R1507, a Monoclonal Antibody to the Insulin-Like Growth Factor 1 Receptor, in Patients With Recurrent or Refractory Ewing Sarcoma Family of Tumors: Results of a Phase II Sarcoma Alliance for Research Through Collaboration Study

Author:

Pappo Alberto S.1,Patel Shreyaskumar R.1,Crowley John1,Reinke Denise K.1,Kuenkele Klaus-Peter1,Chawla Sant P.1,Toner Guy C.1,Maki Robert G.1,Meyers Paul A.1,Chugh Rashmi1,Ganjoo Kristen N.1,Schuetze Scott M.1,Juergens Heribert1,Leahy Michael G.1,Geoerger Birgit1,Benjamin Robert S.1,Helman Lee J.1,Baker Laurence H.1

Affiliation:

1. Alberto S. Pappo, St Jude Children's Research Hospital, Memphis, TN; Shreyaskumar R. Patel and Robert S. Benjamin, MD Anderson Cancer Center, Houston, TX; John Crowley, Cancer Research and Biostatistics, Seattle, WA; Denise K. Reinke, Sarcoma Alliance for Research through Collaboration; Rashmi Chugh, Scott M. Schuetze, and Laurence H. Baker, University of Michigan, Ann Arbor, MI; Klaus-Peter Kuenkele, Roche, Penzberg; Heribert Juergens, University Children's Hospital, Muenster, Germany; Sant P. Chawla,...

Abstract

Purpose The type 1 insulin-like growth factor 1 receptor (IGF-1R) has been implicated in the pathogenesis of the Ewing sarcoma family of tumors (ESFT). We conducted a multicenter phase II study of the fully human IGF-1R monoclonal antibody R1507 in patients with recurrent or refractory ESFT. Patients and Methods Patients ≥ 2 years of age with refractory or recurrent ESFT received R1507 at doses of 9 mg/kg intravenously one a week or 27 mg/kg intravenously every three weeks. Response was measured by using WHO criteria. Tumor imaging was performed every 6 weeks for 24 weeks and then every 12 weeks. Results From December 2007 through April 2010, 115 eligible patients from 31 different institutions were enrolled. The median age was 25 years (range, 8 to 78 years). The location of the primary tumor was bone in 57% of patients and extraskeletal in 43% of patients. A total of 109 patients were treated with R1507 9 mg/kg/wk, and six patients were treated with 27 mg/kg/3 wk. The overall complete response/partial response rate was 10% (95% CI, 4.9% to 16.5%). The median duration of response was 29 weeks (range, 12 to 94 weeks), and the median overall survival was 7.6 months (95% CI, 6 to 9.7 months). Ten of 11 responses were observed in patients who presented with primary bone tumors (P = .016). The most common adverse events of grades 3 to 4 were pain (15%), anemia (8%), thrombocytopenia (7%), and asthenia (5%). Conclusion R1507 was a well-tolerated agent that had meaningful and durable benefit in a subgroup of patients with ESFT. The identification of markers that are predictive of a benefit is necessary to fully capitalize on this approach.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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