252 The Novel Trk Receptor Tyrosine Kinase Inhibitor CEP-701 (KT-5555) Exhibits Antitumor Efficacy against Human Pancreatic Carcinoma (Panc1) Xenograft Growth and In Vivo Invasiveness SHEILA J. MIKNYOCZKI, a CRAIG A. DIONNE, b ANDRES J.P. KLEIN-SZANTO, c AND BRUCE A. RUGGERI b,d a Department of Pathology and Laboratory Medicine, Allegheny University of the Health Sciences, Philadelphia, Pennsylvania, USA b Division of Oncology, Cephalon, Inc., West Chester, Pennsylvania, USA c Fox Chase Cancer Center, Philadelphia, Pennsylvania, USA ABSTRACT: The survival rate for patients with pancreatic ductal adenocar- cinoma (PDAC) is among the poorest for all cancers. The factors that contrib- ute to this poor prognosis are lack of effective early detection, high rate of metastases and a generally refractory response to available treatment modalities. The most commonly used treatment methods—chemotherapy and radiation therapy—are mainly used for symptom palliation, with surgery being the only “curative” treatment option. The use of combinations of treatment modalities is the only therapy available to patients with locally advanced disease or that which is surgically unresectable. These options are still not sufficient to in- crease patient survival time significantly. The aggressive behavior and poor prognosis of this cancer is associated with an increased expression of many growth factors and their cognate receptors. We have demonstrated previously the aberrant expression of the Trk receptors (Trks A, B, and C) in PDAC specimens and human PDAC-derived cell lines and a biphasic, dose-dependent response of specific neurotrophic agents on the in vitro invasiveness of PDAC cells. Based on these data we have evaluated the therapeutic potential of inhibiting neurotrophin-Trk interactions using a selec- tive Trk tyrosine kinase inhibitor (CEP-701) on subcutaneous (s.c.) and trache- al xenografts derived from the poorly differentiated PDAC cell line, Panc1. We demonstrate that CEP-701 administration at 10 mg/kg s.c. BID for 21 days inhibited tumor growth of the Panc1 s.c. xenografts in a statistically-sig- nificant manner (p <0.01) compared to vehicle controls, in the absence of mor- bidity and mortality. A T/C value of 25% was observed for CEP-701-treated s.c. xenografts. In addition, CEP-701 administration inhibited tumor cell inva- sion in the s.c. tracheal xenograft model of in vivo invasiveness. Taken together, these data suggest that further studies are warranted to evaluate CEP-701 as a potential therapeutic agent in the treatment of PDAC. d To whom correspondence and reprint requests should be addressed: Cephalon, Inc. 145 Bran- dywine Parkway, West Chester, PA 19380. Phone, 610/738-6637; fax, 610/344-0065; e-mail, bruggeri@cephalon.com