Cystoprostatectomy Versus Radiotherapy Combined With ADT for the Treatment of cT4 Prostate Cancer With Bladder Invasion (CRADT)
Primary Purpose
Prostate Cancer
Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Cystoprostatectomy
external beam radiotherapy
Sponsored by
About this trial
This is an interventional treatment trial for Prostate Cancer
Eligibility Criteria
Inclusion Criteria:
- 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.
Exclusion Criteria:
- 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
Sites / Locations
- Tongji Hospital of Tongji Medical College, Huazhong University of Science and TechnologyRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Cystoprostatectomy
Radiotherapy
Arm Description
(Open, laparoscopic or robot-assisted ) cystoprostatectomy with urinary diversion surgery and extended pelvic lymph node dissection; without adjuvant androgen deprivation therapy;
Radiotherapy by external beam radiotherapy (81 Gy,2.4-4 Gy per fraction over 4-6 weeks); with adjuvant androgen deprivation therapy for the least 3 years
Outcomes
Primary Outcome Measures
Overall survival (OS)
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.
Secondary Outcome Measures
Biochemical progression-free survival (BPFS)
the interval between randomization and biochemical recurrence or death from any cause or the percentage of subjects in a study who have survived without biochemical recurrence at the endpoint of the observation since randomization
Cancer-specific survival (CSS)
the interval between randomization and tumor recurrence, metastasis, or death from any cause, or the percentage of subjects in a study who have survived without tumor recurrence or metastasis at the endpoint of the observation since randomization
Functional Assessment of Cancer Therapy-General (FACT-G) score
This is a score system assessing cancer patients' quality of life, including four aspects of physical status, social status, emotional status and functional status. The total score ranges from 0-108 and a higher score indicates a better outcome.
Functional Assessment of Cancer Therapy-Prostate (FACT-P) score
This is a score system assessing prostate cancer patients' quality of life. The total score ranges from 0-48 and a higher score indicates a better outcome
complications
the complications and the incidence
Full Information
NCT ID
NCT03482089
First Posted
March 18, 2018
Last Updated
October 19, 2022
Sponsor
Tongji Hospital
Collaborators
Chinese PLA General Hospital, Xiangya Hospital of Central South University, Hubei Cancer Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03482089
Brief Title
Cystoprostatectomy Versus Radiotherapy Combined With ADT for the Treatment of cT4 Prostate Cancer With Bladder Invasion
Acronym
CRADT
Official Title
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
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
June 12, 2018 (Actual)
Primary Completion Date
June 12, 2023 (Anticipated)
Study Completion Date
June 12, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tongji Hospital
Collaborators
Chinese PLA General Hospital, Xiangya Hospital of Central South University, Hubei Cancer Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
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.
Detailed Description
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
The intervention measures were divided into operation group and non-operation group. The operation group was given cystoprostatectomy + expanded pelvic lymph node dissection + urinary diversion. The non-operation group received radiotherapy plus androgen deprivation therapy.
4 Follow-up Process
Follow-up was performed once a month (12 times in total) in the first year after surgery or radiotherapy, once every 3 months (4 times in total) in the second year, and once every six months after 2 years. Follow-up items included the presence of complications, digital rectal examination, PSA and testosterone levels, liver and kidney function. If digital rectal examination is positive and serum PSA continues to rise, pelvic MRI and bone scan should be performed. Bone pain, regardless of PSA level, should be scanned.
FunctionalAssessment of Cancer Therapy-General (FACT-G; FunctionalAssessment of Cancer Therapy-Prostate, FACT-P) and color Doppler ultrasonography of bilateral kidney and ureter were performed once every six months after 1 year.
Pelvic MRI, bone scan, chest radiograph, and color ultrasound of abdomen (liver, bile, pancreas and spleen) were examined once a year after surgery or radiotherapy.
Other follow-up examination items or follow-up time can be selected according to special circumstances. The patients were followed up for at least 10 years after surgery or after the end of radiotherapy.
