Randomized Phase II Study of Carboplatin and Paclitaxel With Either Linifanib or Placebo for Advanced Nonsquamous Non–Small-Cell Lung Cancer

• Type of Material: Article
• Authors: Suresh Ramalingam, Emory University; Mikhail Shtivelband, Ironwood Cancer and Research Centers, Chandler, AZ; Ross A. Soo, National University Cancer Institute, National University Health System, Singapore; Carlos H. Barrios, Pontifícia Universidade Católica do Rio Grande; Anatoly Makhson, Moscow City Oncology Hospital; Jose G. M. Segalla, Hospital Amaral Carvalho, Jau; Kenneth B. Pittman, he Queen Elizabeth Hospital, Woodville, South Australia; Petr Kolman, Hospital Kyjov, Kyjov, Czech Republic; Jose R. Pereira, Instituto Brasileiro de Cancerologia Toracica, Sao Paulo, Brazil; Gordan Srkalovic, Sparrow Regional Cancer Center, Lansing, MI; Chandra P. Belani, Penn State Hershey Cancer Institute; Rita Axelrod, Thomas Jefferson University Hospital, Philadelphia, PA; Taofeek Owonikoko, Emory University; Qin Qin, AbbVie, North Chicago, IL.; Jiang Qian, AbbVie, North Chicago, IL.; Evelyn M. McKeegan, AbbVie, North Chicago, IL.; Viswanath Devanarayan, AbbVie, North Chicago, IL.; Mark D. McKee, AbbVie, North Chicago, IL.; Justin L. Ricker, AbbVie, North Chicago, IL.; Dawn M. Carlson, AbbVie, North Chicago, IL.; VA Gorbunova, N.N. Blokhin Cancer Research Center, Russian Academy of Medical Sciences, Moscow, Russia
• Language: English
• Date: 2015-02-10
• Publisher: American Society of Clinical Oncology
• Publication Version: Final Published Version
• Copyright Statement: © 2015 by American Society of Clinical Oncology.
• Final Published Version (URL): http://dx.doi.org/10.1200/JCO.2014.55.7173
• Title of Journal or Parent Work: Journal of Clinical Oncology
• Volume: 33
• Issue: 5
• Start Page: 433
• End Page: 441
• Grant/Funding Information: None declared
• Keywords: PDGF; Linifanib; nonsquamous NSCLC; advanced stage cancer; chemotherapy; carboplatin; paclitaxel; vascular endothelial growth factor; platelet-derived growth factor; non-small-cell lung cancer; VEGF; toxicity; inhibitor; progression-free survival
• Research Categories: Biology, Cell; Health Sciences, Toxicology; Health Sciences, Rehabilitation and Therapy; Health Sciences, Oncology

Abstract

Purpose: Linifanib, a potent, selective inhibitor of vascular endothelial growth factor (VEGF) and platelet-derived growth factor (PDGF) receptors, has single-agent activity in non–small-cell lung cancer (NSCLC). We evaluated linifanib with carboplatin and paclitaxel as first-line therapy of advanced nonsquamous NSCLC. Patients and Methods: Patients with stage IIIB/IV nonsquamous NSCLC were randomly assigned to 3-week cycles of carboplatin (area under the curve 6) and paclitaxel (200 mg/m2) with daily placebo (arm A), linifanib 7.5 mg (arm B), or linifanib 12.5 mg (arm C). The primary end point was progression-free survival (PFS); secondary efficacy end points included overall survival (OS) and objective response rate. Results: One hundred thirty-eight patients were randomly assigned (median age, 61 years; 57% men; 84% smokers). Median PFS times were 5.4 months (95% CI, 4.2 to 5.7 months) in arm A (n = 47), 8.3 months (95% CI, 4.2 to 10.8 months) in arm B (n = 44), and 7.3 months (95% CI, 4.6 to 10.8 months) in arm C (n = 47). Hazard ratios (HRs) for PFS were 0.51 for arm B versus A (P = .022) and 0.64 for arm C versus A (P = .118). Median OS times were 11.3, 11.4, and 13.0 months in arms A, B, and C, respectively. HRs for OS were 1.08 for arm B versus A (P = .779) and 0.88 for arm C versus A (P = .650). Both linifanib doses were associated with increased toxicity, including a higher incidence of adverse events known to be associated with VEGF/PDGF inhibition. Baseline plasma carcinoembryonic antigen/cytokeratin 19 fragments biomarker signature was associated with PFS improvement and a trend toward OS improvement with linifanib 12.5 mg. Conclusion: Addition of linifanib to chemotherapy significantly improved PFS (arm B), with a modest trend for survival benefit (arm C) and increased toxicity reflective of known VEGF/PDGF inhibitory effects.