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Clinical Trial Summary

To generate meaningful data regarding ctDNA that would infer risk of recurrence in stage III melanoma patients.


Clinical Trial Description

Cancer cells harbor and can acquire potentially hundreds of mutations, many of whom are found in the ctDNA. Circulating tumor DNA (ctDNA) holds the promise for the 50% of participants who do not need adjuvant therapies - participants could be monitored to ensure no increase in ctDNA. Participants treated could then be followed for the earliest possible blood level signs of recurrence (incr. ctDNA) and more quickly be switched to more effective therapies. Further, the treating physician could hold therapy until the first signs of ctDNA based recurrence for those participants that would benefit. Blood sample from a biobank will be used to identify to monitor ctDNA. These blood samples were drawn at baseline, 3 months, 6 months and 18 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05079113
Study type Observational
Source Case Comprehensive Cancer Center
Contact
Status Active, not recruiting
Phase
Start date October 1, 2019
Completion date April 2025

See also
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