Hong Kong Children's Hospital
Hong Kong
Location status: Recruiting
NCT Number: NCT05754684
This is a single-arm clinical trial to evaluate the efficacy and safety of quadruple immunotherapy with natural killer (NK) cells, anti-GD2 antibody, cytokines (interleukin-2 (IL-2) and granulocyte-macrophage colony stimulating factor (GM-CSF)) and retinoid X receptor gamma (RXRg) agonist spironolactone for paediatric patients with relapsed or refractory neuroblastoma.
Interested in participating?
Request InfoUp to 18 year
All sexes
Interventional
Phase 2
Hong Kong
Location status: Recruiting
Included patients will receive intravenous infusion of donor NK cells on day 0, and anti-GD2 antibody (dinutuximab) on day -6 to day -2. IL-2 will be given subcutaneously on day -1, day +1, day +3, day +5, day +7, and day +9. Subcutaneous injection of GM-CSF will be started on day 0, given daily till neutrophil count >1000/mm3. Spironolactone will be started orally on day -1, given three times daily till cessation of GM-CSF.
Alternative anti-GD2 antibody (Naxitamab) can be used instead of dinutuximab, to be given on day -5, day -3, day +1 and day +3.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Natural killer cells isolated from HLA-haploidentical relative donor
Other names: NK cell
Dinutuximab beta iv for 5 days
Other names: Ch14.18
Interleukin-2 sc alternate day for 6 doses
Other names: Aldesleukin
Granulocyte-macrophage colony-stimulating factor sc daily till ANC >2,000/mm3
Other names: Sargramostim
Spironolactone po three time daily
Other names: Aldactone
Naxitamab iv for 4 days (as alternative for dinutuximab)
Other names: hu3F8
Time frame: 1-2 months
Objective response = complete response + partial response + minor response + stable disease
Time frame: up to 1 year
From the date of treatment start until the date of death from any cause, assessed up to 1 year
Time frame: up to 1 year
From date of treatment start until the date of first documented progression or the date of death from any cause, whichever comes first, assessed up to 1 year
Time frame: up to 1 year
relapse = reappearance of tumor after complete response
Time frame: up to 1 month
Adverse events are graded according to Cancer Therapy Evaluation Program Common Terminology Criteria for Adverse Events version 5 (CTCAEv5)
Time frame: up to 1 year
Percentage of donor natural killer cells in the recipient's blood will be evaluated weekly from the date of NK cell infusion for 4 weeks, then every 2 weeks till donor NK cells are undetectable
Contact information is provided by the study sponsor or research team.
Hong Kong Children's Hospital
Other
Quadruple Immunotherapy for Paediatric Patients With Relapsed or Refractory Neuroblastoma
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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