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Precision radiation for prostate cancer shows promise in early trial
NCT ID NCT02470897
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tested a new way to deliver radiation for prostate cancer. The goal was to give a higher dose to the tumor while protecting the urethra and other healthy tissue. 115 men with early-stage prostate cancer took part. The researchers looked at side effects and how well the treatment worked over time.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- radiation therapy (SBRT with IMRT planning)
- What this could lead to
- If successful, this approach could offer a shorter, more precise radiation treatment for prostate cancer with fewer side effects.
- What could go wrong
- This is an early-phase study focused on safety and dosing, so it's not yet proven to be better than standard radiation. There is still a risk of urinary or rectal side effects.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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115 people
The number who actually took part.
- Started
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Jul 2015
- Finished
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Aug 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Male participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Histologically confirmed diagnosis of adenocarcinoma of the prostate and most recent biopsy within 180 days of study enrollment * History/physical examination with digital rectal examination of the prostate within 90 days prior to study enrollment * Gleason score =\< 7, no tertiary pattern \>= 5 * Clinical stage =\< T2b (American Joint Committee on Cancer \[AJCC\] 7th Edition Staging Manual) and no radiographic evidence of T3 or T4 disease * Clinical stage N0, M0 * Most recent prostate specific antigen (PSA) within 60 days of enrollment * Maximum PSA =\< 20 ng/ml (not within 20 days after biopsy) * Eastern Cooperative Oncology Group (ECOG) performance status 0-1 * American Urological Association (AUA) =\< 18 with or without medical management * Up to a total of year of androgen deprivation allowed. * Participant signs study specific informed consent prior to study enrollment Exclusion Criteria: * FOR ARM A: Inability to obtain a planning MRI or a planning MRI of sufficient quality to allow identification of the peripheral zone and urethra, or inability to adequately fuse the MRI to the planning CT scan * FOR BOTH ARM A AND ARM B: * Prior or concurrent invasive malignancy (except non-melanomatous skin cancer) or lymphomatous/hematogenous malignancy unless continually disease free for a minimum of 5 years; (for example, carcinoma in situ of the bladder or oral cavity is permissible) * Prosthetic implants in the pelvic region that the investigator feels will impede treatment, planning, or delivery (e.g., an artificial hip) * =\< 3 months from a transurethral resection of the prostate (TURP) procedure * Significant urinary obstruction (i.e. AUA symptom score \> 18) * Previous pelvic irradiation, prostate brachytherapy * Previous radical surgery (prostatectomy) or cryosurgery for prostate cancer * Severe, active comorbidity, defined as follows: * Acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration * Crohn's disease or ulcerative colitis * Scleroderma
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Swedish American
Rockford, Illinois, 61104, United States
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UW Cancer Center, Johnson Creek
Johnson Creek, Wisconsin, 53038, United States
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University of Wisconsin Carbone Cancer Center
Madison, Wisconsin, 53792, United States
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