As I was part of the Flair trial here in the UK, I see the trial team every six months for monitoring. Today, for the first time the consultant said they are doing MRD blood testing to check if there are any miniscule amounts of CLL. I had FCR in 2018. Telephone consultation in 4-6 weeks when results back from Sheffield test centre.
This has not happened before and now I’m starting to worry. Did he see something in my routine blood tests or is this standard in the Flair trial? Does anyone have any similar experience or explanation to offer?