Dosimetric factors predicting radiation pneumonitis after CyberKnife stereotactic body radiotherapy for peripheral lung cancer

Objective: The aims of this study were to investigate the frequency of symptomatic radiation pneumonitis (RP) after CyberKnife lung stereotactic body radiotherapy (SBRT) and to evaluate predictive factors of symptomatic RP. Methods: 56 patients with peripheral non-small-cell lung cancer were treated using the CyberKnife® VSI System (Accuracy Inc., Sunnyvale, CA) between May 2013 and September 2015. Total radiation doses ranged from 48 to 56Gy, as delivered in four equal fractions. Symptomatic RP was defined as a grade of 2. Predictive factors for symptomatic RP were evaluated using univariate and multivariate analyses. Results: With a median follow-up duration of 12.5 months (range, 3-27 months), symptomatic RP was observed in 6 (10.7%) of the 56 patients. In the univariate analysis, percent vital capacity (p,0.05), maximum tumour diameter (p,0.05), gross tumour volume (p,0.05), planning target volume (p,0.01), mean lung dose (p,0.01) and a normal lung volume receiving 5-50Gy of radiation (V5-50) (p,0.01) were identified as significant predictive factors for symptomatic RP. In the multivariate analysis, only a V25 .3.4% (p50.011) was identified as a significant predictive factor of symptomatic RP. Conclusion: The incidence of symptomatic RP after CyberKnife SBRT was almost identical to the incidences reported in the linear accelerator-based SBRT. A significant association was observed between a V25 .3.4% and the risk of developing symptomatic RP.