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Circulating free plasma tumor DNA in patients with advanced gastric cancer receiving systemic chemotherapy
BACKGROUND: Advanced gastric cancers are usually associated with incurable conditions for which systemic treatments are indicated. Recent studies suggest that circulating cell-free plasma DNA of tumour origin (tDNA) is a promising non-invasive biomarker that can be used to predict the prognosis and...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258437/ https://www.ncbi.nlm.nih.gov/pubmed/30498396 http://dx.doi.org/10.1186/s12907-018-0079-y |
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author | Normando, Sávia Raquel Costa Delgado, Pamela de Oliveira Rodrigues, Ana Katherine Soares Barbosa David Filho, Waldec Jorge Fonseca, Fernando Luiz Affonso Cruz, Felipe José Silva Melo del Giglio, Auro |
author_facet | Normando, Sávia Raquel Costa Delgado, Pamela de Oliveira Rodrigues, Ana Katherine Soares Barbosa David Filho, Waldec Jorge Fonseca, Fernando Luiz Affonso Cruz, Felipe José Silva Melo del Giglio, Auro |
author_sort | Normando, Sávia Raquel Costa |
collection | PubMed |
description | BACKGROUND: Advanced gastric cancers are usually associated with incurable conditions for which systemic treatments are indicated. Recent studies suggest that circulating cell-free plasma DNA of tumour origin (tDNA) is a promising non-invasive biomarker that can be used to predict the prognosis and monitor the efficacy of systemic treatments in patients with certain types of cancer. We conducted a pilot study to analyse the potential role of tDNA as a biomarker in patients with advanced gastric cancer. METHODS: We included 30 patients with locally advanced unresectable or metastatic gastric cancer. We obtained samples (10 mL of total blood) from each patient every 3 months and performed concomitant CT until disease progression or death. Total cell-free circulating DNA (cfDNA) samples were measured using GeneQuant RNA/DNA Calculator-Amersham Pharmacia Biotech (Biochrom) Ltd. The cfDNA was used to evaluate the ALU DNA sequences 247 and 115. The level of tDNA was calculated from the ratio of the expression of ALU DNA sequences and the concentration of total cell-free DNA. We utilized the RECIST criteria 1.1 to evaluate the tumour response. RESULTS: Patients with advanced gastric cancer had significantly higher concentrations of cfDNA compared with normal controls (p = 0.00015), which allowed us to conclude that the cfDNA in the patients originated from the tumour. We did not find any significant correlation between the level of tDNA and OS or tumour response. However, after the first cycles of chemotherapy (at 3 months), we observed that patients with lower tDNA levels had significantly longer DFS compared with those with higher levels (Cox Regression p = 0.0228). CONCLUSIONS: At 3 months after the beginning of chemotherapy, the tDNA levels are correlated with DFS in patients with advanced gastric cancer who receive systemic chemotherapy. tDNA may be a specific, non-invasive and cost effective new biomarker for these patients. |
format | Online Article Text |
id | pubmed-6258437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62584372018-11-29 Circulating free plasma tumor DNA in patients with advanced gastric cancer receiving systemic chemotherapy Normando, Sávia Raquel Costa Delgado, Pamela de Oliveira Rodrigues, Ana Katherine Soares Barbosa David Filho, Waldec Jorge Fonseca, Fernando Luiz Affonso Cruz, Felipe José Silva Melo del Giglio, Auro BMC Clin Pathol Research Article BACKGROUND: Advanced gastric cancers are usually associated with incurable conditions for which systemic treatments are indicated. Recent studies suggest that circulating cell-free plasma DNA of tumour origin (tDNA) is a promising non-invasive biomarker that can be used to predict the prognosis and monitor the efficacy of systemic treatments in patients with certain types of cancer. We conducted a pilot study to analyse the potential role of tDNA as a biomarker in patients with advanced gastric cancer. METHODS: We included 30 patients with locally advanced unresectable or metastatic gastric cancer. We obtained samples (10 mL of total blood) from each patient every 3 months and performed concomitant CT until disease progression or death. Total cell-free circulating DNA (cfDNA) samples were measured using GeneQuant RNA/DNA Calculator-Amersham Pharmacia Biotech (Biochrom) Ltd. The cfDNA was used to evaluate the ALU DNA sequences 247 and 115. The level of tDNA was calculated from the ratio of the expression of ALU DNA sequences and the concentration of total cell-free DNA. We utilized the RECIST criteria 1.1 to evaluate the tumour response. RESULTS: Patients with advanced gastric cancer had significantly higher concentrations of cfDNA compared with normal controls (p = 0.00015), which allowed us to conclude that the cfDNA in the patients originated from the tumour. We did not find any significant correlation between the level of tDNA and OS or tumour response. However, after the first cycles of chemotherapy (at 3 months), we observed that patients with lower tDNA levels had significantly longer DFS compared with those with higher levels (Cox Regression p = 0.0228). CONCLUSIONS: At 3 months after the beginning of chemotherapy, the tDNA levels are correlated with DFS in patients with advanced gastric cancer who receive systemic chemotherapy. tDNA may be a specific, non-invasive and cost effective new biomarker for these patients. BioMed Central 2018-11-26 /pmc/articles/PMC6258437/ /pubmed/30498396 http://dx.doi.org/10.1186/s12907-018-0079-y Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Normando, Sávia Raquel Costa Delgado, Pamela de Oliveira Rodrigues, Ana Katherine Soares Barbosa David Filho, Waldec Jorge Fonseca, Fernando Luiz Affonso Cruz, Felipe José Silva Melo del Giglio, Auro Circulating free plasma tumor DNA in patients with advanced gastric cancer receiving systemic chemotherapy |
title | Circulating free plasma tumor DNA in patients with advanced gastric cancer receiving systemic chemotherapy |
title_full | Circulating free plasma tumor DNA in patients with advanced gastric cancer receiving systemic chemotherapy |
title_fullStr | Circulating free plasma tumor DNA in patients with advanced gastric cancer receiving systemic chemotherapy |
title_full_unstemmed | Circulating free plasma tumor DNA in patients with advanced gastric cancer receiving systemic chemotherapy |
title_short | Circulating free plasma tumor DNA in patients with advanced gastric cancer receiving systemic chemotherapy |
title_sort | circulating free plasma tumor dna in patients with advanced gastric cancer receiving systemic chemotherapy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258437/ https://www.ncbi.nlm.nih.gov/pubmed/30498396 http://dx.doi.org/10.1186/s12907-018-0079-y |
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