Evidence map›Paper›PMID 37199022›Full record

Trial reportPediatric blood & cancer2023

Impact of diagnostic and end-of-induction Curie scores with tandem high-dose chemotherapy and autologous transplants for metastatic high-risk neuroblastoma: A report from the Children's Oncology Group.

Keri A Streby, Marguerite T Parisi, Barry L Shulkin, Brian LaBarre, Rochelle Bagatell, Lisa Diller, Stephan A Grupp, Katherine K Matthay, Stephan D Voss, Alice L Yu and 4 more

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Pediatric blood & cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Effect ofJCO precision oncology · 2026
    Article
  6. Ganglioside Profiling Uncovers Distinct Patterns in High-Risk Neuroblastoma.International journal of molecular sciences · 2025
    Article
  7. Recommendations for the use of nuclear medicine imaging in patients with neuroblastoma.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
  8. The value ofQuantitative imaging in medicine and surgery · 2025
    Article
  9. 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

14 authors at 9 institutions in 3 countries.

Keri A StrebyDivision of Hematology/Oncology/BMT, Department of Pediatrics, Nationwide Children's Hospital, The Ohio State University, Columbus, Ohio, USA.ORCID 0000-0002-2469-2553
Marguerite T ParisiDepartment of Radiology, Seattle Children's Hospital, University of Washington School of Medicine, Seattle, Washington, USA.
Barry L ShulkinDepartment of Radiological Sciences, St. Jude Children's Research Hospital, University of Tennessee Health Science Center, Memphis, Tennessee, USA.ORCID 0000-0003-4784-7914
Brian LaBarreChildren's Oncology Group Statistics & Data Center, Department of Biostatistics, University of Florida, Gainesville, Florida, USA.
Rochelle BagatellDepartment of Pediatrics, Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Lisa DillerDana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, Massachusetts, USA.
Stephan A GruppDepartment of Pediatrics, Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Katherine K MatthayDepartment of Pediatrics, University of California San Francisco School of Medicine, San Francisco, California, USA.ORCID 0000-0002-0146-2499
Stephan D VossDepartment of Radiology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.ORCID 0000-0002-2092-2219
Alice L YuUniversity of California in San Diego, San Diego, California, USA.
Wendy B LondonDana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, Massachusetts, USA.ORCID 0000-0003-3571-6538
Julie R ParkDepartment of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee, USA.
Gregory A YanikDivision of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee, United States.
Arlene NaranjoChildren's Oncology Group Statistics & Data Center, Department of Biostatistics, University of Florida, Gainesville, Florida, USA.
St. Jude Children's Research Hospital · USChildren's Hospital of Philadelphia · USChildren's Oncology Group · CHHarvard University · USBoston Children's Hospital · USNationwide Children's Hospital · USSeattle Children's Hospital · USUniversity of California, San Francisco · USUniversity of San Diego · US

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
NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899
6 · The paper itself

Abstract

backgroundDiagnostic mIBG (meta-iodobenzylguanidine) scans are an integral component of response assessment in children with high-risk neuroblastoma. The role of end-of-induction (EOI) Curie scores (CS) was previously described in patients undergoing a single course of high-dose chemotherapy (HDC) and autologous hematopoietic cell transplant (AHCT) as consolidation therapy.

objectiveWe now examine the prognostic significance of CS in patients randomized to tandem HDC and AHCT on the Children's Oncology Group (COG) trial ANBL0532. STUDY

designA retrospective analysis of mIBG scans obtained from patients enrolled in COG ANBL0532 was performed. Evaluable patients had mIBG-avid, International Neuroblastoma Staging System (INSS) stage 4 disease, did not progress during induction therapy, consented to consolidation randomization, and received either single or tandem HDC (n = 80). Optimal CS cut points maximized the outcome difference (≤CS vs. >CS cut-off) according to the Youden index.

resultsFor recipients of tandem HDC, the optimal cut point at diagnosis was CS = 12, with superior event-free survival (EFS) from study enrollment for patients with CS ≤ 12 (3-year EFS 74.2% ± 7.9%) versus CS > 12 (59.2% ± 7.1%) (p = .002). At EOI, the optimal cut point was CS = 0, with superior EOI EFS for patients with CS = 0 (72.9% ± 6.4%) versus CS > 0 (46.5% ± 9.1%) (p = .002).

conclusionIn the setting of tandem transplantation for children with high-risk neuroblastoma, CS at diagnosis and EOI may identify a more favorable patient group. Patients treated with tandem HDC who exhibited a CS ≤ 12 at diagnosis or CS = 0 at EOI had superior EFS compared to those with CS above these cut points.

Indexed as

Hematopoietic Stem Cell TransplantationNeuroblastoma3-IodobenzylguanidineAntineoplastic Combined Chemotherapy ProtocolsChildDisease-Free SurvivalHumansInfantRetrospective StudiesTransplantation, Autologous3-IodobenzylguanidineCurie scoremIBGneuroblastomatandem

Identifiers

PMID37199022
PMCPMC10511015
OpenAlexW4377010348

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.