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Explore incidence, mortality, types, risk factors, staging, biopsy techniques, workup labs, and prognostic markers of melanoma. Understand the challenges and management strategies in treating this aggressive skin cancer.
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Melanoma By Dr Abeer Elsayed Aly Lecturer of medical oncology SECI 19/03/2013
Melanoma Incidence and Mortality • Incidence (US) • 59,580 new cases • 33,580 new male cases • 26,000 new female cases • 12 per 100,000 population • Mortality (US) • 7,770 total • 4,910 males • 2,860 females American Cancer Society,Cancer Facts and Figures. 2005.
Melanoma: risk factors • Constitutional predisposition • Fair skin/hair color/ freckling • Burn vs tan • >20 benign nevi (moles) or >3 atypical nevi • Family history of dysplastic nevi • Increasing age • Immunosuppression • Xeroderma pigmentosum • H/O solar keratosis, squamous cell carcinoma
Melanoma: risk factors • Risk behaviors • >3 sunburns • Episodic excessive sunlight exposure • Long term continuous sunlight exposure • UV exposure at tanning salons
Melanoma The challenge (historically): • Early detection • Rapid growth/high proliferation rate • Chemotherapy resistant • Radiation resistant • Short anticipated survival
Types of Melanoma • Acral lentiginous • Mucosal melanoma • Superfical spreading melanoma • Lentigo maligna melanoma • Nodular melanoma
Superficial spreading • most common head and neck, 50% • 4th to 5th decade • clinical mixture of brown/tan, pink/white irregular borders, biphasic growth • irregular nests in epidermis • underlying lymphoid infiltrate • enlarged nests and single cells in all epidermal layers
Lentigo maligna • 20% of head and neck • longest radial growth phase >15 yrs • elderly sun exposed areas • clinical dark, irregular ink spot • contiguous lintiginous proliferation, dyshesive, variable shape, atrophic epidermis, infundibular basal cell layer of hair follicles
Nodular melanoma • 30% of head and neck • 5th decade • aggressive monophasic growth • sun-exposed and nonexposed areas • well circumscribed blue/black or nodular with involution in irregular plaque • downward tumorigenic growth, expand papillary dermis into reticular dermis
Mucosal melanoma • 8% head and neck • histologic staging little use • local control predicts survival • neck dissection for clinical N+ • XRT for histo N+ • adjuvant interferon alpha 2-b
Biopsy techniques Excisional biopsy 1-3 mm margins avoid wider margins (accurate lymphatic mapping) Full thickness incisional/punch biopsy for large lesions lesions of the palms, soles, digits, face, ears Deep shave biopsies When suspicion for melanoma is low NCCN Guidelines 2005
Clark staging • Based upon histologic level of invasion • Level I – Epidermis only (in situ) • Level II – Invades the papillary dermis, but not to the papillary-reticular interface • Level III – Invades to the papillary-reticular interface, but not into the reticular dermis • Level IV – Into the reticular dermis • Level V – Into subcutaneous tissue
Breslow staging • Based upon absolute depth of invasion • Stage I – < 0.75 mm • Stage II – 0.76 – 1.5 mm • Stage III – 1.51 – 4.0 mm • Stage IV - > 4.0 mm
Work up Labs LDH Radiology CXR Possible CT for metastasis Possible CT abdomen, MRI brain Possible Lymphoscintigraphy Excision 2 cm margins Adjunctive Therapy Possible elective neck dissection Possible sentinel lymph node biopsy Possible elective radiation
Prognostic indicators Thickness (Breslow depth) Nodal status Ulceration Mitosis Satellite lesions In transit lesions
Prognostic indicators Thickness (Breslow depth) Nodal status Ulceration Mitosis Satellite lesions In transit lesions
Prognostic indicators Thickness (Breslow depth) Nodal status Ulceration Mitosis Satellite lesions In transit lesions
Prognostic Indicators: Nodal status OS for patients with 1 positive sentinel node is 60% at 5 years OS for patients with a single palpable node is 40% at 5 years Gershenwald et al, 2001
Prognostic indicators Thickness (Breslow depth) Nodal status Ulceration Mitosis Satellite lesions In transit lesions
Mitotic Index N = 3661 from the Sydney Melanoma Database Correlated clinical information (survival) primary tumor thickness (Breslow depth) ulcerative state (infiltrative, attenuative, and traumatic) tumor mitotic rate (TMR) (at the invading front, deep border) Conclusion: TMR is a more powerful prognostic indicator than ulceration in patients with primary cutaneous melanoma Azzola et al, Cancer 2003
Prognostic indicators Thickness (Breslow depth) Nodal status Ulceration Mitosis Satellite lesions In transit lesions
Risk of In-Transit Metastasis In- transit metastasis Cutaneous / subcutaneous tissue Between the primary tumor and the draining lymph node basin 5 yr survival rates: 12% - 37% Risk factors: Thicker primary Lower extremity Regional LN metastasis
Other prognostic factors: LDH Elevated levels correlate with: Early recurrence Shorter survival (Newcki et al, 2008) Serum S100 level Early studies suggest: Shorter survival Early distant relapse Poorer response to treatment (Smith et al, 2008) Microvessel Density
Other prognostic factors: LDH Elevated levels correlate with: Early recurrence Shorter survival (Newcki et al, 2008) Serum S100 level Early studies suggest: Shorter survival Early distant relapse Poorer response to treatment (Smith et al, 2008) Microvessel Density
Other prognostic factors: LDH Elevated levels correlate with: Early recurrence Shorter survival (Newcki et al, 2008) Serum S100 level Early studies suggest: Shorter survival Early distant relapse Poorer response to treatment (Smith et al, 2008) Microvessel Density