Radiation Hypofractionation Via Extended Versus Accelerated Therapy (HEAT) For Prostate Cancer
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Purpose
Accelerated Hypofractionation Radiotherapy for prostate cancer of 36.25 Gy delivered in 5 fractions will not be inferior to the standard treatment of 70.2 Gy given in 26 fractions with respect to two-year failure defined as a positive biopsy two years post treatment completion or earlier evidence of biochemical or clinical failure.
| Condition | Intervention | Phase |
|---|---|---|
|
Prostate Cancer |
Radiation: Extended Hypofractionation Radiotherapy Radiation: Accelerated Hypofractionation Radiotherapy Procedure: Fiducial Marker Placement Behavioral: Quality of Life Questionnaires Procedure: Prostate Biopsy Genetic: Biopsy Tissue for Biomarkers Genetic: Biofluids for proteomics and genomics studies |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Randomized Study of Radiation Hypofractionation Via Extended Versus Accelerated Therapy (HEAT) For Prostate Cancer |
- Compare the two-year failure rates (biochemical or clinical failure, or positive biopsy) between the treatment arms (AHRT and EHRT) using a noninferiority margin of 12%. [ Time Frame: 2 years ] [ Designated as safety issue: No ]
- Compare acute toxicity rates of AHRT and EHRT. [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
- Compare Efficacy of AHRT with EHRT [ Time Frame: 2 years ] [ Designated as safety issue: No ]Compare the efficacy of AHRT with EHRT for the treatment of low and early intermediate risk prostate cancer, where efficacy is defined by biochemical failure using Phoenix (Nadir+2) definition or clinical failure.
- Compare AHRT and EHRT overall survival [ Time Frame: 2 years ] [ Designated as safety issue: No ]Compare AHRT and EHRT with respect to prostate cancer mortality and overall survival.
- Compare AHRT and EHRT quality of life [ Time Frame: 2 years ] [ Designated as safety issue: No ]Compare AHRT and EHRT with respect to quality of life (QOL), including erectile dysfunction rates, in generic and organ-specific domains.
- Rates of ASTRO-defined biochemical failure. [ Time Frame: 2 years ] [ Designated as safety issue: No ]
- Relationship of biomarkers from pretreatment diagnostic tissue and blood to the efficacy endpoints, toxicity and QOL. [ Time Frame: 2 years ] [ Designated as safety issue: No ]Examine the relationship of biomarkers from pretreatment diagnostic tissue and blood to the efficacy endpoints, toxicity and QOL.
- Rates of late-occurring grade 2 or greater GI/GU toxicity [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]To compare the rates of late-occurring grade 2 or greater G.I. or GU toxicity.
- Effectiveness of AHRT and EHRT [ Time Frame: 2 years ] [ Designated as safety issue: No ]Evaluate the comparative effectiveness of each treatment regimen.
- Cost utility of AHRT and EHRT [ Time Frame: 2 years ] [ Designated as safety issue: No ]Examine the cost utility of each treatment regimen.
| Estimated Enrollment: | 75 |
| Study Start Date: | March 2013 |
| Estimated Study Completion Date: | February 2018 |
| Estimated Primary Completion Date: | February 2018 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Extended Hypofractionation Radiotherapy (EHRT)
A total dose of 70.2 Gy will be delivered in 26 fractions, 2.7 Gy to the Planning Target Volume (PTV) by Intensity Modulated Radiotherapy (IMRT) with stationary gantry or rotating gantry technique.
|
Radiation: Extended Hypofractionation Radiotherapy
A total dose of 70.2 Gy will be delivered in 26 fractions, 2.7 Gy to the Planning Target Volume (PTV) by Intensity Modulated Radiotherapy (IMRT) with stationary gantry or rotating gantry technique.
Other Name: EHRT
Procedure: Fiducial Marker Placement
All patients will have 3-4 gold fiducial seeds or tracking markers placed in the prostate under ultrasound guidance (biopsy) prior to treatment planning by MRI and/or CT.
Behavioral: Quality of Life Questionnaires
The Expanded Prostate Cancer Index Composite Questionnaire-SF-12 (EPIC-SF-12) at after enrollment, prior to radiation therapy, and post-therapy at 6 weeks, 3 months, 9 months, 15 months, and then yearly to 5.25 years. Memorial Anxiety Scale for Prostate Cancer patients (MAX-PC) at after enrollment, prior to radiation therapy, and post-therapy at at 6 weeks, 3 months, 9 months, 15 months and then yearly to 5.25 years. International Prostate Symptom Index (IPSS) after enrollment, prior to radiation therapy, last week of therapy, and post-therapy at at 6 weeks, 3 months, and then every 6 months for 5.25 years. Other Names:
Procedure: Prostate Biopsy
Prostate biopsy at 2 - 2.5 years post completion of all therapy. Additional as needed.
