Institute of Oncology Ljubljana
Ljubljana, 1000, Slovenia
Location contact
Eva Ćirić, MD
CONTACT
Klavdija Korošec
CONTACT
NCT Number: NCT07540650
This is a prospective, randomized, single-center clinical trial evaluating whether early prophylactic radiotherapy to high-risk asymptomatic or minimally symptomatic bone metastases reduces the 1-year rate of skeletal-related events (SREs) in patients with metastatic solid cancers. Patients will be randomized in a 1:1 ratio to receive either standard of care systemic therapy or observation, or prophylactic radiotherapy in addition to standard of care. The primary endpoint is the 1-year rate of SREs. Secondary endpoints include adverse events, quality of life, economic burden, pain-free survival, and overall survival.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Phase 2
Ljubljana, 1000, Slovenia
Eva Ćirić, MD
CONTACT
Klavdija Korošec
CONTACT
Bone metastases are a common complication in patients with metastatic solid cancers and are associated with significant morbidity, including skeletal-related events (SREs) such as pathological fractures, spinal cord compression, and severe pain requiring intervention. While palliative radiotherapy is an established treatment for symptomatic bone metastases, the role of prophylactic radiotherapy in asymptomatic or minimally symptomatic high-risk lesions remains insufficiently defined.
This prospective, randomized, single-center phase II clinical trial evaluates the effectiveness of early prophylactic radiotherapy in reducing the incidence of SREs. Eligible patients with metastatic solid cancers and up to five high-risk asymptomatic or minimally symptomatic bone metastases will be randomized in a 1:1 ratio into two groups. The control group will receive standard of care systemic therapy or observation according to tumor type and clinical guidelines. The intervention group will receive prophylactic external-beam radiotherapy (25 Gy in 5 fractions) to selected high-risk bone metastases in addition to standard of care.
Patients will be followed from baseline up to 12 months, with assessments conducted at predefined intervals. Study outcomes include the incidence of SREs, adverse events (graded according to CTCAE), patient-reported outcomes using validated questionnaires (EORTC QLQ-C30, EQ-5D-5L, BPI), economic burden, pain-free survival, and overall survival.
This study aims to determine whether early radiotherapy intervention can prevent skeletal complications, reduce healthcare burden, and improve patient outcomes in metastatic bone disease.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
External beam radiotherapy delivered to up to five high-risk asymptomatic or minimally symptomatic bone metastases at a total dose of 25 Gy in 5 fractions.
Systemic therapy or observation according to tumor type and clinical guidelines.
Time frame: From randomization to 12 months after randomization
Number of participants experiencing at least one skeletal-related event (pathological fracture, spinal cord compression, need for radiation to bone, need for surgery to bone, or tumor-related hypercalcemia) within 12 months after randomization.
Time frame: Up to 12 months after randomization
Adverse events assessed and graded according to CTCAE version 6.0
Time frame: Baseline, 3 months, 6 months, and 12 months after randomization
EORTC QLQ-C30 global health status score at each assessment time point (range: 0-100; higher scores indicate better quality of life).
Time frame: Baseline and follow-up visits up to 12 months after randomization
EQ-5D-5L index score at each assessment time point (range typically from <0 to 1; higher values indicate better health status).
Time frame: Baseline and follow-up visits up to 12 months after randomization
Pain intensity score measured using the Brief Pain Inventory (scale 0-10; higher scores indicate worse pain).
Time frame: From randomization to 12 months after randomization
Time from randomization to first occurrence of pain requiring opioid analgesics or death from any cause, whichever occurs first.
Time frame: From randomization to 12 months after randomization
Time from randomization to death from any cause.
Time frame: From randomization to 12 months after randomization
Number and duration of hospitalizations, number of outpatient visits, and associated healthcare costs during the study period.
Contact information is provided by the study sponsor or research team.
Eva Ćirić, MD
CONTACT
Klavdija Korošec
CONTACT
Institute of Oncology Ljubljana
Other
A Randomized Controlled Trial of Early Prophylactic Radiotherapy to Prevent Bone Complications in Patients With Metastatic Solid Cancers
Acronym: pRevenT
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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