
What Is Ocular (Uveal) Melanoma?
If you are newly diagnosed or looking to better understand ocular melanoma, this page provides an overview of what it is, how it develops, and what you need to know moving forward.
Ocular melanoma, also known as uveal melanoma, is a rare cancer that develops in pigment-producing cells (melanocytes) inside the eye. These cells are found in the uvea, the middle layer of the eye that supplies blood and nutrients to the retina.
The uvea has three parts, all of which can be affected:
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Choroid (the most common site)
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Ciliary body
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Iris
Ocular melanoma is the most common primary cancer of the eye in adults, but it remains a rare form of melanoma overall. Because it develops inside the eye, it is often not visible and may not cause symptoms in its early stages. Many cases are detected during routine, dilated eye exams.​​



We have compiled a list of resources created to support individuals after diagnosis:
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Signs & Diagnosis​
Ocular melanoma may not cause symptoms early on. As the tumour grows, some people may experience:
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Blurred or reduced vision in one eye
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Flashes of light or floating spots (“floaters”)
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A dark spot on the iris or changes in pupil shape
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Eye redness, pressure, or pain
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Bulging of the eye or changes in appearance
These symptoms can also be caused by other eye conditions. Any sudden or persistent change in vision should be assessed by an eye care professional.
Primary vs. Metastatic Disease
Primary Ocular Melanoma
When the cancer is confined to the eye, it is referred to as primary ocular melanoma. Treatment at this stage focuses on controlling the tumour while preserving vision whenever possible. Many people live for years after treatment for primary disease.
Metastatic Ocular Melanoma
Ocular melanoma can spread beyond the eye, most commonly to the liver, but also to the lungs, bones, and other organs. This is known as metastatic ocular melanoma.
While not all cases progress to metastatic disease, ongoing monitoring is an important part of care. Even after successful treatment of the primary tumour, metastases can develop years later, making long-term follow-up and surveillance essential.

Risk Factors & Causes
The exact cause of ocular melanoma is not fully understood. It is believed to result from genetic changes that occur in melanocytes within the eye.
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Factors associated with increased risk include:
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Light-coloured eyes (blue or green)
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Fair skin
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Increasing age
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Certain inherited genetic mutations, including BAP1
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Pre-existing pigmentation conditions involving the eye
Many people diagnosed with ocular melanoma have no known risk factors.
Treatment, Care & Moving Forward
Treatment depends on tumour size, location, spread, and individual circumstances. Options may include:
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Radiation therapy, such as plaque brachytherapy or proton beam therapy
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Laser-based treatments for selected small tumours
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Surgery, including tumour removal or, in advanced cases, removal of the eye
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Systemic treatments (affecting the whole body), such as immunotherapy and targeted drug therapies, for metastatic disease
New therapies continue to emerge, and clinical trials play an important role in advancing care for ocular melanoma.
Ocular Melanoma: Innovative Treatments and Beyond
FEBRUARY 2019
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This webinar provides an update on the landscape of metastatic ocular melanoma treatment in Canada and the United States. Dr. Hamid and Dr. Butler share their knowledge of current practices and care pathways, identifying the most pressing needs for patients. They also discuss new and emerging treatment options such as IMCgp100 (now named Tebentafusp or brand name Kimmtrak), as well as clinical trials available to Canadian patients with ocular or uveal melanoma.
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FAQ's
Addtional Information
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Ocular (uveal) melanoma accounts for approximately 3–5% of all melanoma diagnoses.
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In Canada, the estimated incidence is 5–6 cases per million people per year, translating to roughly 200-250 new cases annually.
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About 40–50% of patients will eventually develop metastatic disease, often years after initial diagnosis.
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The liver is involved in up to 90% of metastatic cases.
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Sources:
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Public Health Agency of Canada: https://www.canada.ca/en/public-health
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Rare Disease Database (Orphanet): https://www.orpha.net
NOTE: The information on the Ocumel Canada website is not intended to replace the medical advice of a doctor or healthcare provider. While we make every effort to ensure that the information on our site is as current as possible, please note that information and statistics are subject to change as new research and studies are published.
