Evidence map›Paper›PMID 30444686›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2019

Defining Risk Factors for Chemotherapeutic Intervention in Infants With Stage 4S Neuroblastoma: A Report From Children's Oncology Group Study ANBL0531.

Clare J Twist, Arlene Naranjo, Mary Lou Schmidt, Sheena C Tenney, Susan L Cohn, Holly J Meany, Peter Mattei, E Stanton Adkins, Hiroyuki Shimada, Wendy B London and 3 more

Abstract readClinical Trial, Phase III
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 5% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 61 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
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  11. Article
  12. Advancing therapy for neuroblastoma.Nature reviews. Clinical oncology · 2022
    Review
  13. Review
  14. Article
  15. Review
  16. Revised Neuroblastoma Risk Classification System: A Report From the Children's Oncology Group.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2021
    Article
  17. Article
  18. Article
  19. Article
  20. 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

13 authors at 11 institutions in 1 country.

Clare J Twist1 Roswell Park Cancer Institute, Buffalo, NY.
Arlene Naranjo2 University of Florida, Gainesville, FL.
Mary Lou Schmidt3 University of Illinois at Chicago College of Medicine, Chicago, IL.
Sheena C Tenney2 University of Florida, Gainesville, FL.
Susan L Cohn4 University of Chicago, Chicago, IL.
Holly J Meany5 Children's National Medical Center, Washington, DC.
Peter Mattei6 Children's Hospital of Philadelphia, Philadelphia, PA.
E Stanton Adkins7 Palmetto Health USC Medical Group, Columbia, SC.
Hiroyuki Shimada8 Children's Hospital Los Angeles, Los Angeles, CA.
Wendy B London9 Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, MA.
Julie R Park10 Seattle Children's Hospital, Seattle, WA.
Katherine K Matthay11 University of California San Francisco School of Medicine and UCSF Benioff Children's Hospital, San Francisco, CA.
John M Maris6 Children's Hospital of Philadelphia, Philadelphia, PA.
Children's Hospital of Philadelphia · USUniversity of Florida · USChildren's Hospital of Los Angeles · USChildren's National · USHarvard University · USPalmetto Health Richland · USRoswell Park Comprehensive Cancer Center · USSeattle Children's Hospital · USUCSF Benioff Children's Hospital · USUniversity of Chicago · USUniversity of Illinois Chicago · 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

purposeInfants with stage 4S neuroblastoma usually have favorable outcomes with observation or minimal chemotherapy. However, young infants with symptoms secondary to massive hepatomegaly or with unfavorable tumor biology are at high risk of death. Our aim was to improve outcomes for patients with symptomatic and/or unfavorable biology 4S neuroblastoma with a uniform treatment approach using a biology- and response-based algorithm. PATIENTS AND

methodsThe subset of patients with 4S disease with MYCN-not amplified tumors with impaired or impending organ dysfunction, or with unfavorable histology and/or diploid DNA index, were eligible. Patients were assigned to receive two, four, or eight cycles of chemotherapy on the basis of histology, diploid DNA index, chromosome arm 1p or 11q loss of heterozygosity (LOH) status, and symptoms.

resultsForty-nine eligible patients were enrolled: 41 were symptomatic and 28 had unfavorable biology. Seventeen patients (symptomatic, favorable biology) were assigned two cycles, 21 patients (any unfavorable biologic feature without 1p or 11q LOH) were assigned four cycles, and 11 patients (unfavorable biology including 1p and/or 11q LOH [n = 7] or symptomatic with unknown biology [n = 4]), were assigned eight cycles. The 3-year overall survival was 81.4% ± 5.8%. Eight of nine deaths were in patients younger than 2 months of age at diagnosis (median, 9 days [range, 1 to 68 days]): five acute deaths were a result of hepatomegaly and associated toxicities; two were a result of late relapse in patients with unfavorable biology; and two were a result of treatment complications. No deaths occurred after protocol-mandated pre-emptive treatment of infants younger than 2 months with hepatomegaly, regardless of symptoms. A new scoring algorithm for emergent chemotherapy in patients with 4S disease was developed on the basis of this experience.

conclusionThe outcome for 4S neuroblastoma can be improved with pre-emptive chemotherapy for evolving hepatomegaly or other baseline comorbidities in infants younger than 2 months of age.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarboplatinCyclophosphamideDisease-Free SurvivalDoxorubicinEtoposideFemaleFilgrastimGene AmplificationHepatomegalyHumansInfantInfant, NewbornLoss of HeterozygosityMaleNeoplasm StagingCarboplatinCyclophosphamideDoxorubicinEtoposideFilgrastimMYCN protein, humanN-Myc Proto-Oncogene Protein

Identifiers

PMID30444686
PMCPMC6325354
OpenAlexW2901421585

What OpenQuestion holds

Textmetadata
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.