TY - JOUR
T1 - Dose-Intensified Stereotactic Ablative Radiation for Localized Prostate Cancer
AU - Chen, Lily
AU - Gannavarapu, Bhavani S.
AU - Desai, Neil B.
AU - Folkert, Michael R
AU - Dohopolski, Michael
AU - Gao, Ang
AU - Ahn, Chul
AU - Cadeddu, Jeffrey
AU - Bagrodia, Aditya
AU - Woldu, Solomon
AU - Raj, Ganesh V.
AU - Roehrborn, Claus
AU - Lotan, Yair
AU - Timmerman, Robert D.
AU - Garant, Aurelie
AU - Hannan, Raquibul
N1 - Publisher Copyright:
Copyright © 2022 Chen, Gannavarapu, Desai, Folkert, Dohopolski, Gao, Ahn, Cadeddu, Bagrodia, Woldu, Raj, Roehrborn, Lotan, Timmerman, Garant and Hannan.
PY - 2022/2/21
Y1 - 2022/2/21
N2 - Purpose: Stereotactic ablative radiation (SAbR) has been increasingly used in prostate cancer (PCa) given its convenience and cost efficacy. Optimal doses remain poorly defined with limited prospective comparative trials and long-term safety/efficacy data at higher dose levels. We analyzed toxicity and outcomes for SAbR in men with localized PCa at escalated 45 Gy in 5 fractions. Methods and Materials: This study retrospectively analyzed men from 2015 to 2019 with PCa who received linear-accelerator-based SAbR to 45 Gy in 5 fractions, along with perirectal hydrogel spacer, fiducial placement, and MRI-based planning. Disease control outcomes were calculated from end of treatment. Minimally important difference (MID) assessing patient-reported quality of life was defined as greater than a one-half standard deviation increase in American Urological Association (AUA) symptom score after SAbR. Results: Two-hundred and forty-nine (249) low-, intermediate-, and high-risk PCa patients with median follow-up of 14.9 months for clinical toxicity were included. Acute urinary grade II toxicity occurred in 20.4% of patients. Acute grade II GI toxicity occurred in 7.3% of patients. For follow-up > 2 years (n = 69), late GU and GI grade ≥III toxicity occurred in 5.8% and 1.5% of patients, respectively. MID was evident in 31.8%, 23.4%, 35.8%, 37.0%, 33.3%, and 26.7% of patients at 3, 6, 12, 24, 36, and 48 months, respectively. The median follow-up for biochemical recurrence was 22.6 months with biochemical failure-free survival of 100% at 1 year (n = 226) and 98.7% for years 2 (n = 113) and 3 (n = 54). Conclusions: SAbR for PCa at 45 Gy in 5 fractions shows an encouraging safety profile. Prospective studies with longer follow-up are warranted to establish this dose regimen as standard of care for PCa.
AB - Purpose: Stereotactic ablative radiation (SAbR) has been increasingly used in prostate cancer (PCa) given its convenience and cost efficacy. Optimal doses remain poorly defined with limited prospective comparative trials and long-term safety/efficacy data at higher dose levels. We analyzed toxicity and outcomes for SAbR in men with localized PCa at escalated 45 Gy in 5 fractions. Methods and Materials: This study retrospectively analyzed men from 2015 to 2019 with PCa who received linear-accelerator-based SAbR to 45 Gy in 5 fractions, along with perirectal hydrogel spacer, fiducial placement, and MRI-based planning. Disease control outcomes were calculated from end of treatment. Minimally important difference (MID) assessing patient-reported quality of life was defined as greater than a one-half standard deviation increase in American Urological Association (AUA) symptom score after SAbR. Results: Two-hundred and forty-nine (249) low-, intermediate-, and high-risk PCa patients with median follow-up of 14.9 months for clinical toxicity were included. Acute urinary grade II toxicity occurred in 20.4% of patients. Acute grade II GI toxicity occurred in 7.3% of patients. For follow-up > 2 years (n = 69), late GU and GI grade ≥III toxicity occurred in 5.8% and 1.5% of patients, respectively. MID was evident in 31.8%, 23.4%, 35.8%, 37.0%, 33.3%, and 26.7% of patients at 3, 6, 12, 24, 36, and 48 months, respectively. The median follow-up for biochemical recurrence was 22.6 months with biochemical failure-free survival of 100% at 1 year (n = 226) and 98.7% for years 2 (n = 113) and 3 (n = 54). Conclusions: SAbR for PCa at 45 Gy in 5 fractions shows an encouraging safety profile. Prospective studies with longer follow-up are warranted to establish this dose regimen as standard of care for PCa.
KW - SBRT (stereotactic body radiation therapy)
KW - dose-intense radiation therapy
KW - gastrointestinal (GI)
KW - genitourinary (GU)
KW - prostate
KW - prostate cancer
KW - stereotactic ablative radiation (SAbR)
KW - toxicity
UR - http://www.scopus.com/inward/record.url?scp=85125853113&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85125853113&partnerID=8YFLogxK
U2 - 10.3389/fonc.2022.779182
DO - 10.3389/fonc.2022.779182
M3 - Article
C2 - 35265519
AN - SCOPUS:85125853113
SN - 2234-943X
VL - 12
JO - Frontiers in Oncology
JF - Frontiers in Oncology
M1 - 779182
ER -