Dosimetric comparison of different algorithms in stereotactic body radiation therapy (SBRT) plan for non-small cell lung cancer (NSCLC).

Onco Targets Ther

Department of Radiation and Medical Oncology, Zhongnan Hospital of Wuhan University, Hubei Cancer Clinical Study Center, Hubei 430072, People's Republic of China.

Published: August 2019

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Purposes: The main aim of the study was to investigate the dosimetric difference between acuros XB algorithm (AXB), anisotropic analytic algorithm (AAA), and pencil beam convolution (PBC) algorithm in stereotactic body radiation therapy (SBRT) plan for non-small cell lung cancer (NSCLC).

Patients And Methods: Thirty-eight NSCLC patients were included. GTV, PTV, and organs at risk were delineated by the radiation oncologists. Three optimized SBRT plans for each patients were gained using three algorithms of AXB, AAA, and PBC with the identical plan parameters. Dosimetric endpoints were collected and compared among the three plans, including dosimetric criteria: V100%, V90%, PTV D, D, D, homogeneity index (HI), and Paddick conformity index (CI).

Results: AXB plan resulted in decreased V100% with a mean difference 6.14% compared with PBC plan (For V100%, AXB vs AAA vs PBC=93.44% vs 95.54% vs 99.58%, <0.05). Three plans showed no significant difference as to the parameter V90%. AXB plan leaded to reduced D of PTV compared with other two algorithms (For D of PTV, AXB vs AAA vs PBC=4048cGy vs 4365Gy vs 4873Gy, <0.05). PBC induced the enhanced trend of D of PTV compared with other two algorithms (D among three algorithms, 0.05); and increased the D of PTV in three algorithms with significant difference (For D of PTV, AXB vs AAA vs PBC=5332cGy vs 5330Gy vs 5785Gy, <0.05). AXB algorithm achieved a similar plan conformity with other two algorithms (For CI, AXB vs AAA vs PBC=0.80 vs 0.85 vs 0.71, >0.05).

Conclusion: For SBRT plan of NSCLC, AAA and PBC algorithms overestimate target coverage, AXB algorithm is recommended for the SBRT plan of NSCLC.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6697670PMC
http://dx.doi.org/10.2147/OTT.S201473DOI Listing

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