Prognosis for patients with CML and >10% BCR-ABL1 after 3 months of imatinib depends on the rate of BCR-ABL1 decline

Author:

Branford Susan1234,Yeung David T.1256,Parker Wendy T.13,Roberts Nicola D.1,Purins Leanne1,Braley Jodi A.1,Altamura Haley K.1,Yeoman Alexandra L.1,Georgievski Jasmina1,Jamison Bronte A.1,Phillis Stuart1,Donaldson Zoe1,Leong Mary1,Fletcher Linda1,Seymour John F.678,Grigg Andrew P.689,Ross David M.25610,Hughes Timothy P.25611

Affiliation:

1. Department of Genetics and Molecular Pathology, Centre for Cancer Biology, SA Pathology, Adelaide, Australia;

2. School of Medicine, and

3. School of Molecular and Biomedical Science, University of Adelaide, Adelaide, Australia;

4. School of Pharmacy and Medical Science, University of South Adelaide, Adelaide, Australia;

5. Department of Haematology, Centre for Cancer Biology, SA Pathology, Adelaide, Australia;

6. Australasian Leukaemia and Lymphoma Group, East Melbourne, Australia;

7. Department of Haematology, Peter MacCallum Cancer Centre, East Melbourne, Australia;

8. University of Melbourne, Parkville, Australia;

9. Department of Haematology, Austin Hospital, Melbourne, Australia;

10. Department of Haematology, Flinders University and Medical Centre, Bedford Park, Australia; and

11. Cancer Theme, South Australian Health and Medical Research Institute, Adelaide, Australia

Abstract

Key Points Among patients with >10% BCR-ABL1, at 3 months, the poorest-risk group can be distinguished by the rate of BCR-ABL1 decline from baseline. Patients with BCR-ABL1 values on a constant downward trajectory may rapidly reach the level considered optimal with additional follow-up.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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