- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07635485
VA Induction and Bridging Transplantation for Hypoplastic/Secondary AML
7 giugno 2026 aggiornato da: 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).
Panoramica dello studio
Stato
Non ancora reclutamento
Intervento / Trattamento
Descrizione dettagliata
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.
Tipo di studio
Interventistico
Iscrizione (Stimato)
50
Fase
- Non applicabile
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Contatto studio
- Nome: Zhen Shen, Doctor
- Numero di telefono: 0512-67976802
- Email: zhenshen96@sina.cn
Luoghi di studio
-
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Jiangsu
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Suzhou, Jiangsu, Cina, 215000
- The First Affiliated Hospital of Soochow University
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Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
No
Descrizione
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.
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: A
VA induction+Allo-HSCT consolidation
|
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.
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Overall Survival (OS)
Lasso di tempo: 2 year
|
Time from the date of diagnosis to death due to any cause.
|
2 year
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Complete Remission Rate(CRR)
Lasso di tempo: 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.
|
Day 28 of induction therapy and 56 days post-transplantation
|
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Composite Complete Remission Rate (CCRR)
Lasso di tempo: 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)
Lasso di tempo: 2 year
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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)
Lasso di tempo: 2 year
|
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)
Lasso di tempo: 2 year
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Time from transplant date to disease relapse.
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2 year
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Non-relapse Mortality (NRM)
Lasso di tempo: 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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Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Collaboratori
Investigatori
- Investigatore principale: Suning Chen, Doctor, The First Affiliated Hospital of Soochow University
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Stimato)
1 giugno 2026
Completamento primario (Stimato)
31 maggio 2029
Completamento dello studio (Stimato)
31 agosto 2029
Date di iscrizione allo studio
Primo inviato
1 giugno 2026
Primo inviato che soddisfa i criteri di controllo qualità
7 giugno 2026
Primo Inserito (Effettivo)
9 giugno 2026
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
9 giugno 2026
Ultimo aggiornamento inviato che soddisfa i criteri QC
7 giugno 2026
Ultimo verificato
1 maggio 2026
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- 2026531
- 09021420250003 (Altro numero di sovvenzione/finanziamento: Suzhou University Affiliated First Hospital 'Yanzhen Lingfei' Program)
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
NO
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
No
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
No
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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