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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
IRCCS Azienda Ospedaliero-Universitaria di Bologna
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - 79 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

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

    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
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    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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