About this trial
The goal of this study is to demonstrate that cytokine-induced memory-like natural killer cells (CIML-NK cells) can be generated from donor cells and infused safely into patients with relapsed or refractory neuroblastoma during dinutuximab-based therapy.
Eligibility criteria
Qualifiers
Age 1-39 years at the time of study enrollment
With diagnosis of neuroblastoma with histologic verification
Classified as high-risk neuroblastoma as defined by Children's Oncology Group (COG) risk classification, including patients initially classified as low or intermediate risk at diagnosis with subsequent reclassification as high-risk disease
Recurrent disease at any time after completion of frontline therapy
Disqualifiers
Infectious disease: Active, uncontrolled infection or received a live vaccine within 30 days prior to study enrollment.
Cardiac function: LVEF <50% by echocardiogram, serious uncontrolled cardiac arrhythmias, or history of myocarditis or congestive heart failure (New York Heart Association Functional Classification III or IV)
Pulmonary function: Active interstitial lung disease (ILD)/pneumonitis or history of ILD/pneumonitis requiring systemic corticosteroid treatment.
Renal function: Glomerular Function Rate (GFR) <50 mL/min/1.73 m2 as measured by cystatin C or NM GFR
Trial design
Treatments tested in this trial
- CIML-NK Cells