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Management of Groin in Cancer of the Penis

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Title: Management of Groin in Cancer of the Penis


1
Management of Groin in Cancer of the Penis
  • Hemant B. Tongaonkar
  • Professor Head Urologic
    Oncology Services Tata Memorial
    Hospital, Mumbai

2
Penile Cancer
  • Presence and extent of inguinal nodal metastases
  • most important prognostic factor for survival

3
Penile Cancer
  • Prolonged locoregional phase before mets occur
  • Superficial inguinal LN most frequent site of
    lymphatic mets
  • LN involvement generally stepwise
  • LN mets beyond pelvis considered distant
  • Lymphadenectomy can be curative need not be
    treated as systemic disease

4
Penile cancerProblems in management of groin
  • LN mets single most imp prognostic parameter
  • 10-20 have occult LN mets in patients with
    clinically negative groin
  • 50 of patients with palpable groin nodes do not
    have metastasis
  • Clinical prediction of nodal spread unreliable
    inaccurate

5
Penile CancerAssessment of groin
  • Clinical examination
  • Lymphangiography
  • High resolution USG with FNAC
  • Fine needle aspiration cytology
  • Sentinel node biopsy with patent blue dye or
    lymphoscintigraphy
  • Histological evaluation at surgery is the Gold
    Standard

6
Penile Cancer Management of Groin NodesCrucial
questions
  • Predictors of lymph node mets
  • Indications for lymphadenectomy
  • Prophylactic vs therapeutic
  • Extent of lymphadenectomy
    Superficial vs deep inguinal
    Inguinal or inguinopelvic
    Unilateral vs bilateral

No prospective or randomized trials
7
Inguinopelvic LymphadenectomyGood Prognostic
Factors
  • Minimal nodal disease (2 or less nodes)
  • Unilateral involvement
  • No extranodal extension
  • Absence of pelvic node metastases

8
Penile Cancer
  • Lymphadenectomy is indicated in patients with
    palpable inguinal lymphadenopathy that persists
    after treatment of the primary penile lesion
    following a course of antibiotic therapy
  • Srinivas 1987, Ornellas 1994

9
Penile CancerManagement of No groin
  • Early prophylactic lymphadenectomy
  • Versus
  • Surveillance (delayed lymphadenectomy)

10
Penile CancerEarly Prophylactic Lymphadenectomy
for N0 Groin
  • Cure rate may be as high as 80
  • Lymph node metastases in nearly 30
  • Reluctance due to substantial morbidity
  • Less likely in prophylactic setting
  • Modified extent of dissection
  • Better surgical technique
  • Preservation of dermis, scarpas fascia
    saphenous veins
  • Myocutaneous flap coverage

11
Early vs Delayed LymphadenectomyEarly better
  • Baker 1976 (n37) 59 vs 61
  • McDougal 1986 (n23) 83 vs 36 (66 in patients
    with N1 with GND)
  • Fraley 1989, Johnson Lo 1984, Lynch 1997,
    Ornellas 1999
  • Delayed LND unable to salvage relapses (Fossa
    1987, Fraley 1989, Johnson 1984, Ravi 1993,
    Srinivas 1987)

Early prophylactic better than delayed
therapeutic Window of opportunity Reluctance
due to morbidity
12
Early vs Delayed LymphadenectomyNo difference
  • Ravi 1993 (n371) 100 vs. 76 (NS)
  • Probably due to
  • Patient selection
  • Strict follow up
  • Aggressive treatment at relapse

Can delayed therapeutic dissection reliably
Effectively salvage inguinal recurrences?
13
N0 Groin Treatment Options
  • Fine needle aspiration cytology
  • Isolated node biopsy
  • Sentinel node biopsy
  • Extended sentinel LN dissection
  • Intraoperative lymphatic mapping
  • Superficial dissection
  • Modified complete dissection
  • Is there a role for Spiral CT or PET scan?

