Skin cancer - Melanoma, basal and squamous cell carcinoma
Common and specific risk factors
| Risk factor | Mechanism and context | Type of cancer concerned |
|---|---|---|
| Chronic UV exposure (sun) | UVB (290-320 nm) induces characteristic C→T mutations on the dipyrimidine bases of keratinocyte and melanocyte DNA - dominant UV mutational signature in all skin cancers; cumulative exposure over a lifetime → BCC and CSC; episodes of intense sunburn (especially in childhood and adolescence) → melanoma | BCC, CSC, melanoma |
| Tanning booths (artificial UV) | High-intensity UVA (320-400 nm) - melanoma risk increased by 75 % if first used before age 35 (Boniol 2012 meta-analysis); banned for minors in Quebec since 2012 (Public Health Act) | Melanoma, BCC, CSC |
| Phototype I-II (fair skin) | Low production of protective melanin (eumelanin) → increased sensitivity to UV; redheads, blonds, blue or green eyes, freckles, skin that burns easily without tanning - risk 10 to 20 times greater than phototypes V-VI | BCC, CSC, melanoma |
| Multiple and atypical nevi | > 50 common nevi → 5-fold increased risk of melanoma; dysplastic (atypical) nevi → 10- to 20-fold increased risk; multiple atypical nevi syndrome (MANS) → 10-fold increased lifetime risk compared to general population | Melanoma |
| Personal or family history of melanoma | Personal history → risk of second melanoma ×8; 1st-degree family history → risk ×2-3; CDKN2A (p16) mutations - tumor suppressor gene - in 25-40 % of familial melanomas; CDK4, BAP1, TERT mutations | Melanoma |
| Immunodepression | Transplant recipients (chronic immunosuppression) → risk of BCC ×10, CSC ×65-250 (especially on precancerous lesion), melanoma ×3; advanced HIV; chronic lymphocytic leukemia; prolonged immunosuppressive treatments | CSC +++, BCC, melanoma |
| Occupational and environmental exposure | Inorganic arsenic (contaminated water, old pesticides, wood treatment) → CSC and arsenical keratoses; ionizing radiation (old radiotherapy, radiologist) → CSC in the irradiated field (20-30 years delay); mineral oils, coal tar, soot (chimney sweeps - first occupational cancer described by Percival Pott 1775) | CSC, CBC |
| Chronic precancerous skin lesions | Actinic keratosis (precancerous lesion of CSC - risk of transformation 1-10 % per year); chronic ulcer, burn scar (Marjolin's carcinoma); genital lichen sclerosus; HPV (mucosal and nail carcinomas) | CSC |
Basal cell carcinoma (BCC)
- Epidemiology and location: most common cancer in humans - 75-80 % of skin cancers; located in 85 % of cases on the face and neck (sun-exposed areas); nose (one-third of BCCs), cheeks, forehead, eyelids, peri-auricular region; occurs mainly between the ages of 50 and 80; very rarely metastatic (< 0.1 %) but locally destructive if neglected (ulceration of soft tissue and bone - «ulcus rodens»).
- Clinical forms: nodular BCC (most frequent form - 60 %): translucent pearly papule with rolled edges, telangiectatic vessels visible on surface, center may ulcerate (ulcero-nodular BCC); superficial BCC (20 %): slightly scaly erythematous plaque, fine pearly edges, trunk and limbs - often multifocal; sclerodermiform BCC (morpheiform - 10 %): ill-defined, pearly-white, indurated plaque, highly infiltrative, histological margins difficult to define - form at high risk of recurrence; pigmented BCC: pigmented variant of nodular - differential diagnosis with melanoma (presence of characteristic pearly margins).
- Diagnosis: clinical + dermoscopy (maple leaf structures, egg nests, tree-like telangiectasias, structured white-grey areas); confirmatory skin biopsy before treatment; MRI if there is any doubt about deep invasion (recurrent scleroderma forms).
- Treatment : surgical excision with safety margins (4-6 mm for low-risk forms, 3-5 mm for high-risk forms) - reference treatment with cure rate > 95 %; Mohs surgery (controlled micrography) - for high-risk forms (scleroderma, recurrent, high-risk location - nose, eyelids, lips, ears) - histological margins controlled intraoperatively, recurrence rate < 1 % ; topical treatment (vismodegib - hedgehog inhibitor - for advanced or metastatic unresectable BCCs); topical imiquimod and topical 5-FU for superficial BCCs; cryotherapy and curettage-electrocoagulation for small, low-risk superficial lesions.
