HUDEČKOVÁ, Markéta, Vladimír KOUCKÝ, Jan ROTTENBERG and Břetislav GÁL. Gene Mutations in Circulating Tumour DNA as a Diagnostic and Prognostic Marker in Head and Neck Cancer - A Systematic Review. BIOMEDICINES. BASEL: MDPI, 2021, vol. 9, No 11, p. 1-12. ISSN 2227-9059. Available from: https://dx.doi.org/10.3390/biomedicines9111548.
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Basic information
Original name Gene Mutations in Circulating Tumour DNA as a Diagnostic and Prognostic Marker in Head and Neck Cancer - A Systematic Review
Name in Czech Gene Mutations in Circulating Tumour DNA as a Diagnostic and Prognostic Marker in Head and Neck Cancer - A Systematic Review
Authors HUDEČKOVÁ, Markéta (203 Czech Republic, belonging to the institution), Vladimír KOUCKÝ (203 Czech Republic), Jan ROTTENBERG (203 Czech Republic, belonging to the institution) and Břetislav GÁL (203 Czech Republic, guarantor, belonging to the institution).
Edition BIOMEDICINES, BASEL, MDPI, 2021, 2227-9059.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30206 Otorhinolaryngology
Country of publisher Czech Republic
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 4.757
RIV identification code RIV/00216224:14110/21:00123265
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.3390/biomedicines9111548
UT WoS 000722923900001
Keywords (in Czech) head and neck cancer squamous cell carcinoma (HNSCC); circulating tumour DNA (ctDNA); diagnostic biomarker; liquid biopsy
Keywords in English head and neck cancer squamous cell carcinoma (HNSCC); circulating tumour DNA (ctDNA); diagnostic biomarker; liquid biopsy
Tags 14110126, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 17/5/2022 12:41.
Abstract
Background: Head and Neck Squamous Cell Carcinoma (HNSCC) is one of the most common malignancies globally. An early diagnosis of this disease is crucial, and the detection of gene mutations in circulating tumour DNA (ctDNA) through a liquid biopsy is a promising non-invasive diagnostic method. This review aims to provide an overview of ctDNA mutations in HNSCC patients and discuss the potential use of this tool in diagnosis and prognosis. (2) Methods: A systematic search for articles published in the English language between January 2000 and April 2021 in the Medline and Scopus databases was conducted. (3) Results: A total of 10 studies published in nine publications were selected and analysed. Altogether, 390 samples were obtained from HNSCC patients, and 79 control samples were evaluated. The most often explored gene mutation in ctDNA was TP53. (4) Conclusions: The examination of a larger group of gene mutations and the use of a combination of multiple detection methods contribute to a higher detection rate of mutated ctDNA. More studies are necessary to verify these conclusions and to translate them into clinical practice.
Abstract (in Czech)
Background: Head and Neck Squamous Cell Carcinoma (HNSCC) is one of the most common malignancies globally. An early diagnosis of this disease is crucial, and the detection of gene mutations in circulating tumour DNA (ctDNA) through a liquid biopsy is a promising non-invasive diagnostic method. This review aims to provide an overview of ctDNA mutations in HNSCC patients and discuss the potential use of this tool in diagnosis and prognosis. (2) Methods: A systematic search for articles published in the English language between January 2000 and April 2021 in the Medline and Scopus databases was conducted. (3) Results: A total of 10 studies published in nine publications were selected and analysed. Altogether, 390 samples were obtained from HNSCC patients, and 79 control samples were evaluated. The most often explored gene mutation in ctDNA was TP53. (4) Conclusions: The examination of a larger group of gene mutations and the use of a combination of multiple detection methods contribute to a higher detection rate of mutated ctDNA. More studies are necessary to verify these conclusions and to translate them into clinical practice.
Links
MUNI/A/1002/2018, interní kód MUName: Ztráta sluchu v dětském věku - příčiny, diagnostika, možnosti rehabilitace III
Investor: Masaryk University, Category A
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