Please use this identifier to cite or link to this item: https://repositorio.ufrn.br/jspui/handle/123456789/25924
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dc.contributor.authorBarros, Bruna D. de Figueiredo-
dc.contributor.authorKupper, Bruna E. C.-
dc.contributor.authorAguiar Junior, Samuel-
dc.contributor.authorMello, Celso A. L. de-
dc.contributor.authorBegnam, Maria D.-
dc.contributor.authorChojniak, Rubens-
dc.contributor.authorSouza, Sandro J. de-
dc.contributor.authorTorrezan, Giovana T.-
dc.contributor.authorCarraro, Dirce M.-
dc.date.accessioned2018-10-02T14:29:55Z-
dc.date.available2018-10-02T14:29:55Z-
dc.date.issued2018-08-10-
dc.identifier.citationBARROS, B. D. F. et al. Mutation detection in tumor-derived cell free DNA anticipates progression in a patient with metastatic colorectal cancer. Front. Oncol., v. 8, p. 306, ago/2018.pt_BR
dc.identifier.urihttps://repositorio.ufrn.br/jspui/handle/123456789/25924-
dc.languageengpt_BR
dc.rightsAcesso Abertopt_BR
dc.subjectliquid biopsypt_BR
dc.subjectctDNApt_BR
dc.subjectcolorectal cancerpt_BR
dc.subjectNGSpt_BR
dc.subjectgene panelpt_BR
dc.titleMutation detection in tumor-derived cell free DNA anticipates progression in a patient with metastatic colorectal cancerpt_BR
dc.typearticlept_BR
dc.identifier.doi10.3389/fonc.2018.00306-
dc.description.resumoBackground: The observation of tumor-derived cell-free DNA (ctDNA) in plasma brought new expectations to monitor treatment response in cancer patients. Case presentation: In an exploratory case of a 57-year-old man diagnosed with metastatic sigmoid adenocarcinoma, we used a hotspot panel of cancer-associated gene mutations to identify tumor-specific mutations in the primary tumor and metastasis. Results: Five mutations were detected (KRAS, p.Gly12Val; TP53, p.Arg175His; RB1, p.Ile680Thr; ALK, p.Gly1184Glu; and ERBB2, p.Lys860Lys), of which three were detected in both tissue types (primary tumor and metastasis). All five mutations were monitored in the ctDNA of six serial plasma samples. Only KRAS and TP53 mutations were detected at a high frequency in the first plasma sample. After 1 month of chemotherapy the allele frequencies of both mutations fell below the detection limit. From the third month of systemic treatment onward, the allele frequencies of both mutations were detectable in plasma, displaying a continual increase thereafter. The remaining three mutations were not detected in plasma samples. Signs of disease progression in ctDNA during the treatment period were evident while computed tomography (CT) measurements suggested stable metastatic lesions throughout the treatment. Conclusions: Liquid biopsies revealed tumor heterogeneity and predicted tumor progression, demonstrating the potential of ctDNA analysis to be a sensitive and specific tool for monitoring treatment responsivity and for early identification of treatment resistance.pt_BR
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