TKI Maintenance After Stem-Cell Transplantation for FLT3 -ITD Positive Acute Myeloid Leukemia: A Systematic Review and Meta-Analysis

This analysis aimed to systematically review and synthesize the existing evidence regarding the outcome of tyrosine kinase inhibitor (TKI) maintenance therapy after allogeneic stem-cell transplantation for patients with -ITD-mutated acute myeloid leukemia (AML). We searched publicly available databa...

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Veröffentlicht in:Frontiers in immunology 2021-03, Vol.12, p.630429-630429
Hauptverfasser: Gagelmann, Nico, Wolschke, Christine, Klyuchnikov, Evgeny, Christopeit, Maximilian, Ayuk, Francis, Kröger, Nicolaus
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Sprache:eng
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Zusammenfassung:This analysis aimed to systematically review and synthesize the existing evidence regarding the outcome of tyrosine kinase inhibitor (TKI) maintenance therapy after allogeneic stem-cell transplantation for patients with -ITD-mutated acute myeloid leukemia (AML). We searched publicly available databases, references lists of relevant reviews, registered trials, and relevant conference proceedings. A total of 7 studies comprising 680 patients were included. Five studies evaluated sorafenib and 2 studies evaluated midostaurin, compared with control. The incidence of relapse was significantly reduced after TKI therapy, showing an overall pooled risk ratio (RR) of 0.35 (95% confidence interval [CI], 0.23-0.51; < 0.001), with a marked 65% reduced risk for relapse. The overall pooled RR for relapse-free survival and overall survival showed significantly improved outcome after TKI maintenance therapy, being 0.48 (95% CI, 0.37-0.61; < 0.001) and 0.48 (95% CI, 0.36-0.64; < 0.001). The risk for relapse or death from any cause was reduced by 52% using TKI. No difference in outcome was seen for non-relapse mortality, and the risk for chronic or acute graft-vs. -host disease appeared to be increased, at least for sorafenib. In conclusion, post-transplant maintenance therapy with TKI was associated with significantly improved outcome in relapse and survival in patients with -ITD positive AML.
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2021.630429