Post-transplantation maintenance with sorafenib or midostaurin for FLT3 positive AML patients - a multicenter retrospective observational study.
Shai ShimonyMoshe YeshurunOfir WolachRon RamUri RozovskiLiat Shargian-AlonTsila ZukermanOdelia AmitYael Bar-OnBaher KrayemBatya AvniGalit PeretzPia RaananiOren PasvolskyPublished in: Leukemia & lymphoma (2021)
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.
Keyphrases
- acute myeloid leukemia
- end stage renal disease
- stem cell transplantation
- newly diagnosed
- ejection fraction
- chronic kidney disease
- tyrosine kinase
- rheumatoid arthritis
- cross sectional
- high dose
- clinical trial
- randomized controlled trial
- mesenchymal stem cells
- bone marrow
- advanced non small cell lung cancer
- systemic lupus erythematosus
- cell death
- smoking cessation
- patient reported
- cell cycle arrest