Evidence map›Paper›PMID 41392230›Full record

ArticleJournal of the Egyptian National Cancer Institute2025

Lessons learned from different prognostic factors analysis in intermediate-risk neuroblastoma: ten years' experience at a tertiary center.

Mustafa Selim, Hanafy Hafez, Abeer M Elsayed, Mohamed Shalaby, Abdalwahab R Abdalwahab, Soad A Eltokhy, Mohamed Fawzy

Abstract read
In one paragraph

Article in Journal of the Egyptian National Cancer Institute, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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

7 authors.

Mustafa SelimPediatric Oncology Department, National Cancer Institute (NCI), Cairo University, Giza, Egypt. d_mostafaselim@cu.edu.eg.
Hanafy HafezPediatric Oncology Department, National Cancer Institute (NCI), Cairo University, Giza, Egypt.
Abeer M ElsayedCancer Pathology Department, National Cancer Institute (NCI), Cairo University, Giza, Egypt.
Mohamed ShalabySurgical Oncology Department, National Cancer Institute (NCI), Cairo University, Giza, Egypt.
Abdalwahab R AbdalwahabSurgical Oncology Department, National Cancer Institute (NCI), Cairo University, Giza, Egypt.
Soad A EltokhyClinical Pathology Department, National Cancer Institute (NCI), Cairo University, Giza, Egypt.
Mohamed FawzyPediatric Oncology Department, National Cancer Institute (NCI), Cairo University, Giza, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIntermediate-risk (IR) neuroblastoma represents a biologically and clinically diverse group of tumors. This study evaluates the feasibility of surgical excision and identifies prognostic factors that influence survival in IR-neuroblastoma patients, particularly those with suboptimal responses to induction chemotherapy.

methodsWe conducted a retrospective analysis of 50 pediatric patients diagnosed with IR-neuroblastoma at a tertiary cancer center between 2007 and 2016. Treatment responses, surgical outcomes, and survival data were assessed. Prognostic variables were evaluated using univariable and multivariable models.

resultsAfter four cycles of induction chemotherapy, 26% of patients showed an objective response, increasing to 62% by treatment completion. Surgical resection was performed in 70% of patients, with a higher proportion among non-responders. Initial response to induction chemotherapy was a significant independent predictor of surgical feasibility (p = 0.022) and final disease status (p = 0.026). Five-year overall survival (OS) was 84%, and event-free survival (EFS) was 72%. Surgical resection significantly improved end-of-treatment disease status in slow-responder patients but did not independently affect OS or EFS.

conclusionModerate-intensity chemotherapy with or without surgery provides acceptable survival outcomes in IR-neuroblastoma. An early favorable response to induction therapy may justify avoiding surgery, while surgical resection remains critical for slow-responder patients.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsNeuroblastomaChildChild, PreschoolFemaleHumansInduction ChemotherapyInfantMalePrognosisRetrospective StudiesTertiary Care CentersTreatment OutcomeChemotherapy toxicityDisease statusInduction therapy responseIR-neuroblastomaPrognostic factorsSurgical resectionSurvival outcomes

Identifiers

PMID41392230
PMCPMC13313431

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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 OpenQuestion graph.