RecruitingPhase 2NCT06744556

HAV Versus DAV/IAV Induction Regimen in Elderly Patients With AML

HAV Versus DAV/IAV Induction Regimen in Elderly Patients With Acute Myeloid Leukemia Suitable for Intensive Chemotherapy: a Multicenter, Randomized, Controlled Clinical Trial


Sponsor

Institute of Hematology & Blood Diseases Hospital, China

Enrollment

60 participants

Start Date

Jan 21, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Acute myeloid leukemia (AML) represents the most prevalent leukemia type in China. Elderly patients (≥60 years old) have a high incidence rate, accounting for over half of all AML patients, with a median age of onset approximately 68 years. Elderly AML patients have a poor prognosis and are often accompanied with multiple high-risk factors.The 5-year overall survival (OS) is only 3-8%. Before the advent of new targeted drugs, for elderly patients with newly diagnosed AML who were suitable for intensive chemotherapy, the most commonly used chemotherapy regimen remained the classic "3 + 7" regimen. However, the complete remission (CR) rate after induction was approximately 40-60%. The majority of elderly patients were not eligible for allogeneic hematopoietic stem cell transplantation, resulting in a relatively poor long-term survival for elderly AML patients . With the emergence of new targeted drugs, clinical studies both domestically and internationally have demonstrated that the combination of various targeted drugs and demethylating agents has achieved favorable efficacy in elderly/unsuitable for intensive chemotherapy patients with newly diagnosed AML, prolonging their survival. Previously, we initiated a multicenter, prospective, randomized controlled clinical study (registration number: NCT06066242). The aim was to explore the optimal induction regimen for elderly fit patients with newly diagnosed AML. Preliminary data revealed that the regimen of daunorubicin (DNR) or idarubicin (IDA) combined with cytarabine (Ara - C, DA/IA) + venetoclax (Ven, DAV/IAV) had a higher induction remission rate (77.3% )than the DA/IA "3 + 7" and Ven + azacitidine (AZA) regimens (45% - 59%). However, compared to the induction remission rate of young adult patients with newly diagnosed AML (\> 85%), further improvement is still required. Previous research data show that HHT enhances the inhibitory effect of Ara-c on DNA synthesis in tumor cells by influencing cell cycle regulation. The combination of HHT and Ven can jointly affect the apoptotic pathway and enhance cell apoptosis. Therefore, this study intends to establish a prospective, randomized controlled clinical trial to compare the induction remission rates of the HHT + Ara-c + Ven (HAV) regimen with the DAV/IAV regimen, which,based on previous data, had the highest induction remission rate .


Eligibility

Min Age: 60 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This study compares two chemotherapy combinations — HAV versus DAV or IAV — as initial treatment for elderly patients (aged 60–75) with newly diagnosed acute myeloid leukemia (AML) or a related condition called MDS/AML, to find which is safer and more effective in older adults. **You may be eligible if...** - You are between 60 and 75 years old - You have been newly diagnosed with AML or MDS/AML (confirmed by WHO or ICC criteria) - You are in reasonably good physical condition (ECOG 0–2) - Your liver, kidney, and heart function are within acceptable limits - Your heart pumping function (LVEF) is greater than 50% **You may NOT be eligible if...** - You have previously received treatment for AML (not newly diagnosed) - You have another active cancer requiring treatment - You have significant uncontrolled heart disease - You have severe uncontrolled infection Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGdaunorubicin

Used in combination with cytarabine and venetoclax for induction therapy in DAV.

DRUGVenetoclax

Used in combination with cytarabine and daunorubicin for induction therapy in DAV.

DRUGcytarabine

Used in combination with venetoclax and daunorubicin for induction therapy in DAV or used by intermediate does for consolidation therapy.

DRUGazacitidine

Used in combination with venetoclax for maintenance therapy.

DRUGHomoharringtonine

Used in combination with cytarabine and venetoclax for induction therapy in HAV.

DRUGIdarubicin

Used in combination with cytarabine and venetoclax for induction therapy in IAV.


Locations(1)

Blood Diseases Hospital

Tianjin, Tianjin Municipality, China

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NCT06744556


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