A novel integrated cytogenetic and genomic classification refines risk stratification in pediatric acute lymphoblastic leukemia

Author:

Moorman Anthony V.1,Enshaei Amir1,Schwab Claire1,Wade Rachel2,Chilton Lucy1,Elliott Alannah1,Richardson Stacey1,Hancock Jeremy3,Kinsey Sally E.45,Mitchell Christopher D.6,Goulden Nicholas7,Vora Ajay8,Harrison Christine J.1

Affiliation:

1. Leukaemia Research Cytogenetics Group, Northern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne, United Kingdom;

2. Clinical Trial Service Unit, University of Oxford, Oxford, United Kingdom;

3. Bristol Genetics Laboratory, North Bristol National Health Service Trust, Bristol, United Kingdom;

4. Leeds Institute of Molecular Medicine, University of Leeds, Leeds, United Kingdom;

5. Department of Paediatric Haematology and Oncology, Leeds General Infirmary, Leeds, United Kingdom;

6. Department of Paediatric Oncology, John Radcliffe Hospital, Oxford, United Kingdom;

7. Department of Haematology, Great Ormond Street Hospital, London, United Kingdom; and

8. Department of Haematology, Sheffield Children’s Hospital, Sheffield, United Kingdom

Abstract

Key Points Integrating cytogenetic and genomic data in pediatric ALL reveals 2 subgroups with different outcomes independent of other risk factors. A total of 75% of children on UKALL2003 had a good-risk genetic profile, which predicted an EFS and OS of 94% and 97% at 5 years.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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