Table 2.
Ref.
|
Journal
|
year
|
No. of patients
|
Biomarker
|
Method
|
Main findings
|
Singh et al[91], 2015 | Cancer Invest | 2015 | cfDNA | Higher level of plasma DNA (> 62 ng/mL) was found to associate significantly with lower overall survival time (P = 0.002), presence of vascular encasement (P = 0.030) and metastasis (P = 0.001) | ||
Lapin et al[92], 2018 | J Transl Med | 2018 | 61 | cfDNA | 2100 Bioanalyzer | Pre-treatment cfDNA levels could independently predict prognosis for both PFS (HR = 3.049, P = 0.005) and OS (HR = 2.236, P = 0.028) |
Wang et al[93], 2021 | Pancreas | 2021 | 97 | cfDNA | PCR | The 1- and 5-year survivals for those with high cfDNA were poorer; 70.2% and 21.2%, respectively, as compared with 93.4% and 23.7% for those with low cfDNA level |
Castells et al[94], 1999 | J Clin Oncol | 1999 | 47 | ctDNA | PCR-RFLP and SSCP | Plasma KRAS mutations were identified as the only independent prognostic factor (odds ratio, 1.51; 95%CI: 1.02 to 2.23) |
Ako et al[95], 2017 | Pancreatology | 2017 | 40 | ctDNA | ddPCR | KRAS mutation at G12V in the plasma or serum conferred a significantly poorer prognosis than without the mutation (P < 0.01) |
Hadano et al[96], 2016 | Br J Cancer | 2016 | 105 | ctDNA | ddPCR | Patients who were preoperative ctDNA+ had a significantly poorer prognosis with respect to OS (P < 0.0001) |
Nakano et al[97], 2018 | Br J Cancer | 2018 | 45 | ctDNA | PNA directed, PCR clamping | There were no significant differences in DFS and OS between patients with and without KRAS mutations from preoperative serum |
Watanabe et al[98], 2019 | PLoS One | 2019 | 78 | ctDNA | ddPCR | No effect of the presence of KRAS-mutated ctDNA before surgery on RFS (median: 16.9 mo vs 32.4 mo) was observed |
Bernard et al[99], 2019 | Gastroenterology | 2019 | 34 | ctDNA and exosome DNA | ddPCR | Increased exosome DNA levels after neoadjuvant therapy were significantly associated with disease progression (P = 0.003) |
Kinugasa et al[100], 2015 | Cancer | 2015 | 75 | ctDNA | ddPCR | KRAS mutations in plasma correlated with poor OS (P = 0.002) |
Tjensvoll et al[101], 2016 | Mol Oncol | 2016 | 14 | ctDNA | PNA clamp PCR | Kaplan-Meier survival analyses indicated that patients with a positive ctDNA before or after initiation of chemotherapy had shorter PFS and OS |
Chen et al[102], 2010 | Eur J Surg Oncol | 2010 | 91 | ctDNA | Direct sequencing | KRAS codon 12 mutation from plasma DNA was an independent negative prognostic factor (HR, 7.39; 95%CI: 3.69-14.89) |
Sausen et al[103], 2015 | Nat Commun | 2015 | 101 | ctDNA | Next-generation sequencing and digital PCR | ctDNA was an independent prognostic marker of OS in advanced disease, with OS of 6.5 mo vs 19.0 mo for ctDNA-positive and negative patients, respectively |
Khoja et al[105], 2012 | Br J Cancer | 2012 | 54 | CTC | Cellsearch and ISET | The PFS and OS for patients without vs those with CTCswas 140 d vs 94 d (P = 0.13) and 164 d vs 127 d (P = 0.26), respectively |
Earl et al[106], 2015 | BMC Cancer | 2015 | 45 | CTC | Cellsearch | A Cox regression analysis showed a significant difference in OS for CTC positive vs negative patients with a HR of 3.0 (P = 0.023) |
Zhang et al[107], 2015 | Int J Cancer | 2015 | 61 | CTC | The EpCAM-independent method | CTCs positive pancreatic cancer patients exhibit a worse (P = 0.0458) survival rate |
