Treatment
Surgery
is the first choice therapy for localized cutaneous melanoma. Depending
on the stage a sentinel lymph node biopsy is done as well, although
controversy exists around trial evidence for this procedure. Treatment
of advanced malignant melanoma is performed from a multidisciplinary
approach.
Surgery
Diagnostic
punch or excisional biopsies may appear to excise (and in some cases
may indeed actually remove) the tumor, but further surgery is often
necessary to reduce the risk of recurrence.
Complete
surgical excision with adequate margins and assessment for the presence
of detectable metastatic disease along with short- and long-term followup
is standard. Often this is done by a "wide local excision"
(WLE) with 1 to 2 cm margins. Melanoma-in-situ and lentigo malignas
are treated with narrower surgical margins, usually 0.2 to 0.5 cm. Many
surgeons consider 0.5 cm the standard of care for standard excision
of melanoma-in-situ, but 0.2 cm margin might be acceptable for margin
controlled surgery (Mohs surgery, or the double bladed technique with
margin control). The wide excision aims to reduce the rate of tumour
recurrence at the site of the original lesion. This is a common pattern
of treatment failure in melanoma. Considerable research has aimed to
elucidate appropriate margins for excision with a general trend toward
less aggressive treatment during the last decades.
Mohs
surgery has been reported with cure rate as low as 77% and as high as
98% for melanoma-in-situ.
Melanomas
which spread usually do so to the lymph nodes in the region of the tumor
before spreading elsewhere. Attempts to improve survival by removing
lymph nodes surgically (lymphadenectomy) were associated with many complications
but unfortunately no overall survival benefit. Recently the technique
of sentinel lymph node biopsy has been developed to reduce the complications
of lymph node surgery while allowing assessment of the involvement of
nodes with tumor.
Although
controversial and without prolonging survival, "sentinel lymph
node" biopsy is often performed, especially for T1b/T2+ tumors,
mucosal tumors, ocular melanoma and tumors of the limbs. A process called
lymphoscintigraphy is performed in which a radioactive tracer is injected
at the tumor site in order to localize the "sentinel node(s)".
Further precision is provided using a blue tracer dye and surgery is
performed to biopsy the node(s). Routine H&E staining, and immunoperoxidase
staining will be adequate to rule out node involvement. PCR tests on
nodes, usually performed to test for entry into clinical trials, now
demonstrate that many patients with a negative SLN actually had a small
number of positive cells in their nodes. Alternatively, a fine-needle
aspiration may be performed and is often used to test masses.
If
a lymph node is positive, depending on the extent of lymph node spread,
a radical lymph node dissection will often be performed. If the disease
is completely resected, the patient will be considered for adjuvant
therapy.
Adjuvant
treatment
High
risk melanomas may require adjuvant treatment. In the United States
most patients in otherwise good health will begin up to a year of high-dose
interferon treatment, which has severe side effects but may improve
the patient's prognosis. This claim is not supported by all research
at this time, and in Europe interferon is usually not used outside the
scope of clinical trials.
Metastatic
melanomas can be detected by X-rays, CT scans, MRIs, PET and PET/CTs,
ultrasound, LDH testing and photoacoustic detection.
Chemotherapy
and immunotherapy
Various
chemotherapy agents are used, including dacarbazine (also termed DTIC),
immunotherapy (with interleukin-2 (IL-2) or interferon (IFN)) as well
as local perfusion are used by different centers. They can occasionally
show dramatic success, but the overall success in metastatic melanoma
is quite limited. IL-2 (Proleukin) is the first new therapy approved
for the treatment of metastatic melanoma in 20 years. Studies have demonstrated
that IL-2 offers the possibility of a complete and long-lasting remission
in this disease, although only in a small percentage of patients. A
number of new agents and novel approaches are under evaluation and show
promise.
On
June 23, 2008, Israeli scientists from the Oncology Institute of the
Hadassa Medical Center in Jerusalem announced they developed a vaccine
that prevents recurrences of the disease among previous sufferers and
increases chances of survival for current ones.
Lentigo
maligna treatment
Standard
excision is still being done by most surgeons. Unfortunately, the recurrence
rate is exceeding high (up to 50%). This is due to the ill defined visible
surgical margin, and the facial location of the lesions (often forcing
the surgeon to use a narrow surgical margin). The narrow surgical margin
used, combined with the limitation of the standard bread loafing technique
of fixed tissue histology - result in a high "false negative"
error rate, and frequent recurrences. Margin controlled (peripheral
margins) is necessary to eliminate the false negative errors. If breadloafing
is utilized, distances from sections should approach 0.1 mm to assure
that the method approaches complete margin control.
Mohs
surgery has been done with cure rate reported to be as low as 77% ,
and as high as 95% by another author The "double scalpel"
peripheral margin controlled excision method approximates the Mohs method
in margin control, but requires a pathologist intimately familiar with
the complexity of managing the vertical margin on the thin peripheral
sections and staining methods.
Some
melanocytic nevi, and melanoma-in-situ (lentigo maligna) have resolved
with an experimental treatment, imiquimod (Aldara) topical cream, an
immune enhancing agent. Some dermasurgeons are combining the 2 methods:
surgically excising the cancer and then treating the area with Aldara
cream postoperatively for three months. Considering the very poor cure
rate with standard excision, it might not be a bad idea to follow up
all surgical excisions with topical imiquimod treatments.
Radiation
and other therapies
Radiation
therapy is often used after surgical resection for patients with locally
or regionally advanced melanoma or for patients with unresectable distant
metastases. It may reduce the rate of local recurrence but does not
prolong survival.
In
research setting other therapies, such as gene therapy, may be tested.
Radioimmunotherapy of metastatic melanoma is currently under investigation.
Experimental treatment developed at the National Cancer Institute (NCI),
part of the National Institutes of Health in the US was used in advanced
(metastatic) melanoma with moderate success. The treatment, adoptive
transfer of genetically altered autologous lymphocytes, depends on delivering
genes that encode so called T cell receptors (TCRs), into patient's
lymphocytes. After that manipulation lymphocytes recognize and bind
to certain molecules found on the surface of melanoma cells and kill
them.