An open-label, phase 2 study evaluating the efficacy and safety of the anti-IGF-1R antibody cixutumumab in patients with previously treated advanced or metastatic soft-tissue sarcoma or Ewing family of tumours

被引:67
作者
Schoffski, P. [1 ]
Adkins, D. [2 ]
Blay, J. -Y. [3 ]
Gil, T. [4 ]
Elias, A. D. [5 ]
Rutkowski, P. [6 ]
Pennock, G. K. [7 ]
Youssoufian, H. [8 ]
Gelderblom, H. [9 ]
Willey, R. [10 ]
Grebennik, D. O. [10 ]
机构
[1] Katholieke Univ Leuven, Univ Hosp Leuven, B-3000 Louvain, Belgium
[2] Washington Univ, Sch Med, St Louis, MO USA
[3] Univ Lyon 1, Ctr Leon Berard, F-69365 Lyon, France
[4] Univ Libre Bruxelles, Inst Jules Bordet, Brussels, Belgium
[5] Univ Colorado, Dept Med, Aurora, CO USA
[6] Ctr Onkol Inst Im Marii Sklodowskiej Curie, Warsaw, Poland
[7] MD Anderson Canc Ctr, Orlando, FL USA
[8] Ziopharm Oncol Inc, Boston, MA USA
[9] Leiden Univ, Med Ctr, Dept Clin Oncol, Leiden, Netherlands
[10] ImClone Syst LLC, Bridgewater, NJ USA
关键词
Cixutumumab; Soft-tissue sarcoma; Ewing family of tumours; Rhabdomyosarcoma; Leiomyosarcoma; Adipocytic sarcoma; Synovial sarcoma; Insulin-like growth factor receptor; GROWTH-FACTOR-I; EUROPEAN-ORGANIZATION; MONOCLONAL-ANTIBODY; FACTOR-RECEPTOR; INSULIN; CANCER; BONE; DOXORUBICIN; EXPRESSION; CHEMOTHERAPY;
D O I
10.1016/j.ejca.2013.06.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Cixutumumab (IMC-A12), a fully human immunoglobulin G1 (IgG1) monoclonal antibody, exerts preclinical activity in several sarcoma models and may be effective for the treatment of these tumours. Methods: In this open-label, multicentre, phase 2 study, patients with previously treated advanced or metastatic rhabdomyosarcoma, leiomyosarcoma, adipocytic sarcoma, synovial sarcoma or Ewing family of tumours received intravenous cixutumumab (10 mg/kg) for 1 h every other week until disease progression or discontinuation. The primary end-point was the progression-free survival rate (PFR), defined as stable disease or better at 12 weeks. In each tier of disease histology, Simon's optimum 2-stage design was applied (PFR at 12 weeks P0 = 20%, P1 = 40%, alpha = 0.10, beta = 0.10). Stage 1 enrolled 17 patients in each disease group/tier, with at least four patients with stable disease or better required at 12 weeks to proceed to stage 2. Results: A total of 113 patients were enrolled; all tiers except adipocytic sarcoma were closed after stage 1 due to futility. The 12-week PFR was 12% for rhabdomyosarcoma (n = 17), 14% for leiomyosarcoma (n = 22), 32% for adipocytic sarcoma (n = 37), 18% for synovial sarcoma (n = 17) and 11% for Ewing family of tumours (n = 18). Median progression-free survival (weeks) was 6.1 for rhabdomyosarcoma, 6.0 for leiomyosarcoma, 12.1 for adipocytic sarcoma, 6.4 for synovial sarcoma and 6.4 for Ewing family of tumours. Among all patients, the most frequent treatment-emergent adverse events (AEs) were nausea (26%), fatigue (23%), diarrhoea (23%) and hyperglycaemia (20%). Conclusions: Patients with adipocytic sarcoma may benefit from treatment with cixutumumab. Cixutumumab treatment was well tolerated, with limited gastrointestinal AEs, fatigue and hyperglycaemia. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3219 / 3228
页数:10
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