Tobias Alexander, O'brien Michael P, Agulnik Mark
a Rosalind Franklin University of Medicine and Science , North Chicago , IL , USA.
b Loyola University , Chicago , IL , USA.
Expert Rev Clin Pharmacol. 2017 Jul;10(7):699-705. doi: 10.1080/17512433.2017.1324295. Epub 2017 May 5.
Olaratumab is a humanized IgG1 monoclonal antibody that blocks the platelet-derived growth factor receptor alpha (PDGFRα). Its antagonistic behavior inhibits the receptor's tyrosine kinase activity, thereby, turning off the downstream signaling cascades responsible for soft tissue sarcoma tumorigenesis. In October 2016, olaratumab received Food and Drug Administration (FDA) approval for its use in combination with doxorubicin for treatment of advanced soft tissue sarcoma. Areas covered: This drug profile takes a comprehensive look at the clinical studies leading to FDA approval of olaratumab as well as its safety and efficacy as a front-line treatment option for sarcoma patients. The literature search was primarily conducted using PubMed. Expert commentary: The combination of olaratumab plus doxorubicin has provided a new front-line therapeutic option for soft tissue sarcoma patients. An open-label phase Ib and randomized phase II trial in patients with advanced soft tissue sarcoma demonstrated that the addition of olaratumab to doxorubicin prolonged progression-free survival by 2.5 months and overall survival by 11.8 months when compared to doxorubicin alone. Of importance, this clinically meaningful increase in overall survival did not come at the expense of a significantly greater number of toxicities. A phase III confirmatory trial (ClinicalTrials.gov Identifier NCT02451943) will be completed in 2020.
奥拉单抗是一种人源化IgG1单克隆抗体,可阻断血小板衍生生长因子受体α(PDGFRα)。其拮抗作用可抑制该受体的酪氨酸激酶活性,从而关闭负责软组织肉瘤肿瘤发生的下游信号级联反应。2016年10月,奥拉单抗获得美国食品药品监督管理局(FDA)批准,可与多柔比星联合用于治疗晚期软组织肉瘤。涵盖领域:本药物简介全面审视了促使FDA批准奥拉单抗的临床研究,以及其作为肉瘤患者一线治疗选择的安全性和有效性。文献检索主要通过PubMed进行。专家评论:奥拉单抗加多柔比星的联合用药为软组织肉瘤患者提供了一种新的一线治疗选择。一项针对晚期软组织肉瘤患者的开放标签Ib期和随机II期试验表明,与单独使用多柔比星相比,在多柔比星中添加奥拉单抗可使无进展生存期延长2.5个月,总生存期延长11.8个月。重要的是,总生存期的这种具有临床意义的提高并未以出现明显更多的毒性为代价。一项III期确证性试验(ClinicalTrials.gov标识符NCT02451943)将于2020年完成。