Department of Radiation Oncology, University Medical Center Groningen, Hanzeplein 1, Postbus 30 001, 9700 RB, Groningen, the Netherlands.
Department of Urology, University Medical Center Groningen, Groningen, the Netherlands.
BMC Cancer. 2022 May 2;22(1):482. doi: 10.1186/s12885-022-09523-2.
More than 60% of oligo-recurrent prostate cancer (PCa) patients treated with metastasis-directed radiotherapy (MDRT) develop biochemical recurrence within 2 years. This recurrence rate emphasises the need for improved treatment and patient selection. In line with the treatment of primary PCa, the efficacy of MDRT may be enhanced when combined with androgen-deprivation therapy (ADT). Furthermore, the availability of PSMA PET/CT offers an excellent tool for optimal patient selection for MDRT. This phase III randomised controlled trial will investigate the role of the addition of ADT to MDRT in oligo-recurrent PCa patients selected with PSMA PET/CT to enhance oncological outcome.
Two hundred and eighty patients will be randomised in a 1:1 ratio to the standard treatment arm (MDRT alone) or the experimental arm (MDRT + 6 months ADT). Patients with biochemical recurrence after primary treatment of PCa presenting with ≤ 4 metastases will be included. The primary endpoint is the 2.5-year metastases progression-free survival (MPFS). Secondary endpoints are acute and late toxicity, quality of life, biochemical progression-free survival, overall survival, and the sensitivity of the PSMA PET/CT for detecting oligometastases at low PSA-levels. So far, between March 2020 and December 2021, one hundred patients have been included.
This phase III randomised controlled trial will assess the possible benefit of the addition of 6 months ADT to MDRT on metastases progression-free survival, toxicity, QoL and survival in PCa patients with 1-4 recurrent oligometastatic lesions.
ClinicalTrials.gov, NCT04302454 . Registered 10 March 2020.
超过 60%的寡转移前列腺癌(PCa)患者在接受转移导向放疗(MDRT)后,在 2 年内会出现生化复发。这种复发率强调了需要改进治疗方法和患者选择。与原发性 PCa 的治疗一致,MDRT 联合去势治疗(ADT)可能会提高疗效。此外,PSMA PET/CT 的应用为 MDRT 的最佳患者选择提供了极好的工具。这项 III 期随机对照试验将研究在 PSMA PET/CT 选择的寡转移 PCa 患者中,将 ADT 加入 MDRT 是否会提高肿瘤学结果。
280 名患者将以 1:1 的比例随机分为标准治疗组(单独 MDRT)或实验组(MDRT+6 个月 ADT)。纳入接受原发性 PCa 治疗后出现生化复发且转移灶≤4 个的患者。主要终点是 2.5 年的转移无进展生存率(MPFS)。次要终点是急性和迟发性毒性、生活质量、生化无进展生存率、总生存率,以及 PSMA PET/CT 在低 PSA 水平检测寡转移方面的敏感性。到目前为止,在 2020 年 3 月至 2021 年 12 月之间,已经纳入了 100 名患者。
这项 III 期随机对照试验将评估在 MDRT 中加入 6 个月 ADT 对 1-4 个复发性寡转移病灶的 PCa 患者转移无进展生存率、毒性、生活质量和生存的可能益处。
ClinicalTrials.gov,NCT04302454。于 2020 年 3 月 10 日注册。