| Literature DB >> 15876674 |
Bryan Kim1, Tomas Kron, Jerry Battista, Jake Van Dyk.
Abstract
Loose helical delivery is a potential solution to account for respiration-driven tumour motion inpan> helical tomotherapy (HT). In this approach, a treatmenpan>t is divided inpan>to a set of inpan>terlaced 'loose' helices commenpan>cinpan>g at differenpan>t ganpan>try anpan>gles. Each loose helix covers the enpan>tire target lenpan>gth inpan> onpan>e ganpan>try rotationpan> durinpan>g a sinpan>gle breath-hold. The dosimetric characteristics of loose helical delivery were inpan>vestigated by deliverinpan>g a 6 MV photonpan> beam inpan> a HT-like manpan>ner. Multiple scenpan>arios of conpan>venpan>tionpan>al 'tight' HT anpan>d loose helical deliveries were modelled inpan> treatmenpan>t planpan>ninpan>g software, anpan>d carried out experimenpan>tally with Kodak pan> class="Gene">EDR2 film. The advantage of loose helical delivery lies in its ability to produce a more homogeneous dose distribution by eliminating the 'thread' effect-an inherent characteristic of HT, which results in dose modulations away from the axis of gantry rotation. However, loose helical delivery was also subjected to undesirable dose modulations in the direction of couch motion (termed 'beating' effect), when the ratio between the number of beam projections per gantry rotation (n) and pitch factor (p) was a non-integer. The magnitude of dose modulations decreased with an increasing n/p ratio. The results suggest that for the current HT unit (n = 51), dose modulations could be kept under 5% by selecting a pitch factor smaller than 7. A pitch factor of this magnitude should be able to treat a target up to 30 cm in length. Loose helical delivery should increase the total session time only by a factor of 2, while the planning time should stay the same since the total number of beam projections remains unchanged. Considering its dosimetric advantage and clinical practicality, loose helical delivery is a promising solution for the future HT treatments of respiration-driven targets.Entities:
Mesh:
Year: 2005 PMID: 15876674 DOI: 10.1088/0031-9155/50/10/014
Source DB: PubMed Journal: Phys Med Biol ISSN: 0031-9155 Impact factor: 3.609