Novel Agents in the Treatment of Pancreatic Adenocarcinoma

被引:0
|
作者
Dimou, Anastasios [1 ]
Syrigos, Konstantinos N. [2 ]
Saif, Muhammad Wasif [3 ,4 ,5 ,6 ]
机构
[1] Albert Einstein Med Ctr, Dept Internal Med, Philadelphia, PA 19141 USA
[2] Univ Athens, Sotiria Gen Hosp, Dept Med 3, Oncol Unit, Athens, Greece
[3] Tufts Med Ctr, Ctr Canc, Dept Med, Div Hematol Oncol, Boston, MA 02111 USA
[4] Tufts Med Ctr, Div Hematol Oncol, Boston, MA 02111 USA
[5] Tufts Med Ctr, Dept Med, 800 Washington St Box 245, Boston, MA 02111 USA
[6] Tufts Med Ctr, Ctr Canc, Boston, MA 02111 USA
来源
JOURNAL OF THE PANCREAS | 2013年 / 14卷 / 02期
关键词
Connective Tissue Growth Factor; HSP90 Heat-Shock Proteins; Pancreatic Neoplasms; tanespimycin; Tumor Micro-environment;
D O I
暂无
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The development of new agents and treatment strategies against pancreatic adenocarcinoma is vital, given the poor prognosis of the patients with this particular type of cancer. Three novel compounds were tested at different phases of clinical research and the results were presented in the recent ASCO Gastrointestinal Cancers Symposium. FG-3019 inhibits the connective tissue growth factor which is important in the biology of pancreatic cancer and was shown to be relatively safe in a phase I study (Abstract #213). In addition, ASG-5ME, an antibody specific for SLC44A4 that is universally expressed in pancreatic cancer and also carries a conjugate chemotherapy particle was safe at the appropriate dosing in a phase I trial (Abstract #176). Last but not least, tanespimycin, a molecule that inhibits heat shock protein 90 was not effective in the first line treatment of patients with pancreatic cancer in a phase II study (Abstract #245). Further studying of FG-3019 and ASG-5ME will show the potential activity if any of these compounds in patients with pancreatic cancer.
引用
收藏
页码:138 / 140
页数:3
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