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NCT Number: NCT07540650

Prophylactic Radiotherapy to Prevent Bone Complications in Patients With Metastatic Solid Cancers

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥18 years
  • Histologically confirmed solid malignancy
  • Metastatic disease confirmed by imaging (CT, MRI, or PET-CT)
  • Presence of up to five high-risk bone metastases
  • High-risk bone metastases defined according to protocol criteria
  • Asymptomatic or minimally symptomatic bone metastases (not requiring opioid analgesics)
  • ECOG performance status 0-2
  • Ability to provide written informed consent

Exclusion criteria

  • Prior radiotherapy to the index bone metastases preventing safe treatment planning
  • Symptomatic bone metastases requiring immediate palliative radiotherapy
  • Evidence of spinal cord compression
  • Bone metastases causing significant pain requiring opioid analgesics
  • Oligometastatic disease suitable for radical treatment
  • Leptomeningeal disease
  • ECOG performance status ≥3
  • Life expectancy less than 3 months
  • Any condition that, in the investigator's opinion, would interfere with study participation or assessment

Treatment and study plan

Prophylactic External Beam Radiotherapy

Radiation

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.

Standard of care

Other

Systemic therapy or observation according to tumor type and clinical guidelines.

Primary outcomes

  1. 1-year rate of skeletal-related events (SREs)

    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.

Secondary outcomes

  1. Incidence of adverse events

    Time frame: Up to 12 months after randomization

    Adverse events assessed and graded according to CTCAE version 6.0

  2. EORTC QLQ-C30 global health status score

    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).

  3. EQ-5D-5L index score

    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).

  4. Brief Pain Inventory (BPI) pain intensity score

    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).

  5. Pain-free survival

    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.

  6. Overall survival

    Time frame: From randomization to 12 months after randomization

    Time from randomization to death from any cause.

  7. Healthcare resource utilization

    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.

Study contacts

Contact information is provided by the study sponsor or research team.

Eva Ćirić, MD

CONTACT

[email protected]

+38615879623

Klavdija Korošec

CONTACT

[email protected]

+38631630065

Sponsors and collaborators

Lead sponsor

Institute of Oncology Ljubljana

Other

Registry information

Official study title

A Randomized Controlled Trial of Early Prophylactic Radiotherapy to Prevent Bone Complications in Patients With Metastatic Solid Cancers

Acronym: pRevenT

Important dates

Study start
2026
Primary completion
2029
Study completion
2029
First posted
Apr 20, 2026
Registry last updated
Apr 20, 2026

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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