Immunotherapy and Pancreatic Cancer: Hope for the Future?
The MUC1 immunotherapeutic target may help to enhance the body’s natural response to cancer cells, thereby extending pancreatic cancer survival.
The MUC1 immunotherapeutic target may help to enhance the body’s natural response to cancer cells, thereby extending pancreatic cancer survival.
Abraxane (paclitaxel injection) plus gemcitabine is associated with prolonged survival among patients with metastatic pancreatic cancer.
Important research from the International Cancer Genome Consortium has identified thousands of genetic mutations associated with pancreatic cancer.
Pancreatic adenocarcinoma found in the absence of pancreated intraepithelial neoplasia is more aggressive and associated with poorer prognosis than tumors found in the presence of PanIN.
Specific KRAS mutation subtypes are associated with poorer overall survival times among patients with unresectable pancreatic cancer.
Gemcitabine-based combination therapies for patients with advanced pancreatic cancer offer modestly but statistically-significantly improved overall survival but increased toxicities.
EGFR signaling plays a key role in pancreatic intraepithelial neoplasia and pancreatic ductal adenocarcinoma tumorigenesis and progression, suggesting a new potential therapeutic target.
Hospitalization data will help patients with pancreatic cancer to make more informed choices regarding their care following diagnosis.
Pre-existing T2DM of more than 5 years increases mortality risk in pancreatic adenocarcinoma.
Consuming vitamins C and E decreases risk of developing pancreatic cancer, according to UK-based researchers.