TY - JOUR
T1 - In Silico Trial of Computed Tomography-Guided Stereotactic Adaptive Radiation Therapy (CT-STAR) for the Treatment of Abdominal Oligometastases
AU - Schiff, Joshua P.
AU - Stowe, Hayley B.
AU - Price, Alex
AU - Laugeman, Eric
AU - Hatscher, Casey
AU - Hugo, Geoffrey D.
AU - Badiyan, Shahed N.
AU - Kim, Hyun
AU - Robinson, Clifford G.
AU - Henke, Lauren E.
N1 - Funding Information:
Sources of support: This study was funded by Varian Medical Systems. Disclosures: J.P.S. has no disclosures. H.B.S. has no disclosures. A.P. has a grant from Varian Medical Systems and recieves support for travel from ViewRay and Sun Nuclear Corporation. E.L. recieves honoraria from Varian Medical Systems. C.H. has no disclosures. G.D.H. has grants with Sieman Healthineers, Varian Medical Systems, ViewRay and Mevion. He also has royalties and consulting fees with Varian Medical Systems. S.N.B. recieves honoraria from Mevion. H.K. recieves grants and honoraria from Varian Medical Systems. C.G.R. recieves grants from Varian Medical Systems and Merck, royalties from Varian Medical Systems, consulting fees from Varian Medical Systems, AstraZeneca, EMD Serono, Radialogica, and Quantaras, stock options from radialogica and quantaras, and patent WO 2017078757 A1. L.E.H. recieved funding from Varian Medical Systems paid to the institution for this clinical trial. She also recieves grants from Varian Medical Systems, consulting fees from Varian Medical Systems and Radiologica, honoraria from ViewRay and Varian Medical Systems, and particiapates on a advisory board from ViewRay.
Funding Information:
Disclosures: J.P.S. has no disclosures. H.B.S. has no disclosures. A.P. has a grant from Varian Medical Systems and recieves support for travel from ViewRay and Sun Nuclear Corporation. E.L. recieves honoraria from Varian Medical Systems. C.H. has no disclosures. G.D.H. has grants with Sieman Healthineers, Varian Medical Systems, ViewRay and Mevion. He also has royalties and consulting fees with Varian Medical Systems. S.N.B. recieves honoraria from Mevion. H.K. recieves grants and honoraria from Varian Medical Systems. C.G.R. recieves grants from Varian Medical Systems and Merck, royalties from Varian Medical Systems, consulting fees from Varian Medical Systems, AstraZeneca, EMD Serono, Radialogica, and Quantaras, stock options from radialogica and quantaras, and patent WO 2017078757 A1. L.E.H. recieved funding from Varian Medical Systems paid to the institution for this clinical trial. She also recieves grants from Varian Medical Systems, consulting fees from Varian Medical Systems and Radiologica, honoraria from ViewRay and Varian Medical Systems, and particiapates on a advisory board from ViewRay.
Publisher Copyright:
© 2022 Elsevier Inc.
PY - 2022/12/1
Y1 - 2022/12/1
N2 - Purpose: We conducted a prospective, in silico clinical imaging study (NCT04008537) to evaluate the feasibility of cone beam computed tomography-guided stereotactic adaptive radiation therapy (CT-STAR) for the treatment of abdominal oligometastases. We hypothesized that CT-STAR produces improved dosimetry compared with nonadapted CT-stereotactic body radiation therapy (SBRT). Methods and Materials: Eight patients receiving stereotactic body radiation therapy for abdominal oligometastatic disease received 5 additional kV cone beam CTs on the ETHOS system. These additional cone beam CTs were used for imaging during an emulator treatment session. Initial plans were created based on their simulation (PI) and emulated adaptive plans were based on anatomy-of-the-day. The prescription was 50 Gy out of 5 fractions. Organ-at-risk (OAR) constraints were prioritized over planning target volume coverage under a strict isotoxicity approach. The PI was applied to the patient's anatomy-of-the-day and compared with the reoptimized adaptive plans using dose-volume histogram metrics, with selection of the superior plan. Feasibility was defined as completion of the adaptive workflow and compliance with strict OAR constraints in ≥80% of fractions. Fractions were performed under time pressures by a physician and physicist to mimic the adaptive process. Results: CT-STAR was feasible, with successful workflow completion in 38 out of 40 (95%) fractions. PI application to daily anatomy created OAR constraint violations in 30 out of 40 (75%) fractions. There were 8 stomach, 18 duodenum, 16 small bowel, and 11 large bowel PI OAR constraint violations. In contrast, OAR violations occurred in 2 out of 40 (5%) adaptive plans (both small bowel violations, both improved from the PI). CT-STAR also improved gross tumor volume V100 and D95 coverage in 25 out of 40 (63%) and 20 out of 40 (50%) fractions, respectively. Zero out of 40 (0%) fractions were deemed nonfeasible due to poor image quality and/or inability to delineate structures. Adaptation time per fraction was a median of 22.59 minutes (10.97-47.23). Conclusions: CT-STAR resolved OAR hard constraint violations and/or improved target coverage in silico compared with nonadapted CT-guided stereotactic body radiation therapy for the ablation of abdominal oligometastatic disease. Although limitations of this study include its small sample size and in silico design, the consistently high-quality cone beam CT images captured and comparable timing metrics to prior adaptive studies suggest that CT- STAR is a viable treatment paradigm for the ablation of abdominal oligometastatic disease. Clinical trials are in development to further evaluate CT-STAR in the clinic.
