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Completed

NCT Number: NCT02622841

Stereotactic Body Radiotherapy Followed by Surgical Stabilization for Patients With Unstable Spinal Metastases

The aim of this study is to assess the feasibility and safety of combining stereotactic body radiotherapy (SBRT) and pedicle screw fixation in a 48-hour window for the treatment of painful unstable metastases of the thoracic and/or lumbar spine.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

University Medical Center Utrecht

Utrecht, 3584 CX, Netherlands

About this study

Rationale: Sixty-five percent of cancer patients with terminal illness have bone metastases, with debilitating pain as devastating consequence. The spine is the most common location for bone metastases. Spinal cord compression is present in 10% of patients with vertebral metastases and aggravates pain and performance status even further. Standard treatment of unstable vertebral metastases consists of stabilizing surgery, followed by external beam radiotherapy (8 Gy) after two weeks. Although this approach is effective in 60-70% of patients, it is has several downsides. Firstly, because of the two weeks interval between surgery and external beam radiotherapy, necessary for sufficient wound healing, it takes a long time before radiotherapy induced pain relief is achieved. Scatter artifacts on planning computed tomography images caused by surgical implants prohibit high-resolution imaging and accurate targeting of the lesion. Multiple hospital visits (+/- 10) are needed for administration of external beam irradiation, and in about 30-40% of patients no adequate pain response is achieved. An alternative treatment strategy, which would lead to faster pain relief in a higher proportion of patients with less hospital visits, would be highly desirable from the patient's perspective.

Objective: To assess the feasibility and safety of combining stereotactic body radiotherapy (SBRT) and pedicle screw fixation in a 48-hour window for the treatment of painful unstable metastases of the thoracic and/or lumbar spine.

Study design: Prospective case series (13), first in man study, Phase I and II a study according to the IDEAL recommendations

Study population: All patients, male and female, with impending spinal stability requiring radiation therapy and surgical intervention at the University Medical Center Utrecht

Main study parameters/endpoints: The main outcome of this study is safety of the combined procedure, defined as grade 3 or higher treatment-induced toxicity according to common terminology criteria for adverse events (CTC-AE) 4.0 as a result of the procedure within 60 days after the surgery.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Painful metastases from solid tumors in the thoracic or lumbar spine needing surgical stabilization
  • Histologic proof of malignancy
  • Radiographic evidence of spinal metastases
  • Karnofsky performance status ≤ 50
  • Written informed consent

Exclusion criteria

  • Multiple spinal metastases necessitating bridging more than five vertebral levels during surgery
  • Previous surgery or radiotherapy to index lesion
  • stereotactic body radiotherapy cannot be delivered (Bilsky score 2 and 3)
  • Neurological deficits (ASIA C, B or A)
  • Partial neurological deficits (ASIA D) with rapid progression (hours to days)
  • Inability to lie flat on table for stereotactic body radiotherapy
  • Non-ambulatory patients
  • Patient in hospice or with < 3 months life expectancy
  • Medically inoperable or patient refused surgery

Treatment and study plan

BLEND

Procedure

Stereotactic bodyradiotherapy and surgical stabilization within 48 hours.

Primary outcomes

  1. Occurrence of adverse events

    Time frame: first 90 days post treatment

    Occurrence of adverse events grade 3/4 according to the common terminology criteria for adverse events (CTCAE) 4.0

Secondary outcomes

  1. Pain response

    Time frame: first 90 days post treatment

    Measurement of pain response to combined therapy according to consensus guidelines

  2. Duration of pain relief

    Time frame: first 90 days post treatment

    Measurement of duration of pain relief

  3. Rapidity of pain relief

    Time frame: first 90 days post treatment

    Measurement of rapidity of pain relief

  4. Hospital stay

    Time frame: first 90 days post treatment

    Measurement of length of hospital stay

  5. Early mortality

    Time frame: First 30 days post treatment

    Measurement of 30 days mortality

  6. Neurological status

    Time frame: First 90 days post treatment

    Measurement of neurological deterioration

  7. Quality of life

    Time frame: first 90 days post treatment

    Evaluation of quality of life

  8. Survival

    Time frame: Time from inclusion until date of death from any cause assessed up to 100 months

    Overall survival

Sponsors and collaborators

Lead sponsor

UMC Utrecht

Other

Registry information

Official study title

Stereotactic Body Radiotherapy Followed by Surgical Stabilization for Patients With Unstable Spinal Metastases: First-in-Man Study According to the IDEAL Recommendations

Acronym: BLEND

Important dates

Study start
2015
Primary completion
2017
Study completion
2017
First posted
Dec 7, 2015
Registry last updated
May 8, 2017

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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