Extracranial radiosurgery with volumetric modulated arc therapy: Feasibility evaluation of a phase I trial

  • Authors:
    • Francesco Deodato
    • Savino Cilla
    • Gabriella Macchia
    • Luciana Caravatta
    • Samantha Mignogna
    • Mariangela Massaccesi
    • Vincenzo Picardi
    • Cinzia Digesu
    • Giuseppina Sallustio
    • Pierluigi Bonomo
    • Angelo Piermattei
    • Gabriella Ferrandina
    • Giovanni Scambia
    • Vincenzo Valentini
    • Numa Cellini
    • Alessio G Morganti
  • View Affiliations

  • Published online on: March 29, 2013     https://doi.org/10.3892/ol.2013.1276
  • Pages: 1889-1896
Metrics: Total Views: 0 (Spandidos Publications: | PMC Statistics: )
Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )


Abstract

The aim of this study was to report early clinical experience in stereotactic body radiosurgery (SBRS) delivered using volumetric intensity modulated arc therapy (VMAT) in patients with primary or metastatic tumors in various extracranial body sites. Each enrolled subject was included in a different phase I study arm, depending on the tumor site and the disease stage (lung, liver, bone, metastatic), and sequentially assigned to a particular dose level. Technical feasibility and dosimetric results were investigated. The acute toxicity, tumor response and early local control were also studied. In total, 25 lesions in 20 consecutive patients (male/female, 11/9; median age, 67 years; age range, 47-86 years) were treated. Of these 25 lesions, 4 were primary or metastatic lung tumors, 6 were liver metastases, 8 were bone metastases and 7 were nodal metastases. The dose-volume constraints for organs at risk (OARs) were observed in 19 patients using a single‑arc technique. Only in one patient were two arcs required. The treatment was performed without interruption or any other technical issues. The prescribed dose ranged from 12‑26 Gy to the planning target volume (PTV). Delivery time ranged from 4 min to 9 min and 13 sec (median, 6 min and 6 sec). No incidence of grade 2-4 acute toxicity was recorded. The overall response rate was 48% (95% confidence interval (CI), 24.2-70.2) based on computed tomography (CT)/magnetic resonance imaging (MRI) and 89% (95% CI, 58.6-98.7) based on the positron emission tomography (PET) scan. SBRS delivered by means of VMAT allowed the required target coverage to be achieved while remaining within the normal tissue dose‑volume constraints in the 20 consecutive patients. VMAT‑SBRS resulted in adequate technical feasibility; the maximum tolerable dose has not yet been reached in any study arm.
View Figures
View References

Related Articles

Journal Cover

June 2013
Volume 5 Issue 6

Print ISSN: 1792-1074
Online ISSN:1792-1082

Sign up for eToc alerts

Recommend to Library

Copy and paste a formatted citation
x
Spandidos Publications style
Deodato F, Cilla S, Macchia G, Caravatta L, Mignogna S, Massaccesi M, Picardi V, Digesu C, Sallustio G, Bonomo P, Bonomo P, et al: Extracranial radiosurgery with volumetric modulated arc therapy: Feasibility evaluation of a phase I trial. Oncol Lett 5: 1889-1896, 2013.
APA
Deodato, F., Cilla, S., Macchia, G., Caravatta, L., Mignogna, S., Massaccesi, M. ... Morganti, A.G. (2013). Extracranial radiosurgery with volumetric modulated arc therapy: Feasibility evaluation of a phase I trial. Oncology Letters, 5, 1889-1896. https://doi.org/10.3892/ol.2013.1276
MLA
Deodato, F., Cilla, S., Macchia, G., Caravatta, L., Mignogna, S., Massaccesi, M., Picardi, V., Digesu, C., Sallustio, G., Bonomo, P., Piermattei , A., Ferrandina, G., Scambia, G., Valentini, V., Cellini, N., Morganti, A. G."Extracranial radiosurgery with volumetric modulated arc therapy: Feasibility evaluation of a phase I trial". Oncology Letters 5.6 (2013): 1889-1896.
Chicago
Deodato, F., Cilla, S., Macchia, G., Caravatta, L., Mignogna, S., Massaccesi, M., Picardi, V., Digesu, C., Sallustio, G., Bonomo, P., Piermattei , A., Ferrandina, G., Scambia, G., Valentini, V., Cellini, N., Morganti, A. G."Extracranial radiosurgery with volumetric modulated arc therapy: Feasibility evaluation of a phase I trial". Oncology Letters 5, no. 6 (2013): 1889-1896. https://doi.org/10.3892/ol.2013.1276