Randomised Phase 2 study of maintenance linsitinib (OSI-906) in combination with erlotinib compared with placebo plus erlotinib after platinum-based chemotherapy in patients with advanced non-small cell lung cancer

被引:27
作者
Ciuleanu, Tudor-Eliade [1 ,2 ]
Ahmed, Samreen [3 ]
Kim, Joo-Hang [4 ]
Mezger, Joerg [5 ]
Park, Keunchil [6 ]
Thomas, Michael [7 ]
Chen, Jihong [8 ]
Poondru, Srinivasu [8 ]
VanTornout, Jan M. [8 ]
Whitcomb, Debbie [8 ]
Blackhall, Fiona [9 ]
机构
[1] Oncol Inst I Chiricuta, Cluj Napoca, Romania
[2] UMF Iuliu Hatieganu, Cluj Napoca, Romania
[3] Leicester Royal Infirm, Leicester, Leics, England
[4] CHA Univ, CHA Bundang Med Ctr, Gyeonggi Do, South Korea
[5] St Vincentius Kliniken Karlsruhe, Karlsruhe, Germany
[6] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Seoul, South Korea
[7] German Ctr Lung Res DZL, Translat Lung Res Ctr Heidelberg, Heidelberg, Germany
[8] Astellas Pharma Global Dev, Northbrook, IL USA
[9] Manchester Univ & Christie Hosp NHS Fdn Trust, Manchester, Lancs, England
关键词
linsitinib; erlotinib; NSCLC; maintenance therapy; insulin-like growth factor receptor; GROWTH-FACTOR-I; DOUBLE-BLIND; MONOCLONAL-ANTIBODY; TARGETED THERAPIES; INSULIN-RECEPTORS; IGF-1R INHIBITION; DUAL INHIBITOR; EGFR MUTATIONS; RESISTANCE; METAANALYSIS;
D O I
10.1038/bjc.2017.226
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Maintenance therapy is important in advanced/metastatic non-small cell lung cancer (NSCLC). Erlotinib as switch maintenance following platinum-based chemotherapy increases survival. Cross-talk between the epidermal growth factor receptor and insulin-like growth factor receptor (IGFR) pathways mediate resistance to individual receptor blockade. This study compared maintenance linsitinib plus erlotinib vs erlotinib plus placebo in patients with NSCLC. Methods: In this Phase II randomised trial, patients without progression following four cycles of first-line platinum-based chemotherapy (N = 205) received continuous schedule maintenance oral linsitinib 150mg or placebo BID combined with erlotinib 150mg QD for 21-day cycles. The primary endpoint was progression-free survival (PFS). Results: The study was unblinded early due to linsitinib non-superiority. No difference was found between the two treatment groups in median PFS of 125 days linsitinib vs 129 days placebo (P = 0.601); no difference in overall survival (OS) was observed. Tolerability was similar, although in the linsitinib group, treatment-related adverse events and discontinuations were more frequent. No drug-drug interaction was implicated. Conclusions: Linsitinib maintenance therapy added to erlotinib did not improve PFS or OS in non-progressing NSCLC patients. This highlights the need for robust biomarkers of response for combinations that incorporate IGFR-targeted therapies in maintenance or other therapeutic settings.
引用
收藏
页码:757 / 766
页数:10
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