AB - Purpose: We conducted a prospective, in silico clinical imaging study (NCT04008537) to evaluate the feasibility of cone beam computed tomography-guided stereotactic adaptive radiation therapy (CT-STAR) for the treatment of abdominal oligometastases. We hypothesized that CT-STAR produces improved dosimetry compared with nonadapted CT-stereotactic body radiation therapy (SBRT). Methods and Materials: Eight patients receiving stereotactic body radiation therapy for abdominal oligometastatic disease received 5 additional kV cone beam CTs on the ETHOS system. These additional cone beam CTs were used for imaging during an emulator treatment session. Initial plans were created based on their simulation (PI) and emulated adaptive plans were based on anatomy-of-the-day. The prescription was 50 Gy out of 5 fractions. Organ-at-risk (OAR) constraints were prioritized over planning target volume coverage under a strict isotoxicity approach. The PI was applied to the patient's anatomy-of-the-day and compared with the reoptimized adaptive plans using dose-volume histogram metrics, with selection of the superior plan. Feasibility was defined as completion of the adaptive workflow and compliance with strict OAR constraints in ≥80% of fractions. Fractions were performed under time pressures by a physician and physicist to mimic the adaptive process. Results: CT-STAR was feasible, with successful workflow completion in 38 out of 40 (95%) fractions. PI application to daily anatomy created OAR constraint violations in 30 out of 40 (75%) fractions. There were 8 stomach, 18 duodenum, 16 small bowel, and 11 large bowel PI OAR constraint violations. In contrast, OAR violations occurred in 2 out of 40 (5%) adaptive plans (both small bowel violations, both improved from the PI). CT-STAR also improved gross tumor volume V100 and D95 coverage in 25 out of 40 (63%) and 20 out of 40 (50%) fractions, respectively. Zero out of 40 (0%) fractions were deemed nonfeasible due to poor image quality and/or inability to delineate structures. Adaptation time per fraction was a median of 22.59 minutes (10.97-47.23). Conclusions: CT-STAR resolved OAR hard constraint violations and/or improved target coverage in silico compared with nonadapted CT-guided stereotactic body radiation therapy for the ablation of abdominal oligometastatic disease. Although limitations of this study include its small sample size and in silico design, the consistently high-quality cone beam CT images captured and comparable timing metrics to prior adaptive studies suggest that CT- STAR is a viable treatment paradigm for the ablation of abdominal oligometastatic disease. Clinical trials are in development to further evaluate CT-STAR in the clinic.
UR - http://www.scopus.com/inward/record.url?scp=85136247462&partnerID=8YFLogxK
U2 - 10.1016/j.ijrobp.2022.06.078
DO - 10.1016/j.ijrobp.2022.06.078
M3 - Article
C2 - 35768023
AN - SCOPUS:85136247462
SN - 0360-3016
VL - 114
SP - 1022
EP - 1031
JO - International Journal of Radiation Oncology Biology Physics
JF - International Journal of Radiation Oncology Biology Physics
IS - 5
ER -