Evidence map›Paper›PMID 35655525›Full record

ArticleSarcoma2022

Targeting the FAK-Src Complex in Desmoplastic Small Round Cell Tumors, Ewing Sarcoma, and Rhabdomyosarcoma.

Anke E M van Erp, Melissa H S Hillebrandt-Roeffen, Niek F H N van Bree, Tim A Plüm, Uta E Flucke, Ingrid M E Desar, Emmy D G Fleuren, Winette T A van der Graaf, Yvonne M H Versleijen-Jonkers

Open access · hybridAbstract read
In one paragraph

Article in Sarcoma, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 29% of its field
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

7 citing papers in PubMed, 5 citations in OpenAlex.

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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

9 authors at 3 institutions in 2 countries.

Anke E M van ErpDepartment of Medical Oncology, Radboud University Medical Center, P.O. Box 9101, 6500 HB, Nijmegen, Netherlands.
Melissa H S Hillebrandt-RoeffenDepartment of Medical Oncology, Radboud University Medical Center, P.O. Box 9101, 6500 HB, Nijmegen, Netherlands.
Niek F H N van BreeDepartment of Medical Oncology, Radboud University Medical Center, P.O. Box 9101, 6500 HB, Nijmegen, Netherlands.
Tim A PlümDepartment of Medical Oncology, Radboud University Medical Center, P.O. Box 9101, 6500 HB, Nijmegen, Netherlands.
Uta E FluckeDepartment of Pathology, Radboud University Medical Center, P.O. Box 9101, 6500 HB, Nijmegen, Netherlands.
Ingrid M E DesarDepartment of Medical Oncology, Radboud University Medical Center, P.O. Box 9101, 6500 HB, Nijmegen, Netherlands.
Emmy D G FleurenChildren's Cancer Institute Australia, Lowy Cancer Research Centre, University of NSW, Sydney, NSW, Australia.
Winette T A van der GraafDepartment of Medical Oncology, Netherlands Cancer Institute-Van Leeuwenhoek, 1066 CX, Amsterdam, Netherlands.
Yvonne M H Versleijen-JonkersDepartment of Medical Oncology, Radboud University Medical Center, P.O. Box 9101, 6500 HB, Nijmegen, Netherlands.ORCID https://orcid.org/0000-0001-7623-0505
Radboud University Nijmegen · NLCancer Institute of New South Wales · AUThe Netherlands Cancer Institute · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Desmoplastic small round cell tumors (DSRCTs), Ewing sarcoma (ES), and alveolar and embryonal rhabdomyosarcoma (ARMS and ERMS) are malignant sarcomas typically occurring at young age, with a poor prognosis in the metastatic setting. New treatment options are necessary. Src family kinase inhibitor dasatinib single-agent treatment has been investigated in a phase 2 study in patients with advanced sarcomas including ES and RMS but failed as a single agent in these subtypes. Since previous studies demonstrated high FAK and Src activities in RMS and ES tissue and cell lines, and dasatinib treatment was shown to upregulate activated FAK, we hypothesized that FAK-Src combination treatment could potentially be an interesting treatment option for these tumor types. We examined the effects of targeting the FAK-Src complex by addressing (p)FAK and (p)Src expressions in tumor sections of DSRCT (

Identifiers

PMID35655525
PMCPMC9153931
OpenAlexW4280500959

What OpenQuestion holds

Textmetadata
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.