Intraoperative Radiotherapy in Treating Spinal Metastases

Sponsor
Shanghai Changzheng Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06093854
Collaborator
(none)
132
1
2
36
3.7

Study Details

Study Description

Brief Summary

In order to provide theoretical evidence for the comprehensive and standardized treatment of spinal metastases with pathological fractures and/or spinal cord compression, the investigators conduct this trial to investigate the efficacy and safety of IORT and postoperative SBRT in adjuvant treatment of metastatic spinal tumors after posterior decompression surgery by recruiting patients with spinal metastases who met the inclusion criteria, and randomly divided them into the following treatment cohorts: 1) decompression surgery + IORT (15-20 Gy, 20-50min); 2) decompression surgery and postoperative SBRT(30Gy, 5 fractions, 3 weeks).

Condition or Disease Intervention/Treatment Phase
  • Radiation: Intraoperative radiotherapy (IORT)
  • Radiation: Stereotactic body radiotherapy (SBRT)
N/A

Detailed Description

Spine is the most common metastatic site for advanced malignancies, accounting for about 70% of all patients with bone metastasis. Approximately 40% -70% of patients with advanced cancer eventually develop spinal metastases.

Spinal metastases require multidisciplinary treatments, and surgical decompression surgery is the preferred treatment in managing spinal metastases with bone related events, especially those with spinal cord compression. The purpose of decompression surgery is to directly relieve nerve compression, alleviate pain, rebuild spinal stability, and reduce tumor burden, which improves the quality of life, and extend the life span indirectly.

At the same time, radiotherapy is also an indispensable treatment for spinal metastases after surgical decompression. The purpose of radiotherapy is to remove residual tumor lesions, alleviate pain, and prevent further pathological fractures. Recent years have witnessed the rapid development of stereotactic bone radiotherapy (SBRT). As reported, SBRT can not only increase the radiation dose at the tumor site, but also reduce radiation damage to the spinal cord and surrounding normal tissues, which is the preferred adjuvant treatment for patients with metastatic spinal tumors. However, SBRT has the several risks, including radiation myelitis, delayed vertebral pathological fractures, local skin allergies, radiotherapy side effects in the esophagus and lungs, and duodenal perforation. Moreover, stereotactic radiotherapy technology has higher costs compared to traditional external beam radiotherapy.

Recently, the application of intraoperative radiotherapy (IORT) can effectively reduce the direct radiation for surrounding normal tissues and maximally eliminate the residual tumor cells. The advantages of IORT include: ① immediate reduction of the possibility of tumor cell expansion after surgery; ② Safe direct radiation and effective protection of normal tissues beyond the radiation depth; ③ To effectively protect adjacent normal tissues, light-limiting tubes with different diameters can be selected based on the size and range of tumor; ④ Shortening treatment course with lower costs and better compliance; ⑤ Slight systemic side effects and bone marrow suppression.

To the knowledge, no research focuses on the efficacy of IORT and SBRT in the adjuvant treatment of spinal metastases. Therefore, in order to provide theoretical evidence for the comprehensive and standardized treatment of spinal metastases with pathological fractures and/or spinal cord compression, the investigators conduct this trial to investigate the efficacy and safety of IORT and postoperative SBRT in adjuvant treatment of metastatic spinal tumors after posterior decompression surgery by recruiting patients with spinal metastases who met the inclusion criteria, and randomly divided them into the following treatment cohorts: 1) decompression surgery + IORT (15-20 Gy, 20-50min); 2) decompression surgery and postoperative SBRT(30Gy, 5 fractions, 3 weeks).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
132 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Decompression surgery + IORT (15-20 Gy, 20-50min) Decomression surgery + postoperative SBRT ( 30Gy, 5 fractions, 3 weeks)Decompression surgery + IORT (15-20 Gy, 20-50min) Decomression surgery + postoperative SBRT ( 30Gy, 5 fractions, 3 weeks)
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
The Efficacy and Safety of Intraoperative Radiotherapy Vesus Stereotactic Body Radiotherapy in Managing Spinal Metastases: A Prospective, Single-center, Open-label, Non-inferior, Randomized Controlled Trial
Anticipated Study Start Date :
Jan 1, 2024
Anticipated Primary Completion Date :
Jan 1, 2027
Anticipated Study Completion Date :
Jan 1, 2027

Arms and Interventions

Arm Intervention/Treatment
Experimental: Decompression surgery + IORT

Decompression surgery + IORT (15-20 Gy, 20-50min)

Radiation: Intraoperative radiotherapy (IORT)
Intraoperative radiotherapy (IORT, 15-20 Gy, 20-50min)

Active Comparator: Decompression surgery + postoperative SBRT

Decompression surgery + postoperative SBRT (30Gy, 5 fractions, 3 weeks)

Radiation: Stereotactic body radiotherapy (SBRT)
postoperative stereotactic body radiotherapy (SBRT, 30Gy, 5 fractions, 3 weeks)

Outcome Measures

Primary Outcome Measures

  1. Local control rate [2 years]

    The local control of tumor in the surgical field

Secondary Outcome Measures

  1. Health-related quality of life [2 years]

    The "Functional Assessment of Cancer Therapy -General" (FACT-G) Scale (Minimum: 0; Maximum: 108 ) is utilized to evaluate the health-related quality of life after treatments, and higher scores mean a worse outcome.

  2. Progression-free survival [2 years]

    The survival time between the day after treatments and the date of any evidence proving tumor progression or final follow-up

  3. Overall survival [2 years]

    The survival time between the day after treatments and the date of all-cause death or final follow-up

  4. Radiation-related complications [2 years]

    The complications assciated with the radiation process

Eligibility Criteria

Criteria

Ages Eligible for Study:
35 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Clinical diagnosis of spinal metastases;

  • Estimated survival time more than 3 months;

  • The spinal instability neoplastic score (SINS) >12;

  • The general condition allows to recieve surgery;

  • Single or multiple metastatic lesions with only one site presenting epidural spinal cord compression;

  • signed informed consent.

Exclusion Criteria:
  • Clinical diagnosis of primary spinal tumors;

  • Presence of metastases in central nerve system;

  • Isolated lesion undergoing en bloc resection;

  • Mental disorder and/or intellectual dificiency;

  • Refusing to accept follow-up;

  • without signing informed consent.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Shanghai Changzheng Hospital Shanghai Shanghai China 200003

Sponsors and Collaborators

  • Shanghai Changzheng Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Haifeng Wei, MD, PhD, Professor, Chief Surgeon, Shanghai Changzheng Hospital
ClinicalTrials.gov Identifier:
NCT06093854
Other Study ID Numbers:
  • 2022SL052
First Posted:
Oct 23, 2023
Last Update Posted:
Oct 23, 2023
Last Verified:
Oct 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Haifeng Wei, MD, PhD, Professor, Chief Surgeon, Shanghai Changzheng Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 23, 2023