Image-guided radiotherapy reduces the risk of under-dosing high-risk prostate cancer extra-capsular disease and improves biochemical control

被引:11
作者
af Rosenschold, Per Munck [1 ,2 ]
Zelefsky, Michael J. [3 ]
Apte, Aditya P. [1 ]
Jackson, Andrew [1 ]
Oh, Jung Hun [1 ]
Shulman, Elliot [3 ]
Desai, Neil [3 ,4 ]
Hunt, Margie [1 ]
Ghadjar, Pirus [3 ]
Yorke, Ellen [1 ]
Deasy, Joseph O. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med Phys, New York, NY 10021 USA
[2] Rigshosp, Dept Radiat Oncol, Copenhagen, Denmark
[3] Mem Sloan Kettering Canc Ctr, Dept Radiat Oncol, 1275 York Ave,Box 22, New York, NY 10065 USA
[4] Univ Texas Southwestern, Dept Radiat Oncol, Dallas, TX USA
关键词
Image-guided; Radiotherapy; Prostate cancer; High risk disease; IMRT; Tumor control probability; CONFORMAL RADIATION-THERAPY; RANDOMIZED CONTROLLED-TRIAL; DOSE-RESPONSE; RADICAL PROSTATECTOMY; 68; GY; EXTENSION; FAILURE; IMPACT; ESCALATION; OUTCOMES;
D O I
10.1186/s13014-018-0978-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: To determine if reduced dose delivery uncertainty is associated with daily image-guidance (IG) and Prostate Specific Antigen Relapse Free Survival (PRFS) in intensity-modulated radiotherapy (IMRT) of high-risk prostate cancer (PCa). Methods: Planning data for consecutive PCa patients treated with IMRT (n = 67) and IG-IMRT (n = 35) was retrieved. Using computer simulations of setup errors, we estimated the patient-specific uncertainty in accumulated treatment dose distributions for the prostate and for posterolateral aspects of the gland that are at highest risk for extra-capsular disease. Multivariate Cox regression for PRFS considering Gleason score, T-stage, pre-treatment PSA, number of elevated clinical risk factors (T2c+, GS7+ and PSA10+), nomogram-predicted risk of extra-capsular disease (ECD), and dose metrics was performed. Results: For IMRT vs. IG-IMRT, plan dosimetry values were similar, but simulations revealed uncertainty in delivered dose external to the prostate was significantly different, due to positioning uncertainties. A patient-specific interaction term of the risk of ECD and risk of low dose to the ECD (p = 0.005), and the number of elevated clinical risk factors (p = 0.008), correlate with reduced PRFS. Conclusions: Improvements in PSA outcomes for high-risk PCa using IG-IMRT vs. IMRT without IG may be due to improved dosimetry for ECD.
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页数:8
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