TY - JOUR
T1 - Targeted therapy paves the way for the cure of acute lymphoblastic leukaemia
AU - Rafei, Hind
AU - Kantarjian, Hagop M.
AU - Jabbour, Elias J.
N1 - Publisher Copyright:
© 2019 British Society for Haematology and John Wiley & Sons Ltd
PY - 2020/1/1
Y1 - 2020/1/1
N2 - The past decade has witnessed tremendous progress in the treatment of acute lymphoblastic leukaemia (ALL), primarily due to the development of targeted therapies, including tyrosine kinase inhibitors targeting BCR-ABL1 tyrosine kinase, monoclonal antibodies targeting cell surface antigens (CD19, CD20 and CD22), bispecific antibodies and chimeric antigen receptor T- cell therapy. A number of new therapies have been approved by the US Food and Drug Administration in the past 5 years, including blinatumomab in 2014, inotuzumab ozagamicin in 2017 and tisagenlecleucel in 2017 for relapsed/refractory ALL. This has led to tremendous improvement in long-term survival, of more than 50% in patients with precursor B-ALL [50–70% in patients with Philadelphia chromosome (Ph)-positive ALL)], 50–60% in T-ALL and 80% in mature B-ALL. Research is ongoing to optimize the benefit of targeted therapeutics with the goal of decreasing the use of cytotoxic therapies.
AB - The past decade has witnessed tremendous progress in the treatment of acute lymphoblastic leukaemia (ALL), primarily due to the development of targeted therapies, including tyrosine kinase inhibitors targeting BCR-ABL1 tyrosine kinase, monoclonal antibodies targeting cell surface antigens (CD19, CD20 and CD22), bispecific antibodies and chimeric antigen receptor T- cell therapy. A number of new therapies have been approved by the US Food and Drug Administration in the past 5 years, including blinatumomab in 2014, inotuzumab ozagamicin in 2017 and tisagenlecleucel in 2017 for relapsed/refractory ALL. This has led to tremendous improvement in long-term survival, of more than 50% in patients with precursor B-ALL [50–70% in patients with Philadelphia chromosome (Ph)-positive ALL)], 50–60% in T-ALL and 80% in mature B-ALL. Research is ongoing to optimize the benefit of targeted therapeutics with the goal of decreasing the use of cytotoxic therapies.
KW - acute lymphoblastic leukaemia
KW - bispecific antibodies
KW - chimeric antigen receptor-T cell therapy
KW - monoclonal antibodies
KW - tyrosine kinase inhibitors
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U2 - 10.1111/bjh.16207
DO - 10.1111/bjh.16207
M3 - Review article
C2 - 31566728
AN - SCOPUS:85073927465
SN - 0007-1048
VL - 188
SP - 207
EP - 223
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 2
ER -