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临床试验/CTIS2022-500838-28-00
CTIS2022-500838-28-00进行中(未招募)1 期

A Phase I/II Study of Neoadjuvant, Intra-arterial Administration of [177Lu]Lu-PSMA-617 in Subjects with High-risk, Localised or Locally Advanced Prostate Cancer who are Candidates for Radical Prostatectomy (LUPUS) - LUPUS

niversitaetsklinikum Essen AöR0 个研究点目标入组 22 人开始时间: 2023年9月13日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
22

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 65+(—)
性别
Male

入选标准

  • Histologically confirmed adenocarcinoma of the prostate including the following criteria: - High-risk prostate cancer defined by: a)a total Gleason sum score =4+4 (=ISUP Grade Groups 4 5), or b)any Gleason sum score and serum PSA-level = 20 ng/mL or -Locally advanced high-risk prostate cancer (=pT3a) defined as a)Extracapsular extension confirmed by mpMRI or PSMA-PET scan and/or b)Positive pelvic lymph nodes on pre-study PSMA-PET scan or c)Suspicion of pelvic lymph node involvement (cN1) on conventional imaging, Treatment-naïve patients for adenocarcinoma of the prostate, Eastern Cooperative Oncology Group (ECOG) performance status 0 1, Candidate eligible for intra-arterial treatment as per investigator, Candidate scheduled for radical prostatectomy with pelvic lymph node dissection as per the investigator, Adequate bone marrow function, liver and renal function, Patients must be willing to use a condom for all sexual activities, Patients must have evidence of PSMA-positive disease as seen on a PSMA-PET scan

排除标准

  • Distant metastasis (clinical stage M1), Prior treatment with androgen receptor antagonists. Treatment with GnRH analogues prior to ICF signature, Bilateral orchiectomy, History of prior systemic or local therapy for prostate cancer, including pelvic radiation for prostate cancer, Major surgery =4 weeks prior to inclusion, Previous treatment with radioligands within 6 months before inclusion

研究者

发起方
niversitaetsklinikum Essen AöR

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