Evidence map›Paper›PMID 42613365›Full record

ReviewBritish journal of cancer2026

Paediatric therapeutic development workshop on osteosarcoma.

Joseph S Baxter, Claudia Montiel Equihua, Jan J Molenaar, Pablo Berlanga, Michael W Bishop, Patricia Blanc, Quentin Campbell-Hewson, Michela Casanova, Isidro Cortes-Ciriano, Brian Crompton and 42 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in British journal of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

52 authors.

Joseph S Baxter *LifeArc, Lynton House, London, UK.ORCID http://orcid.org/0000-0002-2336-614X
Claudia Montiel Equihua *LifeArc, Lynton House, London, UK.
Jan J Molenaar *Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Pablo BerlangaDepartement de cancérologie de l'enfant et l'adolescent, Gustave-Roussy, Université Paris-Saclay, Villejuif, France.
Michael W BishopDepartment of Pediatrics, Arkansas Children's Hospital, Little Rock, AR, USA.
Patricia BlancImagine for Margo, Paris, France.
Quentin Campbell-HewsonGreat North Children's Hospital, Newcastle upon Tyne Hospitals NHS, Newcastle, UK.
Michela CasanovaFondazione IRCC Istituto Nazionale dei Tumori di Milano, Milano, Italy.
Isidro Cortes-CirianoEMBL-EBI, European Molecular Biology Laboratory, European Bioinformatics Institute, Cambridge, UK.
Brian CromptonDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID http://orcid.org/0000-0001-9404-6621
Sam DaemsWaterland Private Equity Investments, Antwerp, Belgium.
Laura DanielsonCancer Research UK, London, UK.
Filemon Dela CruzDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-8356-5191
Adrienne FlanaganGenetics and Cell Biology of Sarcoma, UCL Cancer Institute, London, UK.ORCID http://orcid.org/0000-0002-2832-1303
Richard GorlickDivision of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0001-8995-2929
Ann GrahamMIB Agents Osteosarcoma Alliance, Barnard, VT, USA.
Lillian M GuentherDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN, USA.
Stefanie Hecker-NoltingKlinikum Stuttgart - Olgahospital, Stuttgart Cancer Center, Zentrum für Kinder-, Jugend- und Frauenmedizin, Pädiatrie 5 (Onkologie, Hämatologie, Immunologie), Stuttgart, Germany.
Lee HelmanThe Osteosarcoma Institute, Dallas, TX, USA.
Maia Kavanagh-WilliamsonLifeArc, Lynton House, London, UK.
Pamela KearnsCollege of Medicine and Health, University of Birmingham, Birmingham, UK.ORCID http://orcid.org/0000-0003-2756-5813
Geffen LassLifeArc, Lynton House, London, UK.
Christina Ip-TomaMIB Agents Osteosarcoma Alliance, Barnard, VT, USA.
John LigonDepartment of Pediatrics, College of Medicine, The University of Florida, Gainesville, FL, USA.
Jeremy LewinDepartment of Cancer Medicine, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia.
J Andrew LivingstonDepartment of Sarcoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0002-1337-3282
Antonin MarchaisUMR 1360 "Oncogenesis, Resistance and Therapeutic Targets for Pediatric Cancers", Université Paris-Saclay Gustave Roussy, Villejuif, France.
Martin G McCabeDivision of Cancer Sciences, University of Manchester, Manchester, UK.ORCID http://orcid.org/0000-0002-5138-0707
Sybille MittnachtDepartment of Pediatrics and Children's Cancer Research Center, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, Munich, Germany.
Michaela NathrathDepartment of Pediatric Oncology, Klinikum Kassel, Kassel, Germany.
Emanuela PalmeriniSylvester Comprehensive Cancer Center, Miller School of Medicine, University of Miami, Miami, FL, USA.
Pan PantziarkaThe George Pantziarka TP53 Trust, Kingston upon Thames, UK.ORCID http://orcid.org/0000-0002-4676-7835
Seema PatelLifeArc, Lynton House, London, UK.
Sheena PatelCancer Research Horizons, London, UK.
Damon ReedDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-8238-2465
Ryan RobertsCenter for Childhood Cancer, Nationwide Children's Hospital, Columbus, OH, USA.
Katia ScotlandiLaboratory of Oncology Research and Functional Genomics, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
Emily SlotkinDepartment of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-4463-5759
Mandy TsengLifeArc, Lynton House, London, UK.
Walker SmallwoodMIB Agents Osteosarcoma Alliance, Barnard, VT, USA.
Poul H SorensenBritish Columbia Cancer Research Institute and University of British Columbia, Vancouver, BC, Canada.
Claudia ValverdeMedical Oncology Department, Hospital Universitari Vall d'Hebron/Vall d'Hebrón Institute of Oncology, Barcelona, Spain.
Madina WaneLifeArc, Lynton House, London, UK.
Gemma A WilsonLifeArc, Lynton House, London, UK.
Andrew D J PearsonLifeArc, Lynton House, London, UK. andy1pearson@btinternet.com.ORCID http://orcid.org/0000-0002-8738-5913
David JenkinsonLifeArc, Lynton House, London, UK.
Nathalie GasparDepartement de cancérologie de l'enfant et l'adolescent, Gustave-Roussy, Université Paris-Saclay, Villejuif, France.ORCID http://orcid.org/0000-0002-1827-8903
Sandra J StraussDepartment of Oncology, University College London Cancer Institute, London, UK.
LifeArc
Innovative Therapies for Children and Adolescents with Cancer (ITCC)
Cancer Research UK
Cancer Grand Challenge Protect team

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The fourth Paediatric Therapeutic Development Workshop focused on osteosarcoma, the most common primary bone cancer in children and young adults. Current treatment of osteosarcoma comprises surgery and chemotherapy. Outcome has shown very little improvement over the last four decades and there are substantial unmet needs including improving survival, especially in metastatic or relapsed disease, and reducing treatment toxicity. There is a lack of new therapeutics in osteosarcoma, with the evaluation of new treatments challenged by complex biology and variation in chemotherapy standard of care regimens. An antibody-drug conjugate (ADC) targeting LRRC15 with an osteosarcoma-relevant payload is a promising therapeutic approach. Small molecule inhibitors and degraders targeting SMARCAL1 should be considered as a very high priority, as it is a target applicable to several high unmet need malignancies. Preclinical evaluation of KIF18A in osteosarcoma models is required. An early phase study of an eIF4A1 inhibitor is warranted. Further preclinical validation of RUNX2 using PROTACs or ADCs is required. Targeting MYC, either indirectly or directly is a high priority. Osteosarcomas have significant genomic instability and impaired DNA repair mechanisms and efforts are ongoing to exploit this vulnerability therapeutically. The goal is that these therapeutic developments will improve survival for patients with osteosarcoma.

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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.