Squamous cell carcinoma (SCC)
- Epidemiology and localization: 15-20 % of skin cancers; metastatic risk significantly higher than BCC (1-5 % on average, up to 30-40 % for high-risk forms - lip, ear, scar, immunocompromised); localized mainly on photo-exposed areas (lower lip, auricle, dorsum of hands, forearms, scalp of bald men) and on mucous membranes (lips, tongue, genitals - often associated with HPV).
- Forms and clinical presentation : keratotic, crusty, indurated, irregular-edged skin lesion, which may ulcerate - often against a background of sun-damaged skin (dermatoheliosis) or advanced actinic keratosis ; may take on the appearance of an indurated plaque, a chronic non-healing ulcer, or a budding lesion bleeding easily on contact; in situ form (Bowen's disease) - well-defined erythematous scaly plaque without invasion of the dermis - risk of invasive transformation 3-5 % per year
- High-risk criteria (unfavorable prognostic factors): thickness > 2 mm (adapted Breslow) or Clark level IV-V; peri-neuronal or vascular invasion; ear, lip, genitalia, scar localization; poorly differentiated histological grade (grade 3-4); size > 2 cm; immunodepression; recurrence.
- Treatment : surgical excision with safety margins (4-10 mm depending on risk) - reference treatment; Mohs surgery for high-risk forms in functional or aesthetic areas; sentinel node biopsy if high-risk factors; curettage-electrocoagulation for low-risk in situ forms; cryotherapy for multiple actinic keratoses (primary prevention); imiquimod, topical 5-FU or diclofenac 3 gel % for actinic keratoses; systemic chemotherapy (cisplatin ± 5-FU) or cetuxumab (anti-EGFR) for metastatic or unresectable forms; cemiplimab (anti-PD-1, Libtayo) - approved for advanced cutaneous SCC (2018) - objective response rate 47 %
Malignant melanoma
- Clinical forms : melanoma with superficial extension (SSM - 70 %) - flat polychromatic lesion with radial growth at first, then late vertical invasion; nodular melanoma (NM - 15 %) - vertical growth from the start, poorer prognosis because often thick at diagnosis ; Dubreuilh melanoma (lentigo maligna melanoma - 10 %) - elderly subject, face, slow horizontal growth on pre-existing lentigo maligna; acral lentiginous melanoma (ALM - 2-5 %) - palms, soles, under the nails (subungual) - more frequent in dark-skinned subjects, where it is the most common melanoma.
- ABCDE rule for early detection: A = Asymmetry (one half different from the other); B = Irregular, ill-defined, notched or polycyclic edges; C = Multiple colors in the same lesion (beige, brown, black, red, white, blue) - chromatic heterogeneity; D = Diameter > 6 mm (size of a pencil eraser) - caution: melanomas can be small; E = Evolution - any skin lesion that changes size, shape, color, bleeds or itches should be shown to a doctor; criterion E is the most sensitive and the most important - an evolving lesion justifies a consultation even if the other criteria are not present
- Ugly duckling sign: any lesion that stands out from a patient's other nevi - larger, darker, more irregular - merits evaluation independently of ABCDE criteria; some nodular melanomas are symmetrical and monochrome (amelanotic melanoma - pink or flesh) and escape the ABCDE rule.
- TNM staging (AJCC 8th edition 2017): T = Breslow thickness (mm) and ulceration; N = nodes; M = distant metastases; stage T1a ( 97 % at 5 years; stage IV (M1c - visceral metastases) - median survival 6-9 months without treatment, 12-24 months with immunotherapy, 36-48 months with anti-BRAF/MEK (BRAF-mutated) targeted therapies.
