Hadaschik Boris A, Sowery Richard D, Gleave Martin E
The Prostate Centre at Vancouver General Hospital, Canada.
Curr Opin Urol. 2007 May;17(3):182-7. doi: 10.1097/MOU.0b013e3280dd8a4f.
The development of therapeutic resistance is the underlying cause for most cancer deaths. By understanding the molecular basis of resistance to androgen withdrawal and chemotherapy in prostate cancer, the rational design of targeted therapeutics is possible. We review new treatment options for men with advanced prostate cancer.
Although the taxanes currently represent the most active chemotherapeutic agents and standard of care for first-line treatment of metastatic hormone-refractory prostate cancer, most patients eventually progress because of intrinsic or acquired drug resistance. In recent years, increased knowledge of cancer progression and therapeutic resistance has identified many gene targets that regulate apoptosis, proliferation, and cell signalling. To date, numerous novel compounds have entered clinical trials as either single agents or in combination with cytotoxic chemotherapy.
Even though hormone-refractory prostate cancer is still incurable, it is not untreatable. As cancer cells are proficient at adapting to therapeutic stressors, a combination regimen with drugs that target crucial cellular networks like the apoptotic rheostat may be more promising than treatment with highly selective single-target agents. Recent findings are very hopeful, but challenges remain to demonstrate effective antitumour activity in phase III trials with survival as the principal endpoint.
治疗耐药性的发展是大多数癌症死亡的根本原因。通过了解前列腺癌中雄激素剥夺和化疗耐药的分子基础,有可能合理设计靶向治疗药物。我们综述了晚期前列腺癌男性患者的新治疗选择。
尽管紫杉烷目前是转移性激素难治性前列腺癌一线治疗中最有效的化疗药物和标准治疗方法,但大多数患者最终会因内在或获得性耐药而病情进展。近年来,对癌症进展和治疗耐药性的了解不断增加,已确定了许多调节细胞凋亡、增殖和细胞信号传导的基因靶点。迄今为止,众多新型化合物已作为单一药物或与细胞毒性化疗联合进入临床试验。
尽管激素难治性前列腺癌仍然无法治愈,但并非不可治疗。由于癌细胞善于适应治疗应激源,与靶向关键细胞网络(如凋亡调节器)的药物联合使用的方案可能比使用高度选择性单靶点药物治疗更有前景。最近的研究结果很有希望,但在以生存为主要终点的III期试验中证明有效的抗肿瘤活性仍面临挑战。