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前列腺癌的交叉耐药性和药物序贯治疗。

Cross-resistance and drug sequence in prostate cancer.

机构信息

Department of Medical Oncology, Erasmus Medical Center Cancer Institute, Rotterdam, the Netherlands.

Department of Medical Oncology, Erasmus Medical Center Cancer Institute, Rotterdam, the Netherlands; Department of Hospital Pharmacy, Erasmus Medical Center, Rotterdam, the Netherlands.

出版信息

Drug Resist Updat. 2021 May;56:100761. doi: 10.1016/j.drup.2021.100761. Epub 2021 Mar 18.

Abstract

The treatment landscape of advanced prostate cancer has widely expanded over the past years with androgen receptor signaling inhibitors (ARSIs) and taxane chemotherapy moving to earlier disease stages in the treatment of prostate cancer. With the increasing use of ARSIs in earlier disease stages, cross-resistance between treatments has emerged, which is a dominant impediment in current clinical practice. To overcome cross-resistance in the treatment of prostate cancer, it is of paramount importance to decipher the mechanisms of cross-resistance between ARSIs and between ARSIs and chemotherapy. Here, molecular mechanisms of resistance to the available therapies including androgen receptor (AR) splice variants, AR overexpression, AR mutations and glucocorticoid receptor upregulation are described. Based on these underlying mechanisms, clinical data of cross-resistance between ARSIs and chemotherapy have been reported. Only recently these data have been confirmed in prospective randomized trials. From these studies, it has become clear that sequential ARSI treatment has no place in the treatment of advanced prostate cancer due to emerging drug resistance. In addition, based on prospective evidence, we argue that it is worth considering an early switch to cabazitaxel treatment in case of lack of benefit on docetaxel regimen after an ARSI treatment. Based on these new insights from randomized trials, several recommendations for treatment sequence are proposed.

摘要

在过去的几年中,随着雄激素受体信号抑制剂 (ARSIs) 和紫杉烷化疗药物在前列腺癌治疗中向疾病早期阶段推进,晚期前列腺癌的治疗领域已经广泛扩展。随着 ARSIs 在早期疾病阶段的广泛应用,治疗之间出现了交叉耐药性,这是当前临床实践中的主要障碍。为了克服前列腺癌治疗中的交叉耐药性,解析 ARSIs 之间以及 ARSIs 与化疗之间的交叉耐药机制至关重要。在这里,描述了对现有治疗方法的耐药性的分子机制,包括雄激素受体 (AR) 剪接变体、AR 过表达、AR 突变和糖皮质激素受体上调。基于这些潜在的机制,已经报道了 ARSIs 和化疗之间的交叉耐药性的临床数据。直到最近,这些数据才在前瞻性随机试验中得到证实。从这些研究中可以清楚地看出,由于出现药物耐药性,序贯 ARSI 治疗在晚期前列腺癌的治疗中没有地位。此外,基于前瞻性证据,我们认为,如果在 ARSI 治疗后,在多西他赛方案中没有获益,那么早期改用卡巴他赛治疗是值得考虑的。基于这些随机试验的新见解,提出了一些治疗顺序的建议。

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