Evidence map›Paper›PMID 40731087›Full record

SynthesisBritish journal of cancer2025

Prognostic factors in patients with relapsed high-grade osteosarcoma: a systematic review.

Alba Rubio-San-Simón, William Wilson, Giovanna Sironi, Marie-Cécile le Deley, Emanuela Palmerini, Nathalie Gaspar, Sophie Piperno-Neumann, Stefanie Hecker-Nolting, Sandra Strauss, Roelof van Ewijk and 2 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in British journal of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
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

12 authors.

Alba Rubio-San-Simón *Pediatric Oncology and Hematology Department, Hospital Infantil Universitario Niño Jesús, Madrid, Spain. arubiosansimon@gmail.com.ORCID http://orcid.org/0000-0001-6426-7423
William Wilson *Cancer Research UK and UCL Cancer Trials Centre, London, UK.ORCID http://orcid.org/0009-0004-5576-0135
Giovanna SironiPediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID http://orcid.org/0000-0003-2791-2192
Marie-Cécile le DeleyUnité de Méthodologie et Biostatistiques, Centre Oscar Lambret, Lille, France.ORCID http://orcid.org/0000-0002-2946-4592
Emanuela PalmeriniOsteoncology, Bone and Soft Tissue Sarcomas and Innovative Therapies, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.ORCID http://orcid.org/0000-0003-3406-6705
Nathalie GasparDepartment of Oncology for Child and Adolescent, Gustave Roussy Cancer Center, Villejuif, France.ORCID http://orcid.org/0000-0002-1827-8903
Sophie Piperno-NeumannMedical Oncology Department, Institut Curie, Paris, France.ORCID http://orcid.org/0000-0001-9915-2810
Stefanie Hecker-NoltingKlinikum Stuttgart-Olgahospital, Stuttgart, Germany.ORCID http://orcid.org/0000-0002-1815-138X
Sandra StraussLondon Sarcoma Service, University College London Hospitals NHS Trust, London, UK.ORCID http://orcid.org/0000-0001-8328-0260
Roelof van EwijkPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0003-0339-6031
Cristina MeazzaPediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID http://orcid.org/0000-0002-1875-9563
FOSTER Consortium (Fight OsteoSarcoma Through European Research), work package 3 on recurrent/refractory osteosarcoma trials

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe outcome of patients with osteosarcoma after relapse is very poor, with a 5-year overall survival (OS) below 30%. Prognostic factors in this setting remain poorly defined, limiting treatment decisions. This study identifies key clinical and biological prognostic factors to guide future trials.

methodsA systematic review and meta-analysis included studies published between 1976 and 2022 with ≥35 patients. Searches were performed in MEDLINE/PUBMED, EMBASE, and Cochrane. Study quality was assessed using QUIPS tool. Studies reporting any clinical outcomes in the post-relapse setting were included.

resultsNineteen studies involving 3245 patients were analysed. Nine prognostic factors were identified: relapse-free interval, site, number and size of lesions, resectability, sex, age, alkaline phosphatase levels and response to chemotherapy. Meta-analysis confirmed bilateral lung metastases worsened OS (HR 1.68, 95% CI 1.42-1.99). A relapse-free interval >24 months and complete surgical resection were consistently associated with better outcomes. Results on chemotherapy use were inconsistent. Substantial heterogeneity and low methodological quality were noted across studies.

conclusionsKey prognostic factors should address clinical trial design. Stratification by resectability, number and site of lesions and relapse-free interval is essential to evaluate treatment efficacy. Standardised protocols are needed to improve outcomes and provide tailored strategies for relapsed osteosarcoma.

Indexed as

Bone NeoplasmsNeoplasm Recurrence, LocalOsteosarcomaHumansLung NeoplasmsNeoplasm GradingPrognosis

Identifiers

PMID40731087
PMCPMC12480850

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.