Abstract
2 min read14620 Background: Low-dose chemotherapy without scheduled breaks (metronomic chemotherapy) is thought to be anti-angiogenic. Inhibitors of the VEGF and the PDGF signaling pathways may augment this effect. We initiated a prospective, phase I pharmacokinetic (PK) and biomarker study to assess the safety of a rationally designed combination anti-angiogenesis strategy consisting of metronomic CTX, BV (anti-VEGF antibody), and IM (PDGF-receptor inhibitor). Methods: Cycle length was 28 days. Doses: BV 5 mg/kg IV q 14 d, CTX 25–50 mg PO QD, IM 400–800 mg PO QD. DLT was defined as any treatment (tx)-related grade 4 hematologic or grade 3/4 non-hematologic event during cycle 1. Quantification of circulating tumor cells (CTC), endothelial cells (CEC, aEC) and endothelial progenitor cells (EPC) was performed. Parameters measured by CT perfusion were assessed. Results: 13 pts with metastatic colorectal cancer have been enrolled: M/ F= 7/6; ECOG PS 0/1= 8/5; median age=56 (range 33–68). All pts had received prior BV and had disease refractory to standard chemotherapy. Pts have received tx for a median of 56 days (range 28–252 days); 1 cycle (3 pts), 2 cycles (7 pts) and 7+ cycles (2 pts). Dose level 0 (DL 0) was expanded to 6 pts after 1/3 initial pts was removed from the study for a Gr 2 gastrointestinal fistula (after cycle 1). DL+1 and DL+2 had no DLT’s. 1 pt has been enrolled on DL+3. The MTD has not been reached. Tx has been well tolerated; there have been no tx-related Gr 3/4 toxicites. The most common tx-related AE’s have been Gr 1/2 nausea, vomiting, and rash. Two pts (DL 0, DL+1) demonstrated SD lasting > 6 months; 1 pt had a 19% decrease in target lesions by RECIST. Conclusions: The combination of metronomic CTX, IM, and BV can be safely administered. Class related side effects have been seen. Preliminary clinical activity has been observed in a heavily-pretreated patient population. Enrollment to this study continues, with CTX and IM PK to be performed at the MTD. Updated clinical and biomarker data will be presented. Dose Levels DL CTX (D1- 28) IM (D1–28) BV (D1,15) 0 25 mg PO QD 400 mg PO QD 5 mg/kg IV +1 50 mg PO QD 400 mg PO QD 5 mg/kg IV +2 50 mg PO QD 300 mg PO BID 5 mg/kg IV +3 50 mg PO QD 400 mg PO BID 5 mg/kg IV Author Disclosure Employment or Leadership Consultant or Advisory Role Stock Ownership Honoraria Research Expert Testimony Other Remuneration Genentech, Genentech™ BioOncology, Johnson & Johnson, sanofi-aventis Genentech™ BioOncology, Johnson & Johnson Genentech™ BioOncology, Novartis
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