Abstract A105: Phase 2 trials of linifanib (ABT‐869) in advanced hepatocellular, renal cell and non‐small cell lung cancer: Associations of response by CT or DCE‐MRI with patient outcome

Background: Linifanib is a novel orally active and selective inhibitor of VEGF and PDGF families of receptor tyrosine kinases. Linifanib has demonstrated antitumor activity in a variety of advanced solid tumors in phase 1 and 2 trials. The objective of this analysis was to assess associations between pt outcome (PFS or OS) and response by CT (per RECIST or tumor volume change), or DCE‐MRI (per Ktrans), in patients (pts) enrolled in ongoing phase 2 linifanib monotherapy trials. Methods: Three open‐label, phase 2 monotherapy studies were conducted internationally in advanced/metastatic solid tumor pts with hepatocellular carcinoma (HCC), non‐small cell lung cancer (NSCLC) and renal cell carcinoma (RCC). Interim efficacy and safety results have been previously reported. A retrospective exploratory analysis of associations between pt outcome and CT or DCE‐MRI response was conducted. An independent centralized review of tumor response assessment by CT (baseline, and Q8 wks) and DCE‐MRI (baseline, and 2 wks) was performed using a uniform charter. CT assessed tumor volume and best percent change from baseline and pts were classified as PR, SD, or PD by RECIST. Baseline Ktrans and percent change in Ktrans were derived from DCE‐MRI. Statistical analysis was performed using the Cox proportional hazard model and logrank test, and significance considered at the level of P≥0.05. Threshold estimates were determined by the Bootstrapping & Aggregating Thresholds from Trees (BATTing). Results: Across the 3 phase 2 trials, 236 pts were enrolled from 08/07 to 10/08 at 34 centers: 44 pts with HCC, 53 pts with RCC, and 139 pts with NSCLC. Based on the BATTing methodology, 79/191 evaluable pts had a maximum CT tumor volume decrease of >32%. This was associated with improved OS (log‐rank p Conclusions: CT tumor volume reduction and CT response were associated with improved OS and PFS. Greater baseline Ktrans was associated with improved OS but not PFS. Ktrans changes at 2 wks were not associated with improvement in pt outcome. Citation Information: Mol Cancer Ther 2009;8(12 Suppl):A105.