Evidence map›Paper›PMID 30496881›Full record

ArticleInternational journal of radiation oncology, biology, physics2019

Implications of Image-Defined Risk Factors and Primary-Site Response on Local Control and Radiation Treatment Delivery in the Management of High-Risk Neuroblastoma: Is There a Role for De-escalation of Adjuvant Primary-Site Radiation Therapy?

John T Lucas, M Beth McCarville, David A Cooper, Mikhail Doubrovin, Daniel Wakefield, Teresa Santiago, Yimei Li, Xingyu Li, Matthew Krasin, Victor Santana and 2 more

Open access · greenAbstract read
In one paragraph

Article in International journal of radiation oncology, biology, physics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Neuroblastoma.Pediatric blood & cancer · 2021
    Review
  6. Article
  7. 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

12 authors at 2 institutions in 1 country.

John T LucasDepartment of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee. Electronic address: john.lucas@stjude.org.
M Beth McCarvilleDepartment of Diagnostic Imaging, St. Jude Children's Research Hospital, Memphis, Tennessee.
David A CooperDivision of Radiation Oncology, University of Tennessee Health Science Center, Memphis, Tennessee.
Mikhail DoubrovinDepartment of Diagnostic Imaging, St. Jude Children's Research Hospital, Memphis, Tennessee.
Daniel WakefieldDivision of Radiation Oncology, University of Tennessee Health Science Center, Memphis, Tennessee.
Teresa SantiagoDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee.
Yimei LiDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee.
Xingyu LiDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee.
Matthew KrasinDepartment of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee.
Victor SantanaDepartment of Clinical Trials Administration, St. Jude Children's Research Hospital, Memphis, Tennessee.
Wayne FurmanDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee.
Andrew M DavidoffDepartment of Surgery, St. Jude Children's Research Hospital, Memphis, Tennessee.
St. Jude Children's Research Hospital · USUniversity of Tennessee Health Science Center · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
NCI NIH HHS P30 CA021765
6 · The paper itself

Abstract

purposeThe predictive value of Image-Defined Risk Factors (IDRFs) developed by the International Neuroblastoma Risk Group Task Force as it relates to primary-site management is undefined and may aid patient selection for de-escalation of adjuvant radiation therapy to the primary site in high-risk neuroblastoma. METHODS AND MATERIALS: Patients (N = 76) with high-risk neuroblastoma treated on prospective trials at our institution from 1997 to 2014 were eligible for inclusion. IDRFs were defined based on pretherapy imaging. Overall survival, progression-free survival, and locoregional failure-free survival (LRFFS) were described using the Kaplan-Meier estimator and tested across strata by using the log-rank test.

resultsTwenty of 76 patients (26%) experienced local (n = 6), regional (n = 6), or combined locoregional failure (n = 8) with or without distant failure. Ten (50%) of the locoregional failures had concurrent distant relapse. Of patients who completed all therapy, both those with no IDRFs and those with >90% resection had a 3-year LRFFS of 100%, with or without radiation therapy. Patients with either ≥1 IDRF or <Gross Total Resection (GTR) or the inability to complete all therapy had inferior 3-year LRFFS of 77.8% and 14.4% with or without radiation therapy, respectively (P < .04). Patients treated with a dose ≥30.6 Gy as part of therapy for residual disease had an 83.3% locoregional control rate.

conclusionsPatients with >90% tumor resection and no primary site IDRFs at diagnosis may be candidates for de-escalation of adjuvant primary-site radiation therapy, although validation of these findings in future studies is required.

Indexed as

AdolescentChildChild, PreschoolDisease-Free SurvivalFemaleHumansInfantMagnetic Resonance ImagingMaleNeuroblastomaRadiotherapy, AdjuvantRadiotherapy DosageRetrospective StudiesRisk FactorsSurvival AnalysisTomography, X-Ray Computed

Identifiers

PMID30496881
PMCPMC8810202
OpenAlexW2903196234

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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.