- Molecular alterations and biomarkers : BRAF V600E mutation - present in 40-50 % of cutaneous melanomas (50 % V600E, 10-15 % V600K, 5-6 % V600R) - therapeutic target of BRAF/MEK inhibitors; NRAS mutation (15-25 %) - no approved targeted therapy but slightly better prognosis with immunotherapy; KIT mutation (5-10 % - acral and mucosal melanomas) - imatinib possible; CCND1 amplification; uveal melanomas (eye) - GNAQ/GNA11 mutations, highly resistant to treatment
Melanoma treatment by stage
| Stadium | Recommended treatment |
|---|---|
| Stage 0 (in situ) | Surgical excision with 0.5-1 cm margins - cured in 99 % of cases |
| Stage I-II (localized) | Wide excision with margins of 1 cm (T1) to 2 cm (T2-T4) depending on Breslow thickness; sentinel node biopsy recommended if Breslow ≥ 0.8 mm or ulceration (stage T1b and beyond) - major prognostic information and guides adjuvant treatment; no adjuvant systemic treatment if sentinel node negative (stage IIA-B according to AJCC 8e) |
| Stage III (lymph nodes affected) | Wide excision + lymph node dissection if sentinel node positive (debated); 12-month systemic adjuvant therapy: pembrolizumab (anti-PD-1, KEYNOTE-054) or nivolumab (CheckMate-238) - recurrence risk reduced by 40-50 %; if BRAF V600E/K mutated: dabrafenib + trametinib (COMBI-AD) - reduced risk of recurrence by 53 %; 5-year survival: 60-75 % depending on substage |
| Stage IV (metastatic) - BRAF-mutated | Anti-BRAF + anti-MEK targeted therapies: vemurafenib + cobimetinib (coBRIM) or dabrafenib + trametinib (COMBI-d/v) or encorafenib + binimetinib (COLUMBUS) - response rate 65-70 %, median survival 24-30 months; or combined immunotherapy as first-line therapy depending on profile and preference (see below). |
| Stage IV (metastatic) - any BRAF status | Combined immunotherapy ipilimumab (anti-CTLA-4) + nivolumab (anti-PD-1) - CheckMate-067 - response rate 58 %, 5-year survival 52 % (historical), 6.5-year survival 49 %; pembrolizumab monotherapy - KEYNOTE-006 - 5-year survival 35 %; nivolumab monotherapy - CheckMate-066/037; brain metastases: pembrolizumab or ipilimumab+nivolumab with documented intracranial activity; relatlimab + nivolumab (anti-LAG-3, RELATIVITY-047) - approved FDA 2022 |
Prevention and photoprotection
- Daily sun protection: use a broad-spectrum sunscreen (UVA + UVB) with a protection factor of SPF ≥ 30 (ideally SPF 50+) - apply 15 to 30 minutes before exposure, repeat every 2 hours and after each swim or significant perspiration; apply generously (2 mg/cm² of skin - i.e. approximately 35 mL for the entire body of an adult) - most users apply only 25 to 50 % of the required amount, reducing actual effectiveness
- Avoid intense sun exposure during peak hours (10:00 am to 4:00 pm from May to September in Quebec); seek shade; cover-up clothing, wide-brimmed hat (UV protection ≥ 7.5 cm), sunglasses with certified UV filter
- Avoid tanning booths at all costs - in Quebec, they're banned for under-18s; artificial tanning is not a «healthy» tan - it's the result of a DNA defense response to UV damage, and doesn't effectively protect against subsequent sunburns
- Monthly skin self-examination: examine the entire skin surface (with a mirror and the help of a relative for the back and scalp) - note any new or changing lesions according to the ABCDE rule; annual dermatological consultation recommended for high-risk individuals (phototype I-II, numerous nevi, personal or family history of melanoma).
- Protecting children: children's skin is particularly vulnerable - sunburn in childhood and adolescence is the most strongly associated risk factor for melanoma; SPF 50+ for children, avoid direct exposure before 6 months, systematic shade and protective clothing
Consult a doctor as soon as possible if you notice a skin lesion that changes rapidly (within a few weeks or months) in size, shape or color, a lesion that bleeds spontaneously or at the slightest touch, a skin wound that doesn't heal within 4 weeks, or any lesion meeting the ABCDE criteria (asymmetry, irregular borders, multiple colors, diameter > 6 mm, evolution). The speed of evolution is the most important criterion - a melanoma can double in size within a few weeks in its aggressive nodular forms. Detection at stage I (Breslow < 1 mm) confers a 5-year survival of over 97 %, compared with less than 20 % at stage IV - every week counts.
Consult at Clinique Omicron
Clinique Omicron physicians perform a complete skin examination, use dermoscopy to assess suspicious pigmented lesions, prescribe skin biopsies and refer confirmed skin cancers to partner dermatologists and oncologists for surgical and systemic management. Consultations are available at our points of service in Quebec, as well as via telemedicine. To book an appointment, visit cliniqueomicron.ca.
The contents of this page are provided for information purposes only and do not replace the advice of a qualified healthcare professional. Any suspected skin lesion should be evaluated by a physician - biopsy is the only method to confirm or exclude skin cancer.
Omicron Clinic
Need to consult a doctor?
Treatment within 24-48 hours. In-clinic or telemedicine, anywhere in Quebec.
Insurance receipts. 7j/7. No family doctor required.