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临床试验/NCT07100847
NCT07100847进行中(未招募)1 期

Phase 1b Window of Opportunity Study of Peri-prostatic Neurolysis in High-risk Localized Prostate Cancer

University of Texas Southwestern Medical Center1 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2025年8月15日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
21
试验地点
1
主要终点
Peritumoral adrenergic nerve density on final histology

研究概览

简要总结

The purpose of this research study is to assess whether inhibiting nerve activity to the prostate delays progression of disease in men with high-risk clinical features for prostate cancer. Prostate cancer has been shown to invade nerves, a mechanism that is thought to be involved in prostate cancer spread in men with high-risk cancer. When nerve activity to the prostate is blocked in mice with prostate cancer, prostate cancer growth and spread are inhibited. In a previous study we showed that doing so in humans was safe and may have anticancer therapeutic effect. In this study we will test whether one versus two injections of nerve blocking agent is more effective at reducing nerves in the prostate and whether it will slow/stop spread of prostate cancer after treatment.

详细描述

Men with high-risk prostate cancer are at the greatest risk for clinical progression, with 22 to 40% developing metastatic disease within 10 years of initial treatment. Furthermore, the finding of perineural invasion (PNI) on pathology (when prostate cancer cells invade the nerves that innervate the prostate), is associated with higher Gleason grades and an approximate doubling in risk of lethal prostate cancer. As 90% of prostate cancer metastasis involve the bone marrow, and 97% of bone marrow metastasis involve the lumbar vertebrate from which the pre-ganglionic sympathetic nerves that innervate the prostate derive, targeting this neuro-anatomic connection between the prostate and its primary site of metastasis is an active area of investigation. Therefore, development of therapeutic strategies targeting nerves to prevent clinical progression after definitive therapy for prostate cancer are urgently needed. In a Phase 1a dose escalation study (NCT06703437) we recently demonstrated that periprostatic neurolysis with 5mL pure ethanol was well tolerated with no AEs. This resulted in an approximate 30% reduction in prostatic adrenergic nerve density. The goal of this study is to optimize prostatic denervation by comparing the denervation efficiency of 1 vs 2 periprostatic ethanol injections.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者
否

入选标准

  • •High risk prostate cancer as defined by NCCN criteria Desires surgical disease treatment (radical prostatectomy) Surgical candidate (for radical prostatectomy)
  • •≤cT3a on MRI No seminal vesicle, lymph node, or metastatic disease on PSMA PET No prior prostate cancer treatment (including androgen deprivation therapy, radiation therapy, focal therapy, cryo therapy)

排除标准

  • 未提供

研究组 & 干预措施

No injection control

No Intervention

Single injection neurolysis

Experimental

Single injection of ethanol for periprostatic neurolysis

干预措施: Periprostatic neurolysis with dehydrated alcohol (ethanol) (Procedure)

Two injection neurolysis

Experimental

Two temporally separated periprostatic ethanol injections

干预措施: Periprostatic neurolysis with dehydrated alcohol (ethanol) (Procedure)

结局指标

主要结局

Peritumoral adrenergic nerve density on final histology

时间窗: 4 to 6 weeks after treatment initiation

Will quantify degree of neurolysis by measuring decrease in adrenergic nerve density on radical prostatectomy specimen histology

Peritumoral adrenergic nerve density on final histology

时间窗: 4 to 6 weeks after treatment initiation

Will quantify degree of neurolysis by measuring decrease in adrenergic nerve density on radical prostatectomy specimen histology

次要结局

  • Change in post prostatectomy penile length(6months after surgery)
  • Change in International Prostate Symptom Score (IPSS)(4 to 6 weeks after intervention)
  • Change in sexual health inventory for men (SHIM) score(4 to 6 weeks after intervention)
  • Change in sexual health inventory for men (SHIM) score(4 to 6 weeks after intervention)
  • Change in International Prostate Symptom Score (IPSS)(4 to 6 weeks after intervention)
  • Change in post prostatectomy penile length(6months after surgery)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ali Zahalka

Urologic Oncology Fellow

University of Texas Southwestern Medical Center

研究点 (1)

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