Abstract

Resistance to VEGF-targeted therapy is a major challenge in contemporary treatment of mRCC, and endoglin (CD105) activation may be an important mechanism leading to resistance. Endoglin is an essential angiogenic receptor expressed on proliferating tumor vessels and mRCC cancer stem cells, and is upregulated following VEGF inhibition. TRC105 is an endoglin monoclonal antibody that potentiates the anti-tumor activity of bevacizumab and VEGF receptor tyrosine kinase inhibitors in preclinical models. Heavily pretreated mRCC pts with ECOG PS 0-1 and acceptable organ function were treated with TRC105 weekly (8mg/kg and then 10mg/kg) in combination with axitinib (initially at 5 mg BID and then escalated per patient tolerance to a maximum of 10 mg BID). Eighteen mRCC pts (median age = 61.5; M:F 16:2; median number of prior therapies = 3, including > 1 VEGFR TKI, clear cell = 13, prior axitinib = 1) were treated. TRC105 dose escalation proceeded from 8 mg/kg (n = 3) to 10 mg/kg (n = 15) without dose limiting toxicity. Adverse events characteristic of each drug were not increased in frequency or severity when the two drugs were administered concurrently, and most commonly included epistaxis, headache, fatigue, diarrhea, and gingival bleeding. TRC105 and axitinib demonstrated preliminary evidence of activity, including partial responses in 29% of patients by RECIST 1.1, and longer PFS than expected with axitinib as a single agent. The overall disease control rate (CR/PR/SD > 2 months) was 88% (15 of 17). Median PFS overall was 8.4 months, and was 9.6 months among patients with clear cell RCC. Tumor response will be correlated with baseline protein biomarkers. TRC105 pharmacokinetic parameters will be reported. TRC105 at 8 and 10 mg/kg was well tolerated in combination with axitinib, with encouraging evidence of activity in patients with mRCC. A multicenter randomized Phase 2 trial of axitinib +/- TRC105 is actively enrolling at this time (NCT01806064).

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.