Safety and efficacy of imatinib cessation for CML patients with stable undetectable minimal residual disease: results from the TWISTER study

Author:

Ross David M.1234,Branford Susan5,Seymour John F.26,Schwarer Anthony P.27,Arthur Christopher28,Yeung David T.123,Dang Phuong1,Goyne Jarrad M.1,Slader Cassandra9,Filshie Robin J.210,Mills Anthony K.211,Melo Junia V.13,White Deborah L.123,Grigg Andrew P.212,Hughes Timothy P.123

Affiliation:

1. Haematology, SA Pathology, Adelaide, Australia;

2. Australasian Leukaemia and Lymphoma Group, Melbourne, Australia;

3. School of Medicine, University of Adelaide, Adelaide, Australia;

4. School of Medicine, Flinders University, Adelaide, Australia;

5. Genetic Pathology, SA Pathology, Adelaide, Australia;

6. Haematology, Peter MacCallum Cancer Centre, Melbourne, Australia;

7. Haematology, The Alfred Hospital, Melbourne, Australia;

8. Haematology, Royal North Shore Hospital, Sydney, Australia;

9. Novartis Oncology, Sydney, Australia;

10. Haematology, St. Vincent’s Hospital, Melbourne, Australia;

11. Haematology, Princess Alexandra Hospital, Brisbane, Australia; and

12. Haematology, Royal Melbourne Hospital and Austin Hospital, Melbourne, Australia

Abstract

Key Points Approximately 40% of patients with undetectable minimal residual disease on imatinib can stop treatment without loss of molecular response. Patients in treatment-free remission still have detectable BCR-ABL DNA several years after stopping imatinib.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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