Evidence map›Paper›PMID 31115156›Full record

ArticlePediatric blood & cancer2019

Comprehensive evaluation of context dependence of the prognostic impact of MYCN amplification in neuroblastoma: A report from the International Neuroblastoma Risk Group (INRG) project.

Kevin Campbell, Derek Shyr, Rochelle Bagatell, Matthias Fischer, Akira Nakagawara, Adela Canete Nieto, Garrett M Brodeur, Katherine K Matthay, Wendy B London, Steven G DuBois

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in Pediatric blood & cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.0field-weighted citation impact, top 9% of its field
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

20 citing papers in PubMed, 31 citations in OpenAlex.

  1. Observational
  2. Article
  3. Effect ofJCO precision oncology · 2026
    Article
  4. Diagnosis and management of neuroblastoma in children.World journal of pediatric surgery · 2026
    Review
  5. The baselineBMC medical imaging · 2025
    Article
  6. Management and outcome of children with high-risk neuroblastoma: insights from the Spanish Society of Pediatric Hematology and Oncology (SEHOP) neuroblastoma group on refractory and relapse/progressive disease.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Article
  7. Molecular regulation and therapeutic targeting ofFrontiers in cell and developmental biology · 2025
    Review
  8. Review
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  12. Review
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  18. Article
  19. Gangliosides and Neuroblastomas.International journal of molecular sciences · 2020
    Review
  20. 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

10 authors at 6 institutions in 4 countries.

Kevin CampbellDepartment of Pediatric Oncology, Dana-Farber/Boston Children's Cancer and Blood Disorders Center and Harvard Medical School, Boston, Massachusetts.ORCID 0000-0003-1826-4277
Derek ShyrDepartment of Pediatric Oncology, Dana-Farber/Boston Children's Cancer and Blood Disorders Center and Harvard Medical School, Boston, Massachusetts.
Rochelle BagatellDepartment of Pediatrics, Children's Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.
Matthias FischerDepartment of Pediatric Oncology, Children's Hospital and Center for Molecular Medicine Cologne, University of Cologne, Köln, Germany.
Akira NakagawaraSAGA Heavy Ion Medical Accelerator in Tosu (HIMAT) Foundation, Tosu, Japan.
Adela Canete NietoHospital Universitario y Politecnico La Fe, Valencia, Spain.
Garrett M BrodeurDepartment of Pediatrics, Children's Hospital of Philadelphia and Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.
Katherine K MatthayUCSF School of Medicine and UCSF Benioff Children's Hospital, San Francisco, California.ORCID 0000-0002-0146-2499
Wendy B LondonDepartment of Pediatric Oncology, Dana-Farber/Boston Children's Cancer and Blood Disorders Center and Harvard Medical School, Boston, Massachusetts.
Steven G DuBoisDepartment of Pediatric Oncology, Dana-Farber/Boston Children's Cancer and Blood Disorders Center and Harvard Medical School, Boston, Massachusetts.ORCID 0000-0003-0882-738X
Harvard University · USChildren's Hospital of Philadelphia · USHospital Universitari i Politècnic La Fe · ESSAGA Heavy Ion Medical Accelerator in Tosu · JPUCSF Benioff Children's Hospital · USUniversity of Cologne · DE

Funding

Pediatric Scholars ProgramK12HD043245 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI ST. GEME, JOSEPH W. · 2003 to 2022
$7.4M
NICHD NIH HHS K12 HD043245
6 · The paper itself

Abstract

backgroundMYCN amplification (MYCN-A) is an established adverse prognostic factor in neuroblastoma. The extent to which the prognostic impact of MYCN-A depends on other factors has not been fully characterized. PATIENTS AND

methodsUsing the International Neuroblastoma Risk Group database, we constructed Cox models of overall survival (OS) to obtain hazard ratios of the effect of MYCN-A within subgroups defined by other prognostic factors. Cox models assessed the degree to which the prognostic impact of MYCN-A was modulated by each other covariate. We used absolute hazard ratio (HR) differences to construct classification trees to identify subgroups with greatest differential prognostic effect of MYCN-A.

resultsIn a cohort of 6223 patients with known MYCN status, the OS hazard ratio associated with MYCN-A was 6.3 (95% confidence interval 5.7-7.0, P < .001). Age at diagnosis conferred the largest HR absolute difference for MYCN-A between subgroups (HR absolute difference 16.6; HRs for MYCN-A of 19.6 for <18 months, 3.0 for ≥18 months). MYCN-A remained significantly prognostic of OS after controlling for other factors, abrogating their prognostic strength. Patients whose outcome was most impacted by MYCN status were those who were <18 months, had high mitosis karrhyohexis index (MKI) and low ferritin.

conclusionThe prognostic strength of MYCN-A varies depending on which patient subgroup defined by other neuroblastoma risk factors is examined, with greatest strength in patients with otherwise favorable features. MYCN-A has little effect within some subgroups, aiding clinical decision-making if MYCN status cannot be assessed. Subgroups where MYCN-A has large effect may be prioritized for agents targeting Myc family proteins.

Indexed as

Gene AmplificationBiomarkers, TumorBone Marrow NeoplasmsBone NeoplasmsCohort StudiesFemaleFerritinsFollow-Up StudiesHumansInfantMaleMitosisNeuroblastomaN-Myc Proto-Oncogene ProteinPrognosisRisk FactorsBiomarkers, TumorFerritinsMYCN protein, humanN-Myc Proto-Oncogene ProteinamplificationcontextMYCNneuroblastomaprognosis

Identifiers

PMID31115156
PMCPMC7323455
OpenAlexW2946089084

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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 OpenQuestion graph.