Evidence mapPaperPMID 42524535Full record

ArticleHealth science reports2026

The Role of Precision Medicine in Neuroblastoma: Targeted Therapies and Personalized Approaches-A Narrative Review.

Mossamat Jannatul Mawa, Mohammad Shahangir Biswas, Maksudul Haque, Munna Kumar Podder

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Article in Health science reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Mossamat Jannatul MawaDepartment of Biochemistry and Biotechnology University of Science & Technology Chittagong (USTC), Foy's Lake Chittagong Bangladesh.ORCID https://orcid.org/0009-0007-2489-3631
Mohammad Shahangir BiswasDepartment of Biochemistry and Biotechnology University of Science & Technology Chittagong (USTC), Foy's Lake Chittagong Bangladesh.ORCID https://orcid.org/0000-0002-1545-5521
Maksudul HaqueDepartment of Biochemistry and Biotechnology University of Science & Technology Chittagong (USTC), Foy's Lake Chittagong Bangladesh.ORCID https://orcid.org/0009-0001-2317-0948
Munna Kumar PodderDepartment of Biochemistry and Biotechnology Khwaja Yunus Ali University, Enayetpur Chowhali Bangladesh.ORCID https://orcid.org/0000-0003-2350-3439

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: Neuroblastoma is the most common extracranial solid tumor and contributes the most to pediatric oncology deaths worldwide. Its clinical manifestations are heterogeneous, including relapses, and the prognosis remains poor, especially for high-risk patients. The principal interventions-surgery, chemotherapy, and radiotherapy-exacerbate the prognosis due to high morbidity and poor long-term remission rates. This study attempts to integrate available information on the genetic and molecular characteristics of neuroblastoma, focusing on how the potential of precision medicine is improving neuroblastoma diagnosis and treatment. Methods: This review aims to compile recent literature on the genomic, transcriptomic and epigenetic studies of neuroblastoma and its treatment. The review included the most recent molecular markers for the relevant pathway, the therapeutic targets that arise from them and precision medicine approaches that incorporate AI, CRISPR, and neoantigen vaccines at various stages of clinical trials. Results: Targeted medicines such MYCN amplification, ALK mutations, and chromosomal deletions including 1p36 and 11q have revealed important genetic drivers of neuroblastoma. Early-phase studies have shown encouraging reductions in tumor progression with MYCN modulators, ALK inhibitors and immunotherapies (anti-GD2 antibodies, B7-H3 CAR-T cells). Integrating omics-based markers and AI-directed therapy prediction more precisely classifies risk and customizes therapy. Conclusion: Precision medicine has transformed neuroblastoma treatment by improving diagnostic specificity and therapeutic effectiveness while reducing toxicity. Among emerging strategies, ALK-targeted therapies and anti-GD2 immunotherapies show strong clinical potential, although further validation is still required to improve survival and quality of life in affected children.

Indexed as

genetic mutationpatient‐derived organoidpersonalized approachesprecision medicinetargeted therapytumor heterogeneity

Identifiers

PMID42524535
PMCPMC13412545

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.