YOU CAN HELP RESEARCHERS BETTER UNDERSTAND WHO IS AT RISK FOR HEREDITARY CANCER

Welcome to the Prospective Registry Of MultiPlex Testing (PROMPT). This online research registry for patients and their families helps researchers answer the question: “How do genetic variants affect your cancer risk?”

If you’re here, you’ve likely undergone multiplex gene panel testing and were found to have a genetic variant that may be linked to an increased risk of cancer.

Through your participation, you can help researchers collect data to better understand and prevent cancer.

What, exactly, does PROMPT do? We collect information from people who have had multiplex genetic testing so we can all learn more about hereditary cancer risk. Learn more about us and our mission to help researchers eradicate cancer.

By joining the PROMPT registry, administered through our partner site PatientCrossroads, you’ll join hundreds of other families who are helping researchers learn more about gene mutations and their link to hereditary cancers.