ESTRO 2022 - Abstract Book

S1458

Abstract book

ESTRO 2022

Conclusion Agreement in dosimetric parameters between SBRT centres increased with amount of dosimetric details provided in guidelines and trial protocols.

PO-1660 Assessment of biology-guided radiotherapy (BgRT) Accuracy using Emulated delivery technique

S. Khan 1 , M. Surucu 2 , M. Narayanan 3 , M. Haytmyradov 3 , S. Xu 3 , P. Olcott 3 , Y. Voronenko 3 , O.M. Oderinde 4,5 , G. Kuduvalli 3 , S.M. Shirvani 6 1 RefleXIon Medical, Inc, R&D, Hayward, USA; 2 Stanford University, Department of Radiation Oncology, Palo Auto, USA; 3 RefleXion Medical, Inc , R&D, Hayward, USA; 4 RefleXion Medical, Clinical, Hayward, USA; 5 RefleXion Medical, Inc , Clinical, Hayward, USA; 6 RefleXion Medical, Inc, Clinical, Hayward, USA Purpose or Objective New techniques in radiotherapy respond to intra-treatment information to generate machine instructions “dynamically determined during delivery (D4)”. One example is biology-guided radiotherapy (BgRT), an investigational technique that utilizes packets of positron emission tomography (PET) signal that emanate outward from a malignant tumor to direct beamlets of radiotherapy back to the target with subsecond latency. For these novel systems, machine instructions for the linear accelerator (LINAC) and multileaf collimator (MLC) are different for every fraction. Therefore, new forms of physical delivery validation may be needed to complement established physics quality assurance (QA) methods because the latter assume unchanging machine instructions at each fraction. Herein an investigational methodology, “emulated delivery”, is described and physically validated for assessing “D4” system Materials and Methods BgRT plans directed at 18 F-Fluorodeoxyglucose (FDG) phantoms were used to investigate emulated delivery. BgRT treatment plans were created, approved, and quality assured using imaging-only PET acquisitions for both a static and a moving (sinusoidal motion of 2 cm amplitude and 4 s/cycle using CIRS motion platform) FDG phantom. For both experiments, the 22mm diameter spherical target and the background were filled with FDG to achieve a target-background ratio of approximately 8:1. To emulate BgRT treatment delivery, a short duration pre-scan PET image (to confirm stable PET at the delivery timepoint) and a longer duration PET scan were acquired. The PET emission data from the longer scan was binned into limited time-sample packets and converted to partial fluences using the BgRT algorithm. Those fluences were then modeled onto a digital model of the FDG phantom in silico to generate the resultant dose distribution and then physically delivered into QA phantoms. A points-within-bounded-DVH (pwbDVH) metric was used to assess the accuracy of the on-the- fly dose distributions, and 3D Gamma passing criteria (3%/3mm) was used to assess physical deliverability.

Results