SBRT vs. Conventional Fractionation With HDR Boost for Prostate Cancer
Prostate CancerRandom assignment between SBRT and conventionally fractionated boost following HDR brachytherapy for prostate cancer.
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Conditions de participation
-
Sexe:
MALE -
Âges admissibles:
18 and up
Critères de participation
Inclusion Criteria:
* Age 18 or older
* Informed consent for treatment and study participation completed
* Pathologically proven diagnosis of prostate adenocarcinoma
* ECOG Performance Status 0-2
* No prior history of pelvic radiotherapy, brachytherapy, cryosurgery, HIFU, TURP or radical prostatectomy
Exclusion Criteria:
* Presence of nodal or distant metastasis on staging MRI or CT Abdomen/Pelvis and Bone scan within 90 days of enrolment (CT/MRI/Bone Scan are only required if the clinical risk of metastatic disease is sufficient to warrant these scans)
* Plan for adjuvant chemotherapy post-radiotherapy
* Serious medical comorbidities or other contraindications to HDR brachytherapy
* Presence of inflammatory bowel disease
* Presence of connective tissue disorder seen as a contraindication to radiotherapy
* Medically unfit for general/spinal anesthesia
* Unable or unwilling to complete questionnaires
Lieu de l'étude
Sunnybrook Health Sciences Centre
Sunnybrook Health Sciences CentreToronto, Ontario
Canada
Contactez l'équipe d'étude
Gerard Morton, MD, FRCPC
416-480-6100- Étude parrainée par
- Sunnybrook Health Sciences Centre
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT04861415