About this trial
Uveal melanoma (UM) is the most common type of cancer inside the eyes of adults. Almost half of all patients diagnosed with UM will eventually develop metastases. Once metastases occur, the median patient survival is short.
In this trial, we will test if treatment with Melatonin after primary tumor diagnosis can prevent or delay the development of metastases. 100 patients diagnosed with primary UM will be randomized to either treatment with Melatonin tablets (20 mg at night), or to a control group. Both groups will be followed for 5 years. At 5 years, the number of patients that have developed metastases in the Melatonin and control groups will be compared (primary outcome measure).
Eligibility criteria
Qualifiers
The patient is ≥18 years
The patient has given his/her written informed consent to participate in the trial.
The patient has a melanoma originating in the choroid or in the ciliary body, as diagnosed by clinical methods and/or histological examination.
The patient's tumor is of size category T3d or higher, or stage IIIB or IIIC according to the American Joint Committee on Cancer (AJCC, version 8) criteria.
Disqualifiers
Oversensitivity or allergy to Melatonin or any of the excipients in the tablet.
The patient has metastatic disease, detectable with radiological examinations or any other method (development of metastases after recruitment to the trial does not disqualify the patient from participation).
The patient is unable to provide informed consent.
The patient has decreased liver function (e.g., liver cirrhosis or hepatitis)
Trial design
Treatments tested in this trial
- Melatonin
Treatment groups
Sponsors and collaborators
Gustav Stalhammar
Lead sponsor
St. Erik Eye Hospital
Sponsor institution
Karolinska Trial Alliance
Collaborator
The Swedish Eye Foundation (Ögonfonden)
Collaborator
The Swedish Society of Medicine
Collaborator
Swedish Cancer Foundation
Collaborator