Evidence map›Paper›PMID 35665495›Full record

ArticleCancer2022

Efficacy of post-induction therapy for high-risk neuroblastoma patients with end-induction residual disease.

Ami V Desai, Mark A Applebaum, Theodore G Karrison, Akosua Oppong, Cindy Yuan, Katherine R Berg, Kyle MacQuarrie, Elizabeth Sokol, Anurekha G Hall, Navin Pinto and 9 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Cancer, 2022. 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
1.4field-weighted citation impact, top 18% 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, 12 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Article
  7. Treatment of High-Risk Neuroblastoma.Children (Basel, Switzerland) · 2023
    Review
  8. 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

19 authors at 8 institutions in 1 country.

Ami V DesaiDepartment of Pediatrics, University of Chicago, Chicago, Illinois.ORCID 0000-0001-9658-3156
Mark A ApplebaumDepartment of Pediatrics, University of Chicago, Chicago, Illinois.ORCID 0000-0001-9766-8477
Theodore G KarrisonDepartment of Public Health Sciences, University of Chicago, Chicago, Illinois.
Akosua OppongPritzker School of Medicine, University of Chicago, Chicago, Illinois.
Cindy YuanDepartment of Radiology, University of Chicago, Chicago, Illinois.
Katherine R BergChildren's Hospital of Philadelphia and the University of Pennsylvania, Philadelphia, Pennsylvania.
Kyle MacQuarrieAnn and Robert H. Lurie Children's Hospital of Chicago and Northwestern University, Chicago, Illinois.ORCID 0000-0001-9624-7507
Elizabeth SokolAnn and Robert H. Lurie Children's Hospital of Chicago and Northwestern University, Chicago, Illinois.ORCID 0000-0002-1787-6901
Anurekha G HallSeattle Children's Hospital and University of Washington, Seattle, Washington.
Navin PintoSeattle Children's Hospital and University of Washington, Seattle, Washington.
Ian WolfeC. S. Mott Children's Hospital and University of Michigan, Ann Arbor, Michigan.
Rajen ModyC. S. Mott Children's Hospital and University of Michigan, Ann Arbor, Michigan.
Suzanne ShustermanDana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, Massachusetts.
Valeria SmithTexas Children's Hospital and Baylor College of Medicine, Houston, Texas.
Jennifer H FosterTexas Children's Hospital and Baylor College of Medicine, Houston, Texas.ORCID 0000-0002-2126-9768
Michele NassinDepartment of Pediatrics, University of Chicago, Chicago, Illinois.
James L LaBelleDepartment of Pediatrics, University of Chicago, Chicago, Illinois.
Rochelle BagatellChildren's Hospital of Philadelphia and the University of Pennsylvania, Philadelphia, Pennsylvania.
Susan L CohnDepartment of Pediatrics, University of Chicago, Chicago, Illinois.
University of Chicago · USBaylor College of Medicine · USChildren's Hospital of Philadelphia · USNorthwestern University · USSeattle Children's Hospital · USUniversity of Michigan · USChicago Department of Public Health · USHarvard University · US

Funding

VIRAL ONCOLOGY CORE FACILITYP30CA014599 · NCI · UNIVERSITY OF CHICAGO · PI CHIEN-MIN KAO · 1985 to 2026
$122.1M
Elucidating transcription regulation by epigenetics in neuroblastomaK08CA226237 · NCI · UNIVERSITY OF CHICAGO · PI APPLEBAUM, MARK ANDREW · 2018 to 2021
$826k
NCI NIH HHS K08 CA226237NCI NIH HHS P30 CA014599
6 · The paper itself

Abstract

backgroundHigh-risk neuroblastoma patients with end-induction residual disease commonly receive post-induction therapy in an effort to increase survival by improving the response before autologous stem cell transplantation (ASCT). The authors conducted a multicenter, retrospective study to investigate the efficacy of this approach.

methodsPatients diagnosed between 2008 and 2018 without progressive disease with a partial response or worse at end-induction were stratified according to the post-induction treatment: 1) no additional therapy before ASCT (cohort 1), 2) post-induction "bridge" therapy before ASCT (cohort 2), and 3) post-induction therapy without ASCT (cohort 3). χ

resultsThe study cohort consisted of 201 patients: cohort 1 (n = 123), cohort 2 (n = 51), and cohort 3 (n = 27). Although the end-induction response was better for cohort 1 than cohorts 2 and 3, the outcomes for cohorts 1 and 2 were not significantly different (P = .77 for EFS and P = .85 for OS). Inferior outcomes were observed for cohort 3 (P < .001 for EFS and P = .06 for OS). Among patients with end-induction stable metastatic disease, 3-year EFS was significantly improved for cohort 2 versus cohort 1 (P = .04). Cohort 3 patients with a complete response at metastatic sites after post-induction therapy had significantly better 3-year EFS than those with residual metastatic disease (P = .01).

conclusionsProspective studies to confirm the benefits of bridge treatment and the prognostic significance of metastatic response observed in this study are warranted.

Indexed as

Hematopoietic Stem Cell TransplantationNeuroblastomaAntineoplastic Combined Chemotherapy ProtocolsDisease-Free SurvivalHumansInduction ChemotherapyNeoplasm, ResidualPrognosisProspective StudiesRetrospective StudiesTransplantation, AutologousTreatment Outcomeautologous transplantationneuroblastomaprognosissurvivaltreatment response

Identifiers

PMID35665495
PMCPMC10764281
OpenAlexW4281767954

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.