Liquid Biopsy as Surrogate for Tissue for Molecular Profiling in Pancreatic Cancer: A Meta-Analysis Towards Precision Medicine

dc.contributor.authorLuchini, Claudio
dc.contributor.authorVeronese, Nicola
dc.contributor.authorNottegar, Alessia
dc.contributor.authorCappelletti, Vera
dc.contributor.authorDaidone, Maria G.
dc.contributor.authorSmith, Lee
dc.contributor.authorParris, Christopher
dc.contributor.authorBrosens, Lodewijk A. A.
dc.contributor.authorCaruso, Maria G.
dc.contributor.authorCheng, Liang
dc.contributor.authorWolfgang, Christopher L.
dc.contributor.authorWood, Laura D.
dc.contributor.authorMilella, Michele
dc.contributor.authorSalvia, Roberto
dc.contributor.authorScarpa, Aldo
dc.contributor.departmentPathology and Laboratory Medicine, School of Medicineen_US
dc.date.accessioned2020-01-02T15:20:46Z
dc.date.available2020-01-02T15:20:46Z
dc.date.issued2019-08-10
dc.description.abstractLiquid biopsy (LB) is a non-invasive approach representing a promising tool for new precision medicine strategies for cancer treatment. However, a comprehensive analysis of its reliability for pancreatic cancer (PC) is lacking. To this aim, we performed the first meta-analysis on this topic. We calculated the pooled sensitivity, specificity, positive (LR+) and negative (LR-) likelihood ratio, and diagnostic odds ratio (DOR). A summary receiver operating characteristic curve (SROC) and area under curve (AUC) were used to evaluate the overall accuracy. We finally assessed the concordance rate of all mutations detected by multi-genes panels. Fourteen eligible studies involving 369 patients were included. The overall pooled sensitivity and specificity were 0.70 and 0.86, respectively. The LR+ was 3.85, the LR- was 0.34 and DOR was 15.84. The SROC curve with an AUC of 0.88 indicated a relatively high accuracy of LB for molecular characterization of PC. The concordance rate of all mutations detected by multi-genes panels was 31.9%. LB can serve as surrogate for tissue in the molecular profiling of PC, because of its relatively high sensitivity, specificity and accuracy. It represents a unique opportunity to be further explored towards its introduction in clinical practice and for developing new precision medicine approaches against PC.en_US
dc.identifier.citationLuchini, C., Veronese, N., Nottegar, A., Cappelletti, V., Daidone, M. G., Smith, L., … Scarpa, A. (2019). Liquid Biopsy as Surrogate for Tissue for Molecular Profiling in Pancreatic Cancer: A Meta-Analysis Towards Precision Medicine. Cancers, 11(8), 1152. doi:10.3390/cancers11081152en_US
dc.identifier.urihttps://hdl.handle.net/1805/21682
dc.language.isoen_USen_US
dc.publisherMDPIen_US
dc.relation.isversionof10.3390/cancers11081152en_US
dc.relation.journalCancersen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourcePMCen_US
dc.subjectLiquid biopsyen_US
dc.subjectcfDNAen_US
dc.subjectPancreatic canceren_US
dc.subjectPrecision medicineen_US
dc.subjectCirculating tumor cells (CTC)en_US
dc.titleLiquid Biopsy as Surrogate for Tissue for Molecular Profiling in Pancreatic Cancer: A Meta-Analysis Towards Precision Medicineen_US
dc.typeArticleen_US
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