Cancer-specific dose and fractionation schedules in stereotactic body radiotherapy for oligometastatic disease: An interim analysis of the EORTC-ESTRO E2-RADIatE OligoCare study

Details

Serval ID
serval:BIB_9D470E62D475
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Cancer-specific dose and fractionation schedules in stereotactic body radiotherapy for oligometastatic disease: An interim analysis of the EORTC-ESTRO E2-RADIatE OligoCare study
Journal
Radiotherapy and Oncology
Author(s)
Christ Sebastian M., Alongi Filippo, Ricardi Umberto, Scorsetti Marta, Livi Lorenzo, Balermpas Panagiotis, Lievens Yolande, Braam Pètra, Jereczek-Fossa Barbara Alicja, Stellamans Karin, Ratosa Ivica, Widder Joachim, Peulen Heike, Dirix Piet, Bral Samuel, Ramella Sara, Hemmatazad Hossein, Khanfir Kaouthar, Geets Xavier, Jeene Paul, Zilli Thomas, Fournier Beatrice, Ivaldi Giovanni Battista, Clementel Enrico, Fortpied Catherine, Oppong Felix Boakye, Ost Piet, Guckenberger Matthias
ISSN
0167-8140
ISSN-L
0167-8140
Publication state
Published
Issued date
06/2024
Peer-reviewed
Oui
Volume
195
Pages
110235
Language
english
Abstract
Optimal dose and fractionation in stereotactic body radiotherapy (SBRT) for oligometastatic cancer patients remain unknown. In this interim analysis of OligoCare, we analyzed factors associated with SBRT dose and fractionation.
Analysis was based on the first 1,099 registered patients. SBRT doses were converted to biological effective doses (BED) using α/β of 10 Gy for all primaries, and cancer-specific α/β of 10 Gy for non-small cell lung and colorectal cancer (NSCLC, CRC), 2.5 Gy for breast cancer (BC), or 1.5 Gy for prostate cancer (PC).
Of the interim analysis population of 1,099 patients, 999 (99.5 %) fulfilled inclusion criteria and received metastasis-directed SBRT for NSCLC (n = 195; 19.5 %), BC (n = 163; 16.3 %), CRC (n = 184; 18.4 %), or PC (n = 457; 47.5 %). Two thirds of patients were treated for single metastasis. Median number of fractions was 5 (IQR, 3-5) and median dose per fraction was 9.7 (IQR, 7.7-12.4) Gy. The most frequently treated sites were non-vertebral bone (22.8 %), lung (21.0 %), and distant lymph node metastases (19.0 %). On multivariate analysis, the dose varied significantly for primary cancer type (BC: 237.3 Gy BED, PC 300.6 Gy BED, and CRC 84.3 Gy BED), and metastatic sites, with higher doses for lung and liver lesions.
This real-world analysis suggests that SBRT doses are adjusted to the primary cancers and oligometastasis location. Future analysis will address safety and efficacy of this site- and disease-adapted SBRT fractionation approach (NCT03818503).
Keywords
Radiology, Nuclear Medicine and imaging, Oncology, Hematology
Pubmed
Create date
08/04/2024 14:11
Last modification date
23/04/2024 7:00
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