[HTML][HTML] FLT3 inhibitors in acute myeloid leukaemia: assessment of clinical effectiveness, adverse events and future research—a systematic review and meta-analysis

S Majothi, D Adams, J Loke, SP Stevens, K Wheatley… - Systematic reviews, 2020 - Springer
Background FMS-like tyrosine kinase 3 (FLT3) is the most frequent mutation in AML. With
two FLT3 inhibitors recently approved by the FDA (midostaurin and gilteritinib), there is a …

FLT3 inhibitors in acute myeloid leukaemia: assessment of clinical effectiveness, adverse events and future research--a systematic review and meta-analysis.

S Majothi, D Adams, J Loke, SP Stevens… - Systematic …, 2020 - go.gale.com
FLT3 inhibitors in acute myeloid leukaemia: assessment of clinical effectiveness, adverse
events and future research--a systematic review and meta-analysis. - Document - Gale OneFile …

FLT3 inhibitors in acute myeloid leukaemia: assessment of clinical effectiveness, adverse events and future research—a systematic review and meta-analysis.

S Majothi, D Adams, J Loke, SP Stevens… - Systematic …, 2020 - search.ebscohost.com
Background: FMS-like tyrosine kinase 3 (FLT3) is the most frequent mutation in AML. With
two FLT3 inhibitors recently approved by the FDA (midostaurin and gilteritinib), there is a …

FLT3 inhibitors in acute myeloid leukaemia: assessment of clinical effectiveness, adverse events and future research—a systematic review and meta-analysis

S Majothi, D Adams, J Loke, SP Stevens… - Systematic …, 2020 - search.proquest.com
FLT3 inhibitors in acute myeloid leukaemia: assessment of clinical effectiveness, adverse
events and future research—a systema Page 1 RESEARCH Open Access FLT3 inhibitors in …

FLT3 inhibitors in acute myeloid leukaemia: assessment of clinical effectiveness, adverse events and future research-a systematic review and meta-analysis.

S Majothi, D Adams, J Loke, SP Stevens… - Systematic …, 2020 - europepmc.org
FLT3 inhibitors in acute myeloid leukaemia: assessment of clinical effectiveness, adverse
events and future research-a systematic review and meta-analysis. - Abstract - Europe PMC …

[HTML][HTML] FLT3 inhibitors in acute myeloid leukaemia: assessment of clinical effectiveness, adverse events and future research—a systematic review and meta-analysis

S Majothi, D Adams, J Loke… - Systematic …, 2020 - systematicreviewsjournal …
FMS-like tyrosine kinase 3 (FLT3) is the most frequent mutation in AML. With two FLT3
inhibitors recently approved by the FDA (midostaurin and gilteritinib), there is a need to …

FLT3 inhibitors in acute myeloid leukaemia: assessment of clinical effectiveness, adverse events and future research-a systematic review and meta-analysis.

S Majothi, D Adams, J Loke, SP Stevens, K Wheatley… - 2020 - cabidigitallibrary.org
Background: FMS-like tyrosine kinase 3 (FLT3) is the most frequent mutation in AML. With
two FLT3 inhibitors recently approved by the FDA (midostaurin and gilteritinib), there is a …

[PDF][PDF] FLT3 inhibitors in acute myeloid leukaemia: assessment of clinical effectiveness, adverse events and future research—a systematic review and meta-analysis

S Majothi, D Adams, J Loke, SP Stevens, K Wheatley… - 2020 - scholar.archive.org
Background: FMS-like tyrosine kinase 3 (FLT3) is the most frequent mutation in AML. With
two FLT3 inhibitors recently approved by the FDA (midostaurin and gilteritinib), there is a …

FLT3 inhibitors in acute myeloid leukaemia: assessment of clinical effectiveness, adverse events and future research-a systematic review and meta-analysis

S Majothi, D Adams, J Loke… - Systematic …, 2020 - research.birmingham.ac.uk
BACKGROUND: FMS-like tyrosine kinase 3 (FLT3) is the most frequent mutation in AML.
With two FLT3 inhibitors recently approved by the FDA (midostaurin and gilteritinib), there is …

FLT3 inhibitors in acute myeloid leukaemia: assessment of clinical effectiveness, adverse events and future research-a systematic review and meta-analysis

S Majothi, D Adams, J Loke, SP Stevens… - Systematic …, 2020 - pubmed.ncbi.nlm.nih.gov
Background FMS-like tyrosine kinase 3 (FLT3) is the most frequent mutation in AML. With
two FLT3 inhibitors recently approved by the FDA (midostaurin and gilteritinib), there is a …