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Circulating tumour DNA (ctDNA) as a biomarker in metachronous melanoma and colorectal cancer- a case report
BACKGROUND: Circulating tumour DNA (ctDNA) has emerged as a promising blood-based biomarker for monitoring disease status of patients with advanced cancers. The presence of ctDNA in the blood is a result of biological processes, namely tumour cell apoptosis and/or necrosis, and can be used to monito...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857141/ https://www.ncbi.nlm.nih.gov/pubmed/31727009 http://dx.doi.org/10.1186/s12885-019-6336-3 |
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author | Calapre, Leslie Warburton, Lydia Millward, Michael Gray, Elin S. |
author_facet | Calapre, Leslie Warburton, Lydia Millward, Michael Gray, Elin S. |
author_sort | Calapre, Leslie |
collection | PubMed |
description | BACKGROUND: Circulating tumour DNA (ctDNA) has emerged as a promising blood-based biomarker for monitoring disease status of patients with advanced cancers. The presence of ctDNA in the blood is a result of biological processes, namely tumour cell apoptosis and/or necrosis, and can be used to monitor different cancers by targeting cancer-specific mutation. CASE PRESENTATION: We present the case of a 67 year old Caucasian male that was initially treated with BRAF inhibitors followed by anti-CTLA4 and then anti-PD1 immunotherapy for metastatic melanoma but later developed colorectal cancer. The kinetics of ctDNA derived from each cancer type were monitored targeting BRAF V600R (melanoma) and KRAS G13D (colon cancer), specifically reflected the status of the patient’s tumours. In fact, the discordant pattern of BRAF and KRAS ctDNA was significantly correlated with the clinical response of melanoma to pembrolizumab treatment and progression of colorectal cancer noted by PET and/or CT scan. Based on these results, ctDNA can be used to specifically clarify disease status of patients with metachronous cancers. CONCLUSIONS: Using cancer-specific mutational targets, we report here for the first time the efficacy of ctDNA to accurately provide a comprehensive outlook of the tumour status of two different cancers within one patient. Thus, ctDNA analysis has a potential clinical utility to delineate clinical information in patients with multiple cancer types. |
format | Online Article Text |
id | pubmed-6857141 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68571412019-12-05 Circulating tumour DNA (ctDNA) as a biomarker in metachronous melanoma and colorectal cancer- a case report Calapre, Leslie Warburton, Lydia Millward, Michael Gray, Elin S. BMC Cancer Case Report BACKGROUND: Circulating tumour DNA (ctDNA) has emerged as a promising blood-based biomarker for monitoring disease status of patients with advanced cancers. The presence of ctDNA in the blood is a result of biological processes, namely tumour cell apoptosis and/or necrosis, and can be used to monitor different cancers by targeting cancer-specific mutation. CASE PRESENTATION: We present the case of a 67 year old Caucasian male that was initially treated with BRAF inhibitors followed by anti-CTLA4 and then anti-PD1 immunotherapy for metastatic melanoma but later developed colorectal cancer. The kinetics of ctDNA derived from each cancer type were monitored targeting BRAF V600R (melanoma) and KRAS G13D (colon cancer), specifically reflected the status of the patient’s tumours. In fact, the discordant pattern of BRAF and KRAS ctDNA was significantly correlated with the clinical response of melanoma to pembrolizumab treatment and progression of colorectal cancer noted by PET and/or CT scan. Based on these results, ctDNA can be used to specifically clarify disease status of patients with metachronous cancers. CONCLUSIONS: Using cancer-specific mutational targets, we report here for the first time the efficacy of ctDNA to accurately provide a comprehensive outlook of the tumour status of two different cancers within one patient. Thus, ctDNA analysis has a potential clinical utility to delineate clinical information in patients with multiple cancer types. BioMed Central 2019-11-14 /pmc/articles/PMC6857141/ /pubmed/31727009 http://dx.doi.org/10.1186/s12885-019-6336-3 Text en © The Author(s). 2019 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 | Case Report Calapre, Leslie Warburton, Lydia Millward, Michael Gray, Elin S. Circulating tumour DNA (ctDNA) as a biomarker in metachronous melanoma and colorectal cancer- a case report |
title | Circulating tumour DNA (ctDNA) as a biomarker in metachronous melanoma and colorectal cancer- a case report |
title_full | Circulating tumour DNA (ctDNA) as a biomarker in metachronous melanoma and colorectal cancer- a case report |
title_fullStr | Circulating tumour DNA (ctDNA) as a biomarker in metachronous melanoma and colorectal cancer- a case report |
title_full_unstemmed | Circulating tumour DNA (ctDNA) as a biomarker in metachronous melanoma and colorectal cancer- a case report |
title_short | Circulating tumour DNA (ctDNA) as a biomarker in metachronous melanoma and colorectal cancer- a case report |
title_sort | circulating tumour dna (ctdna) as a biomarker in metachronous melanoma and colorectal cancer- a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857141/ https://www.ncbi.nlm.nih.gov/pubmed/31727009 http://dx.doi.org/10.1186/s12885-019-6336-3 |
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