The robustness planning of SBRT for centrally-located non-small cell lung cancer
PO-1876
Abstract
The robustness planning of SBRT for centrally-located non-small cell lung cancer
Authors: Hing Ming Hung1, Wan Shun Leung2
1Pamela Youde Nethersole Eastern Hospital, Clinical Oncology, Chai Wan, Hong Kong (SAR) China; 2The Hong Kong Polytechnic University, Health Technology and Informatics, Kowloon, Hong Kong (SAR) China
Show Affiliations
Hide Affiliations
Purpose or Objective
Stereostatic
Body Radiotherapy (SBRT) of lung cancer is usually deliver a high fraction dose
to a moving target with heterogeneous density gradient. Strategies in
considering setup and dose estimation uncertainties are particularly important.
This study aimed to compare the conventional margin-based target volume
planning with the robust optimization planning approaches in terms of plan
qualities in SBRT of centrally located non-small cell lung cancer (CL-NSCLC).
Material and Methods
Twelve
CT sets for SBRT of CL-NSCLC were recruited retrospectively. Two SBRT plans
will be recomputed by conventional optimization with Planning Target Volume
(PTV-O) and the Robust Optimization with the Internal Target Volume (ITV-RO) for
each CT set. ITV was created by merging Gross Target Volume (GTV) of 10 motion phases
of 4DCT. While 5mm isotropical margin was given to the ITV to form the PTV. The
prescribed scheme was 50 Gy in 5 fractions. For comparison purposes, the prescribed
dose was normalized to ITV after PTV-O. Planning goals were to cover 95% ITV by
varying prescription isodose lines at 70 to 90% in both plans. 5mm isotropic uncertainties
with +/- 2% density error (16 scenarios) was introduced to robustness analysis
for both optimization approaches. The bandwidth measurement at D95% of ITV from
DVH were measured for comparing the robustness. Moreover, worst-case scenarios
of dosimetric parameters e.g., ITV coverage, dose spillage (R50%, the ratio of 25Gy
isodose volume to ITV) and doses to organs at risk (OARs: lungs, spinal cord,
heart, esophagus, trachea and major vessels) were also compared.
Results
Similar target coverage was observed in all
ITV parameters by both approaches but better performance was noted in ITV-RO approach:
conformity of ITV (conformity index: 1.13 vs 1.21, p < 0.05), dose spillage
(R50% ratio 4.18 vs 4.45, p < 0.05). The worst-case scenarios OARs parameters
by ITV-RO were generally lower than that by PTV-O, significant differences were
recorded in maximum dose of heart, major vessels and V20Gy (Lungs). The robustness
of ITV-RO approach was also assured, the bandwidth of D95% of ITV was 39.6%
narrower than that of PTV-O approach (p < 0.01).
Conclusion
ITV-RO approach offering advantages in conformity,
spillage control and OARs sparing while without sacrificing the target coverage.
Moreover, the robustness of ITV-RO also demonstrated superiority of withstanding
setup and dose estimation uncertainties. Overall, it has potential clinical benefit
to SBRT planning of CL-NSCLC.