Evidence map›Paper›PMID 31300807›Full record

ReviewNature reviews. Cancer2019

Molecular characteristics and therapeutic vulnerabilities across paediatric solid tumours.

David T W Jones, Ana Banito, Thomas G P Grünewald, Michelle Haber, Natalie Jäger, Marcel Kool, Till Milde, Jan J Molenaar, Arash Nabbi, Trevor J Pugh and 4 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed
13.3field-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

86 citing papers in PubMed, 155 citations in OpenAlex.

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  20. The landscape of structural variation in pediatric cancer.bioRxiv : the preprint server for biology · 2025
    Article

26 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

14 authors at 8 institutions in 6 countries.

David T W JonesHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Ana BanitoHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.ORCID http://orcid.org/0000-0003-2188-0003
Thomas G P GrünewaldMax-Eder Research Group for Pediatric Sarcoma Biology, Institute of Pathology, Faculty of Medicine, LMU Munich, Munich, Germany.ORCID http://orcid.org/0000-0003-0920-7377
Michelle HaberChildren's Cancer Institute, Lowy Cancer Research Centre, UNSW Australia, Randwick, NSW, Australia.ORCID http://orcid.org/0000-0003-2036-8817
Natalie JägerHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Marcel KoolHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Till MildeHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Jan J MolenaarPrincess Maxima Center for Pediatric Cancer, Utrecht, The Netherlands.
Arash NabbiPrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Trevor J PughPrincess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Gudrun SchleiermacherSIREDO Oncology Center (Care, Innovation and Research for Children and AYA with Cancer), Institut Curie, Paris, France.
Malcolm A SmithCancer Therapy Evaluation Program, National Cancer Institute, Rockville, MD, USA.
Frank WestermannHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.
Stefan M PfisterHopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany. s.pfister@kitz-heidelberg.de.ORCID http://orcid.org/0000-0002-5447-5322
German Cancer Research Center · DEChildren's Cancer Institute Australia · AUDeutschen Konsortium für Translationale Krebsforschung · DEInserm · FRNational Cancer Institute · USOntario Institute for Cancer Research · CAPrincess Máxima Center · NLUniversity Health Network · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The spectrum of tumours arising in childhood is fundamentally different from that seen in adults, and they are known to be divergent from adult malignancies in terms of cellular origins, epidemiology, genetic complexity, driver mutations and underlying mutational processes. Despite the immense knowledge generated through sequencing efforts and functional characterization of identified (epi-)genetic alterations over the past decade, the clinical implications of this knowledge have so far been limited. Novel preclinical platforms such as the European Innovative Therapies for Children with Cancer-Paediatric Preclinical Proof-of-Concept Platform and the US-based Pediatric Preclinical Testing Consortium are being developed to try to change this by aiming to recapitulate the extensive heterogeneity of paediatric tumours and thereby, hopefully, improve the ability to predict clinical benefit. Numerous studies have also been established worldwide to provide patients with access to real-time molecular profiling and the possibility of more precise mechanism-of-action-based treatments. In addition to tumour-intrinsic findings and mechanisms, ongoing studies are investigating features such as the immune microenvironment of paediatric tumours in comparison with adult cancers - currently of very timely clinical relevance. However, there is an ongoing need for rigorous preclinical biomarker and target validation to feed into the next generation of molecularly stratified clinical trials. This Review aims to provide a comprehensive state-of-the-art overview of the molecular landscape of paediatric solid tumours, including their underlying genomic alterations and interactions with the microenvironment, complemented with our current understanding of potential therapeutic vulnerabilities and how these can be preclinically tested using more accurate predictive methods. Finally, we provide an outlook on the challenges and opportunities associated with translating this overwhelming scientific progress into real clinical benefit.

Indexed as

Cell CycleEpigenesis, GeneticEuropeGene Expression Regulation, NeoplasticGenetic Predisposition to DiseaseGenomicsHumansImmune SystemMutationNeoplasmsPediatricsSignal TransductionTumor MicroenvironmentUnited States

Identifiers

PMID31300807
OpenAlexW2961969123

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.