Efficacy and Safety of anti-GD2 monoclonal antibodies in the Management
of High-Risk Neuroblastoma: A Systematic Review and Meta-Analysis
- Muhammad Ahmad,
- Malik Khan,
- Muhammad Maaz Bin Zahid,
- Aizaz Ali,
- Dawood Shehzad,
- Salman Khan,
- Jibran Ikram,
- Muhammad Esmat,
- Amna Hussain
Malik Khan
Yale University Department of Radiology and Biomedical Imaging
Corresponding Author:malik.khan@yale.edu
Author ProfileAmna Hussain
Liaquat University of Medical and Health Sciences
Author ProfileAbstract
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Introduction: Neuroblastoma (NB) is a malignant tumor of the
sympathetic nervous system that usually occurs in children below 5 years
of age. High-risk Neuroblastoma (HR-NB) has a poor prognosis despite
several treatment strategies. Anti-GD2 monoclonal antibodies
(dinutuximab) have recently been added to the standard of care due to
improved prognosis. We aimed to systematically assess the outcomes of
HR-NB patients treated with anti-GD2 monoclonal antibodies and compare
them with those on other treatment regimens. Methods: A
comprehensive search strategy was used to search PubMed and the Cochrane
Library for articles investigating the effect of dinutuximab on the
outcomes of patients with HR-NB. Eligibility criteria included: 1)
Diagnosis of HR-NB based on INSS and INRG staging, and MYCN status. 2)
Dinutuximab or dinutuximab-beta as the primary agent used in
intervention group. 3) Mean/median follow-up time greater than 6 months.
Three investigators independently reviewed and extracted relevant
articles. Any disagreements were addressed through consultation with
other authors. Risk of bias assessment of the selected articles were
conducted using the Cochrane Risk of Bias Tool for randomized controlled
trials (RCTs) and Newcastle-Ottawa scale for observational studies.
Review Manager Software was used to obtain and display the meta-analysis
estimates in forest plots. Random effects models were used to calculate
the mean difference and overall estimated effects for continuous
variables. The main outcomes were all-cause mortality and 5-years
event-free survival (5-year-EFS), while the secondary endpoints were the
incidence of complete remission and adverse events associated with
dinutuximab therapy. Results: Five studies, including two RCTs,
two secondary analyses of clinical trials, and one retrospective cohort
study, comprising 1,393 participants were included in the analysis. 686
of the patients received dinutuximab while the remaining 707 patients
were assigned to other therapies as controls. Dinutuximab was associated
with lower all-cause mortality as compared to control [Pooled RR,
0.41; 95% CI, 0.22-0.75, P=0.004, I 2=31%].
5-year-EFS was also greater for patients treated with dinutuximab [MD:
0.12; 95% CI, 0.09-0.16; P<0.001, I
2=98%]. Dinutuximab was associated with a
nonsignificant increase in the incidence of complete remission (Pooled
RR, 3.63; 95% CI, 0.64-20.53, P=0.15, I2=70%). The common adverse
events associated with dinutuximab therapy included fever, fluid
retention, hypotension, hypoxia, and diarrhea. Keywords:
dinutuximab, anti-GD2 monoclonal antibody, High-risk Neuroblastoma
(HR-NB).