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Efficacy and Safety of anti-GD2 monoclonal antibodies in the Management of High-Risk Neuroblastoma: A Systematic Review and Meta-Analysis

2024· review· en· W4402030972 on OpenAlexaboutno aff
Muhammad Ahmad, Malik Waleed Zeb Khan, Muhammad Maaz Bin Zahid, Aizaz Ali, Dawood Shehzad, Salman Khan, Jibran Ikram, Muhammad Esmat, Amna Hussain

Bibliographic record

Venuenot available
Typereview
Languageen
FieldMedicine
TopicNeuroblastoma Research and Treatments
Canadian institutionsnot available
Fundersnot available
KeywordsMeta-analysisMonoclonal antibodyMedicineRisk analysis (engineering)AntibodyInternal medicineImmunology

Abstract

fetched live from OpenAlex

not-yet-known not-yet-known not-yet-known unknown 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).

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.010
metaresearch head score (Gemma)0.025
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Meta-analysis · Consensus signal: none
GenreCandidate signal: Review · Consensus signal: Review
Teacher disagreement score0.020
Threshold uncertainty score0.054

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0100.025
Meta-epidemiology (narrow)0.0030.001
Meta-epidemiology (broad)0.0200.036
Bibliometrics0.0060.006
Science and technology studies0.0010.001
Scholarly communication0.0030.002
Open science0.0020.001
Research integrity0.0020.002
Insufficient payload (model declined to judge)0.0040.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.066
GPT teacher head0.374
Teacher spread0.308 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designMeta-analysis
Domainnot available
GenreReview

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2024
Admission routes1
Has abstractyes

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