Evidence map›Paper›PMID 40149640›Full record

ReviewBiomedicines2025

Digging Through the Complexities of Immunological Approaches in Emerging Osteosarcoma Therapeutics: A Comprehensive Narrative Review with Updated Clinical Trials.

Consolato M Sergi, Mervin Burnett, Eugeniu Jantuan, Mariam Hakoum, Shawn T Beug, Roger Leng, Fan Shen

Abstract readReview
In one paragraph

Review in Biomedicines, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. 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

7 authors.

Consolato M SergiDivision of Anatomic Pathology, Department of Laboratory Medicine, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, ON K1H 8L1, Canada.ORCID 0000-0002-2779-7879
Mervin BurnettDepartment of Laboratory Medicine, Stollery Children's Hospital, University of Alberta, Edmonton, AB T6G 2R3, Canada.
Eugeniu JantuanDepartment of Laboratory Medicine, Stollery Children's Hospital, University of Alberta, Edmonton, AB T6G 2R3, Canada.ORCID 0000-0002-4645-3617
Mariam HakoumCHEO Research Institute, University of Ottawa, Ottawa, ON K1N 6N5, Canada.
Shawn T BeugCHEO Research Institute, University of Ottawa, Ottawa, ON K1N 6N5, Canada.ORCID 0000-0002-9991-3306
Roger LengDepartment of Laboratory Medicine, Stollery Children's Hospital, University of Alberta, Edmonton, AB T6G 2R3, Canada.ORCID 0000-0001-9652-4703
Fan ShenDepartment of Laboratory Medicine, Stollery Children's Hospital, University of Alberta, Edmonton, AB T6G 2R3, Canada.ORCID 0000-0001-7432-8891

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteosarcoma (OS) is the predominant mesenchymal primary malignant bone tumor in oncology and pathology, impacting a wide age range from adolescents to older adults. It frequently advances to lung metastasis, ultimately resulting in the mortality of OS patients. The precise pathological pathways responsible for OS progression and dissemination are not fully understood due to its heterogeneity. The integration of surgery with neoadjuvant and postoperative chemotherapy has significantly increased the 5-year survival rate to more than 70% for patients with localized OS tumors. However, about 30% of patients experience local recurrence and/or metastasis. Hence, there is a requirement for innovative therapeutic approaches to address the limitations of traditional treatments. Immunotherapy has garnered increasing attention as a promising avenue for tumors resistant to standard therapies, including OS, despite the underlying mechanisms of disease progression and dissemination remaining not well elucidated. Immunotherapy may not have been suitable for use in patients with OS because of the tumor's immunosuppressive microenvironment and limited immunogenicity. Nevertheless, there are immune-based treatments now being developed for clinical use, such as bispecific antibodies, chimeric antigen receptor T cells, and immune checkpoint inhibitors. Also, additional immunotherapy techniques including cytokines, vaccines, and modified-Natural Killer (NK) cells/macrophages are in the early phases of research but will certainly be popular subjects in the nearest future. Our goal in writing this review was to spark new lines of inquiry into OS immunotherapy by summarizing the findings from both preclinical and current clinical studies examining different approaches.

Indexed as

boneimmunologyOmicsOsteosarcomatherapy

Identifiers

PMID40149640
PMCPMC11940054

What OpenQuestion holds

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LicenceCC BY
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.