ARC-LITE

  • Research type

    Research Study

  • Full title

    Assessment of Response to Chemotherapy by Flt-3 Ligand Testing (ARC-LITE)

  • IRAS ID

    334925

  • Contact name

    Nuno Borges

  • Contact email

    nuno.borges@ncl.ac.uk

  • Sponsor organisation

    The Newcastle upon Tyne Hospitals NHS Foundation Trust Newcastle Joint Research Office

  • Duration of Study in the UK

    2 years, 0 months, 1 days

  • Research summary

    Acute myeloid leukaemia (AML) is the most common type of leukaemia. It is a high-risk disease and only 3 out of 10 patients survive. Treatment of AML requires chemotherapy, after which patients must wait several weeks for their blood counts to recover. A bone marrow test is then performed to find out if the treatment has been successful and they have achieved a remission. The anxiety of waiting for a bone marrow test and the test itself cause considerable mental and physical stress.
    We are researching a blood test that can predict the response to treatment day by day. The test is for a growth factor known as Flt3 Ligand (FL) which is essential for normal blood cell development and for nearly all types of AML. When AML cells are present, FL is undetectable. If the AML has been cleared, FL rises to a very high level. Since it is a blood test, FL can be measured often to monitor the response to treatment.
    Previous research has shown that the bone marrow test result could have been predicted by measuring FL. In this study we will perform FL measurement ‘prospectively’ to find out if FL can predict the result of the bone marrow test in advance. We will also find out the best way to measure the FL to get the most accurate prediction.
    We hope that FL testing will prove useful in assessing the response of AML to chemotherapy. In the future we anticipate that FL testing will reduce the stress of treatment by removing anxiety and reducing the number of painful bone marrow tests that need to be performed.

  • REC name

    North East - Newcastle & North Tyneside 2 Research Ethics Committee

  • REC reference

    24/NE/0203

  • Date of REC Opinion

    28 Nov 2024

  • REC opinion

    Further Information Favourable Opinion