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Droplet-based digital PCR and next generation sequencing for monitoring circulating tumor DNA: a cancer diagnostic perspective

Authors :
Pierre Laurent-Puig
Mathilde Postel
Shu-Fang Wang-Renault
Valérie Taly
Alice Roosen
Médecine Personnalisée, Pharmacogénomique, Optimisation Thérapeutique (MEPPOT - U1147)
Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)
Equipe labellisée Ligue contre le Cancer
Service de Biologie [Hôpital Européen Georges Pompidou, APHP]
Hôpital Européen Georges Pompidou [APHP] (HEGP)
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpitaux Universitaires Paris Ouest - Hôpitaux Universitaires Île de France Ouest (HUPO)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpitaux Universitaires Paris Ouest - Hôpitaux Universitaires Île de France Ouest (HUPO)
TALY, Valerie
Source :
Expert Review of Molecular Diagnostics, Expert Review of Molecular Diagnostics, Expert Reviews (formerly Future Drugs), 2018, 18 (1), pp.7-17. ⟨10.1080/14737159.2018.1400384⟩
Publication Year :
2018
Publisher :
HAL CCSD, 2018.

Abstract

International audience; Early detection of cancers through the analysis of ctDNA could have a significant impact on morbidity and mortality of cancer patients. However, using ctDNA for early cancer diagnosis is challenging partly due to the low amount of tumor DNA released in the circulation and its dilution within DNA originating from non-tumor cells. Development of new technologies such as droplet-based digital PCR (ddPCR) or optimized next generation sequencing (NGS) has greatly improved the sensitivity, specificity and precision for the detection of rare sequences. Areas covered: This paper will focus on the potential application of ddPCR and optimized NGS to detect ctDNA for detection of cancer recurrence and minimal residual disease as well as early diagnosis of cancer patients. Expert commentary: Compared to tumor tissue biopsies, blood-based ctDNA analyses are minimally invasive and accessible for regular follow-up of cancer patients. They are also described as a better picture of patients' pathology allowing to highlight both tumor heterogeneity and multiple tumor sites. After a brief introduction on the application of the follow-up of ctDNA using genetic or epigenetic biomarkers for prognosis and surveillance of cancer patients, potential perspectives of using ctDNA for early diagnosis of cancers will be presented.

Details

Language :
English
ISSN :
14737159 and 17448352
Database :
OpenAIRE
Journal :
Expert Review of Molecular Diagnostics, Expert Review of Molecular Diagnostics, Expert Reviews (formerly Future Drugs), 2018, 18 (1), pp.7-17. ⟨10.1080/14737159.2018.1400384⟩
Accession number :
edsair.doi.dedup.....0ea4e4829e270ac7481d092ab4ed3bc7
Full Text :
https://doi.org/10.1080/14737159.2018.1400384⟩