Vyxeos for Induction of Low- or Intermediate-risk.

Leukemia, Myeloid, Acute Clinical Trial

Official title: Vyxeos for Induction of Newly Diagnosed Low- or Intermediate-risk AML Patients, Age 18-70. A Pilot Study

Status Recruiting

Clinical Trial Summary

Vyxeos Vyxeos is a liposomal-encapsulated combination of cytarabine and daunorubicin, at a molar ratio of 5:1. Delivery of the 5:1 molar ratio seems to prevent antagonistic drug-drug interactions and the liposomal encapsulation increases the plasma half-life of cytarabine and daunorubicin and leads to drug accumulation within the bone marrow (BM).

Despite previous results that highlighted the advantage of Vyxeos for sAML, it is intuitively likely that this powerful drug is also suitable for non-sAML. The mechanism of action is relevant for every AML. Following the FDA approval of the drug for sAML we would like to evaluate its efficacy for low or intermediate risk fms-like tyrosine kinase 3 (FLT3)-negative de novo AML patients. This consideration is particularly relevant by the inclusion of young AML patients in the study.

Gemtuzumab ozogamicin (GO) Gemtuzumab ozogamicin (Mylotarg) - an anti-cluster of differentiation 33 (CD33) monoclonal antibody linked to calicheamicin, was approved for the treatment of newly diagnosed AML patients, when given as a combination with the '7+3' regimen.

One of the goals of the current study is to examine the feasibility and efficacy of the combination of Mylotarg plus Vyxeos.

Minimal/ measurable residual disease (MRD) Minimal or measurable residual disease (MRD) denotes the presence of leukemia cells down to levels of 1:10-4 to 1:10-6, compared with 1:20 in morphology-based assessments. MRD can be evaluated using a variety of multiparameter flow cytometry (MFC) and molecular methods. There are no data regarding the achievement or impact of MRD using Vyxeos as induction therapy. The current trial will address this issue.

Purpose of this Trial The current study is designed to examine the response rate of the Vyxeos as induction therapy for newly diagnosed low/intermediate risk AML patients in the 'real world' setting. Patients will receive the same induction therapy that they were to receive had they not entered this study (cytarabine /daunorubicin ± Mylotarg) but the combination of cytarabine /daunorubicin will be given in the unique formulation of Vyxeos. In addition to classic CR+CRi evaluation, MFC MRD evaluation, using an centralized, internationally recognized laboratory, will be done at the end of induction. In addition, this pilot study will also provide clinical safety information about the combination of Vyxeos with Mylotarg.

Clinical Trial Description

Introduction Induction therapy Currently, most physicians treating 'fit' patients with acute myeloid leukemia (AML) employ an anthracycline plus cytarabine ('7+3' regimen) as induction therapy. In the past few years 2 new drugs were approved as adjuncts to the '7+3' regimen for treatment of fit patients; Midostaurin- a FLT3 inhibitor and gemtuzumab ozogamicin- an anti-CD33 monoclonal antibody linked to chemotherapy. It has been postulated that using the same drugs as in the '7+3' regimen but at a fixed molar ratio of cytarabine and daunorubicin will increase the CR rate and improve minimal residual disease and disease free survival (DFS).

Vyxeos

Vyxeos is a liposomal-encapsulated combination of cytarabine and daunorubicin, at a molar ratio of 5:1. Delivery of the 5:1 molar ratio seems to prevent antagonistic drug-drug interactions and the liposomal encapsulation increases the plasma half-life of cytarabine and daunorubicin and leads to drug accumulation within the bone marrow (BM). Two randomized controlled trials have been reported in newly diagnosed AML patients:

A phase II, multicenter, randomized, open-label trial studied the efficacy and safety of Vyxeos among newly diagnosed AML patients, age 60-75. The study compared 1-2 induction courses of Vyxeos with '7+3' (daunorubicin dose of 45-60 mg/m2). Patients were allowed to receive 1-2 consolidation courses of Vyxeos (in the investigational arm) and low dose cytarabine with/without daunorubicin or intermediate dose cytarabine (in the control arm). The primary end-point was defined as response rate; complete remission (CR) + CR with incomplete hematologic recovery (CRi). 127 patients were enrolled and randomized in 2:1 ratio. The study showed an increased response rate (CR+CRi of 66.7% vs. 51.2%) in the investigational arm but without statistical significance (p=0.7). A planned sub-group analysis of secondary AML (sAML) patients revealed a more impressive, still non-significant, response rate advantage to the Vyxeos patients (57.6% vs. 31.6%, p=.06) but with significant overall survival (OS) superiority (median 12.1 vs. 6.1 months, HR = 0.46, p=.01).

