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ID 64314
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Murakami, Hiroyuki Department of Hematology and Oncology, Okayama University Hospital
Matsuoka, Ken-Ichi Department of Hematology and Oncology, Okayama University Hospital
Asano, Takeru Department of Hematology and Oncology, Japanese Red Cross Society Himeji Hospital
Moriyama, Takashi Department of Hematology and Oncology, Okayama University Hospital
Matsumura, Akifumi Department of Hematology and Oncology, Okayama University Hospital
Fujiwara, Hideaki Department of Hematology and Oncology, Okayama University Hospital
Asada, Noboru Department of Hematology and Oncology, Okayama University Hospital Kaken ID researchmap
Ennishi, Daisuke Department of Hematology and Oncology, Okayama University Hospital
Nishimori, Hisakazu Department of Hematology and Oncology, Okayama University Hospital Kaken ID researchmap
Fujii, Keiko Department of Hematology and Oncology, Okayama University Hospital
Fujii, Nobuharu Department of Hematology and Oncology, Okayama University Hospital Kaken ID publons researchmap
Toji, Tomohiro Department of Pathology, Okayama University Hospital
Yoshino, Tadashi Department of Pathology, Okayama University Hospital Kaken ID publons researchmap
Maeda, Yoshinobu Department of Hematology and Oncology, Okayama University Hospital Kaken ID researchmap
Abstract
Venetoclax (VEN) is an oral B-cell lymphoma-2 (BCL-2) inhibitor that has been widely used to treat various hematological disorders. Recent studies have demonstrated that VEN in combination with fludarabine-enhanced high-dose cytarabine (FLA) is effective for treating relapsed or refractory acute myeloid leukemia (AML). In the combination therapy, salvage chemotherapy and VEN are basically concurrently administrated; however, further optimization may enable the treatment to apply to larger numbers of patients with various clinical backgrounds. Here, we describe a case of refractory AML treated with a sequential combination of the intensive chemotherapy (fludarabine, cytarabine, and mitoxantrone; FLAM) and VEN/AZA to bridge to an unrelated cord blood transplantation (uCBT). By continuously adding VEN/AZA after FLAM, the patient achieved morphologic leukemia free state with only minor toxicities. Blood cell counts did not recover until the time of transplantation because of the deep myelosuppression caused by the treatment sequence, but the infection risk was safely managed during this period. After engraftment, maintenance therapy with VEN/AZA was performed, and the patient has survived without disease recurrence for over 9 months after transplantation. Our case suggests that bridging therapy with VEN and AZA from the time of the last chemotherapy to allogeneic transplantation may provide an effective and tolerable treatment strategy for refractory AML. Further studies of larger numbers of cases are needed to validate the effectiveness of this treatment.
Keywords
Refractory acute myeloid leukemia
Transplant
B-cell lymphoma-2
Azacitidine
Venetoclax
Published Date
2022-11-08
Publication Title
Case Reports In Oncology
Volume
volume15
Issue
issue3
Publisher
Karger
Start Page
974
End Page
979
ISSN
1662-6575
NCID
AA12780955
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© 2022 The Author(s).
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Related Url
isVersionOf https://doi.org/10.1159/000526697
License
https://creativecommons.org/licenses/by-nc/4.0/
Funder Name
Japan Society for the Promotion of Science
助成番号
26461449