In a series of preclinical studies, nanoliposomal CPT-11 demonstrated significantly superior efficacy when compared to free CPT-11 at the same or higher dose, including frequent cures in some models. The superiority of nanoliposomal CPT-11 over free CPT-11 has been observed in different tumor models including colorectal, gastric, breast, cervical, glioma, pancreatic and lung cancer models. In addition to superior efficacy, nanoliposomal

CPT-11 has shown a more favorable pharmacologic profile and MLN8237 supplier reduced toxicity in multiple Inhibitors,research,lifescience,medical preclinical models. In order to evaluate this novel agent as a potential therapy for pancreatic cancer, a bioluminescence-based orthotopic xenograft model of pancreas cancer was developed (28). COLO357, a human pancreatic cell line, was passaged multiple times in vivo to generate the subline L3.6pl. This cell line was then modified by lentiviral transduction (L3.6pl-T) to express Inhibitors,research,lifescience,medical firefly luciferase. L3.6pl-T cells were implanted during open surgery directly into the pancreas of a nude mouse to form an orthotopic tumor xenograft. Therapeutic studies in this model compared nanoliposomal CPT-11 versus free drug at the equivalent dose, along with Inhibitors,research,lifescience,medical vehicle control (Figure 1). All treatments were administered intravenously by tail vein beginning at 7 days post-tumor implantation and continued weekly for a total of

3 planned treatments. At 20 mg/kg, free CPT-11 showed some tumor growth inhibition, but all mice required euthanization after 2 doses due to massive tumor progression. In contrast, nanoliposomal CPT-11 at the equivalent 20 mg/kg dose showed potent antitumor Inhibitors,research,lifescience,medical activity, including complete tumor inhibition during the entire post-treatment period. Systemic toxicity was not observed with any treatment. These studies indicated that nanoparticle- mediated delivery via nanoliposomal CPT-11 greatly

enhances antitumor efficacy in the COLO357/L3.6pI-T orthotopic pancreatic xenograft model. Figure 1 Nude mice were orthotopically implanted with COLO357/L3.6pI-T Inhibitors,research,lifescience,medical xenografts into the pancreas. Following ip administration of luciferin, animals were immediately imaged using a Xenogen IVIS 100 bioluminescence Astemizole system, and subsequently imaged at weekly intervals. … In the first-in-human phase I trial, patients with standard therapy-failure solid tumor were enrolled to determine the maximum tolerated dose, safety profile and pharmacokinetics of nanoliposomal CPT-11 (formerly PEP02, PharmaEngine, Inc., Taiwan, and now under the designation of MM-398, Merrimack Pharmaceuticals, Inc, USA). The drug was delivered intravenously for 90 minutes, once every 3 weeks, with starting dose of 60 mg/m2. The maximum tolerated dose was 120 mg/m2. Two patients achieved partial response including cervical cancer in one and pancreatic cancer in one (29).