Miller K, Albers P, Eichenauer R, Geiges G, Grimm M-O, König F, Mickisch G, Pfister D, Schwentner C, Suttmann H, Zastrow S
Klinik für Urologie, Urologische Klinik, Charité-Universitätsmedizin Berlin, Hindenburgdamm 30, 12200, Berlin, Deutschland.
Klinik für Urologie, Universitätsklinikum Düsseldorf, Düsseldorf, Deutschland.
Urologe A. 2016 Sep;55(9):1206-12. doi: 10.1007/s00120-016-0176-4.
Therapies currently available in Germany for metastatic castration-resistant prostate cancer (mCRPC) include docetaxel, cabazitaxel, abiraterone acetate, enzalutamide and radium-223, all of which offer a potential survival benefit that adds up in their sequential application to a significant overall survival benefit. However, the optimal sequencing of these agents is still unclear. In the absence of evidence, treatment selection is based on the particular situation and on comorbid conditions of each individual patient. Furthermore, predictive markers to facilitate the selection of patients for a specific therapy or sequence of therapies remain an unmet need. However, with the recently discovered androgen receptor splice variant V7, which mediates (cross)resistance to or between abiraterone and enzalutamide, the first such marker has been identified. It is critical to monitor the response to treatments at prespecified intervals in order to optimize treatment sequencing so that the patient does not miss a valuable therapeutic window to receive alternative treatment that may prolong his life along with good symptom control and preservation of quality of life.
德国目前用于转移性去势抵抗性前列腺癌(mCRPC)的治疗方法包括多西他赛、卡巴他赛、醋酸阿比特龙、恩杂鲁胺和镭-223,所有这些方法都具有潜在的生存获益,在序贯应用时可累积产生显著的总生存获益。然而,这些药物的最佳序贯方案仍不明确。在缺乏证据的情况下,治疗选择基于每个患者的具体情况和合并症。此外,有助于选择特定治疗或治疗序列的预测标志物仍是未满足的需求。然而,随着最近发现的雄激素受体剪接变体V7介导阿比特龙和恩杂鲁胺之间的(交叉)耐药性,首个此类标志物已被确定。为了优化治疗序贯,在预定间隔监测治疗反应至关重要,这样患者就不会错过接受可能延长其生命并伴有良好症状控制和生活质量保留的替代治疗的宝贵治疗窗口。