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Shifting paradigm of developing biologics for the treatment of pancreatic adenocarcinoma.
Zeng, Ying; Rucki, Agnieszka A; Che, Xu; Zheng, Lei.
Affiliation
  • Zeng Y; Department of Medical Oncology, Geisinger Medical Center, Danville, PA 17822, USA.
  • Rucki AA; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
  • Che X; The Sidney Kimmel Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
  • Zheng L; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
J Gastrointest Oncol ; 8(3): 441-448, 2017 Jun.
Article de En | MEDLINE | ID: mdl-28736631
ABSTRACT
Pancreatic adenocarcinoma is still widely considered as a deadly disease even though there are substantial therapeutic developments in the past decade. Using combinational chemotherapy regimens, represented by gemcitabine plus nab-paclitaxel and FOLFIRINOX, was able to improve overall survival in patients with advanced disease to a limited extent. It has been a challenge to develop targeted therapies that are focused on the neoplasm cells of pancreatic adenocarcinoma. Recently, targeting the stroma and immune compartments of pancreatic adenocarcinoma has shown promising results. The paradigm of biologics drug development therefore has been shifted by extending to these exciting areas. Although some of the preclinical and clinical researches in targeting the tumor microenvironment of pancreatic adenocarcinoma have shown promising results, others have resulted in controversial findings. Both comprehensive and in-depth researches on the basic science of the tumor microenvironment of pancreatic adenocarcinoma are thus warranted for the development of effective biologics that target the tumor microenvironment. Moreover, an ideal treatment for pancreatic adenocarcinoma shall be a combination of targeting both neoplastic cells and the tumor microenvironment.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: J Gastrointest Oncol Année: 2017 Type de document: Article Pays d'affiliation: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: J Gastrointest Oncol Année: 2017 Type de document: Article Pays d'affiliation: États-Unis d'Amérique
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