Approach to Carcinoma Penis 2
Carcinoma Penis
Author
Deepak K Thakur, Ms, MCh (Urology)
Contents
Relevant anatomy
History
Examination
Investigations
Staging
Decision making
Treatment options
Outcome
Follow up
Relevant Anatomy
Penile Anatomy:
Superficial and deep dorsal vein
Dorsal artery
Fascicles of dorsal nerve
Skin and superficial (dartos) fascia
Deep (Buck) fascia
Subtunical space
Cavernosal artery
Erectile tissue
Tunica albuginea: outer longitudinal layer, inner circular layer, corpus spongiosum
Vascular Supply
Arteries:
Internal pudendal artery
Cavernous artery
Bulbourethral artery
Circumflex artery
Dorsal artery
Veins:
Deep dorsal vein
Circumflex vein
Periprostatic vein
Internal pudendal vein
External iliac vein
Cavernous vein
Bulbar vein
Subtunical venous plexus
Lymphatic Drainage
Lymphatics of the prepuce and skin = superficial inguinal nodes
Lymphatics of the glans and corporeal bodies = superficial nodes
Drainage pathway: superficial nodes > deep inguinal nodes > pelvic nodes (external, internal iliac, and obturator nodes)
Multiple cross-connections exist leading to bilateral drainage to both inguinal areas
Risk Factors
Phimosis
Chronic penile inflammations:
Balanoposthitis
Lichen sclerosus
Human Papillomavirus (HPV) types 16 & 18
UV-A therapy
Multiple sexual partners
Smoking
Poor hygiene
Low socioeconomic status
Pathology
Premalignant Conditions
~1/3 malignancy risk
Conditions include:
Intraepithelial neoplasia grade III
Giant condylomata (Buschke-Löwenstein)
Erythroplasia of Queyrat
Bowen’s disease
Paget’s disease (intradermal adenocarcinoma)
Presentation
Commonly affects elderly males
Typical presenting symptom: lesion on the penis
Associated symptoms:
Bleeding
Weakness
Weight loss
Fatigue
Systemic malaise due to chronicity
Lesion Characteristics
May appear as:
Shallow erosion
Deeply excavated ulcer with elevated or rolled-in edges
Phimosis may obscure lesions
Symptoms: erosion through the prepuce, foul odor, and discharge with or without bleeding
Tumor Distribution
Common locations for tumors:
Glans (48%)
Prepuce (21%)
Coronal sulcus (6%)
Shaft (<2%)
Assessment of:
Size
Location
Fixation
Involvement of corporeal bodies
Clinical Examination
Inspect base of penis and scrotum for extension
Rectal and bimanual examination to assess perineal involvement and pelvic mass
Extensive bilateral inguinal palpation for adenopathy is crucial
Diagnosis
Delay in Medical Care: 15% to 50% of patients seek care after a year or more
Requirements before therapy:
Confirmation of diagnosis
Assessment of invasion and histologic grade
Biopsy Procedures: May be separate from definitive treatment; a dorsal slit may be necessary
Diagnosis Indicators: Anemia, leucocytosis, hypoalbuminemia, azotemia, hypercalcemia
Node Assessment
Techniques:
Fine needle aspiration cytology
Sentinel lymph node biopsy
Dynamic sentinel node biopsy
Superficial & modified complete inguinal dissection
Radiological Assessment
Methods:
Penile Ultrasound (USG)
Contrast-enhanced CT (CECT)
MRI
Lymphotropic nanoparticle-enhanced MRI (LNMRI)
FDG-PET/CT
Sensitivity of Diagnostic Methods
FNAC: 93% for palpable nodes; 71% for non-palatable nodes
DSNB: Lower morbidity; sensitivity of 82%, false-negative rate of 18%
Surgical Approaches
Superficial & modified inguinal dissection: Effective in identifying microscopic metastases in clinically normal inguinal findings
Imaging Techniques
USG: Detects 100% of corpus cavernosum invasion; inaccurate in 26% of physical exams
MRI: Sensitive in detecting corporal invasion
LNMRI: Highly sensitive for micrometastasis; effective for nodes <1 cm
Minimal Diagnostic Criteria
Primary Tumor (T): Clinical examination, incisional/excisional biopsy for grade and invasion assessment
Regional Lymph Nodes (N): Clinical examination, CT for palpable adenopathy, superficial inguinal node dissection as indicated
Distant Metastases (M): Clinical examination, chest radiographs, biochemical determinations, MRI, and bone scans
AJCC Staging of Penile Cancer
Primary Tumor (T)
TX, TO, Tis, Ta, T1a, T1b, T2, T3, T4
Lymph Nodes (N)
NX, PNX, NO, N1, N2, N3, pN3
Distant Metastasis (M)
M0, M1
Stage Grouping
Stage 0: Tis, Ta, N0, M0
Stage I: T1a, N0, M0
Stage II: T1b, T2, N0, M0; T3, N0, M0
Stage IIIa: T1-3, N1, M0
Stage IIIb: T1-3, N2, M0
Stage IV: T4, Any N, M0; Any T, N3, M0; Any T, Any N, M1
Treatment Options
Primary Tumor Treatment
Organ-preserving measures
Limited excision strategies:
Topical therapy (5-fluorouracil for Tis)
Mohs micrographic surgery
Laser ablation
Penile amputation
Radiation therapy
Mohs Micrographic Surgery
Layer-by-layer excision with microscopic examination; relevant for CIS & small tumors
Laser Ablation
CO2, argon, Nd:YAG, and KTP lasers; effectively treats T1 tumors
Recurrence rates variable; recurrences require wide local excision or partial amputation
Penile Amputation
Indicated for deeply invasive or high-grade tumors; tumors >4 cm, grade 3 lesions, or invading structures
Treatment of Inguinal Metastasis
Presence and extent of metastasis crucial for prognosis
Lymphadenectomy can be curative for many cases
Risk Assessment for Nodes
Palpable nodes: indication for intervention
Non-palpable nodes categorized into risk groups:
Low risk: CIS, Ta
Intermediate risk: T1, grade 1 and 2
High risk: pT2
Low & Intermediate Risk Group Protocol
Physical examination of lymphatics, observation, antibiotics if needed, further testing as indicated
High-Risk Group Protocol
Surgical approaches more aggressive, including bilateral dissection, FNAC, and imaging studies
Treatment for Metastatic Disease
Strategies depend on the presence and mobility of nodal metastases; might involve:
Induction chemotherapy
Surgical resection if responsive
Palliative options if progressive
Radiation Therapy
Types:
External beam radiation therapy (EBRT)
Brachytherapy
Prior circumcision often necessary before treatment
Efficacy of EBRT
60 Gy to 74 Gy delivered over 5 to 7.5 weeks
Local control rates: 45-70%, preservation rates: 50-65%
Efficacy of Brachytherapy
Isotopes like radium-226 and iridium-192; superior local control rates of 70% to 87%
Chemotherapy
Indications: advanced, recurrent disease
Single agent (Cisplatin, Bleomycin, Methotrexate) and combination therapies
Efficacy rates from studies demonstrate variable response
Follow-up Protocol
For low-risk group: Annual follow-ups; shorter intervals initially
For high-risk group: More frequent assessments and imaging as required.