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一项转移性去势抵抗性前列腺癌寡转移患者中应用发射阿尔法粒子的镭-223进行转移灶定向治疗的 II 期随机试验(MEDAL)。

A phase II randomized trial of metastasis-directed therapy with alpha emitter radium-223 in men with oligometastatic castration-resistant prostate cancer (MEDAL).

机构信息

Department of Urology, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-Ku, Tokyo, 113-8510, Japan.

Department of Biomedical Engineering, Tokai University School of Engineering, Kanagawa, Japan.

出版信息

BMC Urol. 2023 Mar 6;23(1):33. doi: 10.1186/s12894-023-01202-z.

Abstract

BACKGROUND

The significance of metastasis-directed therapy for oligometastatic prostate cancer has been widely discussed, and targeted therapy for progressive sites is a feasible option as a multidisciplinary treatment for castration-resistant prostate cancer (CRPC). When oligometastatic CRPC with only bone metastases progresses after targeted therapy, it tends to progress as multiple bone metastases. The progression of oligometastatic CRPC after targeted therapy may be due in part to the presence of micrometastatic lesions that, though undetected on imaging, were present prior to targeted therapy. Thus the systemic treatment of micrometastases in combination with targeted therapy for progressive sites is expected to enhance the therapeutic effect. Radium-223 dichloride (radium-223) is a radiopharmaceutical that selectively binds to sites of increased bone turnover and inhibits the growth of adjacent tumor cells by emitting alpha rays. Therefore, for oligometastatic CRPC with only bone metastases, radium-223 may enhance the therapeutic effect of radiotherapy for active metastases.

METHODS

This phase II, randomized trial of Metastasis-Directed therapy with ALpha emitter radium-223 in men with oligometastatic CRPC (MEDAL) is designed to assess the utility of radium-223 in combination with metastasis-directed radiotherapy in patients with oligometastatic CRPC confined to bone. In this trial, patients with oligometastatic CRPC with three or fewer bone metastases on whole-body MRI with diffusion-weighted MRI (WB-DWI) will be randomized in a 1:1 ratio to receive radiotherapy for active metastases plus radium-223 or radiotherapy for active metastases alone. The prior use of androgen receptor axis-targeted therapy and prostate-specific antigen doubling time will be used as allocation factors. The primary endpoint will be radiological progression-free survival against progression of bone metastases on WB-DWI.

DISCUSSION

This will be the first randomized trial to evaluate the effect of radium-223 in combination with targeted therapy in oligometastatic CRPC patients. The combination of targeted therapy for macroscopic metastases with radiopharmaceuticals targeting micrometastasis is expected to be a promising new therapeutic strategy for patients with oligometastatic CRPC confined to bone. Trial registration Japan Registry of Clinical Trials (jRCT) (jRCTs031200358); Registered on March 1, 2021, https://jrct.niph.go.jp/latest-detail/jRCTs031200358.

摘要

背景

寡转移前列腺癌的转移导向治疗意义重大,针对进展部位的靶向治疗是去势抵抗性前列腺癌(CRPC)的一种可行的多学科治疗选择。当仅有骨转移的寡转移性 CRPC 在靶向治疗后进展时,往往会发展为多处骨转移。寡转移性 CRPC 在靶向治疗后进展的部分原因可能是存在微转移病灶,这些病灶在影像学上无法检测到,但在靶向治疗前就已经存在。因此,联合靶向治疗进展部位的系统治疗微转移灶有望增强治疗效果。镭-223 二氯化物(镭-223)是一种放射药物,通过发射阿尔法射线,选择性地与骨代谢增加的部位结合,并抑制相邻肿瘤细胞的生长。因此,对于仅有骨转移的寡转移性 CRPC,镭-223 可能会增强针对活跃转移灶的放疗的治疗效果。

方法

这项名为转移性治疗中使用阿尔法发射体镭-223治疗寡转移性 CRPC(MEDAL)的 II 期随机试验旨在评估镭-223联合转移性放疗在局限于骨骼的寡转移性 CRPC 患者中的应用。在这项试验中,全身 MRI 结合弥散加权 MRI(WB-DWI)显示有 3 个或更少骨转移的寡转移性 CRPC 患者将以 1:1 的比例随机分配,接受针对活跃转移灶的放疗加镭-223 治疗或仅接受针对活跃转移灶的放疗。先前使用雄激素受体轴靶向治疗和前列腺特异性抗原倍增时间将作为分配因素。主要终点是在 WB-DWI 上评估骨转移的影像学无进展生存期。

讨论

这将是第一项评估镭-223联合寡转移性 CRPC 患者靶向治疗效果的随机试验。针对宏观转移灶的靶向治疗与针对微转移灶的放射性药物相结合,有望成为一种有前途的新治疗策略,适用于局限于骨骼的寡转移性 CRPC 患者。

试验注册

日本临床试验注册(jRCT)(jRCTs031200358);注册于 2021 年 3 月 1 日,https://jrct.niph.go.jp/latest-detail/jRCTs031200358。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ae1/9987040/e967827fa282/12894_2023_1202_Fig1_HTML.jpg

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