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ID 70952
フルテキストURL
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著者
Sugiura, Hiroyuki Division of Internal Medicine, Fukuyama City Hospital
Asada, Noboru Department of Hematology, Oncology and Respiratory Medicine, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine Kaken ID researchmap
Asano, Takeru Department of Hematology and Oncology, Japanese Red Cross Society Himeji Hospital
Hiramatsu, Yasushi Department of Hematology and Oncology, Japanese Red Cross Society Himeji Hospital
Urata, Tomohiro Department of Hematology and Blood Transfusion, Kochi Health Sciences Center
Imai, Toshi Department of Hematology and Blood Transfusion, Kochi Health Sciences Center
Nakamura, Makoto Department of Hematology, Okayama City Hospital
Yamamoto, Kazuhiko Department of Hematology, Okayama City Hospital
Ishikawa, Tatsunori Department of Hematology, Chugoku Central Hospital of Japan Mutual Aid Association of Public School Teachers
Makita, Masanori Department of Hematology, Chugoku Central Hospital of Japan Mutual Aid Association of Public School Teachers
Yoshioka, Takanori Department of Hematology, NHO Okayama Medical Center
Sunami, Kazutaka Department of Hematology, NHO Okayama Medical Center
Saeki, Kyosuke Division of Hematology, Ehime Prefectural Central Hospital
Nawa, Yuichiro Division of Hematology, Ehime Prefectural Central Hospital
Kimura, Maiko Department of Hematology, Japanese Red Cross Okayama Hospital
Takeuchi, Makoto Department of Hematology, Japanese Red Cross Okayama Hospital
Abe, Masaya Department of Hematology, Oncology and Respiratory Medicine, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine
Asakura, Shoji Department of Internal Medicine, Okayama Rosai Hospital
Yano, Tomofumi Department of Internal Medicine, Okayama Rosai Hospital
Maeda, Yoshinobu Department of Hematology, Oncology and Respiratory Medicine, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine Kaken ID researchmap
抄録
Venetoclax and azacitidine (VEN/AZA), which target BCL-2 and DNA methylation, have demonstrated substantial efficacy, particularly in older or unfit patients with acute myeloid leukemia (AML). Wilms’ Tumor-1 (WT1) mRNA, measurable in peripheral blood (PB), is an established biomarker for monitoring treatment response and predicting AML prognosis. We conducted a retrospective analysis of patients with AML treated with VEN/AZA within the Okayama Hematology Study Group (OHSG). Patients who showed a marked reduction in PB WT1 mRNA levels from baseline after the first or second treatment cycle had significantly improved overall survival (OS) and progression-free survival (PFS). Moreover, achieving PB WT1 mRNA negativity-regardless of whether this occurred early or later in the therapy།was consistently associated with superior OS and PFS. These findings suggest that PB WT1 mRNA is a sensitive and reliable biomarker for predicting treatment response and long-term outcomes in patients with AML receiving VEN/AZA.
キーワード
WT1 mRNA
Acute myeloid leukemia
Venetoclax
Azacitidine
Measurable residual disease
発行日
2026-05-09
出版物タイトル
Annals of Hematology
巻
105巻
号
7号
出版者
Springer Science and Business Media LLC
開始ページ
105
ISSN
1432-0584
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© The Author(s) 2026
論文のバージョン
publisher
PubMed ID
DOI
関連URL
isVersionOf https://doi.org/10.1007/s00277-026-07046-5
ライセンス
http://creativecommons.org/licenses/by-nc-nd/4.0/
Citation
Sugiura, H., Asada, N., Asano, T. et al. WT1 mRNA in peripheral blood enables early prognostic stratification in AML patients receiving venetoclax and azacitidine therapy. Ann Hematol 105, 309 (2026). https://doi.org/10.1007/s00277-026-07046-5
助成情報
( 国立大学法人岡山大学 / Okayama University )