SBRT
RadiationSBRT (all metastatic lesions)
NCT Number: NCT05209243
Phase III study of stereotactic body radiation therapy (SBRT) plus standard of care in castration sensitive oligometastatic prostate cancer patients, defined as androgen deprivation therapy plus radiotherapy to the primary tumor in previously not treated patients and second generation hormonal treatments (Apalutamide/Abiraterone+Prednisone/Enzalutamide) vs androgen deprivation therapy plus radiotherapy to the primary tumor in previously not treated patients plus second generation hormonal treatments, for the treatment of oligometastatic prostate cancer.
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Interventional
Not applicable
Hospital Universitario Ramón y Cajal, Madrid, Spain
A total of 266 patients with a histological diagnosis of metastatic hormone sensitive prostate cancer, with limited disease (≤ 3 lesions based on CT and Bone Scan and ≤ 5 lesions based on Choline or PSMA PET/TC) at the diagnosis or in an oligorrecurrent stage will be included in the study. Candidates will be first screened for metastatic sites through bone scintigraphy and computerised tomography (CT) scans. Those who meet the ≤3 metastatic sites criteria will be second screened for metastatic sites based on Choline or PSMA PET/TC, which will be used to define the treatment volume of metastatic disease with SBRT/HIGRT and to confirm the oligometastatic status before the inclusion in the study.
Once included in the study, patients will be randomize (1:1) to standard of care + SBRT vs standard of care.
Patients will be stratified according to prior local treatment (yes/no) or the new imaging technique used (Choline vs PSMA PET/TC).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
SBRT (all metastatic lesions)
ADT+ RT to the primary tumor (previously not treated) + Second generation hormonal treatment
Time frame: An average of two years
based on RECIST 1.1 criteria
Time frame: 3 years
Defined as the time from trial randomization to the date of death from any cause. Patients not experiencing an event will be censored at the last known time they were alive.
Time frame: An average of two years
Time from trial randomization to start of first cytotoxic chemotherapy
Time frame: An average of two years
Counted from the day of randomization to the day of either first recorded biochemical progression[30]. Patients not experiencing a biochemical failure are censored at time of last assessment
Time frame: 3 years
based on RECIST 1.1 criteria
Time frame: 3 years
Defined as the time from trial randomization until castration resistant status
Time frame: An average of two years
Time from randomization until the occurrence of a skeletal related event (SRE)
Time frame: Three years after the study completion
FACT-P
Time frame: Three years after the study completion
To determine acute and late toxicity due to radiotherapy, scored using the Common Terminology Criteria for Adverse Events (CTCAE) versión 4.3.
Time frame: Three years after the study completion
Evaluate the impact of the treatment on the patient's quality of life using the Brief Pain Inventory (BPI) questionnaire
Contact information is provided by the study sponsor or research team.
Antonio J Conde Moreno, MD PhD
CONTACT
Fernando López Campos, MD PhD
CONTACT
Instituto de Investigación en Oncología Radioterápica - Fundación Española de Oncología Radioterápic
Other
Phase III Study of Stereotactic Body Radiation Therapy (SBRT) Plus Standard of Care in Castration Sensitive Oligometastatic Prostate Cancer Patients.
Acronym: START-MET
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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