Graff Julie N, Thomas George V, Higano Celestia S, Beer Tomasz M
Knight Cancer Institute, Oregon Health & Science University.
Seattle Cancer Care Alliance, University of Washington.
Cureus. 2015 Dec 22;7(12):e426. doi: 10.7759/cureus.426.
The androgen receptor is the main therapeutic target that has been successfully exploited through direct inhibition to extend survival of patients with metastatic castration-resistant prostate cancer (mCRPC). We present a patient who participated in a Phase II study of an antagonist antibody to insulin-like growth factor 1 receptor (IGF-1R) in men with mCRPC and experienced over five years of stable disease. His disease was rapidly progressing before exposure to the antibody and resumed its aggressive behavior following discontinuation of therapy, strongly supporting the attribution of his stable disease to IGF-1R inhibition. His pre-treatment biopsy exhibited increased protein expression of IGF-1R (and its downstream effector, phosphorylated-S6). Consequently, agents that target IGF-1R may provide profound and durable responses in a subset of patients and upfront molecular selection may enable us to identify those most likely to benefit.
雄激素受体是主要的治疗靶点,通过直接抑制该靶点已成功延长了转移性去势抵抗性前列腺癌(mCRPC)患者的生存期。我们报告了一名参与一项针对mCRPC男性患者的胰岛素样生长因子1受体(IGF-1R)拮抗剂抗体II期研究的患者,该患者经历了超过五年的疾病稳定期。在接触该抗体之前,他的疾病进展迅速,而在治疗中断后又恢复了侵袭性,这有力地支持了将其疾病稳定归因于IGF-1R抑制的观点。他治疗前的活检显示IGF-1R(及其下游效应物磷酸化-S6)的蛋白表达增加。因此,靶向IGF-1R的药物可能在一部分患者中产生深刻而持久的反应,而预先进行分子筛选可能使我们能够识别出最有可能受益的患者。