Phase III, randomized, double-blind, placebo-controlled trial of gemcitabine/cisplatin alone or with sorafenib for the first-line treatment of advanced, nonsquamous non-small-cell lung cancer

Luis G. Paz-Ares, Bonne Biesma, David Heigener, Joachim Von Pawel, Timothy Eisen, Jaafar Bennouna, Li Zhang, Meilin Liao, Yan Sun, Steven Gans, Kostas Syrigos, Etienne Le Marie, Maya Gottfried, Johan Vansteenkiste, Vincente Alberola, Uwe Phillip Strauss, Elaine Montegriffo, Teng Jin Ong, Armando Santoro

Research output: Contribution to journalArticle

Abstract

Purpose: This trial evaluated the efficacy and safety of sorafenib plus gemcitabine/cisplatin in chemotherapynaive patients with unresectable stage IIIB to IV nonsquamous non-small-cell lung cancer (NSCLC). Patients and Methods: Between February 2007 and March 2009, 904 patients were randomly assigned to daily sorafenib (400 mg twice a day) or matching placebo plus gemcitabine (1,250 mg/m 2 per day on days 1 and 8) and cisplatin (75 mg/m 2 on day 1) for up to six 21-day cycles. Because of safety findings from the Evaluation of Sorafenib, Carboplatin and Paclitaxel Efficacy in NSCLC (ESCAPE) trial, patients with squamous cell histology were withdrawn from the trial in February 2008 and excluded from analysis. The primary end point was overall survival (OS), and secondary end points included progression-free survival (PFS) and time-to-progression (TTP). Results: The primary analysis population consisted of 772 patients (sorafenib, 385; placebo, 387); the two groups had similar demographic and baseline characteristics. Median OS was similar in the sorafenib and placebo groups (12.4 v 12.5 months; hazard ratio [HR], 0.98; P = .401). By investigator assessment, sorafenib improved median PFS (6.0 v 5.5 months; HR, 0.83; P = .008) and TTP (6.1 v 5.5 months; HR, 0.73; P <.001). Grade 3 to 4 drug-related adverse events more than two-fold higher in the sorafenib group included hand-foot skin reaction (8.6% v 0.3%), fatigue (7.3% v 3.6%), rash (5.7% v 0.5%), and hypertension (4.2% v 1.8%). No unexpected toxicities were observed. Conclusion: This study did not meet its primary end point of improved OS when sorafenib was added to first-line gemcitabine/ cisplatin in patients with advanced nonsquamous NSCLC. Identification of predictive biomarkers is warranted in future trials of sorafenib.

Original languageEnglish
Pages (from-to)3084-3092
Number of pages9
JournalJournal of Clinical Oncology
Volume30
Issue number25
DOIs
Publication statusPublished - Sep 1 2012

ASJC Scopus subject areas

  • Cancer Research
  • Oncology

Fingerprint Dive into the research topics of 'Phase III, randomized, double-blind, placebo-controlled trial of gemcitabine/cisplatin alone or with sorafenib for the first-line treatment of advanced, nonsquamous non-small-cell lung cancer'. Together they form a unique fingerprint.

  • Cite this

    Paz-Ares, L. G., Biesma, B., Heigener, D., Von Pawel, J., Eisen, T., Bennouna, J., Zhang, L., Liao, M., Sun, Y., Gans, S., Syrigos, K., Le Marie, E., Gottfried, M., Vansteenkiste, J., Alberola, V., Strauss, U. P., Montegriffo, E., Ong, T. J., & Santoro, A. (2012). Phase III, randomized, double-blind, placebo-controlled trial of gemcitabine/cisplatin alone or with sorafenib for the first-line treatment of advanced, nonsquamous non-small-cell lung cancer. Journal of Clinical Oncology, 30(25), 3084-3092. https://doi.org/10.1200/JCO.2011.39.7646