The phase III trial was an open-labeled randomized trial that enrolled only sAML patients, age 60-75, with the exception of patients with antecedent myeloproliferative neoplasm. Patients received 2-3 cycles (1-2 induction courses and 1 consolidation) of either '7+3' with daunorubicin 60 mg/m2 or Vyxeos. The primary end-point was defined as OS. A total of 309 patients were enrolled and randomized in a 1:1 ratio. This study showed a significant OS (median of 9.56 vs. 5.95 months, HR=0.69, p=.005) and CR+CRi rate (47.7% vs. 33.3%, p=.016) advantage for the patients who received the Vyxeos. These results led the Food and Drug Administration (FDA), in August 2017, to approve the drug for use in the treatment of newly diagnosed therapy-related AML (tAML) and AML with myelodysplasia-related changes (MRC).

Despite the results that highlighted the advantage of Vyxeos for sAML, it is intuitively likely that this powerful drug is also suitable for non-sAML. The mechanism of action is relevant for every AML. Following the FDA approval of the drug for sAML we would like to evaluate its efficacy for low or intermediate risk FLT3-negative de novo AML patients. This consideration is particularly relevant by the inclusion of young AML patients in the study.

Gemtuzumab ozogamicin (GO) Gemtuzumab ozogamicin (Mylotarg) - an anti-CD33 monoclonal antibody linked to calicheamicin, was approved for the treatment of newly diagnosed AML patients, when given as a combination with the '7+3' regimen.

The French Alfa-0701 study evaluated the safety and efficacy of GO administered in a fractionated dosing regimen (3 mg/m² administered on Days 1, 4, and 7) when added to the standard '7+3' regimen. Patients with a CR or CR with incomplete platelet recovery (CRp) received consolidation therapy with 2 courses of treatment including daunorubicin plus cytarabine with or without GO, based on their initial randomization. The primary end point was event free survival (EFS) which was longer in the GO arm; median of 17.3 months (95% combination index (CI): 13.4-30.0) vs 9.5 months (95% CI: 8.1-12.0). 3-years EFS was achieved by 39.8% of the GO arm compared to 13.6% of the control arm. OS was better in the GO arm (27.5 vs. 21.8 months) but have not reached statistical significance (HR 0.807, 95% CI: 0.596-1.093, p=0.1646)5. A meta-analysis of GO in combination with chemotherapy for newly diagnosed AML patients concluded that GO does not increase the CR rate but decreases the relapse rate and improves the OS. The drug is ineffective in high risk patients.

One of the goals of the current study is to examine the feasibility and efficacy of the combination of Mylotarg plus Vyxeos.

Minimal/ measurable residual disease (MRD) Several factors present at diagnosis of AML, including cytogenetics, molecular genetics, and age, have been associated with prognosis. Increasing evidence now indicates that the ability to identify residual disease far below the morphology-based 5% blast threshold is an important tool for refining the approach to risk classification. Minimal or measurable residual disease (MRD) denotes the presence of leukemia cells down to levels of 1:10-4 to 1:10-6, compared with 1:20 in morphology-based assessments. MRD can be evaluated using a variety of multiparameter flow cytometry (MFC) and molecular methods. There are no data regarding the achievement or impact of MRD using Vyxeos as induction therapy. The current trial will address this issue.

Purpose of this Trial The current study is designed to examine the response rate of the Vyxeos as induction therapy for newly diagnosed low/intermediate risk AML patients in the 'real world' setting. Patients will receive the same induction therapy that they were to receive had they not entered this study (cytarabine /daunorubicin ± Mylotarg) but the combination of cytarabine /daunorubicin will be given in the unique formulation of Vyxeos. In addition to classic CR+CRi evaluation, MFC MRD evaluation, using an centralized, internationally recognized laboratory, will be done at the end of induction. In addition, this pilot study will also provide clinical safety information about the combination of Vyxeos with Mylotarg.

Gender and Ethnicity Entry to this study is open to both men and women, and to persons of any racial or ethnic group. We are aware of no data that would lead us to expect differential treatment effects by gender and ethnicity and therefore have not incorporated separate accrual goals for these subgroups. ;

Related Conditions & MeSH terms

• Leukemia, Myeloid
• Leukemia, Myeloid, Acute

• NCT number: NCT05599360
• Study type: Interventional
• Source: Shaare Zedek Medical Center
• Contact: Chezi Ganzel, DR
• Phone: 026555438
• Email: ganzelc@szmc.org.il
• Status: Recruiting
• Phase: Phase 2
• Start date: August 7, 2022
• Completion date: March 2027