This is a single-arm, uncontrolled, international, multi-center, clinical,phase 2 trial, in patients ≥ 12 months of age with high-risk neuroblastoma in first remission. 120 patients will be enrolled to receive naxitamab + GM-CSF in combination with isotretinoin.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
3.0 mg/kg/day = 9.0 mg/kg/cycle
250 - 500 microgram/m2/day
160 mg/m2/day
Hong Kong Children's Hospital
Kowloon, Hong Kong
National Medical Research Center Pediatric Hematology, Oncology and Immunology n.a Dmitry Rogachev
Moscow, Russia
Research Institute of Pediatric Oncology ad Hematology of N.N. Blokhin National Medical Research Center of Oncology
Moscow, Russia
2-year progression free survival (PFS)
2-year PFS defined as the proportion of patients alive and without progressive disease (PD) or relapse 2 years after enrollment
Time frame: 2 years
Progression free survival
Progression free survival (defined as time from enrollment until progressive disease/relapse or death, whichever comes first)
Time frame: 128 weeks
1-year progression free survival
1-year progression free survival defined as the proportion of patients alive and without progressive disease or relapse 1 year after enrollment
Time frame: 1 year
1-year and 2-year overall survival
1-year and 2-year overall survival defined as the proportion of patients alive 1 year and 2 years after enrollment, respectively
Time frame: 2 years
2-year event-free survival
2-year event-free survival, defined as the proportion of patients alive and without progressive disease, relapse, secondary malignancy or until last contact if no event occurred, 2 years after enrollment
Time frame: 2 years
Proportion of positive to negative minimal residual disease (MRD) after 2 cycles
Proportion of patients changing from minimal residual disease positive in bone marrow at enrollment (defined as patients assessed as minimal residual disease positive by RTqPCR of bone marrow at enrollment) to minimal residual disease negative at completion of Cycle 2
Time frame: 6 weeks
Proportion of patients with MD positive convert to MRD negative
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Raisa Gorbacheva Memorial Institute of Children Hematology and Transplantation Bone marrow Transplant Clinic
Saint Petersburg, Russia
ICON Cancer Centre Novena
Singapore, Singapore
KK Women's and Children's Hospital
Singapore, Singapore
Asan Medical Center Childrens Hospital
Seoul, South Korea
Samsung Medical Center
Seoul, South Korea
Seoul National University Hospital
Soeul, South Korea
Proportion of patients with disease in bone marrow at enrollment (i.e., minimal disease according to INRC) and convert to minimal residual disease negative (assessed by RTqPCR) at completion of Cycle 2
Time frame: 6 weeks