Evidence map›Paper›PMID 40251562›Full record

SynthesisBMC cancer2025

Tyrosine kinase inhibitors in Ewing's sarcoma: a systematic review.

Ahmad Assi, Mohamad Farhat, Rami Mohanna, Maria Catherine Rita Hachem, Ziad Zalaquett, Marven Aoun, Sami Abi Farraj, Mohammad Daher, Amer Sebaaly, Hampig-Raphaël Kourie

Abstract readSystematic Review
In one paragraph

Synthesis in BMC 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. Drug sensitivity testing of patient-derived bone sarcomas identifies selective kinase inhibitors for patients with refractory disease.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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  3. Review
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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

10 authors.

Ahmad AssiHematology-Oncology Department, Hotel Dieu de France, Beirut, Lebanon. a.m.assi@hotmail.com.
Mohamad FarhatHematology-Oncology Department, Hotel Dieu de France, Beirut, Lebanon.
Rami MohannaHematology-Oncology Department, Hotel Dieu de France, Beirut, Lebanon.
Maria Catherine Rita HachemHematology-Oncology Department, Hotel Dieu de France, Beirut, Lebanon.
Ziad ZalaquettHematology-Oncology Department, Hotel Dieu de France, Beirut, Lebanon.
Marven AounOrthopedics Department, Hotel Dieu de France, Beirut, Lebanon.
Sami Abi FarrajHematology-Oncology Department, Hotel Dieu de France, Beirut, Lebanon.
Mohammad DaherOrthopedics Department, Hotel Dieu de France, Beirut, Lebanon. Mohdaher1@hotmail.com.
Amer SebaalyOrthopedics Department, Hotel Dieu de France, Beirut, Lebanon. Amersebaaly@hotmail.com.
Hampig-Raphaël KourieHematology-Oncology Department, Hotel Dieu de France, Beirut, Lebanon.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ewing's sarcoma (ES) is a highly aggressive primary bone malignancy that primarily affects children and adolescents. Several tyrosine kinase receptors (RTKs) have been found to be overexpressed in ES samples, and it was demonstrated that some play significant roles in driving the malignant phenotype of ES. Specifically, ES with insulin-like growth factor 1 (IGF1R) or vascular endothelial growth factor (VEGFR) overexpression were correlated with more aggressive ES and worse outcomes. Other RTKs that were determined to be overexpressed in ES include platelet-derived growth factor receptor, stem cell factor receptor, and hepatocyte growth factor. Overexpression of these molecules suggests their possible tumor-driving role, making them potential targets for intervention. Various tyrosine kinase inhibitors (TKIs), including apatinib, anlotinib, and cabozantinib have shown clinical promise in patients with recurrent ES who have progressed on previous lines of therapy. The findings reported in this review emphasize the importance of assessing IGF1R-focused inhibitors and combinational therapeutic regimens in future research. Furthermore, biomarkers predictive of response are necessary to improve patient outcomes. In order to optimize ES care, considerations for patient eligibility on the basis of positivity for biomarkers predictive of response, and the inclusion of quality-of-life evaluations in studies must be addressed.

Indexed as

Bone NeoplasmsProtein Kinase InhibitorsSarcoma, EwingHumansReceptor, IGF Type 1Tyrosine Kinase InhibitorsIGF1R protein, humanProtein Kinase InhibitorsReceptor, IGF Type 1Tyrosine Kinase InhibitorsEwing’s SarcomaReceptors Tyrosine KinaseSystematic ReviewTyrosine Kinase Inhibitors

Identifiers

PMID40251562
PMCPMC12008964

What OpenQuestion holds

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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.