This tumour register has received approval from an NHMRC accredited ethics committee. Case reporting is based on provision to the Register (by the treating clinician) of deidentified demographic information, histological diagnosis and the submitting clinicians contact details. Whilst ANTIGR does not require a written statement of patient consent, it is the submitting clinician's responsibility to ensure they are satisfied issues relating to informed patient consent have been considered prior to registering case data. The submitting clinician may register as much or as little case demographic information as they feel is appropriate.

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