Okubo et al[108], 2017 | Eur J Surg Oncol | 2017 | 65 | CTC | Cellsearch | A multivariate analysis identified the presence or absence of CTCs as an independent prognostic factor (P = 0.049) |
Ankeny et al[76], 2016 | Br J Cancer | 2016 | 100 | CTC | Microfluidic NanoVelcro CTC chip | A cut-off of 3 CTCs in 4 mL venous blood was able to discriminate between local/regional and metastatic disease (AUROC = 0.885; 95%CI: 0.800-0.969; and P < 0.001) |
Chang et al[109], 2016 | Clin Chem | 2016 | 63 | CTM | anti-EpCAM conjugated supported lipid bilayer-coated microfluidic chips | CTM was an independent prognostic factor of OS and PFS (P 0.0001 and P = 0.003, respectively) |
Bidard et al[110], 2013 | Ann Oncol | 2013 | 79 | CTC | Cellsearch | CTC positivity was associated with poor tumor differentiation (P = 0.04), and with shorter OS in multivariable analysis (P = 0.01) |
Kurihara et al[111], 2008 | J Hepatobiliary Pancreat Surg | 2008 | 47 | CTC | Cellsearch | MST of the CTC-positive and -negative patients were 110.5 and 375.8 d (P < 0.001) |
de Albuquerque et al[112], 2008 | Oncology | 2012 | 74 | CTC | Median PFS time was 66.0 d for patients with baseline CTC positivity and 138.0 days for CTC-negative patients (P = 0.01) | |
Kulemann et al[81], 2015 | Pancreas | 2015 | 21 | CTC | ScreenCell | The presence of CTC did not adversely affect MST: 16 mo in CTC-positive (n = 18) vs 10 mo in CTC-negative (n = 3) patients |
Li et al[116], 2018 | Cell Physiol Biochem | 2018 | 73 | miRNA | Arraystar Human miRCURYTM LNA Array | Multivariate analyses showed that exosomal miR-222 was independent risk factors for PDAC survival (P = 0.046) |
Wang et al[117], 2018 | Cancer Res | 2018 | 50 | miRNA | qRT-PCR | Exosomal miR-301a-3p overexpression predicted late TNM stage and poor survival in human PDAC (P = 0.0182) |
Frampton et al[118], 2018 | Oncotarget | 2018 | 43 | GPC1+ circulating exosomes | ELISA | Patients with high crExos GPC1 levels have significantly larger PDACs (> 4 cm; P = 0.012) |
Costa-Silva et al[119], 2015 | Nat Cell Biol | 2015 | 55 | Exosome | ELISA | Increased levels of MIF in exosomes isolated from patients with PDAC with progression of disease post-diagnosis compared with PDAC patients with no evidence of disease five years post-diagnosis (P < 0.01) and with healthy controls (P < 0.01), but not patients with liver metastasis |
AUROC: Area under the curve; cfDNA: Cell-free DNA; ctDNA: Circulating tumor DNA; CTC: Circulating tumor cell; CTM: Circulating tumor microemboli; DFS: Disease-free survival; ddPCR: Droplet digital polymerase chain reaction; ELISA: Enzyme-linked immuno-sorbent assay; EPCAM: Epithelial cell adhesion molecule; ISET: Isolation by size of epithelial tumor cells; HR: Hazard ratio; MST: Median survival time; MIF: Macrophage migration inhibitory factor; miRNA: microRNA; OS: Overall survival; PFS: Progression-free survival; PCR: Polymerase chain reaction; PCR-RFLP: Polymerase chain reaction-restriction fragment length polymorphism; PNA: Peptide nucleic acid; PDAC: Pancreatic ductal adenocarcinoma; qRT-PCR: Quantitative reverse transcription polymerase chain reaction; RFS: Recurrence-free survival; SSCP: Single-strand conformation polymorphism.