Fizazi K, Blue Ian, Nowak Joel T
Institut Gustave Roussy, Villejuif, France.
Patient author.
Future Oncol. 2021 May;17(14):1699-1707. doi: 10.2217/fon-2020-1291. Epub 2021 Feb 8.
This is a summary of a publication about the ARAMIS (Androgen Receptor Antagonizing Agent for Metastasis-free Survival) trial, which was published in the New England Journal of Medicine in September 2020. The trial was in adult participants with nonmetastatic, castration-resistant prostate cancer (nmCRPC) who received a trial treatment called darolutamide (brand name Nubeqa®). Darolutamide is currently available as an oral treatment for adults with nmCRPC. The ARAMIS trial looked at darolutamide taken by mouth in 1509 participants from 36 countries with nmCRPC (prostate cancer that has not spread to other parts of the body and no longer responds adequately to initial hormone therapy). The trial showed that darolutamide in addition to hormone therapy increased the length of time that the trial participants were still alive for and lowered the risk of death by 31% compared with placebo (sugar pill) and hormone therapy. The participants who received darolutamide and hormone therapy also had longer time to worsening pain, needing chemotherapy, and having cancer-related bone fractures or symptoms related to cancer-related bone fractures compared with those who received placebo and hormone therapy during the trial. In general, the percentage of participants who experienced medical problems (referred to as adverse events) was similar between those who received darolutamide and those who received placebo, in addition to hormone therapy. This summary also includes insights and perspectives from a participant who was in the ARAMIS trial and from a prostate cancer patient advocate. Clinical Trial Registration: NCT02200614 (ClinicalTrials.gov).
这是一篇关于ARAMIS(无转移生存期雄激素受体拮抗剂)试验的出版物总结,该试验于2020年9月发表在《新英格兰医学杂志》上。该试验针对的是患有非转移性去势抵抗性前列腺癌(nmCRPC)的成年参与者,他们接受了一种名为达罗他胺(商品名Nubeqa®)的试验性治疗。达罗他胺目前作为nmCRPC成年患者的口服治疗药物。ARAMIS试验观察了来自36个国家的1509名患有nmCRPC(尚未扩散至身体其他部位且对初始激素治疗不再充分反应的前列腺癌)的参与者口服达罗他胺的情况。试验表明,与安慰剂(糖丸)和激素治疗相比,达罗他胺联合激素治疗可延长试验参与者的存活时间,并将死亡风险降低31%。在试验期间,接受达罗他胺和激素治疗的参与者与接受安慰剂和激素治疗的参与者相比,出现疼痛加重、需要化疗以及发生癌症相关骨折或与癌症相关骨折相关症状的时间也更长。总体而言,除激素治疗外,接受达罗他胺治疗的参与者和接受安慰剂治疗的参与者出现医疗问题(称为不良事件)的百分比相似。本总结还包括一位参与ARAMIS试验的参与者以及一位前列腺癌患者倡导者的见解和观点。临床试验注册号:NCT0****(ClinicalTrials.gov)。 (注:原文中NCT02200614的后几位数字缺失,翻译时保留原文格式)