Evidence map›Paper›PMID 27573428›Full record

Trial reportEuropean journal of cancer (Oxford, England : 1990)2016

Incidence and risk factors for secondary malignancy in patients with neuroblastoma after treatment with (131)I-metaiodobenzylguanidine.

Kelly E Huibregtse, Kieuhoa T Vo, Steven G DuBois, Stephanie Fetzko, John Neuhaus, Vandana Batra, John M Maris, Brian Weiss, Araz Marachelian, Greg A Yanik and 1 more

Open access · greenAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in European journal of cancer (Oxford, England : 1990), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

11 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Advancing therapy for neuroblastoma.Nature reviews. Clinical oncology · 2022
    Review
  6. Article
  7. Article
  8. Review
  9. Current Consensus on I-131 MIBG Therapy.Nuclear medicine and molecular imaging · 2018
    Review
  10. Norepinephrine Transporter as a Target for Imaging and Therapy.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2017
    Review
  11. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 7 institutions in 1 country.

Kelly E HuibregtseUniversity of California San Francisco Benioff Children's Hospital, USA. Electronic address: kelly.huibregtse@ucsf.edu.
Kieuhoa T VoDepartment of Pediatrics, University of California San Francisco Benioff Children's Hospital, USA. Electronic address: Kieuhoa.Vo@ucsf.edu.
Steven G DuBoisDana-Farber/Boston Children's Cancer and Blood Disorders Center, USA. Electronic address: Steven_Dubois@dfci.harvard.edu.
Stephanie FetzkoDepartment of Pediatrics, Baylor University Medical Center, USA. Electronic address: fetzko@bcm.edu.
John NeuhausUniversity of California San Francisco Benioff Children's Hospital, Department of Biostatistics, USA. Electronic address: John.Neuhaus@ucsf.edu.
Vandana BatraChildren's Hospital of Philadelphia, Department of Pediatric Oncology, USA. Electronic address: Batrav@email.chop.edu.
John M MarisChildren's Hospital of Philadelphia, Department of Pediatric Oncology, USA. Electronic address: Maris@email.chop.edu.
Brian WeissCincinnati Children's Hospital Medical Center, Division of Pediatric Oncology, USA. Electronic address: Brian.Weiss@cchmc.org.
Araz MarachelianChildren's Hospital of Los Angeles, New Approaches to Neuroblastoma Research, USA. Electronic address: AMarachelian@chla.usc.edu.
Greg A YanikDepartment of Pediatrics, University of Michigan Medical Center, USA. Electronic address: gyanik@med.umich.edu.
Katherine K MatthayDepartment of Pediatrics, University of California San Francisco Benioff Children's Hospital, USA. Electronic address: kate.matthay@ucsf.edu.
University of California, San Francisco · USChildren's Hospital of Philadelphia · USBaylor University Medical Center · USChildren's Hospital of Los Angeles · USCincinnati Children's Hospital Medical Center · USDana-Farber/Boston Children's Cancer and Blood Disorders Center · USUniversity of Michigan · US

Funding

Vascular endothelial cell integrins in angiogenesisP01CA081403 · NCI · CHILDREN'S HOSPITAL OF LOS ANGELES · PI SEEGER, ROBERT CHARLES · 2000 to 2014
$28.5M
NCI NIH HHS P01 CA081403NIH HHS PO1 81403
6 · The paper itself

Abstract

Several reports of second malignant neoplasm (SMN) in patients with relapsed neuroblastoma after treatment with (131)I-MIBG suggest the possibility of increased risk. Incidence of and risk factors for SMN after (131)I-MIBG have not been defined. This is a multi-institutional retrospective review of patients with neuroblastoma treated with (131)I-MIBG therapy. A competing risk approach was used to calculate the cumulative incidence of SMN from time of first exposure to (131)I-MIBG. A competing risk regression was used to identify potential risk factors for SMN. The analytical cohort included 644 patients treated with (131)I-MIBG. The cumulative incidence of SMN was 7.6% (95% confidence interval [CI], 4.4-13.0%) and 14.3% (95% CI, 8.3-23.9%) at 5 and 10 years from first (131)I-MIBG, respectively. No increase in SMN risk was found with increased number of (131)I-MIBG treatments or higher cumulative activity per kilogram of (131)I-MIBG received (p = 0.72 and p = 0.84, respectively). Thirteen of the 19 reported SMN were haematologic. In a multivariate analysis controlling for variables with p < 0.1 (stage, age at first (131)I-MIBG, bone disease, disease status at time of first (131)I-MIBG), patients with relapsed/progressive disease had significantly lower risk of SMN (subdistribution hazard ratio 0.3, 95% CI, 0.1-0.8, p = 0.023) compared to patients with persistent/refractory neuroblastoma. The cumulative risk of SMN after (131)I-MIBG therapy for patients with relapsed or refractory neuroblastoma is similar to the greatest published incidence for high-risk neuroblastoma after myeloablative therapy, with no dose-dependent increase. As the number of patients treated and length of follow-up time increase, it will be important to reassess this risk.

Indexed as

3-IodobenzylguanidineAdolescentAdultAge of OnsetAntineoplastic AgentsChildChild, PreschoolCombined Modality TherapyFemaleHematologic NeoplasmsHumansInfantMaleMyelodysplastic SyndromesNeoplasms, Second PrimaryNeuroblastoma3-IodobenzylguanidineAntineoplastic AgentsRadiopharmaceuticalsCancerChemotherapyI-metaiodobenzylguanidineMIBGNeuroblastomaPaediatricsSecond malignancySMNSolid tumourSurvivorship

Identifiers

PMID27573428
PMCPMC7523915
OpenAlexW2517407182

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.