AflacLL1901 (CHOA-AML)

Acute Myeloid Leukemia Clinical Trial

Official title:

CHOA-AML: A Pilot Study for Newly Diagnosed Pediatric Patients With Acute Myeloid Leukemia (AML)

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT04326439
• Other study ID #: IRB00111627
• Status: Terminated
• Phase: Phase 2
• Start date: January 24, 2020
• Est. completion date: March 15, 2022

Study information

• Verified date: May 2022
• Source: Emory University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The investigators propose to study an Aflac-AML chemotherapy backbone prospectively to validate its use in all pediatric AML and to further evaluate the cardiotoxicity with this approach for low risk AML.

Description:

Advances in risk stratification and therapy, have improved the event-free survival (EFS) and overall survival (OS) for pediatric acute myeloid leukemia (AML) to approximately 50% and 65% respectively, with current treatment strategies. Patients with good response to induction and/or those who lack high-risk cytogenetic and molecular features [classified as low-risk AML (LR-AML)] have even better outcomes with EFS and OS approaching 70% and 85% respectively; however, treatment-related toxicities remain a major concern. Anthracycline-based therapeutic regimens expose patients to the risk of anthracycline-induced cardiotoxicity. Therefore, strategies that reduce cardiac toxicities using tailored approaches while maintaining and/or improving outcomes are needed for all patients with AML. The Children's Oncology Group (COG) regimens AAML1031 and AAML0531 utilized an anthracycline-intensive backbone for LR-AML with cumulative anthracycline doxorubicin-equivalent doses of up to 492mg/m2. However, high-risk patients treated with chemotherapy alone received an intensified induction chemotherapy (using mitoxantrone-cytarabine) but with overall reduced doses of anthracycline-equivalent (342mg/m2). The investigators piloted an institutional practice to treat all LR-AML patients with four cycle regimen (Aflac-AML) with the goal of reducing cumulative anthracycline exposure, thereby reducing the risk of cardiotoxicity, while providing three high-dose cytarabine courses. In this pilot institutional experience with this approach, they were able to maintain excellent outcomes for this low-risk group with 3-year event-free survival (EFS) and OS of 70.0% ± 0.1% and 85.5% ± 0.08% respectively, from end of course 1. Recent evolution in cytogenetic classification has further delineated risk groups in AML. Gemtuzumab ozogamicin (GO), an antibody-drug conjugate was shown to reduce relapse risk in patients with CC genotype with de-novo AML on COG study AAML0531. The investigators propose to study an Aflac-AML chemotherapy backbone prospectively to validate its use in all pediatric AML and to further evaluate the cardiotoxicity with this approach for low risk AML.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 8
• Est. completion date: March 15, 2022
• Est. primary completion date: March 15, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A to 21 Years

Eligibility

Inclusion Criteria:

• Age: Patients must be less than 21 years of age at the time of study enrollment

• Diagnosis: Patients must be newly diagnosed with AML

• Patients with previously untreated primary AML who meet the customary criteria for AML with = 20% bone marrow blasts as set out in the 2016 WHO Myeloid Neoplasm Classification are eligible.

• Attempts to obtain bone marrow either by aspirate or biopsy must be made unless clinically prohibitive. In cases where it is clinically prohibitive, peripheral blood with an excess of 20% blasts and in which adequate flow cytometric and cytogenetics/FISH testing is feasible can be substituted for the marrow exam at diagnosis.

• Patients with <20% bone marrow blasts are eligible if they have:

• A karyotypic abnormality characteristic of de novo AML (t(8;21)(q22;q22), inv(16)(p13q22) or t(16;16)(p13;q22) or 11q23 abnormalities,

• the unequivocal presence of megakaryoblasts, or

• Biopsy proven isolated myeloid sarcoma (myeloblastoma; chloroma, including leukemia cutis)

• Performance Level: Patients with acceptable organ function and any performance status are eligible for enrollment

Exclusion Criteria:

• Patients with any of the following constitutional conditions are not eligible:

• Fanconi anemia

• Shwachman syndrome

• Any other known bone marrow failure syndrome

• Patients with constitutional trisomy 21 or with constitutional mosaicism of trisomy 21 Note: Enrollment may occur, pending results of clinically indicated studies to exclude these conditions.

• Other Excluded Conditions:

• Any concurrent malignancy

• Juvenile myelomonocytic leukemia (JMML)

• Philadelphia chromosome positive AML

• Biphenotypic or bilineal acute leukemia

• Acute promyelocytic leukemia (APL)

• Acute myeloid leukemia arising from myelodysplasia

• Therapy-related myeloid neoplasms

Related Conditions & MeSH terms

• Acute Myeloid Leukemia
• AML, Childhood
• Leukemia
• Leukemia, Myeloid
• Leukemia, Myeloid, Acute

Intervention

Drug:
• Cytarabine
100 mg/m²/dose every 12 hours IV Days 1-10
• Daunorubicin
50 mg/m²/dose IV Days 1, 3, 5
• Erwinase
25,000 International Units/m²/dose IM Days 2, 9
• Etoposide
150 mg/m²/dose IV Days 1-5
• Gemtuzumab ozogamicin
Administered as a single 3 mg/m2 dose of GO to be given between days 6-10 during Induction I for patients with CC genotype, in addition to ADE therapy.

Procedure:
• Stem cell transplantation (SCT)
Transplantation of multipotent hematopoietic stem cells from bone marrow

Drug:
• Sorafenib
200 mg/m2/dose daily, rounded to accommodate tablet size. The maximum dose will be 400 mg. Days 7 through 34.

Locations

Country	Name	City	State
United States	Egleston Hospital	Atlanta	Georgia

Sponsors (1)

Lead Sponsor	Collaborator
Emory University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Event-free Survival (EFS) in Low Risk Patients and High Risk Patients	Event-free survival defined as the time from on study to death, failure to achieve remission or relapse in newly diagnosed patients with pediatric acute myeloid leukemia in the Low risk stratification group and High risk stratification group	Up to 2 years post-intervention
Secondary	Overall Survival (OS)	Time from study entry and from end of first course of therapy for newly diagnosed patients with pediatric acute myeloid leukemia	Up to 2 years post-intervention
Secondary	Minimal Residual Disease (MRD) Negative Status	Number of patients that are in remission (MRD negative) after course 1 in participants receiving GO and those that did not receive GO.	Post-induction I, an average of 28 days
Secondary	Disease-free Survival (DFS) for Patients Who Are MRD Negative	Disease-free survival for patients who are MRD negative but lack high or low risk molecular and cytogenetic features, defined as time from end of first course of therapy to death or relapse	Up to 2 years post-intervention
Secondary	Cardiotoxicity in Patients With de Novo AML That Receive the Four-cycle Aflac-AML Regimen With the Inclusion of Dexrazoxane	Number of patients that develop cardiac ejection fraction <50% (CTCAE V5.0 grade 2 or greater dysfunction) either during therapy (early cardiotoxicity) or after completion of therapy (late cardiotoxicity)	At completion of Cycle 4 (each cycle average is 28 days)
Secondary	Proportion of Patients Who Develop Infection and/or Febrile Neutropenia During Each Treatment Course	Number of participants that developed infection and/or febrile neutropenia at the end of each treatment cycle.	At the end of each cycle (each cycle average is 28 days)
Secondary	Duration of Hospital Admission in Patients That Developed Infection and Febrile Neutropenia at the End of Each Treatment Cycle	Duration of hospital admission in patients that developed infection and febrile neutropenia at the end of each treatment cycle	At the end of each cycle (each cycle average is 28 days)