14
Fine needle aspiration cytology
  • Requires pedal / penile lymphangiograhy for node
    localization aspiration under fluoroscopy
    guidance
  • Multiple nodes to be sampled
  • Sensitivity 71 (Scappini 1986, Horenblas 1993)
  • Can provide useful information to plan therapy
    when ve

15
Sentinel Node Biopsy
  • Based on penile lymphangiographic studies of
    Cabanas (1977)
  • Accuracy questioned False ve 1050 (Cabanas
    1977, McDougal 1986, Fossa 1987)
  • Extended sentinel node biopsy 25 false ve
  • False ve due to anatomic variation in position
    of sentinel node
  • Unreliable method Not recommended

16
Intraoperative Lymphatic Mapping
  • Potential for precise localization of sentinel
    node
  • Intradermal inj of vital blue dye or Tc- labeled
    colloid adjacent to the lesion
  • Horenblas 11/55 All ve False ve in 3
  • Pettaway 3/20 All ve No false ve
  • Tanis (2002) 18/23 ve detected (Sensitivity
    78)
  • Promising technique for early localization of
    nodal metastases
  • Long-term data needed

17
Superficial Inguinal LND
  • Removal of nodes superficial to fascia lata
  • If nodes ve on FS Complete inguino-pelvic LND
  • Rationale No spread to deep inguinal nodes when
    superficial nodes ve (Pompeo 1995, Parra 1996)
  • No clinical evidence of direct deep node mets
    when corporal invasion present

18
Complete Modified LND(Catalona 1988)
  • Smaller incision
  • Limited inguinal dissection (superficial fossa
    ovalis)
  • Preservation of saphenous vein
  • Thicker skin flaps
  • No sartorius transposition

Identifies microscopic mets without morbidity
(Colberg 1997, Parra 1996)
19
Limited Inguinal LND Advantages
  • Provides more information than does biopsy of a
    single node or group of nodes
  • Avoids missing the sentinel node by removing all
    potential first echelon nodes
  • Spares patients the morbid consequences
    associated with traditional LND
  • Can be performed by any surgeon

20
Penile CancerPredictors of lymph node metastases
  • Tumour histology
  • Corporal invasion
  • Urethral involvement
  • Tumour grade
  • Lymphatic vascular invasion
  • DNA ploidy

21
Penile CancerLN mets in stage T1 G1-2 cancers
Author Stage/Grade N LN mets
Fraley T1G1 19 1 (5.2)
Theodorescu T1G1 8 2 (25)
Solsona T1G1-2 23 1 (4.3)
McDougal T1G1-2 24 1 (4)
Heyns T1G1-2 91 5 (6)
Solsona T1G1 17 1 (6)
Total 182 11 (6)
22
Penile CancerCorporal Invasion vs. LN Mets
Author N ve nodes
McDougal 23 11 (48)
Fraley 29 26 (90)
Theodorescu 18 12 (67)
Villavicencio 37 14 (38)
Lopes 44 28 (64)
Heyns 32 15 (47)
Solsona 42 27 (64)
Total 225 133 (59)
23
Penile CancerRisk Grouping for Inguinal Nodal
Metastases
  • Low risk
  • Tis / Ta
  • T1 Grade I-II
  • No vascular invasion
  • lt10 LN mets
  • Surveillance
  • High risk
  • T2-T3
  • Grade III
  • Vascular invasion
  • Non-compliance
  • gt50 LN mets
  • Early lymphadenectomy

24
Penile Cancer N0 High Risk GroupGoals of
Treatment
  • To determine whether occult metastases exist in
    inguinal nodes
  • To maximise detection treatment for those with
    proven nodal metastases
  • To limit treatment morbidity in those with
    histologically negative nodes

25
Management High risk patients
  • Bilateral N0 groin
  • Bilateral superficial or modified inguinal LND
  • Node -ve Unilat ve Bilat ve
  • Conclude Unilat inguino- Bilat inguino-
  • pelvic LND pelvic LND

