TY - JOUR
T1 - Vertebral metastases reirradiation with volumetric-modulated arc radiotherapy
AU - Navarria, Pierina
AU - Mancosu, Pietro
AU - Alongi, Filippo
AU - Pentimalli, Sara
AU - Tozzi, Angelo
AU - Reggiori, Giacomo
AU - Ascolese, Anna Maria
AU - Arcangeli, Stefano
AU - Lobefalo, Francesca
AU - Baena, Riccardo Rodriguez Y
AU - Castiglioni, Simona
AU - Pessina, Federico
AU - Tancioni, Flavio
AU - Santoro, Armando
AU - Fogliata, Antonella
AU - Cozzi, Luca
AU - Scorsetti, Marta
PY - 2012/3
Y1 - 2012/3
N2 - Purpose: To assess the feasibility, acute toxicity, clinical improvement, local control and survival for spinal metastatic patients re-irradiated using volumetric-modulated-arc-radiotherapy (VMAT). Methods and materials: Between February 2009 and November 2010, 31 patients were treated. Surgery was performed in six before re-irradiation. The clinical target volume (CTV) was defined as the whole vertebrae with recurrence excluding the central section of spinal canal. Planning target volume was defined as CTV + 0-5 mm in the three directions. Dose was prescribed in order to have biological equivalent dose to the spinal cord from the two courses lower than 120 Gy 2 to 1 cc of the volume. Clinical improvement, toxicity and recurrence were evaluated. All patients had back pain before treatment and 15 (48%) neurological deficit. Results: Clinical remission of pain was obtained in 29 patients (93%). Neurological improvement was observed in 73% of patients. No acute or late toxicities were recorded. No recurrence occurred. Median survival was 10 months (range 6-24). At the last follow-up 19 patients (61%) were alive and 12 (39%) dead from systemic disease progression. The 1 and 2 year survival were 55% and 35%, respectively. Conclusion: In patients with spinal metastases recurrence re-irradiation with VMAT is feasible and provides clinical benefit in most patients.
AB - Purpose: To assess the feasibility, acute toxicity, clinical improvement, local control and survival for spinal metastatic patients re-irradiated using volumetric-modulated-arc-radiotherapy (VMAT). Methods and materials: Between February 2009 and November 2010, 31 patients were treated. Surgery was performed in six before re-irradiation. The clinical target volume (CTV) was defined as the whole vertebrae with recurrence excluding the central section of spinal canal. Planning target volume was defined as CTV + 0-5 mm in the three directions. Dose was prescribed in order to have biological equivalent dose to the spinal cord from the two courses lower than 120 Gy 2 to 1 cc of the volume. Clinical improvement, toxicity and recurrence were evaluated. All patients had back pain before treatment and 15 (48%) neurological deficit. Results: Clinical remission of pain was obtained in 29 patients (93%). Neurological improvement was observed in 73% of patients. No acute or late toxicities were recorded. No recurrence occurred. Median survival was 10 months (range 6-24). At the last follow-up 19 patients (61%) were alive and 12 (39%) dead from systemic disease progression. The 1 and 2 year survival were 55% and 35%, respectively. Conclusion: In patients with spinal metastases recurrence re-irradiation with VMAT is feasible and provides clinical benefit in most patients.
KW - Re-irradiation
KW - Spinal metastases
KW - Volumetric-modulated-arc-therapy
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U2 - 10.1016/j.radonc.2011.11.005
DO - 10.1016/j.radonc.2011.11.005
M3 - Article
C2 - 22192479
AN - SCOPUS:84857917070
VL - 102
SP - 416
EP - 420
JO - Radiotherapy and Oncology
JF - Radiotherapy and Oncology
SN - 0167-8140
IS - 3
ER -