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临床试验/NCT03365297
NCT03365297已完成2 期

Targeted Drug Intervention to Inhibit Cancer Progression in Men on Active Surveillance for Prostate Cancer. Therapeutics in Active Prostate Cancer Surveillance (TAPS01)

CCTU- Cancer Theme1 个研究点 分布在 1 个国家目标入组 11 人开始时间: 2018年6月5日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
11
试验地点
1
主要终点
Physiological Response

研究概览

简要总结

Testing if short-term use of apalutamide can reduce image defined tumour volumes in men with detectable lesion on multi-parametric Magnetic Resonance Imaging (mpMRI) and being managed by Active Surveillance. The trial will also evaluate the tolerability and side effect profile of men on AS using short term apalutamide and patient acceptability as a therapeutic strategy, as well as determining feasibility of a larger prospective randomised trial of apalutamide.

详细描述

The numbers of men diagnosed with prostate cancer in the United Kingdom (UK) and worldwide is increasing. In the UK 46,690 men were diagnosed in 2014 alone and it is estimated this figure will be closer to 70,000 by 2030. A significant proportion of these men will present with organ confined and low or intermediate risk disease. There is increasing recognition that many men with low and intermediate risk prostate cancer do not need immediate radical therapy.

There is sufficient evidence that pharmacological intervention used as short-term therapy in men with low to intermediate-risk disease can inhibit the growth of prostate tumours and delay or remove the need for radical therapy in men managed by active surveillance. Given the irrefutable role of the androgen receptor in prostate cancer pathogenesis it is logical to target this pathway as a method of inhibiting or delaying disease progression.

This window study will be built on the known anti-androgen effects of apalutamide and investigate the efficacy of using it as a short intervention strategy to cause a physiological change in the tumour by reducing its volume. Tumour volume can be measured using the well-established place of mpMRI defined tumour volumes as a surrogate of disease presence and change. The rationale for a short duration treatment is that it will not have the long term debilitating effects of androgen deprivation on general health and prevent the onset of androgen resistance.

It is anticipated that if successful, this approach could be a new therapeutic strategy for these men who otherwise are living and waiting for their disease to progress or not.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
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

入选标准

  • Given Informed Consent (IC) to participate
  • Age 18 or over
  • Eastern Cooperative Oncology Group (ECOG) status 0-2
  • Diagnosed with prostate cancer
  • Patient selection of active surveillance as a management option
  • mpMRI detectable lesion
  • Prostate cancer on biopsy from a mpMRI defined lesion
  • No contraindications to apalutamide
  • Normal full blood count and normal renal and liver function tests
  • At least 6 months since initiation of active surveillance and/or last rebiopsy date.
  • Low or intermediate risk prostate cancer according to National Institute for Health and Care Excellence (NICE) classification
  • M score of ≥ 3 using Prostate Imaging Reporting and Data System (PIRADS) version 2 reporting criteria

排除标准

  • Contraindications to apalutamide or its excipients
  • Concurrent medication that can lower seizure threshold
  • Prior localised therapy for prostate cancer
  • Any prior use of androgen deprivation therapy or androgen receptor targeting agents
  • Any prior systemic therapy for prostate cancer
  • Patient unable to have prostate 3T mpMRI scan
  • Presence of any pelvic or hip metalwork

研究组 & 干预措施

Treatment

Experimental

apalutamide, 240mg (4x60mg tablets) orally, daily for a max. duration of 90 continuous days.

干预措施: Apalutamide (Drug)

结局指标

主要结局

Physiological Response

时间窗: over a 90 day treatment period

Tumour volume downsizing/absence of lesion, as determined by mpMRI

次要结局

  • Patient Reported Outcomes(over 120 days)
  • Adverse Events(over 120 days)

研究者

发起方
CCTU- Cancer Theme
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

CCTU- Cancer Theme

CCTU Cancer Theme

Cambridge University Hospitals NHS Foundation Trust

研究点 (1)

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