
Validation of the clinical applicability of knowledge‐based planning models in single‐isocenter volumetric‐modulated arc therapy for multiple brain metastases
Author(s) -
Kishi Noriko,
Nakamura Mitsuhiro,
Hirashima Hideaki,
Mukumoto Nobutaka,
Takehana Keiichi,
Uto Megumi,
Matsuo Yukinori,
Mizowaki Takashi
Publication year - 2020
Publication title -
journal of applied clinical medical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.83
H-Index - 48
ISSN - 1526-9914
DOI - 10.1002/acm2.13022
Subject(s) - isocenter , wilcoxon signed rank test , nuclear medicine , radiation treatment planning , medicine , radiation therapy , radiology , imaging phantom , mann–whitney u test
Purpose To validate the clinical applicability of knowledge‐based (KB) planning in single‐isocenter volumetric‐modulated arc therapy (VMAT) for multiple brain metastases using the k ‐fold cross‐validation (CV) method. Methods This study comprised 60 consecutive patients with multiple brain metastases treated with single‐isocenter VMAT (28 Gy in five fractions). The patients were divided randomly into five groups (Groups 1–5). The data of Groups 1–4 were used as the training and validation dataset and those of Group 5 were used as the testing dataset. Four KB models were created from three of the training and validation datasets and then applied to the remaining Groups as the fourfold CV phase. As the testing phase, the final KB model was applied to Group 5 and the dose distributions were calculated with a single optimization process. The dose‐volume indices (DVIs), modified Ian Paddick Conformity Index (mIPCI), modulation complexity scores for VMAT plans (MCSv), and the total number of monitor units (MUs) of the final KB plan were compared to those of the clinical plan (CL) using a paired Wilcoxon signed‐rank test. Results In the fourfold CV phase, no significant differences were observed in the DVIs among the four KB plans (KBPs). In the testing phase, the final KB plan was statistically equivalent to the CL, except for planning target volumes (PTVs) D 2% and D 50% . The differences between the CL and KBP in terms of the PTV D 99.5% , normal brain, and D max to all organs at risk (OARs) were not significant. The KBP achieved a lower total number of MUs and higher MCSv than the CL with no significant difference. Conclusions We demonstrated that a KB model in a single‐isocenter VMAT for multiple brain metastases was equivalent in dose distribution, MCSv, and total number of MUs to a CL with a single optimization.