
| ID | 70952 |
| フルテキストURL | |
| 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
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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
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| 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.
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| キーワード | WT1 mRNA
Acute myeloid leukemia
Venetoclax
Azacitidine
Measurable residual disease
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| 発行日 | 2026-05-09
|
| 出版物タイトル |
Annals of Hematology
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| 巻 | 105巻
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| 号 | 7号
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| 出版者 | Springer Science and Business Media LLC
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| 開始ページ | 105
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| ISSN | 1432-0584
|
| 資料タイプ |
学術雑誌論文
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| 言語 |
英語
|
| OAI-PMH Set |
岡山大学
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| 著作権者 | © The Author(s) 2026
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| 論文のバージョン | publisher
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| PubMed ID | |
| DOI | |
| 関連URL | isVersionOf https://doi.org/10.1007/s00277-026-07046-5
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| ライセンス | http://creativecommons.org/licenses/by-nc-nd/4.0/
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| 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
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| 助成情報 |
( 国立大学法人岡山大学 / Okayama University )
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