Are there any implications if a patient chooses to opt out of the cancer registration scheme?
Patients have the right to be informed about the processing and uses of their information, and the right to object to their information being used in certain circumstances. When a patient expresses a wish to “opt out” of cancer registration, it is important that they understand what the cancer registry is, what information is collected, and what the information is used for. It is important for patients to be fully informed of the potential consequences of their “opting out” before they make this choice. It must also be made clear, however, that this will not affect their treatment and care.
