Dose-intensified SBRT for vertebral oligometastases: Results from a prospective clinical trial.
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BORIS DOI
Date of Publication
May 14, 2025
Publication Type
Article
Division/Institute
Contributor
Guckenberger, Matthias | |
Wilke, Lotte | |
Billiet, Charlotte | |
Rogers, Susanne | |
Franzese, Ciro | |
Schnell, Daniel | |
Spałek, Mateusz | |
Zilli, Thomas | |
Boda-Heggemann, Judit | |
Baumert, Brigitta G | |
Stelmes, Jean-Jacques | |
Nägler, Franziska | |
Bruni, Alessio | |
Zimmermann, Frank | |
Zimmer, Jörg | |
Madani, Indira |
Subject(s)
Series
Radiotherapy & Oncology
ISSN or ISBN (if monograph)
1879-0887
0167-8140
Publisher
Elsevier
Language
English
Publisher DOI
PubMed ID
40378895
Uncontrolled Keywords
Description
Purpose
To prospectively evaluate safety and efficacy of dose-intensified multiple-fraction SBRT using a simultaneous-integrated boost concept for vertebral oligometastases.Material And Methods
Data from 128 patients with 143 vertebral oligometastases (≤5 distant metastases in total) treated with dose-intensified SBRT (48.5 Gy/10 [with epidural involvement] or 40 Gy/5 [without epidural involvement]) in the randomized and non-randomized arms of a phase 3 clinical trial conducted in 18 international centers between 2016 and 2023 were analyzed.Results
The median age of all patients was 68 years; 77 patients (60.2 %) had breast and prostate cancer. Of 143 vertebral metastases, 23 (16.1 %) and 22 metastases (15.4 %) had epidural and paraspinal tumor involvement, respectively. The median follow-up time was 24 months. At 2 years, cumulative incidence of local failure (4 failures) was 5.3 %. There were 4 (2.8 %) baseline and 8 (5.6 %) de novo vertebral compression fractures (VCFs). Two-year OS was 82.2 % (95 % CI, 74.9-89.6 %). There was no grade ≥ 4 adverse events (AE) and the crude rate of grade 3 AEs was 5.5 %; no myelopathy or plexopathy was observed. On multivariate analysis, only non-breast or non-prostate cancer (HR, 7.91; 95 %, CI 1.79-35.03; 2-sided P = 0.01) were found to be prognostic for adverse OS. No prognostic factors for VCF were identified. Epidural and paraspinal involvement were not found to be prognostic for treatment outcome.Conclusions
Dose-intensified SBRT for vertebral oligometastases is effective and safe, even in high-risk patients with epidural or paraspinal involvement.
To prospectively evaluate safety and efficacy of dose-intensified multiple-fraction SBRT using a simultaneous-integrated boost concept for vertebral oligometastases.Material And Methods
Data from 128 patients with 143 vertebral oligometastases (≤5 distant metastases in total) treated with dose-intensified SBRT (48.5 Gy/10 [with epidural involvement] or 40 Gy/5 [without epidural involvement]) in the randomized and non-randomized arms of a phase 3 clinical trial conducted in 18 international centers between 2016 and 2023 were analyzed.Results
The median age of all patients was 68 years; 77 patients (60.2 %) had breast and prostate cancer. Of 143 vertebral metastases, 23 (16.1 %) and 22 metastases (15.4 %) had epidural and paraspinal tumor involvement, respectively. The median follow-up time was 24 months. At 2 years, cumulative incidence of local failure (4 failures) was 5.3 %. There were 4 (2.8 %) baseline and 8 (5.6 %) de novo vertebral compression fractures (VCFs). Two-year OS was 82.2 % (95 % CI, 74.9-89.6 %). There was no grade ≥ 4 adverse events (AE) and the crude rate of grade 3 AEs was 5.5 %; no myelopathy or plexopathy was observed. On multivariate analysis, only non-breast or non-prostate cancer (HR, 7.91; 95 %, CI 1.79-35.03; 2-sided P = 0.01) were found to be prognostic for adverse OS. No prognostic factors for VCF were identified. Epidural and paraspinal involvement were not found to be prognostic for treatment outcome.Conclusions
Dose-intensified SBRT for vertebral oligometastases is effective and safe, even in high-risk patients with epidural or paraspinal involvement.
File(s)
File | File Type | Format | Size | License | Publisher/Copright statement | Content | |
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1-s2.0-S016781402500235X-main.pdf | text | Adobe PDF | 733.33 KB | published |