Evidence map›Paper›PMID 35188340›Full record

ArticlePediatric blood & cancer2022

Pattern and predictors of sites of relapse in neuroblastoma: A report from the International Neuroblastoma Risk Group (INRG) project.

Kieuhoa T Vo, Steven G DuBois, John Neuhaus, Steve E Braunstein, Brent R Weil, Arlene Naranjo, Sabine Irtan, Julia Balaguer, Katherine K Matthay

Open access · greenAbstract read
In one paragraph

Article in Pediatric blood & cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Diagnosis and management of neuroblastoma in children.World journal of pediatric surgery · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Role of surgery in neuroblastoma.Pediatric surgery international · 2023
    Review
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

9 authors at 6 institutions in 4 countries.

Kieuhoa T VoUCSF Benioff Children's Hospital and Departments of Pediatrics, University of California, San Francisco School of Medicine, San Francisco, California, USA.ORCID 0000-0002-9281-7485
Steven G DuBoisDana-Farber/Boston Children's Cancer and Blood Disorders Center and Harvard Medical School, Boston, Massachusetts, USA.ORCID 0000-0003-0882-738X
John NeuhausEpidemiology and Biostatistics, University of California, San Francisco School of Medicine, San Francisco, California, USA.
Steve E BraunsteinRadiation Oncology, University of California, San Francisco School of Medicine, San Francisco, California, USA.ORCID 0000-0002-9841-9357
Brent R WeilDepartment of Surgery, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Arlene NaranjoDepartment of Biostatistics, University of Florida, Children's Oncology Group Statistics and Data Center, Gainesville, Florida, USA.
Sabine IrtanDepartment of Pediatric Surgery, Hôpital d'enfants Armand-Trousseau, Assistance Publique-Hôpitaux de Paris, Sorbonne University, Paris, France.ORCID 0000-0001-5596-9570
Julia BalaguerPediatric Oncology Unit, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
Katherine K MatthayUCSF Benioff Children's Hospital and Departments of Pediatrics, University of California, San Francisco School of Medicine, San Francisco, California, USA.ORCID 0000-0002-0146-2499
University of California, San Francisco · USBoston Children's Hospital · USChildren's Oncology Group · CHHarvard University · USHospital Universitari i Politècnic La Fe · ESSorbonne Université · FR

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
Clinical and Translational Science InstituteUL1TR001872 · NCATS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COLLARD, HAROLD R, JACOBY, VANESSA · 2016 to 2025
$112.1M
Institutional Career Development Core SupplementKL2TR001870 · NCATS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KANAYA, ALKA M., SARKAR, URMIMALA · 2016 to 2025
$19.7M
NCATS NIH HHS KL2 TR001870NCATS NIH HHS UL1 TR001872NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899
6 · The paper itself

Abstract

purposeWe sought to analyze biologic, clinical, and prognostic differences according to pattern of failure at the time of first relapse in neuroblastoma. PATIENTS AND

methodsChildren <21 years diagnosed with neuroblastoma between 1989 and 2017 with known site of first relapse (isolated local vs. distant only vs. combined local and distant sites) were identified from the International Neuroblastoma Risk Group (INRG) database. Data were compared between sites of relapse according to clinical features, biologic features, initial treatment, time to first relapse, and overall survival (OS) from time of first relapse.

resultsPattern of first relapse among 1833 children was 19% isolated local; 65% distant only; and 16% combined sites. All evaluated clinical and biologic variables with exception of tumor diagnosis differed statistically by relapse pattern, with patients with isolated local failure having more favorable prognostic features. Patients with stage 3 disease were more likely to have isolated local failure compared to all other stages (49% vs. 16%; p < .001). OS significantly differed by relapse pattern (5-year OS ± SE): isolated local: 64% ± 3%; distant only: 23% ± 2%; and combined: 26% ± 4% (p < .001). After controlling for age, stage, and MYCN status, patients with isolated local failure (adjusted hazard ratio [HR] = 0.46; 95% confidence interval [CI]: 0.33-0.62; p < .001) and distant-only failure (adjusted HR = 0.57; 95% CI: 0.45-0.71; p < .001) remained at decreased risk for death as compared to patients with combined failure.

conclusionPatients with distant-only and combined failures have a higher proportion of unfavorable clinical and biological features, and a lower survival than those with isolated local relapse.

Indexed as

Biological ProductsNeuroblastomaChildHumansInfantNeoplasm Recurrence, LocalNeoplasm StagingPrognosisBiological Productsneuroblastomapattern of failurerelapsesurvival

Identifiers

PMID35188340
PMCPMC9329207
OpenAlexW4212831409

What OpenQuestion 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 OpenQuestion graph.