Combined, Intensified and Modulated Adjuvant Therapy in Prostate Carcinoma
Primary Purpose
Prostate Cancer
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Combined, intensified and modulated adjuvant radiotherapy
Sponsored by

About this trial
This is an interventional treatment trial for Prostate Cancer focused on measuring adjuvant, androgen suppressive therapy, literature review, phase II, prostate neoplasms, radiotherapy
Eligibility Criteria
Inclusion Criteria:
- < 80 years old
- histological diagnosis of prostate adenocarcinoma
- no distant metastases
- stage pT2-4
- N0-1
- ECOG performance status of 0-2
- One of these pathologic features: extracapsular extension, positive surgical margins, or seminal vesicle invasion. extracapsular extension, positive surgical margins or seminal vesicle invasion, or positive lymph-nodes
- No surgical complications such as pelvic infections or lymphocele, intraoperative rectal injury or severe urinary incontinence
- Preoperative and postoperative PSA test, bone scan and CT-scan or MRI of abdomen and pelvis prior to enrolment
- Normal bone marrow function
Exclusion Criteria:
- Previously treated with Radiotherapy
- Previously treated with androgen deprivation therapy
- Previously treated with chemotherapy for prostate cancer. They also had to be free
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
intensified and modulated adjuvant RT
Arm Description
All patients underwent combined, intensified and modulated adjuvant radiotherapy for 5 days a week with the following doses: 1) pelvic node irradiation (45 Gy; 1.8 Gy/fraction) followed by boost on the prostate bed (19.8-25.2 Gy; 1.8 Gy/fraction; total dose: 64.8-70.2 Gy) or 2) exclusive prostate bed irradiation (64.8 -70.2 Gy; 1.8 Gy/fraction).
Outcomes
Primary Outcome Measures
Biochemical relapse free survival
Survival free from increase of PSA level exceeding 0.2 ng/mL for those with postsurgical PSA level of 0.2 ng/mL or lower, and as two consecutive PSA increases for patients with a postsurgical PSA level of > 0.2 ng/ml
Secondary Outcome Measures
Incidence of early treatment-emergent adverse events
Adverse events after radiotherapy . Acute side effects were scored according to the Radiation Therapy Oncology Group (RTOG) scale.
Incidence of late treatment-emergent adverse events were assessed with Radiation Morbidity Scoring Scheme of the RTOG/European Organization for Research and Treatment of Cancer (EORT)
Late complications were assessed with the Late Radiation Morbidity Scoring Scheme of the RTOG/European Organization for Research and Treatment of Cancer (EORT)
First evidence of any pelvic recurrence
First evidence of any pelvic recurrence
Metastasis-free survival
The first evidence of any extra pelvic recurrence of disease.
Full Information
NCT ID
NCT03169933
First Posted
May 17, 2017
Last Updated
March 5, 2018
Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Collaborators
Catholic University of the Sacred Heart, Howard University, University of Bologna, Michigan State University
1. Study Identification
Unique Protocol Identification Number
NCT03169933
Brief Title
Combined, Intensified and Modulated Adjuvant Therapy in Prostate Carcinoma
Official Title
Combined, Intensified and Modulated Adjuvant Therapy in Prostate Carcinoma: a Phase II Trial
Study Type
Interventional
2. Study Status
Record Verification Date
March 2018
Overall Recruitment Status
Completed
Study Start Date
January 2, 2004 (Actual)
Primary Completion Date
January 10, 2009 (Actual)
Study Completion Date
January 2, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Collaborators
Catholic University of the Sacred Heart, Howard University, University of Bologna, Michigan State University
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
Patients with high risk prostate cancer may benefit from radiotherapy after radical prostatectomy. The investigators postulated that adjuvant androgen deprivation therapy (ADT), radiation dose escalation, and selective pelvic irradiation may improve outcome. A phase II trial was designed to prove that combined-intensified-modulated-adjuvant (CIMA) treatment may improve 5-year biochemical relapse free survival (bRFS) from 75% to 90% in high risk patients. The delivered dose to tumor bed and pelvic nodes was 64.8-70.2 Gy and 45 Gy (57% of patients), respectively, and 69% received ADT.
Detailed Description
Prostate cancer patients at high risk of loco-regional recurrences may benefit from postoperative radiotherapy (RT) following radical prostatectomy (EORTC trial 22911). However, despite an improvement in biochemical relapse-free survival (bRFS), the risk of recurrences remained high for those patients. The investigators postulated that adjuvant androgen deprivation therapy (ADT), radiation dose escalation, and selective pelvic irradiation for patients at risk for regional failures may improve the outcome. The combined-intensified-modulated-adjuvant (CIMA) as described may improve survival through a reduction of loco-regional and systemic failures.
