Hagop Kantarjian's research has led to significant advancements in leukemia treatment, particularly in improving prognosis and survival rates for patients with
chronic myeloid leukemia (CML) and
acute lymphoblastic leukemia (ALL). His work contributed to the development of targeted therapies, including
tyrosine kinase inhibitors such as
imatinib,
dasatinib,
nilotinib, and
bosutinib, which have increased 10-year survival rates for CML from 20% to 90%. He also played a key role in developing the HYPER-CVAD regimen for ALL, replacing radiation therapy with spinal fluid chemotherapy to prevent central nervous system involvement. Kantarjian has been instrumental in the development and
FDA approval of several leukemia treatments, including
decitabine and
clofarabine for
myelodysplastic syndromes and leukemia. He has authored over 2,400 peer-reviewed publications and contributed to the approval of more than 20 leukemia drugs, including
hypomethylating agents (HMAs) combined with
venetoclax for older and unfit patients with acute myeloid leukemia (AML). His research has also advanced the use of
FLT3 inhibitors,
IDH inhibitors, and
monoclonal antibodies such as
inotuzumab and
blinatumomab in the treatment of ALL. == Selected publications ==