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Gilteritinib as Bridging and Posttransplant Maintenance for Relapsed Acute Myeloid Leukemia with FLT3-ITD Mutation Accompanied by Extramedullary Disease in Elderly

A 69-year-old woman was diagnosed with acute myeloid leukemia (AML) with an FMS-like tyrosine kinase 3-internal tandem duplication (FLT3-ITD) mutation. Complete remission (CR) was achieved after induction therapy, but AML resulted in a hematological relapse two months after the consolidation chemoth...

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Autores principales: Saburi, Masuho, Sakata, Masanori, Maruyama, Rika, Kodama, Yosuke, Takata, Hiroyuki, Miyazaki, Yasuhiko, Kawano, Katsuya, Wada, Junpei, Urabe, Shogo, Ohtsuka, Eiichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10468783/
https://www.ncbi.nlm.nih.gov/pubmed/37662831
http://dx.doi.org/10.1155/2023/7164742
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author Saburi, Masuho
Sakata, Masanori
Maruyama, Rika
Kodama, Yosuke
Takata, Hiroyuki
Miyazaki, Yasuhiko
Kawano, Katsuya
Wada, Junpei
Urabe, Shogo
Ohtsuka, Eiichi
author_facet Saburi, Masuho
Sakata, Masanori
Maruyama, Rika
Kodama, Yosuke
Takata, Hiroyuki
Miyazaki, Yasuhiko
Kawano, Katsuya
Wada, Junpei
Urabe, Shogo
Ohtsuka, Eiichi
author_sort Saburi, Masuho
collection PubMed
description A 69-year-old woman was diagnosed with acute myeloid leukemia (AML) with an FMS-like tyrosine kinase 3-internal tandem duplication (FLT3-ITD) mutation. Complete remission (CR) was achieved after induction therapy, but AML resulted in a hematological relapse two months after the consolidation chemotherapy. Relapse was accompanied by multiple skin lesions that demonstrated leukemic cell infiltration as well as a drooping right eyelid with extroversion of the eye due to right oculomotor palsy. Gilteritinib was started as salvage therapy, and bone marrow blasts decreased to 0.8% after one month. Two months later, the eye symptoms improved, and the patient underwent cord blood transplantation (CBT). The skin lesions disappeared after the conditioning regimen, and the patient achieved CR status with complete donor chimerism at day 28. Gilteritinib was restarted as posttransplant maintenance therapy on day 53 of CBT. No adverse events other than mild hepatotoxicity were observed, and the patient was alive and in CR status, while continuing gilteritinib at one year and seven months after CBT. Bridging and posttransplant maintenance therapy with gilteritinib may be a promising therapeutic option for relapsed AML with the FLT3-ITD mutation in elderly patients.
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spelling pubmed-104687832023-09-01 Gilteritinib as Bridging and Posttransplant Maintenance for Relapsed Acute Myeloid Leukemia with FLT3-ITD Mutation Accompanied by Extramedullary Disease in Elderly Saburi, Masuho Sakata, Masanori Maruyama, Rika Kodama, Yosuke Takata, Hiroyuki Miyazaki, Yasuhiko Kawano, Katsuya Wada, Junpei Urabe, Shogo Ohtsuka, Eiichi Case Rep Hematol Case Report A 69-year-old woman was diagnosed with acute myeloid leukemia (AML) with an FMS-like tyrosine kinase 3-internal tandem duplication (FLT3-ITD) mutation. Complete remission (CR) was achieved after induction therapy, but AML resulted in a hematological relapse two months after the consolidation chemotherapy. Relapse was accompanied by multiple skin lesions that demonstrated leukemic cell infiltration as well as a drooping right eyelid with extroversion of the eye due to right oculomotor palsy. Gilteritinib was started as salvage therapy, and bone marrow blasts decreased to 0.8% after one month. Two months later, the eye symptoms improved, and the patient underwent cord blood transplantation (CBT). The skin lesions disappeared after the conditioning regimen, and the patient achieved CR status with complete donor chimerism at day 28. Gilteritinib was restarted as posttransplant maintenance therapy on day 53 of CBT. No adverse events other than mild hepatotoxicity were observed, and the patient was alive and in CR status, while continuing gilteritinib at one year and seven months after CBT. Bridging and posttransplant maintenance therapy with gilteritinib may be a promising therapeutic option for relapsed AML with the FLT3-ITD mutation in elderly patients. Hindawi 2023-08-23 /pmc/articles/PMC10468783/ /pubmed/37662831 http://dx.doi.org/10.1155/2023/7164742 Text en Copyright © 2023 Masuho Saburi et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Saburi, Masuho
Sakata, Masanori
Maruyama, Rika
Kodama, Yosuke
Takata, Hiroyuki
Miyazaki, Yasuhiko
Kawano, Katsuya
Wada, Junpei
Urabe, Shogo
Ohtsuka, Eiichi
Gilteritinib as Bridging and Posttransplant Maintenance for Relapsed Acute Myeloid Leukemia with FLT3-ITD Mutation Accompanied by Extramedullary Disease in Elderly
title Gilteritinib as Bridging and Posttransplant Maintenance for Relapsed Acute Myeloid Leukemia with FLT3-ITD Mutation Accompanied by Extramedullary Disease in Elderly
title_full Gilteritinib as Bridging and Posttransplant Maintenance for Relapsed Acute Myeloid Leukemia with FLT3-ITD Mutation Accompanied by Extramedullary Disease in Elderly
title_fullStr Gilteritinib as Bridging and Posttransplant Maintenance for Relapsed Acute Myeloid Leukemia with FLT3-ITD Mutation Accompanied by Extramedullary Disease in Elderly
title_full_unstemmed Gilteritinib as Bridging and Posttransplant Maintenance for Relapsed Acute Myeloid Leukemia with FLT3-ITD Mutation Accompanied by Extramedullary Disease in Elderly
title_short Gilteritinib as Bridging and Posttransplant Maintenance for Relapsed Acute Myeloid Leukemia with FLT3-ITD Mutation Accompanied by Extramedullary Disease in Elderly
title_sort gilteritinib as bridging and posttransplant maintenance for relapsed acute myeloid leukemia with flt3-itd mutation accompanied by extramedullary disease in elderly
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10468783/
https://www.ncbi.nlm.nih.gov/pubmed/37662831
http://dx.doi.org/10.1155/2023/7164742
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