A phase II trial was designed to test the hypothesis that CIMA treatment may improve 5-year bRFS by 15%. Patients less than 80 years old, with a histological diagnosis of prostate adenocarcinoma without distant metastases, stage pT2-4 N0-1, no previous treatments and an ECOG performance status of 0-2 were selected. All patients had at least one of these pathologic features: extracapsular extension, positive surgical margins, or seminal vesicle invasion. Radiation dose to the tumor bed ranged from 64.8 to 70.2 Gy. Pelvic lymph nodes were treated to 45 Gy in selected patients at risk of regional failures (57%). Selected patients at risk for distant metastases (69.1%) received hormonal therapy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
adjuvant, androgen suppressive therapy, literature review, phase II, prostate neoplasms, radiotherapy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
123 (Actual)
8. Arms, Groups, and Interventions
Arm Title
intensified and modulated adjuvant RT
Arm Type
Other
Arm Description
All patients underwent combined, intensified and modulated adjuvant radiotherapy for 5 days a week with the following doses: 1) pelvic node irradiation (45 Gy; 1.8 Gy/fraction) followed by boost on the prostate bed (19.8-25.2 Gy; 1.8 Gy/fraction; total dose: 64.8-70.2 Gy) or 2) exclusive prostate bed irradiation (64.8 -70.2 Gy; 1.8 Gy/fraction).
Intervention Type
Radiation
Intervention Name(s)
Combined, intensified and modulated adjuvant radiotherapy
Other Intervention Name(s)
adjuvant androgen deprivation therapy
Primary Outcome Measure Information:
Title
Biochemical relapse free survival
Description
Survival free from increase of PSA level exceeding 0.2 ng/mL for those with postsurgical PSA level of 0.2 ng/mL or lower, and as two consecutive PSA increases for patients with a postsurgical PSA level of > 0.2 ng/ml
Time Frame
Five years
Secondary Outcome Measure Information:
Title
Incidence of early treatment-emergent adverse events
Description
Adverse events after radiotherapy . Acute side effects were scored according to the Radiation Therapy Oncology Group (RTOG) scale.
Time Frame
< 90 days.
Title
Incidence of late treatment-emergent adverse events were assessed with Radiation Morbidity Scoring Scheme of the RTOG/European Organization for Research and Treatment of Cancer (EORT)
Description
Late complications were assessed with the Late Radiation Morbidity Scoring Scheme of the RTOG/European Organization for Research and Treatment of Cancer (EORT)
Time Frame
5 years
Title
First evidence of any pelvic recurrence
Description
First evidence of any pelvic recurrence
Time Frame
5 years
Title
Metastasis-free survival
Description
The first evidence of any extra pelvic recurrence of disease.
Time Frame
5 years
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
79 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
< 80 years old
histological diagnosis of prostate adenocarcinoma
no distant metastases
stage pT2-4
N0-1
ECOG performance status of 0-2
One of these pathologic features: extracapsular extension, positive surgical margins, or seminal vesicle invasion. extracapsular extension, positive surgical margins or seminal vesicle invasion, or positive lymph-nodes
No surgical complications such as pelvic infections or lymphocele, intraoperative rectal injury or severe urinary incontinence
Preoperative and postoperative PSA test, bone scan and CT-scan or MRI of abdomen and pelvis prior to enrolment
Normal bone marrow function
Exclusion Criteria:
Previously treated with Radiotherapy
Previously treated with androgen deprivation therapy
Previously treated with chemotherapy for prostate cancer. They also had to be free
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alessio G Morganti, MD
Organizational Affiliation
Radiation Oncology Center, Department of Experimental, Diagnostic and Speciality Medicine-DIMES, University of Bologna, S. Orsola-Malpighi Hospital, Bologna, Italy
Official's Role
Study Director
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
30038390
Citation
Mantini G, Siepe G, Alitto AR, Buwenge M, Nguyen NP, Farioli A, Schiavina R, Catucci F, Deodato F, Fionda B, Frascino V, Macchia G, Ntreta M, Padula GDA, Arcelli A, Cammelli S, Rambaldi GZ, Cilla S, Valentini V, Morganti AG. Tailored postoperative treatment of prostate cancer: final results of a phase I/II trial. Prostate Cancer Prostatic Dis. 2018 Nov;21(4):564-572. doi: 10.1038/s41391-018-0064-7. Epub 2018 Jul 23.
Results Reference
derived
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Combined, Intensified and Modulated Adjuvant Therapy in Prostate Carcinoma
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