Phase II Study to Evaluate Conventional Radiation Therapy Followed by Radiosurgical Boost in Clinically Localized Prostate Cancer
Status: | Active, not recruiting |
---|---|
Conditions: | Prostate Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/17/2018 |
Start Date: | November 2009 |
End Date: | January 2019 |
Phase II Study to Evaluate the Efficacy of Intensity Modulated Radiation Therapy With Hypofractionated Radiosurgical Boosts in the Treatment of Clinically Localized Prostate Cancer
This phase II study designed to prospectively evaluate the efficacy and morbidity of IMRT
with CyberKnife radiosurgical boosts for clinically localized prostate cancer. Patients will
be treated with three radiosurgical treatments (6.5 Gy per fraction) followed by IMRT (45 Gy
in 25 fractions).
with CyberKnife radiosurgical boosts for clinically localized prostate cancer. Patients will
be treated with three radiosurgical treatments (6.5 Gy per fraction) followed by IMRT (45 Gy
in 25 fractions).
This is a phase II study designed to prospectively evaluate the efficacy and morbidity of
IMRT with CyberKnife radiosurgical boosts for clinically localized prostate cancer. Patients
with clinically localized prostate cancer will be treated with three radiosurgical treatments
(6.5 Gy per fraction to the PTV) followed by IMRT (45 Gy in 25 fractions). Treatment will be
completed over a 6-7 week period.
The hypothesis is that for patients with clinically localized adenocarcinoma of the prostate,
CyberKnife Radiosurgery delivered to the prostate is efficacious with acceptable toxicity in
combination with IMRT.
Subjects will have toxicity evaluation and AUA score on the last day of treatment. At 1 month
following treatment, subjects will be assessed for acute toxicity and will fill out AUA form,
SF-12, EPIC-26, SHIM and Utilization of Sexual Rx/Devices. At 3, 6, 12, 18 and 24 month
intervals (and every 6 months thereafter, through year 5, and annually through year 10, if
investigators opt to continue past year 5), subjects will be seen and evaluated, including a
history, physical exam, performance status, PSA, toxicity evaluation, and AUA score. In
addition, at 6 months, 12 months and annually thereafter, the SF-12, EPIC-26, SHIM and
Utilization of Sexual Medications/Devices will be administered. A prostate biopsy will be
performed at time of biochemical or local clinical failure, and is encouraged at 2 years
following treatment and at time of distant failure. A bone scan will be performed at the time
of biochemical failure, or when the subject develops signs of symptoms suggesting metastatic
disease.
Acute side effects (≤ 90 days of treatment start) will be assessed using the NCI Toxicity
Criteria version 3.0.
IMRT with CyberKnife radiosurgical boosts for clinically localized prostate cancer. Patients
with clinically localized prostate cancer will be treated with three radiosurgical treatments
(6.5 Gy per fraction to the PTV) followed by IMRT (45 Gy in 25 fractions). Treatment will be
completed over a 6-7 week period.
The hypothesis is that for patients with clinically localized adenocarcinoma of the prostate,
CyberKnife Radiosurgery delivered to the prostate is efficacious with acceptable toxicity in
combination with IMRT.
Subjects will have toxicity evaluation and AUA score on the last day of treatment. At 1 month
following treatment, subjects will be assessed for acute toxicity and will fill out AUA form,
SF-12, EPIC-26, SHIM and Utilization of Sexual Rx/Devices. At 3, 6, 12, 18 and 24 month
intervals (and every 6 months thereafter, through year 5, and annually through year 10, if
investigators opt to continue past year 5), subjects will be seen and evaluated, including a
history, physical exam, performance status, PSA, toxicity evaluation, and AUA score. In
addition, at 6 months, 12 months and annually thereafter, the SF-12, EPIC-26, SHIM and
Utilization of Sexual Medications/Devices will be administered. A prostate biopsy will be
performed at time of biochemical or local clinical failure, and is encouraged at 2 years
following treatment and at time of distant failure. A bone scan will be performed at the time
of biochemical failure, or when the subject develops signs of symptoms suggesting metastatic
disease.
Acute side effects (≤ 90 days of treatment start) will be assessed using the NCI Toxicity
Criteria version 3.0.
Inclusion Criteria:
- Histologically confirmed adenocarcinoma of the prostate (Biopsy within one year of
enrollment)
- Signed Study-Specific COnsent
- PSA within 60 days of registration
- Baseline AUA score is less than 20
Exclusion Criteria:
- Prior Pelvic radiotherapy
- Prior Radical Prostate surgery
- Recent (within 5 years) or concurrent cancers other than non-melanoma skin cancer
- Medical or psychiatric illness that would interfere with treatment or follow-up
- Implanted hardware adjacent to the prostate that would prohibit appropriate treatment
planning and/or treatment delivery.
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