Evidence map›Paper›PMID 22589483›Full record

ReviewClinical cancer research : an official journal of the American Association for Cancer Research2012

Promising therapeutic targets in neuroblastoma.

Katherine K Matthay, Rani E George, Alice L Yu

Open access · bronzeAbstract readReview
In one paragraph

Review in Clinical cancer research : an official journal of the American Association for Cancer Research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed, 2 pooled it
11.7field-weighted citation impact, top 1% 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

89 citing papers in PubMed, 2 syntheses or guidelines pooled it, 188 citations in OpenAlex.

  1. Pooled it
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  5. Immunotherapeutic Strategies Targeting GD2-Expressing Malignancies.Advances in experimental medicine and biology · 2026
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29 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

3 authors at 2 institutions in 1 country.

Katherine K MatthayDepartment of Pediatrics, UCSF Helen Diller Family Comprehensive Cancer Center, and UCSF Benioff Children's Hospital, UCSF Medical Center, University of California, San Francisco, CA 94143-0106, USA. matthayk@peds.ucsf.edu
Rani E George
Alice L Yu
UCSF Benioff Children's Hospital · USUniversity of California, San Francisco · US

Funding

Vascular endothelial cell integrins in angiogenesisP01CA081403 · NCI · CHILDREN'S HOSPITAL OF LOS ANGELES · PI SEEGER, ROBERT CHARLES · 2000 to 2014
$28.5M
The ALK receptor tyrosine kinase as a therapeutic target in neuroblastomaR01CA148688 · NCI · DANA-FARBER CANCER INST · PI GEORGE, RANI E. · 2011 to 2021
$4.1M
131IMIBG Escalating Dose Rapid Sequence Double InfusionR21CA097758 · NCI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI MATTHAY, KATHERINE KURSHAN · 2003 to 2004
$522k
NCI NIH HHS P01 CA081403NCI NIH HHS P01 CA81403NCI NIH HHS R01 CA148688NCI NIH HHS R21 CA097758
6 · The paper itself

Abstract

Neuroblastoma, the most common extracranial solid tumor in children, is derived from neural crest cells. Nearly half of patients present with metastatic disease and have a 5-year event-free survival of <50%. New approaches with targeted therapy may improve efficacy without increased toxicity. In this review we evaluate 3 promising targeted therapies: (i) (131)I-metaiodobenzylguanidine (MIBG), a radiopharmaceutical that is taken up by human norepinephrine transporter (hNET), which is expressed in 90% of neuroblastomas; (ii) immunotherapy with monoclonal antibodies targeting the GD2 ganglioside, which is expressed on 98% of neuroblastoma cells; and (iii) inhibitors of anaplastic lymphoma kinase (ALK), a tyrosine kinase that is mutated or amplified in ~10% of neuroblastomas and expressed on the surface of most neuroblastoma cells. Early-phase trials have confirmed the activity of (131)I-MIBG in relapsed neuroblastoma, with response rates of ~30%, but the technical aspects of administering large amounts of radioactivity in young children and limited access to this agent have hindered its incorporation into treatment of newly diagnosed patients. Anti-GD2 antibodies have also shown activity in relapsed disease, and a recent phase III randomized trial showed a significant improvement in event-free survival for patients receiving chimeric anti-GD2 (ch14.18) combined with cytokines and isotretinoin after myeloablative consolidation therapy. A recently approved small-molecule inhibitor of ALK has shown promising preclinical activity for neuroblastoma and is currently in phase I and II trials. This is the first agent directed to a specific mutation in neuroblastoma, and marks a new step toward personalized therapy for neuroblastoma. Further clinical development of targeted treatments offers new hope for children with neuroblastoma.

Indexed as

3-IodobenzylguanidineAnaplastic Lymphoma KinaseAntibodies, MonoclonalChildChild, PreschoolCombined Modality TherapyCrizotinibGangliosidesHumansMolecular Targeted TherapyNeural CrestNeuroblastomaNorepinephrine Plasma Membrane Transport ProteinsPrecision MedicinePyrazolesPyridines3-IodobenzylguanidineALK protein, humanAnaplastic Lymphoma KinaseAntibodies, MonoclonalCrizotinibganglioside, GD2GangliosidesNorepinephrine Plasma Membrane Transport ProteinsPyrazolesPyridinesRadiopharmaceuticalsReceptor Protein-Tyrosine Kinases

Identifiers

PMID22589483
PMCPMC3382042
OpenAlexW2102118318

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.