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用于增强由磁共振波谱成像定义的前列腺内主要病灶的高剂量率前列腺近距离治疗逆向计划。

Inverse planning for HDR prostate brachytherapy used to boost dominant intraprostatic lesions defined by magnetic resonance spectroscopy imaging.

作者信息

Pouliot Jean, Kim Yongbok, Lessard Etienne, Hsu I-Chow, Vigneron Daniel B, Kurhanewicz John

机构信息

Department of Radiation Oncology, University of California San Francisco, 1600 Divisadero Street, Suite H1031, San Francisco, CA 94143-1708, USA.

出版信息

Int J Radiat Oncol Biol Phys. 2004 Jul 15;59(4):1196-207. doi: 10.1016/j.ijrobp.2004.02.055.

Abstract

PURPOSE

To dose escalate selected regions inside the prostate without compromising the dose coverage of the prostate and the protection to the urethra, rectum, and bladder for prostate cancer patients treated with high-dose-rate brachytherapy.

METHODS AND MATERIALS

Magnetic resonance imaging combined with magnetic resonance spectroscopy imaging was used to differentiate between normal and malignant prostate and define cancer-validated dominant intraprostatic lesions (DIL) on 10 patients. The DILs were then contoured on the planning scans (CT or MRI based, 5 patients each), and our inverse planning dose optimization algorithm (called IPSA) was used to generate dose distributions for 3 different boost levels. Dose-volume histograms of the target and each organ at risk were compared with optimized plans without DIL boost.

RESULTS

Combined MRI/magnetic resonance spectroscopic imaging identified 2 DILs in 8/10 of the 10 patients studied and a single DIL in the remaining 2 patients. The average prostate dose coverage V100 was 97% (sigma = 1.0%). When the minimum DIL dose requested was 120% of the prescribed dose, the average DIL V120 was 97.1% (sigma = 1.8%). For a boost value of 150%, the average V150 ranged from 77.8% to 86.1%, depending on the upper limit of the dose constraints. The bladder V50 increased by 1%, independently of the boost levels. The absolute increases in V50 for the rectum varied from 1% to 3%, depending on the boost level. The urethra V120 were increased by 13.4% and 32.5% for the lowest and highest boost levels, respectively.

CONCLUSION

The DIL dose can be escalated to a minimum of 120% while the entire prostate is treated simultaneously, without increasing the dose to surrounding normal tissues. Higher boost levels between 150% and 170% are feasible, but with slightly larger doses delivered to the rectum and urethra.

摘要

目的

在不影响前列腺癌患者高剂量率近距离放射治疗中前列腺剂量覆盖以及对尿道、直肠和膀胱保护的前提下,逐步增加前列腺内选定区域的剂量。

方法和材料

利用磁共振成像结合磁共振波谱成像对10例患者的正常前列腺和恶性前列腺进行区分,并确定经癌症验证的前列腺内主要病变(DIL)。然后在计划扫描(基于CT或MRI,各5例患者)上勾勒出DIL的轮廓,并使用我们的逆向计划剂量优化算法(称为IPSA)生成3种不同增加剂量水平的剂量分布。将靶区和每个危及器官的剂量体积直方图与未进行DIL增加剂量的优化计划进行比较。

结果

在研究的10例患者中,8例患者通过磁共振成像/磁共振波谱成像联合检查发现2个DIL,其余2例患者发现1个DIL。前列腺平均剂量覆盖V100为97%(标准差=1.0%)。当要求的最小DIL剂量为处方剂量的120%时,平均DIL V120为97.1%(标准差=1.8%)。对于150%的增加剂量值,平均V150范围为77.8%至86.1%,具体取决于剂量限制的上限。膀胱V50增加了1%,与增加剂量水平无关。直肠V50的绝对增加量因增加剂量水平而异,从1%到3%不等。尿道V120在最低和最高增加剂量水平时分别增加了13.4%和32.5%。

结论

在同时治疗整个前列腺的情况下,DIL剂量可逐步增加至至少120%,而不会增加周围正常组织的剂量。150%至170%之间的更高增加剂量水平是可行的,但会使直肠和尿道接受稍大的剂量。

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