Melanoma

– a very serious form of skin cancer and once diagnosed the advancement of the disease is classified by what is referred to as “staging.” Melanoma begins in the melanocytes, the cells responsible for giving color to the skin. In cases of skin cancer, those cells are damaged.  Typically, there are three main types of melanoma: Cutaneous, Mucosal, and Ocular. Cutaneous Melanoma is the most commonly diagnosed type of skin cancer and falls into five separate sub-classification to further describe the findings of the damaged pigmented cells.

  • Superficial Spreading Melanoma
  • Nodular Melanoma
  • Acral Lentiginous Melanoma
  • Desmoplastic Melanoma
  • Lentigo Melanoma

The causes of melanoma vary, but the experts link the cause to significant exposure to UV rays. While a melanoma is distinctly worrisome especially if not caught within the early stages, the good news is that it has visible indicators. The early warning signs helps to detect melanoma to facilitate successful treatments and recovery. In cases of early detected melanoma, traditional treatment typically includes surgery.

Should you worry about recurrence?

These are questions best answered by treating physicians. However successful the surgery, individual cases vary. There could still be an inherent risk of recurrence. The AJCC report that there is a 36% chance of recurrence in cases of Stage 1 and 2 cancers respectively, and that most occur within 3 years followiing the nitial diagnosis. Statistics indicate that even with systemic treatment choices I.e. chemotherapy, there remains a probable amount of risk though much depends upon the type and stage. Given the statistical data, regular check-ups are a recommended protocol post cancer treatment.

Melanoma staging is basically an assigned description of where the affected cancer stands at the time of diagnosis. Here are some guidelines to help you understand what it means when a physician assigns melanoma staging terminology.

Staging- A Guide to Understanding the Visual Presentation of Melanoma

Localized Stage 1

Classified as a local melanoma (tumor thickness) up to 2mm thick. [Melanomas are measured in millimeters and referred to as a scoring system called the Breslow Depth.] The melanoma is probably not ulcerated, but can be.   A Stage 1 melanoma (tumor) at this point has not spread to lymph nodes. Patients at this diagnostic stage are considered to be at a statistically minimal risk for a reoccurrence or metastasis. Treatment at this stage is surgery. A procedure called sentinel lymph node biopsy the normal recommended action. Stage 1 melanoma can also fall into two sub-classes:

Stage 1a Stage 1b
>0.8mm thick Tumor is 0.8 – 2.0mm thick; no ulceration o
Has not spread to nearby lymph nodes Tumor is less than 2.0mm thick with ulceration
No indication of metastasis to other locations Has not spread to nearby lymph nodes
No indication of metastasis to other locations

 

Localized Stage 2

Classified as a local melanoma measuring between 1.0mm-4mm thick. The melanoma has reached slightly below the dermis of the skin. Ulceration may or may not be present. Stage 2 melanoma is divided into the following subclassifications:

Stage 2a Stage 2b Stage 2c
Tumor is 1.0-2mm thick with ulceration or Tumor is 2.01 -4mm thick with ulceration or Tumor is <4.0mm thick with ulceration
No indication of metastasis. Tumor is <4.0mm thick without ulceration Has not spread to lymph nodes
Has not spread to lymph nodes No indication of lymph node
No indication of metastasis

 

Regional Stage 3

Described as melanomas of various thicknesses having reached regional areas (one or more lymph node locations). The extent of penetration within the lymph areas is of significant value when assigning a stage and prognosis. Stage 3 is divided into the following subclassifications:

