Schwartz Gary K, Dickson Mark A, LoRusso Patricia M, Sausville Edward A, Maekawa Yoshimi, Watanabe Yasuo, Kashima Naomi, Nakashima Daisuke, Akinaga Shiro
Herbert Irving Comprehensive Cancer Center, Columbia University, New York, NY, USA, USA.
Memorial Sloan-Kettering Cancer Center, New York, NY, USA, USA.
Cancer Sci. 2016 Apr;107(4):499-506. doi: 10.1111/cas.12906. Epub 2016 Mar 28.
Numerous solid tumors overexpress or have excessively activated insulin-like growth factor receptor-1 (IGF-1R). We summarize preclinical studies and the first-in-human study of KW-2450, an oral tyrosine kinase inhibitor with IGF-1R and insulin receptor (IR) inhibitory activity. Preclinical activity of KW-2450 was evaluated in various in vitro and in vivo models. It was then evaluated in a phase I clinical trial in 13 patients with advanced solid tumors (NCT00921336). In vitro, KW-2450 inhibited human IGF-1R and IR kinases (IC50 7.39 and 5.64 nmol/L, respectively) and the growth of various human malignant cell lines. KW-2450 40 mg/kg showed modest growth inhibitory activity and inhibited IGF-1-induced signal transduction in the murine HT-29/GFP colon carcinoma xenograft model. The maximum tolerated dose of KW-2450 was 37.5 mg once daily continuously; dose-limiting toxicity occurred in two of six patients at 50 mg/day (both grade 3 hyperglycemia) and in one of seven patients at 37.5 mg/day (grade 3 rash). Four of 10 evaluable patients showed stable disease. Single-agent KW-2450 was associated with modest antitumor activity in heavily pretreated patients with solid tumors and is being further investigated in combination therapy with lapatinib/letrozole in patients with human epidermal growth factor receptor 2-postive metastatic breast cancer.
许多实体瘤过度表达或过度激活胰岛素样生长因子受体-1(IGF-1R)。我们总结了KW-2450的临床前研究和首次人体研究,KW-2450是一种具有IGF-1R和胰岛素受体(IR)抑制活性的口服酪氨酸激酶抑制剂。在各种体外和体内模型中评估了KW-2450的临床前活性。然后在13例晚期实体瘤患者中进行了I期临床试验(NCT00921336)。在体外,KW-2450抑制人IGF-1R和IR激酶(IC50分别为7.39和5.64 nmol/L)以及各种人恶性细胞系的生长。在小鼠HT-29/GFP结肠癌异种移植模型中,40 mg/kg的KW-2450显示出适度的生长抑制活性并抑制IGF-1诱导的信号转导。KW-2450的最大耐受剂量为每日一次连续37.5 mg;6例患者中有2例在50 mg/天出现剂量限制性毒性(均为3级高血糖),7例患者中有1例在37.5 mg/天出现剂量限制性毒性(3级皮疹)。10例可评估患者中有4例病情稳定。单药KW-2450在经过大量预处理的实体瘤患者中具有适度的抗肿瘤活性,目前正在对人表皮生长因子受体2阳性转移性乳腺癌患者与拉帕替尼/来曲唑联合治疗进行进一步研究。