5. Monitoring and management of recurrence, metastasis and complications
If biochemical recurrence after surgery (PSA level two consecutive acuity 0.2 ng/ml, two test interval of 2 weeks) or local recurrence, choose save radiotherapy, 8 Gy single, range is the whole pelvic, continued progress or control again after recurrence after radiotherapy are endocrine therapy, and its solution for than carew amine (50 mg 1 time, 1 times a day, Orally) + Goserelin (3.6mg once every 28 days, subcutaneously injected into the anterior abdominal wall); Patients with extensive metastasis after surgery were treated directly with endocrine therapy (bicalutamide 50mg once daily, orally) plus gosererin (3.6mg once every 28 days, subcutaneously injected into the anterior abdominal wall). The remaining tumor progression was managed according to the recommendations of authoritative guidelines at home and abroad.
The time of occurrence, name of complication, patient status, Clavien-Dindo complication classification, treatment measures and procedures, and treatment results were recorded. Complications were managed according to the recommendations of the guidelines and the experience of our unit.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
70 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Cystoprostatectomy
Arm Type
Experimental
Arm Description
(Open, laparoscopic or robot-assisted ) cystoprostatectomy with urinary diversion surgery and extended pelvic lymph node dissection; without adjuvant androgen deprivation therapy;
Arm Title
Radiotherapy
Arm Type
Active Comparator
Arm Description
Radiotherapy by external beam radiotherapy (81 Gy,2.4-4 Gy per fraction over 4-6 weeks); with adjuvant androgen deprivation therapy for the least 3 years
Intervention Type
Procedure
Intervention Name(s)
Cystoprostatectomy
Intervention Description
Patients with bladder infiltrating T4 prostate cancer receive cystoprostatectomy with urinary diversion surgery and extended pelvic lymph node dissection
Intervention Type
Radiation
Intervention Name(s)
external beam radiotherapy
Intervention Description
Patients with bladder infiltrating T4 prostate cancer are treated with adjuvant androgen deprivation therapy
Primary Outcome Measure Information:
Title
Overall survival (OS)
Description
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.
Time Frame
10 years
Secondary Outcome Measure Information:
Title
Biochemical progression-free survival (BPFS)
Description
the interval between randomization and biochemical recurrence or death from any cause or the percentage of subjects in a study who have survived without biochemical recurrence at the endpoint of the observation since randomization
Time Frame
10 years
Title
Cancer-specific survival (CSS)
Description
the interval between randomization and tumor recurrence, metastasis, or death from any cause, or the percentage of subjects in a study who have survived without tumor recurrence or metastasis at the endpoint of the observation since randomization
Time Frame
10 years
Title
Functional Assessment of Cancer Therapy-General (FACT-G) score
Description
This is a score system assessing cancer patients' quality of life, including four aspects of physical status, social status, emotional status and functional status. The total score ranges from 0-108 and a higher score indicates a better outcome.
Time Frame
10 years
Title
Functional Assessment of Cancer Therapy-Prostate (FACT-P) score
Description
This is a score system assessing prostate cancer patients' quality of life. The total score ranges from 0-48 and a higher score indicates a better outcome
Time Frame
10 years
Title
complications
Description
the complications and the incidence
Time Frame
10 years
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
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.
Exclusion Criteria:
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zhiqiang Chen, M.D.,Ph.D
Phone
008613995512271
Email
zhqchen8366@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Peng Yuan, M.D.
Phone
008615927679790
Email
mwyuanpeng@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zhiqiang Chen, M.D.,Ph.D
Organizational Affiliation
Tongji Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Tongji Hospital of Tongji Medical College, Huazhong University of Science and Technology
City
Wuhan
State/Province
Hubei
ZIP/Postal Code
430030
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zhiqiang Chen, M.D.,Ph.D
12. IPD Sharing Statement
Learn more about this trial
Cystoprostatectomy Versus Radiotherapy Combined With ADT for the Treatment of cT4 Prostate Cancer With Bladder Invasion
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