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临床试验/NCT03482089
NCT03482089招募中不适用

Cystoprostatectomy Versus Radiotherapy Combined With Androgen Deprivation Therapy for the Treatment of Clinical T4 Prostate Cancer With Bladder Invasion: a Multicentre, Prospective, Open, Randomized Clinical Trial

Tongji Hospital1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2018年6月12日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
70
试验地点
1
主要终点
Overall survival (OS)

研究概览

简要总结

Prostate cancer is the most common male cancer in global, which accounts for 19% of the total and poses great hazards to male health. Unfavorable factors including prostatic specific antigen (PSA) >20 ng/ml, Gleason score >8, and T3/4 are significantly associated with biological recurrence, metastatic progression and poor survival in prostate cancer. In clinical T4(cT4) prostate cancer with bladder invasion patients, symptoms of hematuria, urinary urgency, bladder outlet and ureteral obstruction, and pelvic pain led to a poor quality of life.

Radical prostatectomy is crucial for the multimodal treatment of prostate cancer, but limited proof demonstrated enough advantages of the surgery in T4 tumor with bladder invasion. Radical prostatectomy could hardly meet both demands of local tumor control and urinary function. Treatment trends suggest that patients with T4 prostate cancer be treated with radiotherapy combined with androgen deprivation therapy (ADT). However, surgery enables a full pathological assessment of the tumor characteristics and thus a better estimation of the risk of recurrence. Cystoprostatectomy offers an option of surgical treatment for T4 prostate cancer with bladder invasion,which can well remove the bladder and urethra, decrease the risk of positive surgical margins and avoid urination complications.

There is no consensus regarding optimal treatment of T4 prostate cancer and no evidence of oncological outcomes of cystoprostatectomy from clinical trials. A randomized clinical trial comparing two multimodal treatment regimens of cystoprostatectomy and radiotherapy for T4 prostate cancer with bladder invasion is therefore warranted.

详细描述

  1. Determine the subjects

Patients were determined in strict accordance with the inclusion and exclusion criteria, and the trial process and significance were explained to the patients, and informed consent was signed.

2 Randomization

The patients were randomly assigned to surgery group or radiotherapy group according to the random number table.

3 Implementation Process

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 75 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Age ≤75, at the time of randomization
  • Newly diagnosed primary prostatic adenocarcinoma confirmed by pathological examination of biopsy;diagnosed within 6 months prior to randomization
  • Untreated for surgery, radiotherapy, or androgen deprivation therapy
  • Eastern Cooperative Oncology Group (ECOG) performance status 0- 2; American Standards Association (ASA) classification I-III
  • A life expectation of at least 10 years
  • Tumor stage (T, M, N): Clinical T4N0M0 with bladder invasion (confirmed by MRI)
  • Eligible for either treatment of cystoprostatectomy or radiotherapy
  • Signed informed consent should be obtained from both the patient or one authorized legal relative.

排除标准

  • Patients with a history of other cancer diagnoses except non-melanoma skin cancer
  • Patients with pelvic surgery
  • Patients with severe systemic diseases
  • severe kidney function -glomerular filtration rate (GFR) < 30 ml/min or elevated liver transaminases above > 10 upper limit of normal (ULN)
  • Patients who are not able comply with scheduled follow-up visits and examinations with the consideration of patients' physical or mental condition

结局指标

主要结局

Overall survival (OS)

时间窗: 10 years

The percentage of subjects in a study who have survived at the the endpoint of the observation since randomization or the interval between randomization and death from any cause.

次要结局

  • Functional Assessment of Cancer Therapy-General (FACT-G) score(10 years)
  • Functional Assessment of Cancer Therapy-Prostate (FACT-P) score(10 years)
  • complications(10 years)
  • Biochemical progression-free survival (BPFS)(10 years)
  • Cancer-specific survival (CSS)(10 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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