TY - JOUR
T1 - Post-transplantation maintenance with sorafenib or midostaurin for FLT3 positive AML patients–a multicenter retrospective observational study
AU - Shimony, Shai
AU - Yeshurun, Moshe
AU - Wolach, Ofir
AU - Ram, Ron
AU - Rozovski, Uri
AU - Shargian, Liat
AU - Zukerman, Tsila
AU - Amit, Odelia
AU - Bar-On, Yael
AU - Krayem, Baher
AU - Avni, Batya
AU - Peretz, Galit
AU - Raanani, Pia
AU - Pasvolsky, Oren
N1 - Publisher Copyright:
© 2021 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2021
Y1 - 2021
N2 - The role of post allogeneic stem-cell transplantation (AlloSCT) FLT3 inhibition for acute myeloid leukemia in the real-world setting is unclear, especially in the era of widespread pre-transplant use of tyrosine kinase inhibitors (TKIs). In a multicenter nationwide study, we assessed 41 patients who were treated with post-transplant TKIs (sorafenib, n = 23, midostaurin, n = 18). The majority also received TKIs pre-transplant (n = 32, 79%). After a median follow up of 10 months post-transplant (range 3–53.6), 29 patients (71%) were alive and in complete remission. Similar results were seen in a subgroup analysis of pre-transplant TKI recipients (78%). In Univariate analysis, HCT-CI score < 4 and Type of TKI (sorafenib versus midostaurin) predicted longer overall survival. Seventeen patients (41%) suffered from side effects and seven patients (17%) stopped TKI therapy due to adverse events. Overall, our data suggest that post-transplant use of TKIs is safe and effective in an era of their widespread use prior to AlloSCT.
AB - The role of post allogeneic stem-cell transplantation (AlloSCT) FLT3 inhibition for acute myeloid leukemia in the real-world setting is unclear, especially in the era of widespread pre-transplant use of tyrosine kinase inhibitors (TKIs). In a multicenter nationwide study, we assessed 41 patients who were treated with post-transplant TKIs (sorafenib, n = 23, midostaurin, n = 18). The majority also received TKIs pre-transplant (n = 32, 79%). After a median follow up of 10 months post-transplant (range 3–53.6), 29 patients (71%) were alive and in complete remission. Similar results were seen in a subgroup analysis of pre-transplant TKI recipients (78%). In Univariate analysis, HCT-CI score < 4 and Type of TKI (sorafenib versus midostaurin) predicted longer overall survival. Seventeen patients (41%) suffered from side effects and seven patients (17%) stopped TKI therapy due to adverse events. Overall, our data suggest that post-transplant use of TKIs is safe and effective in an era of their widespread use prior to AlloSCT.
KW - Acute myeloid leukemia
KW - FLT3 inhibitors
KW - post-transplantation maintenance
UR - http://www.scopus.com/inward/record.url?scp=85104787719&partnerID=8YFLogxK
U2 - 10.1080/10428194.2021.1913145
DO - 10.1080/10428194.2021.1913145
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C2 - 33879026
AN - SCOPUS:85104787719
SN - 1042-8194
VL - 62
SP - 2475
EP - 2481
JO - Leukemia and Lymphoma
JF - Leukemia and Lymphoma
IS - 10
ER -