Evidence map›Paper›PMID 20879880›Full record

Trial reportThe New England journal of medicine2010

Outcome after reduced chemotherapy for intermediate-risk neuroblastoma.

David L Baker, Mary L Schmidt, Susan L Cohn, John M Maris, Wendy B London, Allen Buxton, Daniel Stram, Robert P Castleberry, Hiroyuki Shimada, Anthony Sandler and 6 more

Registry-linked trialAbstract readClinical Trial, Phase III
In one paragraph

Trial report in The New England journal of medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00003093 (Treatment for Infants and Children With Intermediate Risk Neuroblastoma), which is not on this map. Cited by 133 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
133citing papers in PubMed, 4 pooled it
9.7field-weighted citation impact, top 2% 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.

NCT00003093 phase3completednot on this map

Treatment for Infants and Children With Intermediate Risk Neuroblastoma: A Phase III Intergroup CCG/POG Study

TypeinterventionalSponsorChildren's Oncology GroupRan1988 to 2011Enrolled573ConditionsNeuroblastomaArmsfilgrastim, sargramostim, carboplatin, cyclophosphamide, doxorubicin hydrochloride
3 · Its place in the literature

Who cites it

133 citing papers in PubMed, 4 syntheses or guidelines pooled it, 298 citations in OpenAlex.

  1. Pooled it
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  3. Platinum-induced hearing loss after treatment for childhood cancer.The Cochrane database of systematic reviews · 2016
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73 more citing papers are in PubMed but not listed here.

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

16 authors at 14 institutions in 2 countries.

David L BakerPrincess Margaret Hospital for Children, Perth, Australia.
Mary L Schmidt
Susan L Cohn
John M Maris
Wendy B London
Allen Buxton
Daniel Stram
Robert P Castleberry
Hiroyuki Shimada
Anthony Sandler
Robert C Shamberger
A Thomas Look
C Patrick Reynolds
Robert C Seeger
Katherine K Matthay
Children’s Oncology Group
University of Southern California · USArcadia · USBoston Children's Hospital · USChildren's Hospital of Los Angeles · USChildren's Hospital of Philadelphia · USComer Children's Hospital · USGeorge Washington University · USHarvard University · USPrincess Margaret Hospital for Children · AUSt. Jude Children's Research Hospital · USTexas Tech University Health Sciences Center · USUniversity of Alabama at Birmingham · USUniversity of California, San Francisco · USUniversity of Illinois Chicago · US

Funding

COG FOREIGN ACCRUALU10CA098543 · NCI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI ADAMSON, PETER C. · 2003 to 2013
$335.5M
Children's Oncology Group Statistics &Data Center GrantU10CA098413 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI ANDERSON, JAMES R · 2003 to 2013
$67.5M
PEDIATRIC ONCOLOGY GROUP STATISTICAL OFFICEU10CA029139 · NCI · UNIVERSITY OF FLORIDA · PI DEVIDAS, MEENAKSHI · 1985 to 2002
$7.3M
CHILDRENS CANCER STUDY GROUPU10CA017829 · NCI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI MATTHAY, KATHERINE KURSHAN · 1985 to 2002
$576k
NCI NIH HHS U10 CA017829NCI NIH HHS U10 CA029139NCI NIH HHS U10 CA098413NCI NIH HHS U10 CA098543NCI NIH HHS UI0-CA29139NCI NIH HHS UI0-CA98413NCI NIH HHS UI0-CA98543
6 · The paper itself

Abstract

backgroundThe survival rate among patients with intermediate-risk neuroblastoma who receive dose-intensive chemotherapy is excellent, but the survival rate among patients who receive reduced doses of chemotherapy for shorter periods of time is not known.

methodsWe conducted a prospective, phase 3, nonrandomized trial to determine whether a 3-year estimated overall survival of more than 90% could be maintained with reductions in the duration of therapy and drug doses, using a tumor biology-based therapy assignment. Eligible patients had newly diagnosed, intermediate-risk neuroblastoma without MYCN amplification; these patients included infants (<365 days of age) who had stage 3 or 4 disease, children (≥365 days of age) who had stage 3 tumors with favorable histopathological features, and infants who had stage 4S disease with a diploid DNA index or unfavorable histopathological features. Patients who had disease with favorable histopathological features and hyperdiploidy were assigned to four cycles of chemotherapy, and those with an incomplete response or either unfavorable feature were assigned to eight cycles.

resultsBetween 1997 and 2005, a total of 479 eligible patients were enrolled in this trial (270 patients with stage 3 disease, 178 with stage 4 disease, and 31 with stage 4S disease). A total of 323 patients had tumors with favorable biologic features, and 141 had tumors with unfavorable biologic features. Ploidy, but not histopathological features, was significantly predictive of the outcome. Severe adverse events without disease progression occurred in 10 patients (2.1%), including secondary leukemia (in 3 patients), death from infection (in 3 patients), and death at surgery (in 4 patients). The 3-year estimate (±SE) of overall survival for the entire group was 96±1%, with an overall survival rate of 98±1% among patients who had tumors with favorable biologic features and 93±2% among patients who had tumors with unfavorable biologic features.

conclusionsA very high rate of survival among patients with intermediate-risk neuroblastoma was achieved with a biologically based treatment assignment involving a substantially reduced duration of chemotherapy and reduced doses of chemotherapeutic agents as compared with the regimens used in earlier trials. These data provide support for further reduction in chemotherapy with more refined risk stratification. (Funded by the National Cancer Institute; ClinicalTrials.gov number, NCT00003093.)

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarboplatinChildChild, PreschoolCyclophosphamideDoxorubicinEtoposideHumansInfantIntention to Treat AnalysisNeoplasm StagingNeuroblastomaProspective StudiesSurvival AnalysisTreatment OutcomeCarboplatinCyclophosphamideDoxorubicinEtoposide

Identifiers

PMID20879880
PMCPMC2993160
OpenAlexW1967139222

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Registered trials

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.