Combination Chemotherapy (FLAG-Ida) Followed Immediately by Reduced-Intensity Total Body Radiation Therapy and Donor Hematopoietic Cell Transplant for the Treatment of Adults Age 60 and Older With Newly Diagnosed Adverse-Risk Acute Myeloid Leukemia or Other High-Grade Myeloid Cancer

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorFred Hutchinson Cancer Center

About this trial

This phase II trial tests the safety, side effects, and how well combination chemotherapy with fludarabine, high-dose cytarabine, granulocyte colony-stimulating factor (G-CSF), and idarubicin (FLAG-Ida) followed immediately by reduced-intensity total body radiation therapy, called total body irradiation (TBI), and donor hematopoietic cell transplant (HCT) works in treating adults age 60 and older with newly diagnosed adverse-risk acute myeloid leukemia (AML) or other high-grade myeloid cancer. Despite advances in supportive care and the approval of more than 10 new drugs since 2017, the outcomes of older adults with adverse-risk acute myeloid leukemia and other high-grade myeloid cancers remains poor. Most patients are expected to die from their cancer or the consequences of treatment-related side effects. Donor HCT is a very important part of any curative-cancer treatment for these patients. However, while accepted as standard care for decades, this treatment exposes patients to long periods of drug-induced low blood cell counts and the problems associated with low blood counts, like infections and bleeding, which are associated with significant risk of chronic side effects and death. This study will use a different approach to the upfront curative-cancer treatment of older adults with an adverse-risk AML or other high-grade myeloid cancer. This study will use intense chemotherapy followed a few days later by lower-dose TBI and donor HCT. Chemotherapy drugs, such as idarubicin, fludarabine, high-dose cytarabine work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. G-CSF helps the bone marrow make more white blood cells in patients with low white blood cell count due to cancer treatment. This approach allows effective treatment of cancer cells and overall reduction of the period of low blood cells counts. This decreases the risk for problems associated with low blood counts, such as infection and chronic side effects. Decreasing these are important for older adults who undergo HCT. This treatment strategy may improve treatment outcomes by allowing more patients to successfully undergo donor HCT and reduce the risk of low blood cell counts and the problems associated with low blood counts. Giving chemotherapy followed immediately by reduced-intensity TBI and donor HCT may be safe, tolerable and/or effective in treating adults age 60 and older with newly diagnosed adverse-risk AML or other high-grade myeloid cancer.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

PARTICIPANTS: Age ≥ 60 years. Adults age < 60 years are eligible if they are felt to be unsuitable candidates for myeloablative conditioning as per physician assessment

PARTICIPANTS: Ability to understand and willingness to sign a written informed consent document. Legally authorized representatives may sign and give informed consent on behalf of potential study participants

Adverse-risk AML (using 2022 International Consensus Classification for disease categorization and 2022 European LeukemiaNet [ELN] criteria for molecular/cytogenetic risk assignment)

Acute leukemia of ambiguous lineage (using 2022 International Consensus Classification for disease categorization)

Disqualifiers

PARTICIPANTS: Active central nervous system (CNS) disease

PARTICIPANTS: Decompensated congestive heart failure and/or uncontrolled arrhythmia and/or significant medical history of cardiac disease precluding allogeneic HCT

PARTICIPANTS: Significant medical history of pulmonary disease and/or symptoms suggestive of pulmonary disease precluding allogeneic HCT

PARTICIPANTS: Treatment with any other approved or investigational anti-leukemia agent(s) at the time of initiation of study treatment

Trial design

Design model

Single group

Treatments tested in this trial

  • Allogeneic Hematopoietic Stem Cell Transplantation

    Procedure/Surgery

    Undergo allogeneic HCT

  • Biospecimen Collection

    Procedure/Surgery

    Undergo blood sample collection

  • Bone Marrow Aspiration

    Procedure/Surgery

    Undergo bone marrow biopsy and/or aspiration

  • Bone Marrow Biopsy

    Procedure/Surgery

    Undergo bone marrow biopsy and/or aspiration

  • Cytarabine

    Drug

    Given IV

  • Echocardiography Test

    Procedure/Surgery

    Undergo ECHO

  • Fludarabine

    Drug

    Given IV

  • Idarubicin

    Drug

    Given IV

  • Multigated Acquisition Scan

    Procedure/Surgery

    Undergo MUGA

  • Peripheral Blood Stem Cell

    Biological/Vaccine

    Given IV

  • Questionnaire Administration

    Other intervention

    Ancillary studies

  • Recombinant Granulocyte Colony-Stimulating Factor

    Biological/Vaccine

    Given SC

  • Total-Body Irradiation

    Radiation

    Undergo TBI

Treatment groups

20 Participants
are divided into 1 treatment group
Group A: Treatment (FLAG-Ida, TBI, HCT)Experimental treatment 13 interventions

Trial outcomes

Primary outcomes

1

Proportion of participants starting study treatment with FLAG-Ida within 42 days of the date of informed consent

Will evaluate the proportion of participants starting study treatment with FLAG-Ida within 42 days of the date of informed consent.

Time frame
Up to 42 days after informed consent

Secondary outcomes

1

Number of patients transplanted

Will evaluate the number of patients transplanted.

Time frame
Up to 2 years
2

Time from day of consent to day of allogeneic hematopoietic cell transplant (HCT)

Will evaluate time from day of consent to day of allogeneic HCT.

Time frame
From day of consent to day of allogeneic hematopoietic cell transplant (HCT)
3

Reasons for failure to undergo allogeneic transplantation (allo-HCT)

Identified reasons for failure to undergo allogeneic transplantation (e.g., lack of suitable donor, complications of disease) will be systematically categorized and quantitatively reported.

Time frame
Up to 2 years following Screening enrollment
4

Incidence of adverse events

Will evaluate the number of participants with non-hematologic adverse events ≥ grade 3. Will use the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 for toxicity and adverse event reporting.

Time frame
From start of conditioning (Day -9) to study-defined neutrophil engraftment, or adversely, to graft failure

Other outcomes

Sponsors and contacts

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