2022
DOI: 10.3389/fonc.2022.946597
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Research hotspots and trends of chordoma: A bibliometric analysis

Abstract: BackgroundChordoma is a type of mesenchymal malignancy with a high recurrence rate and poor prognosis. Due to its rarity, the tumorigenic mechanism and optimal therapeutic strategy are not well known.MethodsAll relevant articles of chordoma research from 1 January 2000 to 26 April 2022 were obtained from Web of Science Core Collection database. Blibliometrix was used to acquire basic publication data. Visualization and data table of collaboration network, dynamic analysis, trend topics, thematic map, and facto… Show more

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Cited by 4 publications
(7 citation statements)
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“…Skull base chordomas often present with headaches, dysphagia or bucking caused by cranial nerve palsies, and even hemiplegia [ 17 ]. Mobile spine or sacral chordomas often result in chronic back pain or urinary/bowel dysfunction due to nerve root compression [ 7 , 18 ]. There is little research on postoperative management of chordomas, although they show relatively poor prognosis [ 19 ].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Skull base chordomas often present with headaches, dysphagia or bucking caused by cranial nerve palsies, and even hemiplegia [ 17 ]. Mobile spine or sacral chordomas often result in chronic back pain or urinary/bowel dysfunction due to nerve root compression [ 7 , 18 ]. There is little research on postoperative management of chordomas, although they show relatively poor prognosis [ 19 ].…”
Section: Discussionmentioning
confidence: 99%
“…High-dose radiation therapy is recommended to lower the risk of recurrence [ 6 ]. To date, neurosurgeons and scientists have mainly focused on the molecular signaling pathway of and the targeted therapy for chordoma, the surgical treatment of chordoma, and the optimization of radiotherapy and immunotherapy of chordoma [ 7 ].…”
Section: Introductionmentioning
confidence: 99%
“…Considering also the contribution of less cited recent biomolecular studies, it would seem clear that (1) cell lines obtained from sacral and clival chordomas constitute a fundamental and useful tool for researchers to obtain further biomolecular information; (2) conventional and poorly differentiated chordomas express brachyury while dedifferentiated types do not, and this characteristic limits the potential of an antibrachyury vaccine [ 10 , 11 ]; (3) identification of epigenetic changes such as miR hyper-hypo-expression in recurrent tumors might furnish new therapeutic options [ 3 , 9 ]. Genetic and gene expression changes identified using NGS could provide further potential therapeutic targets [ 39 ].…”
Section: Discussionmentioning
confidence: 99%
“…There are still many open issues about the optimal treatment, mostly related to recurrence management. The natural history of chordomas entails a relatively poor survival of 0.9 years without any treatment [ 9 , 10 , 11 ]. As first treatment, the gold standard is gross total resection (GTR) with either open or endoscopic surgical approaches, though tumor location and proximity to nervous and vascular structures make GTR challenging, followed by particle therapy [ 6 , 12 ].…”
Section: Introductionmentioning
confidence: 99%
“…All records and cited references from the WOS were analyzed using the bibliometrix package of R software (version 4.2.1), CiteSpace (version 6.1.6), VOSviewer (version 1.6.18) and an online analytical platform ( https://bibliometric.com/ ). The biblimetrix package can convert and output simplified bibliographic information and complete data analysis and visualization ( 16 ). VOSviewer can generate the collaboration and co-citation networks.…”
Section: Methodsmentioning
confidence: 99%