penile cancer.

 

Pathology

95 % of penile cancers are squamous cell carcinoma.

Other tumours include melanomas, lymphoma, Kaposi sarcoma, BCC or metastases.

There are multiple subtypes of SCC:

Good prognosis Intermediate prognosis Poor prognosis
 

Verrucous

Papillary

Warty

 

Usual type

Mixed

Pleomorphic warty

Basaloid

Sarcomatoid

 

Pathological grading is important and helps determine TNM staging.

Grading is graded 1 – 3 (or sarcomatoid) based on cytological atypia, keratinisation, intercellular bridges, mitotic activity and tumour margins.

2022 WHO classification divides to HPV-associated and HPV-independent.

Pathological factors portending poorer prognosis:

  • Perineural invasion
  • Lymphovascular invasion
  • Depth of invasion
  • Grade

These factors all increase the risk of lymph node metastases, which is the single most important factor affecting survival and development of metastases.

 

Staging

Tx Tumour can’t be assessed
T0 No evidence primary tumour
Tis Carcinoma in situ
Ta Non invasive verrucous carcinoma
T1a Invades subepithelial tissue – no LVI, not poorly differentiated
T1b Invades subepithelial tissue – LVI or poorly differentiated
T2 Invades corpus spongiosum (+/- urethra)
T3 Invades corpus cavernosum
T4 Invades other adjacent structures
   
cNx Nodes can’t be assessed
cN0 No palpable or visibly enlarged nodes
cN1 Palpable mobile unilateral inguinal node
cN2 Palpable mobile multiple or bilateral inguinal node
cN3 Fixed inguinal nodal mass or pelvic lymphadenopathy
   
pNx Nodes can’t be assessed
pN0 No regional lymph nodes
pN1 Metastasis in one or two inguinal lymph nodes
pN2 Metastasis in more than two unilateral, or bilateral inguinal nodes
pN3 Extranodal extension in inguinal nodes, or pelvic lymph node mets
   
Mx Distant mets can’t be assessed
M0 No distant mets
M1 Distant mets
   
Gx Grade of differentiation can’t be assessed
G1 Well differentiated
G2 Moderately differentiated
G3 Poorly differentiated
G4 Undifferentiated