Evidence map›Paper›PMID 21108439›Full record

ArticlePediatric blood & cancer2011

Incidence, survival, and prevalence of neuroendocrine tumors versus neuroblastoma in children and young adults: nine standard SEER registries, 1975-2006.

Pournima Navalkele, M Sue O'Dorisio, Thomas M O'Dorisio, Gideon K D Zamba, Charles F Lynch

Open access · greenAbstract readComparative Study
In one paragraph

Article in Pediatric blood & cancer, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

33 citing papers in PubMed, 93 citations in OpenAlex.

  1. Safety and dosimetry of [European journal of nuclear medicine and molecular imaging · 2025
    Trial
  2. Approach to the Preoperative Pharmacological Management of Catecholamine-Secreting Tumors in Children: A Case Series and Review.The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG · 2026
    Article
  3. Molecular radiotherapy for adult type metastatic neuroendocrine tumours in children.European journal of nuclear medicine and molecular imaging · 2025
    Observational
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  20. Theragnostic Aspects and Radioimmunotherapy in Pediatric Tumors.International journal of molecular sciences · 2020
    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

5 authors at 3 institutions in 1 country.

Pournima NavalkeleDepartment of Epidemiology, College of Public Health, University of Iowa, Iowa City, Iowa, USA.
M Sue O'Dorisio
Thomas M O'Dorisio
Gideon K D Zamba
Charles F Lynch
University of Iowa · USIowa City Public Library · USUniversity of Iowa Holden Comprehensive Cancer Center

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
DOSIMETRY IN CHILDREN AND YOUNG ADULTS WITH NEUROBLASTOMA OR NEUROENDOCRINE TUMORR21CA134198 · NCI · UNIVERSITY OF IOWA · PI BUSHNELL, DAVID L, O'DORISIO, M. SUE · 2008 to 2009
$615k
Dosimetry Guided Phase II of 90Y-DOTA-tyr3-Octreotide + Retinoic Acid in KidsR21CA141840 · NCI · UNIVERSITY OF IOWA · PI O'DORISIO, M. SUE · 2009 to 2010
$536k
NCI NIH HHS P30 CA016058NCI NIH HHS R21 CA134198NCI NIH HHS R21 CA141840
6 · The paper itself

Abstract

backgroundThe incidence, survival, and prevalence of neuroendocrine tumors (NETs) in children were determined as a first step in improving diagnosis and therapy. Outcomes were compared with neuroblastoma, a pediatric malignancy that shares several biomarkers.

methodsIncidence rates, observed survival rates and 31-year limited duration prevalence counts were obtained from SEER*Stat for diagnosis years 1975 to 2006. These rates were compared between and within NETs and neuroblastoma for demographic and tumor-related variables from nine standard SEER registries for ages 0-29 years. Multivariate Cox regression was performed to identify prognostic factors for survival in NETs.

resultsThe number of NETs was 1,073 compared to 1,664 neuroblastomas. The most common NET sites were lung, breast, and appendix. NET 5-year observed survival rates increased from 83% between 1975 and 1979 to 84% for the 2000-2006 period, while analogous neuroblastoma survival rates steadily increased from 45-73%. Five-year observed survival was less than 30% in females with NETs of the cervix and ovary. The estimated 31-year limited duration prevalence for NETs as of January 1, 2006 in the U.S. population was 7,724 compared to 9,960 for neuroblastomas. Age-adjusted multivariate Cox Regression demonstrated small cell histology, primary location in the breast, and distant stage as major predictors of decreased survival.

conclusionsWhile survivorship has significantly increased for neuroblastoma, those diagnosed with NETs have shown no increase in survival during this 31-year period. NETs constitute an unrecognized cancer threat to children and young adults comparable to neuroblastoma in both number of affected persons and disease severity.

Indexed as

AdolescentAdultChildChild, PreschoolFemaleHumansIncidenceInfantInfant, NewbornMaleNeuroblastomaNeuroendocrine TumorsPrevalencePrognosisRegistriesSEER Program

Identifiers

PMID21108439
PMCPMC4251713
OpenAlexW2084360244

What OpenQuestion holds

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Registered trials

None linked

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.