Definition / Overview
Skin cancer is the most commonly diagnosed cancer in Australia. The three main types encountered in general practice are:
- Basal cell carcinoma (BCC): most common; arises from basal keratinocytes; low metastatic potential
- Cutaneous squamous cell carcinoma (cSCC): second most common; arises from keratinocytes; higher metastatic potential than BCC; can arise from premalignant lesions
- Melanoma: least common of the three but highest mortality; arises from melanocytes
Premalignant conditions seen in general practice include actinic (solar) keratoses (AKs) and Bowen disease (cSCC in-situ).
The GP is the primary point of triage for the vast majority of skin lesions in Australia. Early detection and appropriate management or referral are core competencies.
Pathophysiology / Risk Factors
Ultraviolet Radiation (UVR) as the Central Driver
- Cumulative UV exposure drives keratinocyte mutations, particularly in TP53, NOTCH1/2, CDKN2A, and NRAS
- Intermittent intense UV exposure (sunburns) is more strongly linked to BCC and melanoma
- Chronic cumulative UV damage has a clearer correlation with cSCC
Shared Risk Factors Across Skin Cancers
| Risk Factor | BCC | cSCC | Melanoma |
|---|---|---|---|
| Fair skin (Fitzpatrick I-II) | ++ | ++ | ++ |
| Chronic UV / outdoor occupation | ++ | +++ | + |
| Sunbed use | + | ++ | ++ |
| Immunosuppression (e.g., organ transplant) | ++ | +++ (65-100x risk) | + |
| Previous skin cancer | ++ | ++ | ++ |
| AKs / Bowen disease | - | +++ | - |
| Family history / genetics | + | + | +++ |
| Older age / male sex | ++ | ++ | + |
Clinical Features and Diagnosis
Actinic Keratoses (AKs)
- Rough, scaly papules or plaques on sun-damaged skin; may be white, yellow, red, or pigmented
- Often easier to palpate than visualise; feel like sandpaper
- Some become hyperkeratotic; cutaneous horns may develop
- Multiple confluent AKs in a sun-damaged field = field cancerisation
- Usually diagnosed clinically and on dermoscopy
- Biopsy indicated if an AK becomes tender, rapidly enlarging, ulcerates, or fails to respond to treatment (to exclude cSCC)
- Malignant transformation of a single AK is rare ($\approx 0.1\%$); however, patients with $\geq 10$ AKs have approximately 10% lifetime risk of developing cSCC
Bowen Disease (cSCC In-Situ)
- Well-defined, erythematous, scaly plaque; can resemble eczema or psoriasis
- Full-thickness epidermal dysplasia without dermal invasion
- May progress to invasive cSCC if untreated
Basal Cell Carcinoma (BCC)
- Nodular (most common): pearly, translucent papule or nodule with rolled borders and telangiectasia; may ulcerate centrally ("rodent ulcer")
- Superficial BCC: erythematous, scaly patch; may resemble eczema; common on trunk
- Morphoeic/sclerosing BCC: flat, scar-like, ill-defined; highest risk of incomplete excision
- Pigmented BCC: may resemble melanoma; blue-grey/brown pigmentation
- Slow-growing; rarely metastasises; but can cause significant local destruction if neglected
Cutaneous Squamous Cell Carcinoma (cSCC)
- Firm, hyperkeratotic nodule or plaque; may ulcerate
- Arising on a background of sun-damaged skin, chronic AKs, or Bowen disease
- Higher-risk features requiring urgent referral:
- Rapidly growing or enlarging
- Diameter $> 2\,\text{cm}$
- Poorly differentiated on histology
- Perineural or lymphovascular invasion
- Located on ear, lip, or within a scar
- Immunocompromised patient
- Recurrent lesion
Melanoma
- Superficial spreading: most common; flat or slightly raised; ABCDE changes
- Nodular: fast-growing, often amelanotic or dark; most dangerous subtype at presentation
- Lentigo maligna / lentigo maligna melanoma: slow-growing macular pigmentation on chronically sun-damaged skin of elderly patients; common on face
