Dana-Farber Cancer Institute, Boston, Massachusetts, USA
Massachusetts General Hospital, Boston, Massachusetts, USA.
Oncologist. 2019 Feb;24(2):202-210. doi: 10.1634/theoncologist.2018-0299. Epub 2018 Sep 6.
TRC105 is an IgG1 endoglin monoclonal antibody that potentiates VEGF inhibitors in preclinical models. We assessed safety, pharmacokinetics, and antitumor activity of TRC105 in combination with axitinib in patients with metastatic renal cell carcinoma (mRCC).
SUBJECTS, MATERIALS, AND METHODS: Heavily pretreated mRCC patients were treated with TRC105 weekly (8 mg/kg and then 10 mg/kg) in combination with axitinib (initially at 5 mg b.i.d. and then escalated per patient tolerance to a maximum of 10 mg b.i.d.) until disease progression or unacceptable toxicity using a standard 3 + 3 phase I design.
Eighteen patients (median number of prior therapies = 3) were treated. TRC105 dose escalation proceeded to 10 mg/kg weekly without dose-limiting toxicity. Adverse event characteristics of each drug were not increased in frequency or severity when the two drugs were administered concurrently. TRC105 and axitinib demonstrated preliminary evidence of activity, including partial responses (PR) by RECIST in 29% of patients, and median progression-free survival (11.3 months). None of the patients with PR had PR to prior first-line treatment. Lower baseline levels of osteopontin and higher baseline levels of TGF-β receptor 3 correlated with overall response rate.
TRC105 at 8 and 10 mg/kg weekly was well tolerated in combination with axitinib, with encouraging evidence of activity in patients with mRCC. A multicenter, randomized phase II trial of TRC105 and axitinib has recently completed enrollment (NCT01806064).
TRC105 is a monoclonal antibody to endoglin (CD105), a receptor densely expressed on proliferating endothelial cells and also on renal cancer stem cells that is implicated as a mediator of resistance to inhibitors of the VEGF pathway. In this Phase I trial, TRC105 combined safely with axitinib at the recommended single agent doses of each drug in patients with renal cell carcinoma. The combination demonstrated durable activity in a VEGF inhibitor-refractory population and modulated several angiogenic biomarkers. A randomized Phase II trial testing TRC105 in combination with axitinib in clear cell renal cell carcinoma has completed accrual.
TRC105 是一种 IgG1 内皮糖蛋白单克隆抗体,可增强临床前模型中 VEGF 抑制剂的作用。我们评估了 TRC105 联合阿昔替尼治疗转移性肾细胞癌(mRCC)患者的安全性、药代动力学和抗肿瘤活性。
受试者、材料和方法:既往接受过大量治疗的 mRCC 患者接受每周一次的 TRC105 治疗(起始剂量为 8mg/kg,然后为 10mg/kg),联合阿昔替尼(初始剂量为 5mg bid,然后根据患者的耐受程度递增至最大剂量 10mg bid),直至疾病进展或出现不可接受的毒性,采用标准的 3+3 期 I 设计。
18 名患者(中位既往治疗数=3)接受了治疗。TRC105 剂量递增至每周 10mg/kg 而无剂量限制毒性。当两种药物同时给药时,每种药物的不良反应特征在频率或严重程度上均未增加。TRC105 和阿昔替尼显示出初步的活性证据,包括 29%的患者按 RECIST 标准出现部分缓解(PR),中位无进展生存期(11.3 个月)。没有 PR 的患者之前对一线治疗有反应。较低的基线骨桥蛋白水平和较高的基线转化生长因子-β受体 3 水平与总缓解率相关。
每周 8mg/kg 和 10mg/kg 的 TRC105 联合阿昔替尼耐受性良好,在 mRCC 患者中具有令人鼓舞的活性证据。一项关于 TRC105 和阿昔替尼的多中心、随机 II 期试验最近已完成入组(NCT01806064)。
TRC105 是一种内皮糖蛋白(CD105)的单克隆抗体,内皮糖蛋白是一种在增殖的内皮细胞上高度表达的受体,也在肾癌细胞干细胞上表达,被认为是对 VEGF 通路抑制剂耐药的介质。在这项 I 期试验中,TRC105 与阿昔替尼联合应用于肾癌患者,剂量分别为各药物的推荐单药剂量,安全性良好。该联合方案在 VEGF 抑制剂耐药人群中显示出持久的活性,并调节了几种血管生成生物标志物。一项测试 TRC105 联合阿昔替尼在透明细胞肾细胞癌中的随机 II 期试验已完成入组。