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Stereotactic Radiosurgery Prognosis Assessment for Spinal Tumors Based on Radiomics

Stereotactic Radiosurgery Prognosis Assessment for Spinal Tumors Based on Radiomics

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05369689
Enrollment
300
Registered
2022-05-11
Start date
2022-06-01
Completion date
2027-06-01
Last updated
2022-05-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prognosis, Radiomics, Spinal Tumor, Stereotactic Radiosurgery

Brief summary

This study aims to assess multimodal Radiomics-based prediction model for prognostic prediction in spinal tumors.

Detailed description

Sensitivity for prediction recurrence and survival of currently available prognostic scores is limited. This study proposes to establish a multimodal radiomics model for identifying tumor recurrence and prognostic prediction of spinal tumors. The study will investigate the relationship between the radiomics and the tumor microenvironment. The study includes the construction of multimodal radiomics-based prediction model and the validation of the prediction model.

Interventions

OTHERNo interventions

As this is a prognosis evaluation study, there are no interventions.

Sponsors

Zhuang Hongqing
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

A diagnosis of spinal tumors for which SBRT is appropriate Karnofsky Performance Status \>60 Life expectancy of at least 3 months No contraindication to undergoing MR imaging Age \>18 Complete the CT MRI or PET-CT examination before and after treatment Accept stereotactic radiosurgery

Exclusion criteria

Subjects unable to undergo MRI (includes non-MRI compatible material or devices and severe claustrophobia) Subjects with prior procedural intervention to the involved vertebral body that would result in artifact (kyphoplasty, screw and/or rod placement); minimally invasive surgery without instrumentation of the involved vertebral body and instrumentation immediately above or below the index lesion is allowed. Subjects with spinal cord compression; minimally invasive separation surgery to first resect the epidural component is allowed Pregnant or breast-feeding women Allergy to standard IV contrast agents used in MRI

Design outcomes

Primary

MeasureTime frameDescription
PFS1 yearsprogression-free survival

Secondary

MeasureTime frameDescription
Overall survival (OS)1 yearsdefined as the time from the beginning of diagnosis of spinal tumors to the death with any causes
ORR3 monthsobjective response rate
DCR3 monthsdisease control rate
Recurrence free survival (RFS)1 yeardefined as time between randomization and the time of any recurrence of ipsilateral chest, breast, regional lymph node recurrence, distant metastases, or death occurred

Countries

China

Contacts

Primary ContactHongqing zhuang
hongqingzhuang@163.com82264910
Backup ContactMingqing Wang
wangronggang.love@163.com82264917

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026