Other Name: Prostate Biopsy
Genetic: Biopsy Tissue for Biomarkers
Biomarker analysis of the DNA content (image analysis) and immunohistochemical analyses of Ki-67/MIB-1, p53, bcl-2, bax, MDM2, and PKA in biopsy tissue.
Genetic: Biofluids for proteomics and genomics studies
Blood and urine samples. Four tubes of approximately 10 cc of blood each will be collected prior to treatment. Approximately 50 mL of urine will be collected.
|
|
Active Comparator: Accelerated Hypofractionation Radiotherapy (AHRT)
A total dose of 36.25 Gy will be delivered in 5 fractions, 7.25 Gy each to the Planning Target Volume (PTV), by Stereotactic Body Radiotherapy (SBRT) techniques.
|
Radiation: Accelerated Hypofractionation Radiotherapy
A total dose of 36.25 Gy will be delivered in 5 fractions, 7.25 Gy each to the Planning Target Volume (PTV), by Stereotactic Body Radiotherapy (SBRT) techniques.
Other Name: AHRT
Procedure: Fiducial Marker Placement
All patients will have 3-4 gold fiducial seeds or tracking markers placed in the prostate under ultrasound guidance (biopsy) prior to treatment planning by MRI and/or CT.
Behavioral: Quality of Life Questionnaires
The Expanded Prostate Cancer Index Composite Questionnaire-SF-12 (EPIC-SF-12) at after enrollment, prior to radiation therapy, and post-therapy at 6 weeks, 3 months, 9 months, 15 months, and then yearly to 5.25 years. Memorial Anxiety Scale for Prostate Cancer patients (MAX-PC) at after enrollment, prior to radiation therapy, and post-therapy at at 6 weeks, 3 months, 9 months, 15 months and then yearly to 5.25 years. International Prostate Symptom Index (IPSS) after enrollment, prior to radiation therapy, last week of therapy, and post-therapy at at 6 weeks, 3 months, and then every 6 months for 5.25 years. Other Names:
Procedure: Prostate Biopsy
Prostate biopsy at 2 - 2.5 years post completion of all therapy. Additional as needed.
Other Name: Prostate Biopsy
Genetic: Biopsy Tissue for Biomarkers
Biomarker analysis of the DNA content (image analysis) and immunohistochemical analyses of Ki-67/MIB-1, p53, bcl-2, bax, MDM2, and PKA in biopsy tissue.
Genetic: Biofluids for proteomics and genomics studies
Blood and urine samples. Four tubes of approximately 10 cc of blood each will be collected prior to treatment. Approximately 50 mL of urine will be collected.
|
Eligibility| Ages Eligible for Study: | 35 Years to 85 Years |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Histologically proven prostate adenocarcinoma.
- Gleason score 2-7 (reviewed by reference lab at UM).
- Biopsy within one year of date of enrollment.
Clinical stage ≤T2 based on DRE and ≤T3a based on MRI; N0-Nx; M0-Mx (AJCC 7th Edition)
- T-stage and N-stage determined by physical exam and available imaging studies (CT, and/or MRI of the pelvis; see section 4.5). For MRI, questionable extracapsular extension is permitted. To distinguish blood from tumor the ideal study would be to acquire T2, T1 noncontrast and T1 dynamic contrast enhanced sequence, although this is not required. A small amount of extracapsular extension is permitted, as long as it can be included in the CTV and the constraints are met.
- M-stage determined by physical exam, CT or MRI. Bone scan not required unless clinical findings suggest possible osseous metastases.
- PSA ≤ 15 ng/ml, obtained no greater than 3 months prior to enrollment.
Patients belonging in one of the following risk groups:
Low:
- Clinical stage* T1-T2; Gleason ≤ 6, PSA ≤ 10 & <50% biopsy cores positive.
Intermediate:
- Clinical stage T2b-T2c; Gleason ≤ 6, PSA ≤ 10 & <50% biopsy cores positive.
- Clinical stage T1-T2; Gleason ≤ 6, PSA ≤ 10 & ≥50% biopsy cores positive.
- Clinical stage T1-T2; Gleason = 7, PSA ≤ 10 & <50% biopsy cores positive or T1-T2; Gleason ≤ 6 & PSA >10 and ≤15 & <50% biopsy cores positive.
