Stereotactic MRI-guided Radiation Therapy for Localized prostatE Cancer (SMILE)
Primary Purpose
Prostate Cancer
Status
Recruiting
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
MR-guided Radiotherapy
Sponsored by
About this trial
This is an interventional treatment trial for Prostate Cancer
Eligibility Criteria
Inclusion Criteria:
- Histologically confirmed prostate carcinoma with tissue classification according to Gleason score and PSA
- low- or intermediate-risk carcinoma according to d'Amico criteria or early high-risk Carcinoma (cT3a and / or GS ≤ 8 and / or PSA ≤ 20ng / ml)
- IPSS (International Prostate Symptom Score) max. 12
- Prostate volume <80cm³
- Karnofsky index ≥ 70%
- Age ≥ 18 years
- Patient information provided and written consent
- Ability of the patient to give consent
Exclusion Criteria:
- Previous radiotherapy in the pelvis
- Previous local therapy of the prostate
- lymphogenic metastasis
- Stage IV (distant metastases)
- Contraindication to MRI
- Simultaneous participation in another clinical study which could influence results of either of the respective study
Sites / Locations
- University Hospital of Heidelberg, Radiation OncologyRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
MR-guided Radiotherapy (5 x 7,5 Gy)
Arm Description
5 x 7,5 Gy prescribed on the PTV
Outcomes
Primary Outcome Measures
Toxicity or Discontinuation of Therapy
One of the the following events are counted as an Event (Number of Participants affected):
any urogenital or gastrointestinal grade ≥ 2 toxicity within one year after the start of RT (according to NCI CTCAE Version 5.0)
Discontinuation of therapy, with a connection to the study treatment
Secondary Outcome Measures
Mortality
Mortality due to study treatment or due to prostate Cancer (Number of Participants deceased)
Number of Toxicities
Number and severity of urogenital or gastrointestinal toxicity
bPFS
biochemical progression free survival
Hormone therapy-free Survival
Hormone therapy-free Survival
OS
overall survival
Quality of life according to EORTC QLQ-C30
Quality of life according to EORTC QLQ-C30
Quality of life according to EORTC QLQ-PR25
Quality of life according to EORTC QLQ-PR25
Symptoms and Toxicity
Symptoms and Toxicity according to NCI CTCAE (Rate)
Full Information
NCT ID
NCT04845503
First Posted
March 5, 2021
Last Updated
May 12, 2023
Sponsor
University Hospital Heidelberg
Collaborators
Ludwig-Maximilians - University of Munich, University Hospital, Zürich
1. Study Identification
Unique Protocol Identification Number
NCT04845503
Brief Title
Stereotactic MRI-guided Radiation Therapy for Localized prostatE Cancer
Acronym
SMILE
Official Title
Stereotactic MRI-guided Radiation Therapy for Localized prostatE Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 25, 2021 (Actual)
Primary Completion Date
March 25, 2023 (Actual)
Study Completion Date
March 25, 2028 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Heidelberg
Collaborators
Ludwig-Maximilians - University of Munich, University Hospital, Zürich
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
As the most common carcinoma in men, prostate cancer is a significant tumor entity in oncology. In addition to the surgical approach, definitive radiotherapy is an equivalent therapy alternative in the non-metastatic primary situation. However, radiotherapy usually stretches over a period of several weeks (7 to 8 weeks) during which the patient receives irradiation on a daily basis. For this reason and for radiobiological considerations the total treatment time is increasingly shortened. It has been shown in several randomized phase III studies that shorting radiotherapy to about 4 weeks by increasing the single dose (so-called hypofractionation) is possible. Meanwhile there is also more data on extreme hypofractionation (max. 10 radiation sessions) available, however often times, extensive preparations are necessary (such as the invasive introduction of markers into the prostate). The current, prospective, non-randomized, multicentric, Phase II SMILE study is now testing whether the MRI-guided radiotherapy with a greatly shortened radiotherapy of the prostate over 5 radiation sessions is possible and safe.
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
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
68 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
MR-guided Radiotherapy (5 x 7,5 Gy)
Arm Type
Experimental
Arm Description
5 x 7,5 Gy prescribed on the PTV
Intervention Type
Radiation
Intervention Name(s)
MR-guided Radiotherapy
Intervention Description
Total Dose 37,5 Gy, Single Dose 7,5 Gy, 5 Fractions applied in 1-2 weeks
Primary Outcome Measure Information:
Title
Toxicity or Discontinuation of Therapy
Description
One of the the following events are counted as an Event (Number of Participants affected):
any urogenital or gastrointestinal grade ≥ 2 toxicity within one year after the start of RT (according to NCI CTCAE Version 5.0)
Discontinuation of therapy, with a connection to the study treatment
Time Frame
Within 1 Year
Secondary Outcome Measure Information:
Title
Mortality
Description
Mortality due to study treatment or due to prostate Cancer (Number of Participants deceased)
Time Frame
Within 1 year and within 5 years
Title
Number of Toxicities
Description
Number and severity of urogenital or gastrointestinal toxicity
Time Frame
Within 1 year and within 5 years after start of radiotherapy
Title
bPFS
Description
biochemical progression free survival
Time Frame
from start of radiotherapy (day 1) until PSA-relapse according to Phoenix-Criteria (Prostate-specific antigen (PSA) nadir + 2 ng/mL after radiotherapy), assessed up to 5 years
Title
Hormone therapy-free Survival
Description
Hormone therapy-free Survival
Time Frame
from start of radiotherapy until start of hormon treatment; maximum 3 months neoadjuvant
Title
OS
Description
overall survival
Time Frame
from start of radiotherapy (day 1) until death or censoring assessed up to 5 years
Title
Quality of life according to EORTC QLQ-C30
Description
Quality of life according to EORTC QLQ-C30
Time Frame
from start of radiotherapy (day 1) until end of follow-up (up to 5 years)
Title
Quality of life according to EORTC QLQ-PR25
Description
Quality of life according to EORTC QLQ-PR25
Time Frame
from start of radiotherapy (day 1) until end of follow-up (up to 5 years)
Title
Symptoms and Toxicity
Description
Symptoms and Toxicity according to NCI CTCAE (Rate)
Time Frame
from start of radiotherapy (day 1) until end of follow-up (up to 5 years)
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Histologically confirmed prostate carcinoma with tissue classification according to Gleason score and PSA
low- or intermediate-risk carcinoma according to d'Amico criteria or early high-risk Carcinoma (cT3a and / or GS ≤ 8 and / or PSA ≤ 20ng / ml)
IPSS (International Prostate Symptom Score) max. 12
Prostate volume <80cm³
Karnofsky index ≥ 70%
Age ≥ 18 years
Patient information provided and written consent
Ability of the patient to give consent
Exclusion Criteria:
Previous radiotherapy in the pelvis
Previous local therapy of the prostate
lymphogenic metastasis
Stage IV (distant metastases)
Contraindication to MRI
Simultaneous participation in another clinical study which could influence results of either of the respective study
Facility Information:
Facility Name
University Hospital of Heidelberg, Radiation Oncology
City
Heidelberg
ZIP/Postal Code
69120
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stefan Körber, PD Dr.
Phone
+496221568202
Email
Studien.Radonk@med.uni-heidelberg.de
First Name & Middle Initial & Last Name & Degree
Stefan Körber, PD Dr.
12. IPD Sharing Statement
Learn more about this trial
Stereotactic MRI-guided Radiation Therapy for Localized prostatE Cancer
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