Early Use of Dinutuximab Beta in Patients with High-Risk Neuroblastoma.
Neofit Juriev SpasovMariya SpasovaPublished in: Case reports in pediatrics (2021)
Neuroblastoma is the most common extracranial solid tumor in children, accounting for 15% of all pediatric cancer deaths. High-risk neuroblastoma (HRNB) is a particularly difficult-to-treat form of the disease that requires aggressive multimodality therapy, including induction chemotherapy, consolidation therapy with high-dose chemotherapy and autologous stem cell transplant, and maintenance therapy with dinutuximab beta. Despite treatment advances, the prognosis of these patients remains poor. As a better response to induction therapy has been associated with prolonged survival in patients with HRNB, we hypothesized that early use of dinutuximab beta-post-induction chemotherapy-may improve patient outcomes. We describe here our experience of administering at least one cycle of dinutuximab beta post-induction and prior to surgery in three children with HRNB who did not demonstrate a complete response to induction chemotherapy. All three patients achieved complete remission. Early use of dinutuximab beta may therefore have the potential to improve outcomes in patients with HRNB.
Keyphrases
- end stage renal disease
- stem cells
- ejection fraction
- high dose
- newly diagnosed
- chronic kidney disease
- locally advanced
- prognostic factors
- minimally invasive
- low dose
- cell therapy
- squamous cell carcinoma
- papillary thyroid
- patient reported outcomes
- systemic lupus erythematosus
- adipose tissue
- acute coronary syndrome
- radiation therapy
- metabolic syndrome
- patient reported
- percutaneous coronary intervention
- disease activity
- surgical site infection