- MRI stage T3a with evidence of extraprostatic extension is allowed.
- Clinical stage is based on digital rectal exam (DRE). Seminal vesicle invasion on MRI is not eligible. T1a should be permitted if subsequent peripheral zone biopsies show tumor.
Prostate volume: ≤ 80 cc.
- Determined using: volume = π/6 x length x height x width.
- Measured from CT or MRI ≤90 days prior to enrollment.
- Zubrod performance status 0-1.
No prior total prostatectomy or cryotherapy of the prostate.
-- Prior suprapubic prostatectomy, transurethral resection and laser ablation are permitted.
- No prior radiotherapy to the prostate or lower pelvis.
- No implanted hardware or other material that would prohibit appropriate treatment planning or treatment delivery, in the investigator's opinion.
- No chemotherapy for a malignancy in the last 5 years.
- No history of an invasive malignancy (other than this prostate cancer, or nonmetastatic basal or squamous skin cancers) in the last 5 years.
- No androgen deprivation therapy (ADT) for six months prior to enrollment, and no planned ADT during treatment or adjuvantly.
- Patient must be able to have gold fiducial markers placed in the prostate (if on anticoagulants, must be cleared by a primary care physician or cardiologist).
- Ability to understand and the willingness to sign a written informed consent document.
- Willingness to fill out quality of life/psychosocial forms.
- Age >= 35 and =< 85 years.
- IPSS (AUA) score ≤12
Exclusion Criteria:
- Does not have a diagnosis of prostate adenocarcinoma.
- Patient has clinical T3a or any evidence of T3b disease.
- Patient has stage N1 or M1 disease.
- Patients has a PSA of greater than 15 ng/ml.
- Patient does not meet any of the risk groups outlined in section 3.1.4.
- Prostate volume greater than 80 cc.
- Zubrod performance status 2 or greater.
- Prior total prostatectomy.
- Prior radiation therapy to the prostate or lower pelvis.
- Implanted hardware which limits treatment planning or delivery (determined by the investigator).
- Chemotherapy within the past 5 years.
- Diagnosis of an invasive malignancy within 5 years (other than current prostate cancer or non-metastatic basal or squamous skin cancers).
- The use of androgen deprivation therapy (ADT) within the past 6 months prior to enrollment or the planned use of ADT during or after treatment.
- Inability to have gold fiducial markers placed in the prostate.
- Unwilling or inability to give informed consent.
- Not willing to fill out quality of life/psychosocial questionnaires.
- IPSS score > to 12.
- Age < 35 and > 85 years.
Contacts and Locations| United States, Florida | |
| University of Miami Sylvester Comprehensive Cancer Center | Recruiting |
| Miami, Florida, United States, 33136 | |
| Contact: Matthew C Abramowitz, MD 305-243-4200 mabramowitz@med.miami.edu | |
| Contact: University of Miami Sylvester Comprehensive Cancer Center 866-574-5124 sylvester@emergingmed.com | |
| Principal Investigator: Matthew Abramowitz, MD | |
| Sub-Investigator: Saleem Umar, MD | |
| Sub-Investigator: Radka Stoyanova, PhD | |
| Sub-Investigator: Javier Casillas, MD | |
| Sub-Investigator: Charles Lynne, MD | |
| Sub-Investigator: Margaret Byrne, PhD | |
| Principal Investigator: | Matthew Abramowitz, MD | University of Miami Sylvester Comprehensive Cancer Center |
| Principal Investigator: | Alan Pollack, MD, PhD | University of Miami Sylvester Comprehensive Cancer Center |
More Information
No publications provided
| Responsible Party: | University of Miami Sylvester Comprehensive Cancer Center |
| ClinicalTrials.gov Identifier: | NCT01794403 History of Changes |
| Other Study ID Numbers: | EPROST-20110491 |
| Study First Received: | February 14, 2013 |
| Last Updated: | March 25, 2013 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by University of Miami Sylvester Comprehensive Cancer Center:
|
Prostate Cancer Prostate Radiation Therapy Hypofractionation Radiotherapy |
Extended Hypofractionation Radiotherapy Accelerated Hypofractionation Radiotherapy AHRT EHRT |
Additional relevant MeSH terms:
|
Prostatic Neoplasms Genital Neoplasms, Male Urogenital Neoplasms Neoplasms by Site |
Neoplasms Genital Diseases, Male Prostatic Diseases |
ClinicalTrials.gov processed this record on May 22, 2013