Page 370 - Read Online
P. 370

Salleh et al. J Cancer Metastasis Treat 2020;6:31  I  http://dx.doi.org/10.20517/2394-4722.2020.70                         Page 7 of 9

               combination of TFFs with CA19-9 appeared to be a potential diagnostic tool for distinguishing between
               early-stage pancreatic cancer, benign controls, and chronic pancreatitis. Notably, the sensitivity of CA
                                                          [52]
               19-9 was improved by its combination with TFFs . In addition, the combination of TFFs and CA 19-9
               was associated with an increased overall efficacy of CA 19-9 to discriminate early pancreatic cancer from
               chronic pancreatitis, which indicated the exceptional capabilities of TFFs to differentiate this highly
               aggressive disease at the early stages of progression.


               CONCLUSION
               Based on the findings of various studies, CA 19-9 has proven to be an essential tool in the diagnosis of
               pancreatic cancer, and most importantly in monitoring patient responses to various treatment modalities.
               The validation of CA 19-9 as exhibiting excellent parameters, such as higher sensitivity and specificity
               compared to other biomarkers, has confirmed its potential as a promising clinical tool in this field.
               However, despite its undeniable benefits in the predictive analysis of treatment efficacy and responses in
               PDAC patients, there are still a number of limitations that warrant further investigation in the future.


               DECLARATIONS
               Authors’ contributions
               Involved in the writing, editing, revising, and approving the final version of the manuscript: Salleh S,
               Thyagarajan A, Sahu RP


               Availability of data and materials
               Not applicable.

               Financial support and sponsorship
               None.


               Conflicts of interest
               All authors declared that there are no conflicts of interest.


               Ethical approval and consent to participate
               Not applicable.


               Consent for publication
               Not applicable.


               Copyright
               © The Author(s) 2020.


               REFERENCES
               1.   Luna J, Boni J, Cuatrecasas M, Bofill-De Ros X, Núñez-Manchón E, et al. DYRK1A modulates c-MET in pancreatic ductal
                   adenocarcinoma to drive tumour growth. Gut 2019;68:1465-76.
               2.   Siegel RL, Miller KD, Jemal A. Cancer statistics, 2016. CA Cancer J Clin 2016;66:7-30.
               3.   Sideras K, Braat H, Kwekkeboom J, Van Eijck CH, Peppelenbosch MP, et al. Role of the immune system in pancreatic cancer progression
                   and immune modulating treatment strategies. Cancer Treat Rev 2014;40:513-22.
               4.   Ischenko I, Petrenko O, Hayman MJ. A MEK/PI3K/HDAC inhibitor combination therapy for KRAS mutant pancreatic cancer cells.
                   Oncotarget 2015;6:15814.
               5.   Mielgo A, Schmid MC. Impact of tumour associated macrophages in pancreatic cancer. BMB Rep 2013;46:131.
               6.   Chen J, Chen L, Yu J, Xu Y, Wang X, et al. Meta-analysis of current chemotherapy regimens in advanced pancreatic cancer to prolong
                   survival and reduce treatment-associated toxicities. Mol Med Rep 2019;19:477-89.
               7.   Zhang Y, Hochster H, Stein S, Lacy J. Gemcitabine plus nab-paclitaxel for advanced pancreatic cancer after first-line FOLFIRINOX:
   365   366   367   368   369   370   371   372   373   374   375