26
Cancer PenisManagement of N groin
  • Surgical treatment recommended for operable
    inguinal metastatic disease
  • Most patients with inguinal LN mets will die if
    untreated.
  • 20-67 patients with metastatic inguinal LN
    disease free 5 years after LND. Better survival
    82-88 with single / limited mets

27
Resectable Inguinal Lymphadenopathy
  • Complete inguinopelvic lymphadenectomy
  • Therapeutic value justifies morbidity
  • Goals
  • To eradicate all cancer
  • To cover the vasculature
  • To ensure rapid wound healing

28
LymphadenectomyUnilateral vs. Bilateral
  • Anatomic crossover well-established bilateral
    drainage a rule (Lymphangiography IOLM studies)
  • Synchronous Contralateral nodes in 50
    (Ekstrom 58) Bilateral LND must
    Contralateral side Superficial
    FS
  • Metachronous Unilateral may be justified if
    RFS gt12 mo

29
Should pelvic lymphadenectomy be performed in
patients with positive inguinal nodes?
  • Pelvic LN mets related to inguinal LN mets (Ravi
    1993, Srinivas 1987, Kamat 1993)
  • Inguinal nodes Pelvic nodes
  • -ve -ve
  • 1-3 ve 22
  • gt3 ve 57
  • Although overall survival 10, occasional
  • long-term survivals reported

30
Pelvic Lymphadenectomy
  • Staging tool
  • Identifies patients likely to benefit from
    adjuvant chemo
  • Adds to locoregional control
  • No additional morbidity
  • If pre-op pelvic node identified NACT followed
    by surgery in responders
  • Value of pelvic LND unproven
  • Patients with minimal inguinal disease limited
    pelvic LN mets may benefit

31
Inguinopelvic LymphadenectomyPathologic criteria
for long-term survival
  • Minimal nodal metastases (upto 2)
  • Unilateral involvement
  • No extranodal extension
  • Absence of pelvic node metastases

80 five year survival
32
Penile CancerPelvic LN Mets vs. Survival
Author Pts with ve LN 5 yr survival
Dekernion 2 1 (50)
Horenblas 2 0
Srinivas 11 0
Pow-Sang 3 2 (66)
Kamat 6 2 (33)
Ravi 30 0
Total 54 5 (10)
33
Cancer PenisSubstratification of LN vs survival
  • Survival with metastatic inguinal LN 20-25
  • Survival related to
    - No. of metastatic nodes
    - Bilaterality
    - Level of metastatic nodes
    - Perinodal extension
  • (Srinivas 1989, Tongaonkar 1992)

34
Inguinopelvic LymphadenectomyIndications for
adjuvant therapy
  • gt2 metastatic inguinal nodes
  • Extranodal extension of disease
  • Pelvic lymph node metastases

35
Penile CancerManagement of fixed nodes
  • Neoadjuvant chemo surgery in responders
  • Palliative chemotherapy
  • Chemotherapy radiation therapy

36
Complications of lymphadenectomy
  • Persistent lymphorrhoea
  • Wound breakdown, necrosis, infection
  • Lymphocyst
  • Femoral blowout
  • Lymphangitis
  • Lymphoedema of lower extremity

37
Cancer PenisMeasures to reduce morbidity of GND
  • Choice of incision
  • Downscaling of template
  • Saphenous vein sparing
  • Reconstructive techniques
  • Lymphovenous shunts

38
Tensor fascia lata myocutaneous flap
39
Measures to reduce morbidity of GNDTMH
experience (n 100)
  • Elective excision of skin overlying the lymph
    node area
  • Reconstruction with TFL or anterolateral thigh
    flap
  • Significant reduction in early late morbidity
  • ? Improved disease control

40
Penile Cancer Conclusions
  • Uncommon disease
  • No systematic study complete absence of RCTs
  • Small no of patients over a long time
  • Poor decision making, treatment delays, poor
    compliance to treatment follow up
  • RCTs to develop guidelines essential
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