VA Induction and Bridging Transplantation for Hypoplastic/Secondary AML
2026年6月7日 更新者:The First Affiliated Hospital of Soochow University
A Multicenter, Single-arm Clinical Study of Venetoclax Combined With Azacitidine Induction and Bridging to Allogeneic Hematopoietic Stem Cell Transplantation for the Treatment of Hypoplastic or Secondary Acute Myeloid Leukemia
The purpose of this study is to explore the efficacy and safety of venetoclax combined with azacitidine(VA) induction followed by bridging allogeneic hematopoietic stem cell transplantation (allo-HSCT) in the treatment of hypoplastic and secondary acute myeloid leukemia (AML).
調査の概要
状態
まだ募集していません
詳細な説明
Under the traditional intensive chemotherapy model, patients with hypoplastic or secondary acute myeloid leukemia (AML) often have poor bone marrow reserve and prolonged post-chemotherapy cytopenia, leading to high early mortality, low remission rates, and short median survival.
To address this, the use of venetoclax combined with a hypomethylating agent (the VA regimen) as induction therapy significantly improves complete remission (CR) and overall survival (OS).
Subsequent bridging to allogeneic hematopoietic stem cell transplantation (allo-HSCT) as consolidation further enhances OS and relapse-free survival (RFS).
This combined strategy demonstrates a clear synergistic effect: the VA regimen effectively increases the transplantation rate, and for patients with relapsed/refractory (R/R) AML, a low-intensity regimen followed by bridging transplantation is non-inferior to traditional intensive chemotherapy, achieving a "1+1>2" therapeutic benefit.
Therefore, the investigators conducted a prospective study to evaluate the efficacy and safety of VA regimen induction followed by allo-HSCT in patients with hypoplastic and secondary AML.
研究の種類
介入
入学 (推定)
50
段階
- 適用できない
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究連絡先
- 名前:Zhen Shen, Doctor
- 電話番号:0512-67976802
- メール:zhenshen96@sina.cn
研究場所
-
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Jiangsu
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Suzhou、Jiangsu、中国、215000
- The First Affiliated Hospital of Soochow University
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参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
いいえ
説明
Inclusion Criteria:
- Age ≥18 years.
- Previously untreated acute myeloid leukemia (AML) diagnosed according to the 2022 ELN guidelines. Patients with isolated extramedullary disease (i.e., no evidence of AML in bone marrow or peripheral blood) are not eligible.
- Bone marrow biopsy demonstrating cellularity <20% or concurrent myelofibrosis; Or a prior history of an antecedent hematologic disorder, radiotherapy/chemotherapy-related history, or presence of myelodysplasia-related changes (AML-MRC according to WHO-HEAM5).
- The patient is deemed suitable for allogeneic hematopoietic stem cell transplantation as assessed by the treating physician.
- Adequate organ function, defined as follows: a. Good liver function: serum total bilirubin ≤2.0 × upper limit of normal (ULN); if considered due to Gilbert's disease or leukemia, serum total bilirubin <3.0 × ULN. Aspartate aminotransferase (AST), alanine aminotransferase (ALT), and alkaline phosphatase (ALP) ≤3.0 × ULN, unless considered due to leukemia. b. Good renal function: serum creatinine ≤2.0 × ULN or creatinine clearance >30 mL/min calculated using the Cockcroft-Gault formula. c. No history of chronic lung disease and no dyspnea. Otherwise, documented diffusing capacity of the lung for carbon monoxide ≤40% (adjusted for hemoglobin if available) and forced expiratory volume in 1 second/forced vital capacity ≥50%.
- ECOG performance status score 0-2.
- Ability to understand and voluntarily sign informed consent.
- Women of childbearing potential must have a negative serum pregnancy test before initiation of study treatment.
Exclusion Criteria:
- Prior treatment for AML, except non-cytotoxic therapy given to stabilize disease.
- White blood cell count ≥10×10⁹/L, or presence of proliferation-associated gene mutations such as FLT3.
- Favorable risk group according to the 2022 ELN prognostic stratification, e.g., t(8;21), inv(16)/t(16;16), NPM1 mutation, or CEBPA bZIP in-frame mutation.
- No suitable stem cell donor available.
- Acute promyelocytic leukemia (APL).
- Clinical symptoms suggestive of active central nervous system (CNS) leukemia or known CNS leukemia.
- Life-threatening immediate complications of leukemia, such as uncontrolled bleeding, hypoxic pneumonia, sepsis, and/or disseminated intravascular coagulation (DIC). Expected survival <12 weeks.
