TY - JOUR
T1 - Simultaneous integrated boost intensity-modulated radiotherapy for treatment of bone metastases: analysis of a breast cancer cohort
AU - Marazzi, F.
AU - Masiello, V.
AU - Fabi, A.
AU - Manfrida, S.
AU - Corvari, B.
AU - Lancellotta, V.
AU - Mazzarella, C.
AU - Longo, S.
AU - De, Angeli M.
AU - Moschella, F.
AU - Di Leone, Alba
AU - Orlandi, A.
AU - Bracci, S.
AU - Colloca, G. F.
AU - Massaccesi, M.
AU - Boldrini, Luca
AU - Tagliaferri, Luca
AU - Bria, Emilio
AU - Masetti, R.
AU - Franceschini, Gianluca
AU - Valentini, V.
AU - Gambacorta, Maria Antonietta
AU - Cellini, Francesco
PY - 2025
Y1 - 2025
N2 - Background: Bone metastases occur in up to 75% of metastatic breast cancer (MBC) cases. Advances in imaging now allow earlier detection, even during the oligometastatic phase. Radiotherapy (RT) is increasingly used in asymptomatic patients with <= 5 bone lesions, however standardised guidelines for dose and target volumes remain lacking.This study evaluates the outcomes ofa simultaneous integrated boost (SIB) using intensity-modulated radiotherapy (IMRT) to deliver ablative doses to macroscopic bone lesions. Methods: This retrospective study analysed MBC patients treated with SIB-IMRT for bone metastases between January 2014 and January 2022. The primary endpoint was freedom from local progression (FFLP); secondary endpoints included disease progression after radiotherapy (DP-AR) and overall survival (OS). Subgroup analyses were performed according to age, immunophenotype, and line of therapy. Results: Among 954 patients treated with RT, 85 received SIB-IMRT(6-8 Gy per fraction, 5 fractions). Median follow-up was 41 months. Nineteen patients (22.4%) had a single bone metastasis, 23.5% were oligometastatic, and 54.1% were plurimetastatic. Median FFLP was 17 months; only 7% experienced local relapse at the SIB site. While DP-AR was 13.2 months, median OS reached 82.7 months. No significant correlation was found between local relapse and age, immunophenotype, or systemic therapy. Immunophenotype significantly influenced DP-AR (p = 0.002), while DP-AR and OS were not significantly associated with local progression. Interpretation: SIB-IMRT for bone metastases in MBC is feasible and effective, with encouraging local control and minimal toxicity. Prospective studies are warranted to optimise dose escalation and explore synergistic effects with systemic therapies.
AB - Background: Bone metastases occur in up to 75% of metastatic breast cancer (MBC) cases. Advances in imaging now allow earlier detection, even during the oligometastatic phase. Radiotherapy (RT) is increasingly used in asymptomatic patients with <= 5 bone lesions, however standardised guidelines for dose and target volumes remain lacking.This study evaluates the outcomes ofa simultaneous integrated boost (SIB) using intensity-modulated radiotherapy (IMRT) to deliver ablative doses to macroscopic bone lesions. Methods: This retrospective study analysed MBC patients treated with SIB-IMRT for bone metastases between January 2014 and January 2022. The primary endpoint was freedom from local progression (FFLP); secondary endpoints included disease progression after radiotherapy (DP-AR) and overall survival (OS). Subgroup analyses were performed according to age, immunophenotype, and line of therapy. Results: Among 954 patients treated with RT, 85 received SIB-IMRT(6-8 Gy per fraction, 5 fractions). Median follow-up was 41 months. Nineteen patients (22.4%) had a single bone metastasis, 23.5% were oligometastatic, and 54.1% were plurimetastatic. Median FFLP was 17 months; only 7% experienced local relapse at the SIB site. While DP-AR was 13.2 months, median OS reached 82.7 months. No significant correlation was found between local relapse and age, immunophenotype, or systemic therapy. Immunophenotype significantly influenced DP-AR (p = 0.002), while DP-AR and OS were not significantly associated with local progression. Interpretation: SIB-IMRT for bone metastases in MBC is feasible and effective, with encouraging local control and minimal toxicity. Prospective studies are warranted to optimise dose escalation and explore synergistic effects with systemic therapies.
KW - breast cancer
KW - SIB-IMRT
KW - bone metastases
KW - precision medicine
KW - breast cancer
KW - SIB-IMRT
KW - bone metastases
KW - precision medicine
UR - https://publicatt.unicatt.it/handle/10807/317576
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=105005822913&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105005822913&origin=inward
U2 - 10.2340/1651-226X.2025.42933
DO - 10.2340/1651-226X.2025.42933
M3 - Article
SN - 0284-186X
VL - 64
SP - 685
EP - 692
JO - Acta Oncologica
JF - Acta Oncologica
IS - N/A
ER -