Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
University of Iowa, Holden Comprehensive Cancer Center, Iowa City, Iowa, USA.
Oncologist. 2021 Jul;26(7):560-e1103. doi: 10.1002/onco.13777. Epub 2021 Apr 29.
The combination of carotuximab with axitinib did not provide a benefit over axitinib monotherapy in patients with metastatic clear cell renal cell carcinoma who had previously progressed on one or more vascular endothelial growth factor (VEGF)-targeted therapies. Exploratory evaluation of pretreatment circulating biomarkers suggested the combination might benefit patients who have low baseline VEGF levels.
Endoglin is an angiogenic receptor expressed on proliferating tumor vessels and renal cell carcinoma (RCC) stem cells that is implicated as a mechanism of resistance to vascular endothelial growth factor receptor (VEGFR) inhibitors. This study evaluated an antiendoglin monoclonal antibody (carotuximab, TRC105) combined with axitinib in patients with advanced or metastatic clear cell renal cell carcinoma (mccRCC) who had progressed following one or more prior VEGF inhibitors.
TRAXAR was a multicenter, international randomized 1:1 (stratified by ECOG, 0 vs. 1), phase II study of carotuximab combined with axitinib versus axitinib alone in mccRCC patients who had progressed following one or more prior VEGF inhibitors. The primary endpoint was progression-free survival (PFS) assessed by independent central review (ICR) per RECIST 1.1 RESULTS: A total of 150 patients were randomized. The combination therapy resulted in shorter median PFS by RECIST 1.1 than axitinib monotherapy (6.7 vs. 11.4 months). The combination was tolerated similarly to axitinib monotherapy, and there were no treatment related deaths. Exploratory evaluation of pretreatment circulating biomarkers suggested the combination might benefit patients who have low baseline VEGF levels.
The combination of carotuximab with axitinib did not demonstrate additional efficacy over single agent axitinib in patients with mccRCC who progressed following one or more prior VEGF inhibitor treatment.
在先前接受过一种或多种血管内皮生长因子(VEGF)靶向治疗后进展的转移性透明细胞肾细胞癌(mccRCC)患者中,卡妥昔单抗联合阿昔替尼治疗并未优于阿昔替尼单药治疗。对预处理循环生物标志物的探索性评估表明,该联合治疗可能对基线 VEGF 水平较低的患者有益。
内皮糖蛋白是一种在增殖性肿瘤血管和肾细胞癌(RCC)干细胞上表达的血管生成受体,被认为是对血管内皮生长因子受体(VEGFR)抑制剂产生耐药的机制。这项研究评估了一种抗内皮糖蛋白单克隆抗体(卡妥昔单抗,TRC105)联合阿昔替尼在先前接受过一种或多种 VEGF 抑制剂治疗后进展的晚期或转移性透明细胞肾细胞癌(mccRCC)患者中的疗效。
TRAXAR 是一项多中心、国际随机 1:1(按 ECOG 分层,0 与 1)、二期研究,评估了卡妥昔单抗联合阿昔替尼与阿昔替尼单药治疗在先前接受过一种或多种 VEGF 抑制剂治疗后进展的 mccRCC 患者中的疗效。主要终点是根据 RECIST 1.1 由独立中心审查(ICR)评估的无进展生存期(PFS)。
共 150 例患者被随机分组。联合治疗组的中位 RECIST 1.1 PFS 短于阿昔替尼单药组(6.7 与 11.4 个月)。联合治疗与阿昔替尼单药治疗的耐受性相似,且无治疗相关死亡。对预处理循环生物标志物的探索性评估表明,该联合治疗可能对基线 VEGF 水平较低的患者有益。
在先前接受过一种或多种 VEGF 抑制剂治疗后进展的 mccRCC 患者中,卡妥昔单抗联合阿昔替尼治疗并未显示出优于阿昔替尼单药治疗的额外疗效。