Stereotactic Body Radiation Therapy for Localized Prostate Cancer
Image-Guidance and Online Adaptation With Stereotactic Body Radiation Therapy for the Treatment of Localized Prostate Cancer, MANTICORE Trial
Recruiting
N/AInterventional Study
Localized Prostate AdenocarcinomaStage I Prostate Cancer AJCC v8Stage II Prostate Cancer AJCC v8Stage III Prostate Cancer AJCC v8
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Male
Study type
Interventional
Purpose
Treatment
Participants needed
186 (estimated)
Sponsor
Jonsson Comprehensive Cancer Center · Other
Who this trial is looking for
This trial is looking for adults with localized prostate cancer. Participants will receive a special type of radiation treatment that is guided by images of their cancer.
Are You a Good Fit for This Trial?
You may be able to join if
I am at least 18 years old
I have localized adenocarcinoma of the prostate
I have completed the required staging tests for my cancer
I have no evidence of cancer spread to lymph nodes above the renal arteries
I have a performance status of 2 or less
I do not need immediate radiation treatment
I can provide written consent to participate in the study
You may not be able to join if
I have neuroendocrine or small cell carcinoma of the prostate
I have evidence of distant metastases, except for certain lymph nodes
I have had prior treatments like cryosurgery or brachytherapy on my prostate
I have had previous radiation treatment to my pelvis
I have a history of Crohn's disease or ulcerative colitis
I have a health condition that could compromise my safety or the study's data
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
This clinical trial studies the side effects of image-guidance and online adaptation with stereotactic body radiation therapy (SBRT) for the treatment of patients with prostate adenocarcinoma that has not spread to other parts of the body (localized). Image-guided SBRT is a standard treatment for localized prostate cancer. This treatment uses imaging of the cancer within the body to define and loc…
This clinical trial studies the side effects of image-guidance and online adaptation with stereotactic body radiation therapy (SBRT) for the treatment of patients with prostate adenocarcinoma that has not spread to other parts of the body (localized). Image-guided SBRT is a standard treatment for localized prostate cancer. This treatment uses imaging of the cancer within the body to define and localize the area to be treated with the radiation. Imaging can be obtained using either computed tomography (CT), magnetic resonance imaging (MRI), or a combination of the two. Typically, with SBRT, a radiation plan is developed based on the CT or MRI images obtained before treatment begins and adjustments are not made to the plan during treatment. However, anatomy can be different from day-to-day which may cause radiation to be delivered to the normal surrounding structures and possibly more side effects. During image-guided SBRT with online adaptation, the initial radiation plan is designed similarly; however, when the patient presents for radiation, the attending radiation oncologist, a dosimetrist, and a medical physicist "re-optimize" the radiation plan using the current anatomy of the day, meaning the changes in bladder and prostate size/shape are taken into account. The initial plan and the re-optimized plan are then compared, and the plan that has the optimal balance between delivering a tumor killing dose of radiation and minimizing radiation dose to normal surrounding structures is delivered. Image-guidance and online adaptation with SBRT may lower side effects and be a safer way to treat localized prostate adenocarcinoma.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Age ≥ 18
* Histologically confirmed, clinically localized adenocarcinoma of the prostate
* Staging workup as recommended by the National Comprehensive Cancer Network (NCCN) on the basis of risk grouping
* Advanced imaging studies (i.e. prostate-specific membrane antigen \[P…
Inclusion Criteria:
* Age ≥ 18
* Histologically confirmed, clinically localized adenocarcinoma of the prostate
* Staging workup as recommended by the National Comprehensive Cancer Network (NCCN) on the basis of risk grouping
* Advanced imaging studies (i.e. prostate-specific membrane antigen \[PSMA\] positron emission tomography \[PET\]/CT and fluciclovine PET/CT scan) can supplant a bone scan if performed first
* No evidence of metastatic disease in lymph nodes above the bifurcation of the renal arteries, or in bones or visceral organs (nodal disease identified on a PSMA PET/CT scan below the bifurcation of the renal arteries are amenable)
* Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2
* No indication for urgent or emergent radiation
* Written informed consent obtained from participant or participant's legal representative and ability for participant to comply with the requirements of the study
Exclusion Criteria:
* Patients with neuroendocrine or small cell carcinoma of the prostate
* Patients with any evidence of distant metastases except that evidence of lymphadenopathy below the level of the renal arteries can be deemed locoregional per the discretion of the investigator
* Prior cryosurgery, high-intensity focused ultrasound (HIFU), brachytherapy, or other ablative treatments of the whole prostate
* Prior pelvic radiotherapy
* History of Crohn's disease, ulcerative colitis, or ataxia telangiectasia
* Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the participant or the quality of the data
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