Clinical Trials / Research Studies
Cytokine-Induced Memory-Like Natural Killer Cells (CIML-NK) for Relapsed & Refractory Acute Myeloid Leukemia (AML)
Why are we doing this research?
The goal of treatment of relapsed or refractory acute myeloid leukemia (AML) is to achieve remission and proceed to hematopoietic stem cell transplant (HSCT). Unfortunately, standard protocols have limited success. In this study the investigators will identify patients with relapsed or refractory AML who are unlikely to benefit from standard chemotherapy protocols and do not qualify for, or do not wish to participate in, institutional chemotherapy trials. Peripheral blood from a related haploidentical donor will be collected for the isolation of natural killer (NK) cells. NK cells will be induced into a memory-like state using cytokine supplementation only. In this Phase I/II study, patients will receive a lymphodepleting chemotherapy regimen, after which the cytokine-induced memory-like NK cells (CIML-NKs) will be infused. The primary study endpoint is the feasibility and safety of infusion of the cells. The secondary endpoints are efficacy, as measured by clinical response per standard criteria and ability to subsequently undergo allogeneic HSCT, and the persistence of memory-like NK cells in the blood.
Who can participate?
Inclusion Criteria:
- Of age ≥ 18 years at the time of study enrollment
- With AML diagnosed per 2016 WHO criteria
- With relapsed or refractory AML in their bone marrow
- Refractory disease: Patients must have ≥ 5% blasts in the bone marrow after 2 courses of intensive induction treatment
- Relapsed disease: Patients must have ≥ 5% blasts in the bone marrow, or reappearance of blasts in the blood, within 6 months of initial complete remission
- With available haploidentical related donors
- With performance level of ≥ 50% on Karnofsky scale
Exclusion Criteria:
- Disease: isolated central nervous system (CNS) disease, or isolated extramedullary disease, or diagnosis of acute promyelocytic leukemia (APML). Patients with extramedullary disease in combination with bone marrow disease are eligible for enrollment.
- Infectious Disease: Active uncontrolled infection
- Renal function: Radioisotope determined Glomerular Function Rate <50 mL/min/1.73m2
- Cardiac function: Systolic ejection fraction <45% by echocardiogram
- Pulmonary Function: Oxygen saturation <92% on room air
- Hepatic function: Total bilirubin > 2mg/dL, AST and ALT more than three times the upper limit of normal
- Concomitant medications: receiving either >10mg prednisone equivalent daily, or >0.5mg/kg prednisone equivalent daily, whichever is less
- Concomitant investigational treatments: receiving other investigational therapies
- Known allergy or hypersensitivity reaction to IL-2 injections
- Pregnant or breastfeeding women will not be entered on this study due to risks of fetal and teratogenic adverse events with lymphodepleting chemotherapy. Pregnancy tests must be obtained for female patients. Males or females of reproductive potential may not participate unless they have agreed to use an effective contraceptive method while on study treatment and for six months following completion. Effective contraceptive methods include oral contraceptive pills, patches, or injections, intrauterine devices, having a tubal ligation, having a partner who has had a vasectomy, or not having sex.
Ages
- 18 Years and older
Conditions
- Adult - Leukemia AML Relapse - Refractory
Contact
Cincinnati Children’s Hospital Medical CenterDivision of Hematology/Oncology
3333 Burnet Ave., Cincinnati, OH 45229-3039
Phone: 513-636-2799
cancer@cchmc.org
3333 Burnet Avenue, Cincinnati, Ohio 45229-3026
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