Evidence map›Paper›PMID 40442778›Full record

ReviewMolecular cancer2025

Targeting metastasis in paediatric bone sarcomas.

Emma C Bull, Archana Singh, Amy M Harden, Kirsty Soanes, Hala Habash, Lisa Toracchio, Marianna Carrabotta, Christina Schreck, Karan M Shah, Paulina Velasco Riestra and 22 more

Abstract readReview
In one paragraph

Review in Molecular cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

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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

32 authors.

Emma C BullNorwich Medical School, University of East Anglia, Norwich Research Park, Norwich, UK.
Archana SinghNorwich Medical School, University of East Anglia, Norwich Research Park, Norwich, UK.
Amy M HardenNorwich Medical School, University of East Anglia, Norwich Research Park, Norwich, UK.
Kirsty SoanesNorwich Medical School, University of East Anglia, Norwich Research Park, Norwich, UK.
Hala HabashChildhood Cancer Research Unit, Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
Lisa ToracchioLaboratory of Experimental Oncology, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
Marianna CarrabottaLaboratory of Experimental Oncology, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
Christina SchreckChildren's Cancer Research Center, Klinikum Rechts Der Isar, Technical University of Munich, Munich, Germany.
Karan M ShahSchool of Medicine and Population Health, The University of Sheffield, Sheffield, UK.
Paulina Velasco RiestraBiomedical and Clinical Sciences, Division of Surgery, Orthopaedics and Oncology, Linköping University, Linköping, Sweden.
Margaux ChantoiseauGustave Roussy Institute, Villejuif, France.
Maria Eugénia Marques Da CostaGustave Roussy Institute, Villejuif, France.
Gaël Moquin-BeaudryGustave Roussy Institute, Villejuif, France.
Pan PantziarkaAnticancer Fund, Meise, Belgium.
Edidiong Akanimo EssietOrthopaedic Oncology, Royal National Orthopaedic Hospital, Stanmore, UK.
Craig GerrandOrthopaedic Oncology, Royal National Orthopaedic Hospital, Stanmore, UK.
Alison GartlandSchool of Medicine and Population Health, The University of Sheffield, Sheffield, UK.
Linda BojmarBiomedical and Clinical Sciences, Division of Surgery, Orthopaedics and Oncology, Linköping University, Linköping, Sweden.
Anna FahlgrenBiomedical and Clinical Sciences, Division of Cell and Neurobiology, Linköping University, Linköping, Sweden.
Antonin MarchaisGustave Roussy Institute, Villejuif, France.
Evgenia PapakonstantinouPediatric Hematology-Oncology, Ippokratio General Hospital of Thessaloniki, Thessaloniki, Greece.
Eleni M TomazouSt. Anna Children's Cancer Research Institute, Vienna, Austria.
Didier SurdezFaculty of Medicine, Balgrist University Hospital, University of Zurich, Zurich, Switzerland.
Dominique HeymannSchool of Medicine and Population Health, The University of Sheffield, Sheffield, UK.
Florencia Cidre-AranazHopp Children's Cancer Center (KiTZ), Heidelberg, Germany.
Olivia FromigueInserm UMR981, Gustave Roussy Cancer Campus, Université Paris Saclay, Villejuif, France.
Darren W SextonSchool of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Liverpool, UK.
Nikolas HeroldChildhood Cancer Research Unit, Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
Thomas G P GrünewaldHopp Children's Cancer Center (KiTZ), Heidelberg, Germany.
Katia ScotlandiLaboratory of Experimental Oncology, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
Michaela NathrathChildren's Cancer Research Center, Klinikum Rechts Der Isar, Technical University of Munich, Munich, Germany.
Darrell GreenNorwich Medical School, University of East Anglia, Norwich Research Park, Norwich, UK. d.green@uea.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paediatric bone sarcomas (e.g. Ewing sarcoma, osteosarcoma) comprise significant biological and clinical heterogeneity. This extreme heterogeneity affects response to systemic therapy, facilitates inherent and acquired drug resistance and possibly underpins the origins of metastatic disease, a key component implicit in cancer related death. Across all cancers, metastatic models have offered competing accounts on when dissemination occurs, either early or late during tumorigenesis, whether metastases at different foci arise independently and directly from the primary tumour or give rise to each other, i.e. metastases-to-metastases dissemination, and whether cell exchange occurs between synchronously growing lesions. Although it is probable that all the above mechanisms can lead to metastatic disease, clinical observations indicate that distinct modes of metastasis might predominate in different cancers. Around 70% of patients with bone sarcoma experience metastasis during their disease course but the fundamental molecular and cell mechanisms underlying spread are equivocal. Newer therapies such as tyrosine kinase inhibitors have shown promise in reducing metastatic relapse in trials, nonetheless, not all patients respond and 5-year overall survival remains at ~ 50%. Better understanding of potential bone sarcoma biological subgroups, the role of the tumour immune microenvironment, factors that promote metastasis and clinical biomarkers of prognosis and drug response are required to make progress. In this review, we provide a comprehensive overview of the approaches to manage paediatric patients with metastatic Ewing sarcoma and osteosarcoma. We describe the molecular basis of the tumour immune microenvironment, cell plasticity, circulating tumour cells and the development of the pre-metastatic niche, all required for successful distant colonisation. Finally, we discuss ongoing and upcoming patient clinical trials, biomarkers and gene regulatory networks amenable to the development of anti-metastasis medicines.

Indexed as

Bone NeoplasmsOsteosarcomaSarcoma, EwingBiomarkers, TumorChildHumansMolecular Targeted TherapyNeoplasm MetastasisPrognosisTumor MicroenvironmentBiomarkers, TumorBoneEwing sarcomaMetastasisOsteosarcomaSarcoma

Identifiers

PMID40442778
PMCPMC12121159

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Registered trials

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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.