Spatially fractionated stereotactic body radiation therapy (Lattice) for large tumors.
Spatially fractionated stereotactic body radiation therapy (Lattice) for large tumors.
复制标题
DOI:
10.1016/j.adro.2020.100639
复制
发表时间:
2021-05
影响因子:
2.3
通讯作者:
Spraker MB
中科院分区:
文献类型:
--
作者:
Duriseti S;Kavanaugh J;Goddu S;Price A;Knutson N;Reynoso F;Michalski J;Mutic S;Robinson C;Spraker MB
Stereotactic body radiation therapy (SBRT) has demonstrated clinical benefits for patients with metastatic and/or unresectable cancer. Technical considerations of treatment delivery and nearby organs at risk can limit the use of SBRT in large tumors or those in unfavorable locations. Spatially fractionated radiation therapy (SFRT) may address this limitation because this technique can deliver high-dose radiation to discrete subvolume vertices inside a tumor target while restricting the remainder of the target to a safer lower dose. Indeed, SFRT, such as GRID, has been used to treat large tumors with reported dramatic tumor response and minimal side effects. Lattice is a modern approach to SFRT delivered with arc-based therapy, which may allow for safe, high-quality SBRT for large and/or deep tumors. Herein, we report the results of a dosimetry and quality assurance feasibility study of Lattice SBRT in 11 patients with 12 tumor targets, each ≥10 cm in an axial dimension. Prior computed tomography simulation scans were used to generate volumetric modulated arc therapy Lattice SBRT plans that were then delivered on clinically available Linacs. Quality assurance testing included external portal imaging device and ion chamber analyses. All generated plans met the standard SBRT dose constraints, such as those from the American Association of Physicists in Medicine Task Group 101. Additionally, we provide a step-by-step approach to generate and deliver Lattice SBRT plans using commercially available treatment technology. Lattice SBRT is currently being tested in a prospective trial for patients with metastatic cancer who need palliation of large tumors (NCT04553471, NCT04133415).
登录
查看更多内容
影响因子:
10.3
作者:
Hartsell, WF;Scott, CB;DeSilvio, M
通讯作者:
DeSilvio, M
影响因子:
3.8
作者:
Miften, Moyed;Olch, Arthur;Low, Daniel A.
通讯作者:
Low, Daniel A.
影响因子:
2.1
作者:
Sheikh, Khadija;Hrinivich, William T.;Meyer, Jeffrey
通讯作者:
Meyer, Jeffrey
DOI:
10.1016/j.ijrobp.2013.08.020
发表时间:
2013-12-01
影响因子:
7
作者:
Allibhai, Zishan;Taremi, Mojgan;Cho, B. C. John
通讯作者:
Cho, B. C. John
影响因子:
20.4
作者:
Shiue, Kevin;Cerra-Franco, Alberto;Lautenschlaeger, Tim
通讯作者:
Lautenschlaeger, Tim