- Prior allogeneic hematopoietic stem cell transplantation for a hematologic disorder.
- Current use of strong CYP3A4 inducers or narrow-therapeutic-window CYP3A4 substrates; enrollment is allowed only if these drugs can be switched to alternatives ≥5 half-lives before the first dose of study treatment.
- Active, uncontrolled systemic fungal, bacterial, or viral infection despite appropriate antibiotic, antiviral, or other therapy.
- Known infection with human immunodeficiency virus (HIV) or active hepatitis B virus (HBV) or hepatitis C virus (HCV) that cannot be controlled by therapy.
- Another active malignancy, unless the patient has been disease-free for ≥5 years before initiation of study treatment. However, patients with the following history/concurrent conditions or similar indolent cancers are eligible: Basal cell or squamous cell carcinoma of the skin Carcinoma in situ of the cervix Carcinoma in situ of the breast Prostate cancer found incidentally on histology.
- Significant active cardiac disease within 6 months before initiation of study treatment, including New York Heart Association (NYHA) Class III or IV congestive heart failure, myocardial infarction, unstable angina, and/or stroke.
- Uncontrolled hypertension (systolic blood pressure >180 mmHg or diastolic blood pressure >100 mmHg).
- Dysphagia, short-bowel syndrome, gastroparesis, or other conditions that limit oral intake or gastrointestinal absorption.
- Known history of progressive multifocal leukoencephalopathy (PML).
- Known hypersensitivity to any component of venetoclax or azacitidine.
- Female patient who is pregnant or breastfeeding.
- Any other medical or psychological condition that, in the investigator's opinion, could interfere with the patient's ability to sign informed consent or participate in the study.
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:A
VA induction+Allo-HSCT consolidation
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Venetoclax was administered at 100 mg on day 1, 200 mg on day 2, and 400 mg on days 3-28 of cycle 1.
Azacitidine was administered at 75 mg/m² on days 1-7 of cycle 1.
All patients proceeded directly to allogeneic HSCT after cycle 1, regardless of remission.
Myeloablative or intensified conditioning was preferred; reduced-intensity conditioning was allowed for intolerant patients.
Donor source and transplant type were not restricted.
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Overall Survival (OS)
時間枠:2 year
|
Time from the date of diagnosis to death due to any cause.
|
2 year
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Complete Remission Rate(CRR)
時間枠:Day 28 of induction therapy and 56 days post-transplantation
|
Bone marrow blasts <5%, absence of extramedullary disease, no circulating blasts, peripheral blood neutrophil count ≥1.0×10⁹/L, platelet count ≥100×10⁹/L, independent of transfusion or growth factor support.
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Day 28 of induction therapy and 56 days post-transplantation
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Composite Complete Remission Rate (CCRR)
時間枠:Day 28 of induction therapy and 56 days post-transplantation
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The proportion of patients achieving complete remission (CR), complete remission with incomplete hematologic recovery (CRi), or complete remission with partial hematologic recovery (CRh).
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Day 28 of induction therapy and 56 days post-transplantation
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Disease-free Survival (DFS)
時間枠:2 year
|
Time from achieving disease remission to disease relapse or death from any cause.
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2 year
|
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GVHD-free and Relapse-free Survival (GRFS)
時間枠:2 year
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Time from transplant date to the first occurrence of grade III-IV acute GVHD, chronic GVHD requiring systemic treatment, disease relapse, or death from any cause.
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2 year
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Cumulative Incidence of Relapse (CIR)
時間枠:2 year
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Time from transplant date to disease relapse.
|
2 year
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Non-relapse Mortality (NRM)
時間枠:2 year
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Time from transplant date to death due to non-relapse/progression causes.
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2 year
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協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
協力者
捜査官
- 主任研究者:Suning Chen, Doctor、The First Affiliated Hospital of Soochow University
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (推定)
2026年6月1日
一次修了 (推定)
2029年5月31日
研究の完了 (推定)
2029年8月31日
試験登録日
最初に提出
2026年6月1日
QC基準を満たした最初の提出物
2026年6月7日
最初の投稿 (実際)
2026年6月9日
学習記録の更新
投稿された最後の更新 (実際)
2026年6月9日
QC基準を満たした最後の更新が送信されました
2026年6月7日
最終確認日
2026年5月1日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- 2026531
- 09021420250003 (その他の助成金/資金番号:Suzhou University Affiliated First Hospital 'Yanzhen Lingfei' Program)
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
いいえ
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いいえ
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