跳至主要内容
临床试验/NL-OMON56209
NL-OMON56209尚未招募不适用

A FEASIBILITY STUDY OF 177LU-PSMA RADIOLIGAND THERAPY ALTERNATED WITH RADIUM-223 IN PATIENTS WITH BONE-METASTATIC, OLIGO-METASTATIC HORMONE-SENSITIVE PROSTATE CANCER AFTER CURATIVE THERAPY. THE DUET STUDY - DUET trial

Amsterdam UMC0 个研究点目标入组 6 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
6

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • - Histological proven adenocarcinoma of the prostate
  • - Previous radical prostatectomy
  • - Biochemical recurrence (PSA > 0.5 µg/l).
  • - PSA*doubling time < 6 months. Serum PSA progression is defined as 2
  • consecutive rising PSA
  • values measured at least 1 week apart.
  • - 18F*PSMA*PET*CT positive metastases in bones and/or lymph nodes
  • (miN1/miM1ab): Minimally 2 bone metastases, maximally 5 bone metastases.
  • - Local treatment for oligo*metastases with radiotherapy or surgery appears to
  • be no option
  • anymore (due to prior treatment or the location of the metastatic lesions or if
  • the patient refuse
  • these treatments).
  • - No prior hormonal therapy (including any androgen directed treatment such as
  • finasteride,
  • dutasteride, bicalutamide, apalutamide, abiraterone or enzalutamide) or taxane
  • chemotherapy (docetaxel or cabazitaxel);
  • Exception: local prostate cancer treated with local radiotherapy plus adjuvant
  • androgen deprivation therapy (ADT); these
  • patients need to be stopped with ADT at least 12 months.
  • - Testosterone > 1.7 nmol/l.
  • - A detectable lesion on the 18F*PSMA PET/CT with significant PSMA avidity,
  • defined by a SUVmax > 15 (partial volume corrected).
  • - ECOG 0*1
  • - Patients must have a life expectancy >12 months.
  • - Laboratory values:
  • White blood cells > 4.0 x 109/l
  • Platelet count > 150 x 109/l
  • Hemoglobin > 7.0 mmol/l
  • MDRD*GFR >= 60 ml/min
  • - Signed informed consent.

排除标准

  • A potential subject who meets any of the following criteria will be excluded
  • from participation in
  • this study in case of:
  • - A known subtype other than prostate adenocarcinoma.
  • - Previous PSMA based radioligand treatment.
  • - Visceral or brain metastases.
  • - Any medical condition present that in the opinion of the investigator will
  • negatively affect patients* clinical
  • status when participating in this trial.
  • - Prior hip replacement surgery potentially influencing performance of PSMA
  • - Sjögrens syndrome
  • - A second active malignancy other than prostate cancer.

研究者

发起方
Amsterdam UMC

相似试验