TY - JOUR
T1 - Infant acute lymphoblastic leukaemia—Progress from worldwide clinical efforts
AU - Barrett, Neil
AU - Gruber, Tanja A.
AU - Miyamura, Takako
AU - Duguid, Alasdair
AU - Stutterheim, Janine
N1 - © 2025 British Society for Haematology and John Wiley & Sons Ltd.
PY - 2025/12
Y1 - 2025/12
N2 - Infant acute lymphoblastic leukaemia (ALL) is a rare and aggressive type of leukaemia, especially when a KMT2A rearrangement is involved. Historical treatment strategies have included intensification of conventional ALL chemotherapy in combination with acute myeloid leukaemia treatment elements. However, outcomes have remained consistently poor compared to the advances that have been seen in childhood ALL. The emergence of novel immunotherapies has transformed treatment strategies, with blinatumomab now incorporated into clinical trials for infants with KMT2A-rearranged ALL, promising significant advancements. Additionally, deeper insights into the unique biology of KMT2A-rearranged ALL have facilitated the development of targeted therapies, such as venetoclax and menin inhibitors, which are under clinical evaluation. These efforts offer renewed hope for better outcomes. This review highlights the substantial progress in understanding and treating KMT2A-rearranged ALL, fuelling optimism for future therapeutic success. In addition, we highlight the challenges that might be faced by using immunotherapy.
AB - Infant acute lymphoblastic leukaemia (ALL) is a rare and aggressive type of leukaemia, especially when a KMT2A rearrangement is involved. Historical treatment strategies have included intensification of conventional ALL chemotherapy in combination with acute myeloid leukaemia treatment elements. However, outcomes have remained consistently poor compared to the advances that have been seen in childhood ALL. The emergence of novel immunotherapies has transformed treatment strategies, with blinatumomab now incorporated into clinical trials for infants with KMT2A-rearranged ALL, promising significant advancements. Additionally, deeper insights into the unique biology of KMT2A-rearranged ALL have facilitated the development of targeted therapies, such as venetoclax and menin inhibitors, which are under clinical evaluation. These efforts offer renewed hope for better outcomes. This review highlights the substantial progress in understanding and treating KMT2A-rearranged ALL, fuelling optimism for future therapeutic success. In addition, we highlight the challenges that might be faced by using immunotherapy.
KW - KMT2A-rearranged
KW - acute lymphoblastic leukaemia
KW - infant
KW - Myeloid-Lymphoid Leukemia Protein/genetics
KW - Immunotherapy/methods
KW - Humans
KW - Infant
KW - Antibodies, Bispecific/therapeutic use
KW - Histone-Lysine N-Methyltransferase/genetics
KW - Molecular Targeted Therapy
KW - Precursor Cell Lymphoblastic Leukemia-Lymphoma/genetics
KW - Gene Rearrangement
KW - Bridged Bicyclo Compounds, Heterocyclic/therapeutic use
UR - https://www.scopus.com/pages/publications/105017814468
UR - https://www.mendeley.com/catalogue/73031c23-0cb6-3acd-8fe0-c25939a04397/
U2 - 10.1111/bjh.70166
DO - 10.1111/bjh.70166
M3 - Review article
C2 - 41033852
AN - SCOPUS:105017814468
SN - 0007-1048
VL - 207
SP - 2246
EP - 2260
JO - British journal of haematology
JF - British journal of haematology
IS - 6
ER -