Stage 3a Stage 3b
Non-Ulcerated Tumor >2.0mm thick and has spread to 1-3 lymph nodes, lymph nodes not felt. Non-Ulcerated Tumor >2.0mm thick and has spread to 1-3 lymph nodes 1 of the lymph nodes can be seen or felt. OR
Ulcerated Tumor >1.0mm thick and has spread to 1-3 lymph nodes; lymph nodes can be felt. Non-ulcerated tumor is 2.0mm -4.0 thick and has spread to 1-3 lymph nodes and 1 of the lymph nodes can be seen or felt OR
Non-ulcerated tumor ranges up to 4.0mm thick and there aren’t any affected lymph nodes but there are in transit tumor
Ulcerated tumor is >1.0mm and has spread to 1-3 lymph nodes and 1 can be seen or felt
Ulcerated tumor is 1-2.0mm thick and has spread to 1-3 lymph nodes or 1 of the lymph nodes can be seen or fel
Ulcerated tumor is less than 2.0mm thick and there is no melanoma in lymph nodes

 

Metastasized Melanoma Stage 4

Distinctly different from prior stages, this is classified as a melanoma that has left the site of origin and has spread to other locations within the body such as the internal organs (liver, brain, lungs). Considered to be the most serious and a varied recommendations of treatment options may apply such as targeted therapies, immunotherapies, and surgery. There are subclasses within the stage 4 diagnosis:

M1a: Tumor has metastasized to subcutaneous layer or to distant lymph nodes. LDH is normal
M1b: Tumor has metastasized to the lungs. LDH is normal
M1c: Tumor has metastasized to organs other than the lungs, LDH is normal, or distant metastases with elevated LDH
M1d: Tumor has metastasized to the central nervous system

 

 Treating Aggressive Melanoma

Traditional treatments include surgery for removal of the melanoma. However successful the surgery, there is a risk of recurrence. Risk factors can include independent health risk variables such as prior cancer diagnosis, individual health at time of diagnosis and of course age. As a preventive measure, Oncologists have begun to incorporate a regimen of modern scientific treatments into the fight. Revolutionizing the fight for prolonged life and lessening the risk of re-emergence are three game-changing innovations: immunotherapy options, check-point inhibitors, and oncolytic viral-therapy.

Oncolytic viral therapies are viruses that are introduced into the body to infect and kill off cancer cells. Viruses being used in oncolytic therapies include the ECHO-7 Virus, Adenovirus, HSV virus, and many others. They have gained a lot of positive attention from the scientific community primarily because they are working in cases where traditional methodologies have failed. Prioritizing patient outcome is one of the reasons why oncologists are fast-tracking their patients into clinical trials and also treating with the treatments that have already gained FDA approval.

Checkpoint Inhibitors and Immunotherapy work by enlisting the help of our own immune systems to fight and kill cancer cells. In cases of advanced or rare melanomas, studies have shown checkpoint inhibitors to be very effective at shrinking the tumor.

Targeted Therapies include two different options or types for therapy. One is the use of monoclonal antibodies. Monoclonal antibodies basically assist other traditional therapy modalities by helping them target the cancer cells better. The other form of targeted therapy are small molecule drugs. They work by disabling the process that causes cancer to spread. Both of these targeted types of therapies are proving to be far more effective beyond that of standard measures used alone.  Examples of how targeted therapies are being used, can be found here.

Further Reading:

  1. Balch CM, Soong SJ, Gershenwald JE, et al. Age as a prognostic factor in patients with localized melanoma and regional metastases. Ann Surg Oncol. 2013;20(12):3961-8.

 

  1. Kyrgidis A, Tzellos T, Mocellin S, Apalla Z, Lallas A, Pilati P, Stratigos A. Sentinel lymph node biopsy followed by lymph node dissection for localisedprimary cutaneous melanoma. Cochrane Database Syst Rev. 2015 May 16;(5):CD010307.doi: 10.1002/14651858.CD010307.pub2. Review. PubMed PMID: 25978975.

 

  1. Van den Brom RRH, van der Geest KSM, Brouwer E, Hospers GAP, Boots AMH. Enhanced expression of PD-1 and other activation markers by CD4+ T cells of young but not old patients with metastatic melanoma. Cancer Immunol Immunother. 2018;67(6):925-933.