- Acral lentiginous: palms, soles, subungual; may occur in people with darker skin tones
ABCDE criteria for clinical assessment:
| Feature | Concern |
|---|---|
| Asymmetry | One half does not mirror the other |
| Border | Irregular, notched, or poorly defined |
| Colour | Multiple shades or uneven colour distribution |
| Diameter | $> 6\,\text{mm}$ (though early melanomas can be smaller) |
| Evolving | Change in size, shape, colour, or new symptom (bleed, itch) |
Investigation and Dermoscopy
Dermoscopy in General Practice
Dermoscopy significantly improves diagnostic accuracy for pigmented lesions. GP registrars should have basic competency:
- Melanocytic vs non-melanocytic: look for melanocytic structures (pigment network, dots, globules, streaks) vs non-melanocytic features (milia-like cysts in seborrhoeic keratoses; leaf-like structures in BCC)
- BCC dermoscopy: arborising telangiectasia, blue-grey ovoid nests, shiny white areas, spoke-wheel structures
- AK dermoscopy: strawberry pattern (red pseudo-network with hair follicle openings); surface scaling
- Melanoma red flags on dermoscopy: atypical pigment network, regression structures (white scar-like areas, blue-grey peppering), irregular dots/globules, atypical vascular pattern
When to Biopsy
- Excision biopsy: preferred for pigmented lesions suspected of melanoma; complete excision with $1\text{-}2\,\text{mm}$ margins
- Shave or punch biopsy: acceptable for BCCs, cSCCs, or when diagnosis uncertain; avoid shave biopsy for suspected melanoma
- Incisional biopsy acceptable only when a lesion is very large and full excision not feasible at initial visit
Management
Actinic Keratoses
Step 1: Photoprotection always - Broad-spectrum SPF 50+ sunscreen, sun-protective clothing, behavioural change - Consistent photoprotection reduces AK burden and risk of cSCC
Step 2: Lesion-directed treatment
| Treatment | Indication / Notes |
|---|---|
| Liquid nitrogen cryotherapy | Single or few lesions; 1-2 freeze-thaw cycles |
| Curettage ± diathermy | Hyperkeratotic AKs |
| Topical 5-fluorouracil (5-FU) | Field therapy; applied bd for 2-4 weeks |
| Topical imiquimod 5% | Field therapy; 3x/week for 4-16 weeks (PBS restricted) |
| Ingenol mebutate | Field therapy; 2-3 day course (now less commonly used) |
| Diclofenac 3% gel | Mild AKs; applied bd for 60-90 days |
| Photodynamic therapy (PDT) | Specialist/dermatologist; good cosmetic outcome for facial AKs |
Combination and sequential therapy is often used for field cancerisation.
Bowen Disease
- Cryotherapy, curettage, topical 5-FU, or imiquimod
- PDT particularly effective for large lesions
- Refer if diagnosis uncertain or lesion on face/genitalia
Basal Cell Carcinoma
Low-risk BCC (small, nodular, well-defined, primary lesion on trunk/limb): - Surgical excision with $3\text{-}5\,\text{mm}$ clinical margins: treatment of choice - Curettage and electrodesiccation: for small, low-risk superficial BCCs - Topical imiquimod or 5-FU: PBS-listed for superficial BCC only; appropriate when surgery is not feasible
Higher-risk BCC (morphoeic, large, facial, recurrent, or in high-risk sites such as H-zone of face): - Mohs micrographic surgery: gold standard for tissue-sparing, highest cure rate; refer to dermatologist or Mohs surgeon - Radiotherapy: elderly patients or those unable to undergo surgery
Advanced / metastatic BCC: - Hedgehog pathway inhibitors (vismodegib, sonidegib): specialist-initiated; PBS-listed for locally advanced or metastatic BCC - Immunotherapy (cemiplimab): when hedgehog inhibitors have failed
After first BCC: approximately 30-50% of patients will develop another keratinocyte cancer within 5 years. Advise regular self-skin checks and ongoing photoprotection.
