Pancreatic ductal adenocarcinoma (PDAC) is a type of cancer with one of the highest mortality rates, a statistic that has remained virtually unchanged for the past forty years.
Pancreatic ductal adenocarcinoma (PDAC) remains one of the most difficult-to-treat cancers, with a 5-year survival rate of only 8%, one of the lowest of all cancers.
Pancreatic ductal adenocarcinoma (PDAC), is an aggressive cancer surrounded by a highly immuno-suppressive tumor microenvironment (TME) which limits efficacy of most available therapies
One of the reasons for the dismal prognosis resides in its impressive ability to alter the nutritional status of patients who develop malnutrition, cachexia, anorexia, and sarcopenia in most cases.
In addition, most PDAC patients experience Pancreatic exocrine insufficiency (PEI) that contributes to the complex puzzle of malnutrition and that can be treated with Pancreatic Enzyme Replacement Therapy (PERT).
Prevalent intratumoral and intertumoral heterogeneity in pancreatic cancer has been revealed as an essential cause of its poor prognosis.
There is growing evidence supporting the significance of subtyping pancreatic tumors based on their molecular characteristics for improving the accuracy of clinical decision-making on treatment.
Pancreatic Ductal Adenocarcinoma (PDAC) / Pancreatic Cancer is expected to be the second most deadly cancer by 2040, owing to the high incidence of metastatic disease and limited responses to treatment
The two main types of pancreatic cancer are pancreatic ductal adenocarcinoma (PDAC) and pancreatic neuroendocrine tumor affecting less than 5% of patients.
The development of pancreatic cancer is triggered through many factors, including genetic background (mutations of genes), lifestyle (high-fat diet, smoking), gut microbiota dysbiosis, the occurrence of other diseases/conditions (obesity, type 2 diabetes, pancreatitis), and many others
Pancreatic Ductal Adenocarcinoma (PDAC) / Pancreatic Cancer is a high mortality malignancy with a 5-year survival rate of 9% for all stages, and ~90% of patients are at advanced settings exhibiting a 5-year survival rate of 3% when diagnosed
Activating mutations of the KRAS oncogene are the earliest genetic changes in transformation to pancreatic cancer (over 90% of diagnosed pancreatic cancers)
Mutations in brca gene account for approximately 5% of all Pancreatic Ductal Adenocarcinoma (PDAC) / Pancreatic Cancer
BRCA2 gene mutation account for up to 20% of all cases of familial PDAC
PDAC is expected to become the second leading cause of cancer-related mortality worldwide within the next decade due to its gradually increasing mortality rates
see also:
Cancer microbiome / Tumor microbiota
Pancreatic Ductal Adenocarcinoma (PDAC) (Mismatch Repair Deficiency (MMR-d) / DNA Mismatch Repair / Microsatellite Instability (MSI))
Pancreatic Ductal Adenocarcinoma (PDAC) / Pancreatic Cancer (BRCA m)
Pancreatic Ductal Adenocarcinoma (PDAC) / Pancreatic Cancer (HER1 m)
Pancreatic Ductal Adenocarcinoma (PDAC) / Pancreatic Cancer (KRAS m)
Pancreatic Ductal Adenocarcinoma (PDAC) / Pancreatic Cancer (NRG1 +)