Abstract
The B&D Committee membership includes all participating international study groups. It provides a bridge between the other I-BFM Committees in terms of integration of technical developments, collaborative studies to determine the clinical and prognostic relevance of novel genetic abnormalities in childhood leukaemia and lymphoma. This Committee is most closely aligned with the Genetic Variation, Acute Lymphoblastic Leukaemia, Acute Myeloid Leukaemia and Resistant Disease Committees, with which joint and overlapping meetings are carried out. There has been major focus over the years on studies of minimal residual disease (MRD) and validation of new technologies for their integration into clinical practice.
Scientific aims
- to validate the clinical and prognostic relevance of new genetic subtypes of childhood leukaemia and lymphoma
- to explore the relevance of biological factors in these diseases
- to explore biological studies in relation to improving therapies for these diseases
- to validate emerging new technologies in the field for clinical application
B&D Committee ongoing collaborative studies
-
Consensus diagnostic approaches for clinically actionable genetic abnormalities in ALL
Coordinated by C. Harrison
-
Down syndrome ALL Registry
Coordinated by M. Den Boer and S. Izraeli
-
ETV6::RUNX1-like ALL
Coordinated by M. Zaliova
-
Harmony
Coordinated by A. Moorman
-
IGH translocation partners
Coordinated by L. Russell
-
NUTM1 and other non-MLL Infant-ALL
Coordinated by G. Cazzaniga and J. Boer
-
TP53 in hypodiploid ALL
Coordinated by G. Cazzaniga