Long-term outcome of magnetic resonance spectroscopic image-directed dose escalation for prostate brachytherapy

被引:9
|
作者
King, Martin T. [1 ]
Nasser, Nicola J. [1 ]
Mathur, Nitin [2 ]
Cohen, Gil'ad N. [2 ]
Kollmeier, Marisa A. [1 ]
Yuen, Jasper [3 ]
Vargas, Hebert A. [4 ]
Pei, Xin [1 ]
Yamada, Yoshiya [1 ]
Zakian, Kristen L. [2 ]
Zaider, Marco [2 ]
Zelefsky, Michael J. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Radiat Oncol, 1275 York Ave, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Med Phys, 1275 York Ave, New York, NY 10065 USA
[3] Carlo Fidani Reg Canc Ctr, Dept Radiat Oncol, Mississauga, ON, Canada
[4] Mem Sloan Kettering Canc Ctr, Dept Radiol, 1275 York Ave, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
MR spectroscopy; Prostate; Brachytherapy; Dose escalation; DOMINANT INTRAPROSTATIC LESIONS; DISTANT METASTASES; RADIATION-THERAPY; TUMOR-CONTROL; CANCER; IMPLANTATION; BOOST; RADIOTHERAPY; FEASIBILITY; TOXICITY;
D O I
10.1016/j.brachy.2016.02.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE: To report the long-term control and toxicity outcomes of patients with clinically localized prostate cancer, who underwent low-dose-rate prostate brachytherapy with magnetic resonance spectroscopic image (MRSI) directed dose escalation to intraprostatic regions. METHODS AND MATERIALS: Forty-seven consecutive patients between May 2000 and December 2003 were analyzed retrospectively. Each patient underwent a preprocedural MRSI, and MRS-positive voxels suspicious for malignancy were identified. Intraoperative planning was used to determine the optimal seed distribution to deliver a standard prescription dose to the entire prostate, while escalating the dose to MRS-positive voxels to 150% of prescription. Each patient underwent transperineal implantation of radioactive seeds followed by same-day CT for postimplant dosimetry. RESULTS: The median prostate D-90 (minimum dose received by 90% of the prostate) was 125.7% (interquartile range [IQR], 110.3-136.5%) of prescription. The median value for the MRS-positive mean dose was 229.9% (IQR, 200.0-251.9%). Median urethra D-30 and rectal D-30 values were 142.2% (137.5-168.2%) and 56.1% (40.1-63.4%), respectively. Median followup was 86.4 months (IQR, 49.8-117.6). The 10-year actuarial prostate-specific antigen relapse-free survival was 98% (95% confidence interval, 93-100%). Five patients (11%) experienced late Grade 3 urinary toxicity (e.g., urethral stricture), which improved after operative intervention. Four of these patients had dose-escalated voxels less than 1.0 cm from the urethra. CONCLUSIONS: Low-dose-rate brachytherapy with MRSI-directed dose escalation to suspicious intraprostatic regions exhibits excellent long-term biochemical control. Patients with dose-escalated voxels close to the urethra were at higher risk of late urinary stricture. (C) 2016 American Brachytherapy Society. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:266 / 273
页数:8
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