Prostate Cancer - Localized Adenocarcinoma Proton Therapy
Primary Purpose
Prostate Adenocarcinoma
Status
Recruiting
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Proton Therapy
Sponsored by
About this trial
This is an interventional treatment trial for Prostate Adenocarcinoma
Eligibility Criteria
Inclusion Criteria:
- Biopsy proven prostate adenocarcinoma Stage: T1-T2cN0M0
- ECOG performance status:0-1
- Signed study specific informed consent prior to study entry.
Exclusion Criteria:
- Postoperative residual or recurrent tumor
- Evidence of distant metastasis previous irradiation for the tumor in the same location
- Adjuvant anti-androgenic hormonal therapy High risk group (NCCN guide line)
Sites / Locations
- Kwanho ChoRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Proton Therapy 60 CGE
Proton Therapy 47 CGE
Arm Description
60 CGE (3CGE X 20) for 4wks
47 CGE (4.7CGE X 10) for 2wks
Outcomes
Primary Outcome Measures
BCFFS
To evaluate biochemical failure-free survival (BCFFS)
Secondary Outcome Measures
Acute/late toxicity (CTCAE v4.0)
Common Terminology Criteria for Adverse Events (CTCAE) V 4.0
Disease specific survival
follow-up
EPIC (Extended Prostate Cancer Index Composite)
questionnaire
Full Information
NCT ID
NCT03285815
First Posted
September 12, 2017
Last Updated
September 15, 2017
Sponsor
National Cancer Center, Korea
1. Study Identification
Unique Protocol Identification Number
NCT03285815
Brief Title
Prostate Cancer - Localized Adenocarcinoma Proton Therapy
Official Title
A Phase II Randomized Trial of Hypofractionated Proton Therapy in Patients With a Localized Prostate Adenocarcinoma
Study Type
Interventional
2. Study Status
Record Verification Date
September 2017
Overall Recruitment Status
Recruiting
Study Start Date
May 2016 (undefined)
Primary Completion Date
May 2024 (Anticipated)
Study Completion Date
December 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National Cancer Center, Korea
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
A Phase II Randomized Trial of Hypofractionated Proton Therapy in Patients With A Localized Prostate Adenocarcinoma
Detailed Description
For Proton therapy with prostate adenocarcinoma patients.
Arm 1: Proton therapy 3CGE x 20days = Total 60 CGE for 4 weeks.
Arm 2: Proton therapy 4.7CGE x 10days = Total 47 CGE for 2 weeks.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Adenocarcinoma
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
156 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Proton Therapy 60 CGE
Arm Type
Experimental
Arm Description
60 CGE (3CGE X 20) for 4wks
Arm Title
Proton Therapy 47 CGE
Arm Type
Experimental
Arm Description
47 CGE (4.7CGE X 10) for 2wks
Intervention Type
Device
Intervention Name(s)
Proton Therapy
Primary Outcome Measure Information:
Title
BCFFS
Description
To evaluate biochemical failure-free survival (BCFFS)
Time Frame
up to 5 years from a initial follow-up
Secondary Outcome Measure Information:
Title
Acute/late toxicity (CTCAE v4.0)
Description
Common Terminology Criteria for Adverse Events (CTCAE) V 4.0
Time Frame
up to 5 years from a initial follow-up
Title
Disease specific survival
Description
follow-up
Time Frame
up to 5 years from a initial follow-up
Title
EPIC (Extended Prostate Cancer Index Composite)
Description
questionnaire
Time Frame
up to 5 years from a initial follow-up
10. Eligibility
Sex
Male
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Biopsy proven prostate adenocarcinoma Stage: T1-T2cN0M0
ECOG performance status:0-1
Signed study specific informed consent prior to study entry.
Exclusion Criteria:
Postoperative residual or recurrent tumor
Evidence of distant metastasis previous irradiation for the tumor in the same location
Adjuvant anti-androgenic hormonal therapy High risk group (NCCN guide line)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kwanho Cho
Phone
82-31-920-1720
Email
kwancho@ncc.re.kr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kwanho Cho
Organizational Affiliation
National Cancer Center, Korea
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kwanho Cho
City
Ilsan
State/Province
Gyenggi-do
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kwanho Cho
Phone
82-31-920-1720
Email
kwancho@ncc.re.kr
First Name & Middle Initial & Last Name & Degree
Taehyun Kim
First Name & Middle Initial & Last Name & Degree
Yeonjoo Kim
First Name & Middle Initial & Last Name & Degree
Kanghyun Lee
First Name & Middle Initial & Last Name & Degree
Youngkyung Lim
First Name & Middle Initial & Last Name & Degree
Jaeyoung Jung
First Name & Middle Initial & Last Name & Degree
Byungho Nam
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Prostate Cancer - Localized Adenocarcinoma Proton Therapy
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