This is an prospective study to evaluate the safety and efficacy of naxitamab monotherapy or combined with chemotherapy or combined with chemotherapy and checkpoint inhibitor in the treatment of pediatric high-risk and refractory/relapsed neuroblastoma in Sun Yat-sen University Cancer Center.
Patients with high risk neuroblastoma who obtain CR after chemotherapy combined with surgery, radiotherapy and/or hematopoietic stem cell transplantation received axitamab and GM-CSF. Patients with high-risk neuroblastoma treated by chemotherapy combined with surgery, radiotherapy and or hematopoietic stem cell transplantation patients with tumor residual or progression during treatment (refractory) received naxitamab and GM-CSF in combination with irinotecan and temozolomide or naxitamab and GM-CSF in combination with irinotecan and temozolomide and PD-1 antibody.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
120
Naxitamab is administered on days 1, 3, and 5
Each treatment cycle is 28 days and is started with five days (days -4 to 0) of GM-CSF administered at 250 mcg/m2/day in advance of the start of naxitamab infusion. GM-CSF is thereafter administered at 500 mcg/m2/day on days 1 to 5.
Each HITS treatment cycle is 21 days. Irinotecan intravenously (IV) at 50 mg/m2/day will be administered from Day 1-5 concurrently with temozolomide orally at 150 mg/m2/day or 100 mg/m2/day.
Sun Yat-sen University Cancer Center
Guangzhou, Guangdong, China
RECRUITINGORR
The proportion of patients who achieved CR or PR
Time frame: from start of naxitamab treatment to 1.5 years after EOT
DCR
The proportion of patients who achieved CR or PR or SD
Time frame: from start of naxitamab treatment to 1.5 years after EOT
EFS
The time from from start of naxitamab treatment to disease progression, recurrence
Time frame: from start of naxitamab treatment to 1.5 years after EOT
OS
The time from from start of naxitamab treatment to death or loss of follow-up
Time frame: from start of naxitamab treatment to 1.5 years after EOT
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Each HITS treatment cycle is 21 days. Irinotecan intravenously (IV) at 50 mg/m2/day will be administered from Day 1-5 concurrently with temozolomide orally at 150 mg/m2/day or 100 mg/m2/day.
Naxitamab 2.25mg/kg IV will be administered on Days 2, 4, 8 and 10.
GM-CSF 250 mcg/m2/day will be administered subcutaneously on Days 6-10.
Sintilimab was administerd with 3mg/kg (max 200mg) on day 11 every 3 weeks.