Cutaneous Squamous Cell Carcinoma
Low-risk cSCC: - Surgical excision with $4\,\text{mm}$ clinical margins for low-risk lesions $< 2\,\text{cm}$ - Pathology review of margins essential
High-risk cSCC (see features above): - Wider excision margins ($6\,\text{mm}$ or more); Mohs surgery for head and neck - Refer to specialist: dermatologist, plastic surgeon, or head and neck surgeon - Consider sentinel lymph node biopsy and/or imaging in high-risk cases - Radiotherapy as adjuvant or for inoperable disease - Cemiplimab (anti-PD-1): PBS-listed for locally advanced or metastatic cSCC not amenable to surgery or radiotherapy (specialist-initiated)
Immunocompromised patients (organ transplant, haematological malignancy): - Increased frequency of skin surveillance (at least 6-monthly) - Lower threshold for biopsy and treatment - Refer to dermatologist for co-management
Melanoma
Confirmed or suspected melanoma on biopsy:
- Do not perform staged excision in general practice without histological confirmation
- Once confirmed on excision biopsy, re-excise with definitive margins based on Breslow thickness:
| Breslow Thickness | Recommended Excision Margin |
|---|---|
| In-situ | $5\,\text{mm}$ |
| $\leq 1\,\text{mm}$ | $1\,\text{cm}$ |
| $1.01\text{-}2\,\text{mm}$ | $1\text{-}2\,\text{cm}$ |
| $> 2\,\text{mm}$ | $2\,\text{cm}$ |
- Refer all invasive melanoma to a specialist (dermatologist, plastic surgeon, or melanoma multidisciplinary team)
- Sentinel lymph node biopsy: considered for Breslow $> 0.8\,\text{mm}$ or with high-risk features; specialist decision
- Staging imaging (CT or PET-CT): for Stage III/IV disease
- Adjuvant therapy (immunotherapy: nivolumab, pembrolizumab; targeted therapy: BRAF/MEK inhibitors for BRAF-mutant melanoma): oncologist-initiated, PBS-listed
Complications and Special Considerations
Field Cancerisation
- Multiple AKs on a background of chronic UV damage represent a "field" at high risk
- Treat the field, not just individual lesions
- Patients with field cancerisation require ongoing surveillance: 6-12 monthly skin checks in general practice
Immunosuppressed Patients
- Organ transplant recipients: cSCC risk is 65-100 times that of the general population; BCC risk is also markedly elevated
- Consider referral to dermatology for formal surveillance program
- Advise about strict photoprotection from time of transplantation
Perineural Invasion and Recurrence
- Perineural invasion in cSCC or BCC indicates high-risk disease
- Requires specialist management; adjuvant radiotherapy often considered
Psychological Impact
- Diagnosis of skin cancer, particularly melanoma, carries significant psychological burden
- Consider GP Mental Health Treatment Plan (MBS item 2715) for patients with adjustment disorder or anxiety following diagnosis
Long-Term Care, Surveillance, and Prevention in General Practice
Surveillance After Treatment
| Skin Cancer Type | Recommended GP Follow-up |
|---|---|
| AKs (multiple) | 6-12 monthly skin checks |
| BCC (first) | 6-monthly for 2 years, then annually |
| cSCC (low-risk) | 6-monthly for 2 years, then annually |
| cSCC (high-risk) or melanoma | Specialist-led; GP co-management |
MBS Items Relevant to Skin Cancer in General Practice
- MBS Item 31355: Excision of skin lesion and repair (varies by size and site)
- MBS Item 30071 / 30072: Skin lesion destruction (cryotherapy, curettage)
- GP Management Plan (Item 721) / Team Care Arrangement (Item 723): consider for patients with complex needs, including immunocompromised patients with multiple skin cancers requiring allied health input (e.g., wound care nurses, lymphoedema physiotherapy)
- 75+ Health Assessment (Item 703): opportunistic skin check as part of the annual health assessment for older patients, who carry the highest burden of AKs, BCC, and cSCC
Prevention and Patient Education
- Broad-spectrum SPF 50+ sunscreen applied daily (not just beach days)
- Sun-protective clothing: UPF 50+ where possible
- Avoid peak UV hours (10 am-2 pm standard time)
- No sunbed use
- Regular self-skin examination monthly; know what is new or changing
- Educate patients that after one skin cancer, risk of another is significantly elevated
Aboriginal and Torres Strait Islander Health
- Skin cancer incidence is lower in Aboriginal and Torres Strait Islander people due to higher melanin content providing some UV protection; however, skin cancers do occur and may present at more advanced stages
- Acral lentiginous melanoma may occur on palms, soles, and subungual areas and can be missed
- Ensure culturally safe skin examination; consider gender concordance for full skin checks
- Close the Gap PBS co-payment scheme supports access to treatments including topical therapies
Key Red Flags Requiring Urgent Referral
- Any lesion suspicious for melanoma
- Rapidly enlarging, ulcerated, or bleeding lesion
- cSCC in immunocompromised patient
- High-risk cSCC features (size $> 2\,\text{cm}$, perineural invasion, ear/lip location)
- Any lesion where the GP is uncertain of the diagnosis and biopsy is not immediately feasible