Screening
Is screening for skin melanoma useful?
The working group is of the opinion that routine checking for pigmented lesions warrants recommendation in cases with a known familial increased risk of melanoma. One check-up every 6 to 12 months is considered sufficient.
According to the working group, increased attentiveness is advisable for individuals with a combination of risk factors resulting in a substantially increased risk of melanoma.
The working group is of the opinion that population-based screening for melanoma is not warranted in the Netherlands.
Diagnosis
Does dermatoscopy increase the accuracy of clinical diagnosis?
Dermatoscopy has an established role in the clinical diagnosis of pigmented skin disorders. Physicians who are unfamiliar with dermatoscopy are advised to become proficient with the technique before applying it.
Pathological assessment of diagnostic excisions
Each pigmented skin lesion removed should be submitted for histopathological diagnostic evaluation.
The pathology request form should include at least the following information: personal details, location of the lesion, reason for removal (cosmetic versus diagnostic) and the excisional margin. For excisions made for diagnostic purposes, the reason why malignancy was suspected should be included (e.g., irregular macroscopic features, changes over time, itching).
The pathology report should contain a conclusion statement which, for cases of melanoma, should include at least the following information:
- Anatomical location
- Type of procedure (shave, punch, elliptical or incisional biopsy)
- Excisional margin
- Diagnosis of melanoma (including the histologic subtype, if possible)
- Breslow thickness
- Presence/absence of ulceration
- Clark level
- Presence/absence of microsatellitosis
- Presence/absence of regression or partial regression
- Completeness of the removal
If the diagnosis of melanoma is uncertain, the case should be presented to a pathologist with special expertise in the diagnosis of melanocytic tumours.
Sentinel Node Procedure
What is the indication for sentinel node biopsy?
According to the working group, sentinel node biopsy should be reserved for patients who desire the most complete information possible regarding their prognosis. This procedure is not considered part of standard diagnostic evaluation. If sentinel node biopsy is proposed, the low risk of complications, the rather high percentage of false-negative results, and the possible increased incidence of in-transit metastases should be considered.
How should pathological assessment of the sentinel node be conducted?
Intraoperative frozen section assessment of the sentinel node is contraindicated in melanoma.
In addition to haematoxylin-eosin (HE) stained sections, evaluation of the sentinel node requires immunostaining for S-100 and at least one additional, more specific marker, preferably MART-1.
Assessment of more than one section of the sentinel node is necessary for optimal detection of melanoma metastases. At this time, definitive statements cannot be made regarding the optimal number of sections to assess or the optimal distance between sections. The working group advises that at least three sections from each paraffin block are assessed, including immunohistochemistry of each section; however, assessment of six sections is preferred, in accordance with the European Organisation for Research and Treatment of Cancer (EORTC) guidelines.
The optimal distance between sections depends on the total number of sections and varies between 50 microns for six sections and 150 microns for three sections. Measuring the number and size of melanoma metastases in the sentinel node is not necessary at this time, as confirmation of the possible therapeutic relevance of these findings is pending.
The sentinel node should be fixed in toto and prepared completely for microscopic histopathological evaluation.
Supplemental Investigation
For localised melanoma (American Joint Committee of Cancer [AJCC] stage I and II), does supplemental testing (other than sentinel node evaluation) influence the prognosis?
Supplemental tests for staging assessment are not routinely indicated for patients with clinically localized melanoma. Supplemental testing can be used when indicated, such as the use of lymph node ultrasound when palpation of the lymph node regions yields inconclusive results.
Treatment
What are the recommended margins for therapeutic re-excision of a primary melanoma?
The following margins of unaffected skin surrounding the biopsy are recommended for the therapeutic re-excision of melanoma:
- Melanoma in situ: 0.5 cm
- Breslow thickness <2 mm: 1 cm
- Breslow thickness >2 mm: 2 cm
Pathological Assessment of Re-excised Skin Sections
- Assessment of three blocks of scar tissue in re-excised sections of skin/subcutis is sufficient following complete excision of the melanoma.
- Complete embedment of the scar tissue is required if the melanoma is not removed completely during diagnostic excision and residual tumour is revealed by the resection margin analysis of the re-excision.
- Pigmented lesions and other focal abnormalities should always be evaluated histologically.
Adjuvant Treatment
Is adjuvant radiation therapy indicated following lymph node dissection?
Adjuvant radiation therapy is not considered standard treatment following lymph node dissection. Whether radiation therapy is applied and how it is applied depends on the prognosis and the risk of recurrent disease in the area of the removed lymph nodes.
Is there a systemic adjuvant therapy that has proven efficacy in patients with prognostically unfavourable characteristics?
Systemic adjuvant treatment of patients with melanoma is not recommended outside the context of a clinical trial. This also applies to adjuvant treatment with interferon a (IFNa).
Treatment of Metastases
Which systemic therapy is the treatment of choice for melanoma with distant metastases?
Patients with metastatic melanoma are preferably treated in a clinical trial. If treatment outside the context of a clinical trial is to be considered, there is no better alternative to dacarbazine (DTIC).
Follow-Up
What is adequate follow-up for primary melanoma?
Breslow thickness <1 mm:
- A single check-up 1 month after treatment for primary melanoma, providing the patient with the opportunity to ask questions and learn self-checking techniques. It should be explained to the patient that additional check-ups do not improve the chance of cure, but that an appointment can always be made at short notice if symptoms occur.
- If desired, additional check-ups can be scheduled for counselling, checking one's own work, educational purposes, or scientific research.
- The frequency and extent of evaluation is then determined by need.
Breslow thickness >1 mm:
- Year 1: check-up once every 3 months
- Year 2: check-up once every 4 months
- Years 3 to 5: check-up once every 6 months
Breslow thickness >2 mm:
- Same as Breslow thickness > 1 mm plus annual check-ups years 6 to 10.
Supplemental tests as indicated.
Staging
Which staging system should be used for melanoma in the Netherlands?
The working group is of the opinion that the American Joint Committee of Cancer (AJCC) staging system — unabridged and unmodified — should be adopted in the Netherlands.