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图像引导的自适应放射治疗(IGART):前列腺局限性癌的放射生物学和剂量递增考量

Image-guided adaptive radiation therapy (IGART): Radiobiological and dose escalation considerations for localized carcinoma of the prostate.

作者信息

Song William, Schaly Bryan, Bauman Glenn, Battista Jerry, Van Dyk Jake

机构信息

Department of Medical Biophysics, University of Western Ontario, and Radiation Treatment Program, London Regional Cancer Program, London Health Sciences Centre, London, Ontario, Canada.

Department of Oncology, University of Western Ontario, and Radiation Treatment Program, London Regional Cancer Program, London Health Sciences Centre, London, Ontario, Canada.

出版信息

Med Phys. 2005 Jul;32(7Part1):2193-2203. doi: 10.1118/1.1935775.

Abstract

The goal of this work was to evaluate the efficacy of various image-guided adaptive radiation therapy (IGART) techniques to deliver and escalate dose to the prostate in the presence of geometric uncertainties. Five prostate patients with 15-16 treatment CT studies each were retrospectively analyzed. All patients were planned with an 18 MV, six-field conformal technique with a 10 mm margin size and an initial prescription of 70 Gy in 35 fractions. The adaptive strategy employed in this work for patient-specific dose escalation was to increase the prescription dose in 2 Gy-per-fraction increments until the rectum normal tissue complication probability (NTCP) reached a level equal to that of the nominal plan NTCP (i.e., iso-NTCP dose escalation). The various target localization techniques simulated were: (1) daily laser-guided alignment to skin tattoo marks that represents treatment without image-guidance, (2) alignment to bony landmarks with daily portal images, and (3) alignment to the clinical target volume (CTV) with daily CT images. Techniques (1) and (3) were resimulated with a reduced margin size of 5 mm to investigate further dose escalation. When delivering the original clinical prescription dose of 70 Gy in 35 fractions, the "CTV registration" technique yielded the highest tumor control probability (TCP) most frequently, followed by the "bone registration" and "tattoo registration" techniques. However, the differences in TCP among the three techniques were minor when the margin size was 10 mm (⩽1.1%). Reducing the margin size to 5 mm significantly degraded the TCP values of the "tattoo registration" technique in two of the five patients, where a large difference was found compared to the other techniques (⩽11.8%). The "CTV registration" technique, however, did maintain similar TCP values compared to their 10 mm margin counterpart. In terms of normal tissue sparing, the technique producing the lowest NTCP varied from patient to patient. Reducing the margin size seemed the only sure way to reduce the NTCP significantly, irrespective of the IGART technique employed. In escalating the dose with the iso-NTCP constraint, the largest average gain in dose was observed with the "tattoo registration" technique, followed by the "CTV registration" and "bone registration" techniques. This is attributed to the fact that in three of the five patients, the "tattoo registration" technique yielded the lowest NTCP, hence a greater window of opportunity to escalate the dose was possible with this technique. However, the variation among the five patients was also largest with the "tattoo registration" technique where, in the case of one patient, the required dose actually needed to be below the original prescription dose of 70 Gy to satisfy the iso-NTCP constraint. This was not the case with the "CTV registration" technique where positive and similar dose escalation was allowed on all five patients. Based on these data, an attractive dose escalation strategy may be to implement the "CTV registration" technique (for consistent dosimetric coverage) for daily target localization in combination with a margin reduction (for increased normal tissue sparing).

摘要

这项工作的目标是评估各种图像引导自适应放射治疗(IGART)技术在存在几何不确定性的情况下向前列腺输送并增加剂量的疗效。对五名前列腺癌患者进行了回顾性分析,每名患者有15 - 16次治疗CT研究。所有患者均采用18 MV六野适形技术进行计划,边缘大小为10 mm,初始处方剂量为70 Gy,分35次照射。本研究中用于患者特异性剂量增加的自适应策略是每次以2 Gy的增量增加处方剂量,直到直肠正常组织并发症概率(NTCP)达到与标称计划NTCP相等的水平(即等NTCP剂量增加)。模拟的各种靶区定位技术包括:(1)每日激光引导对准皮肤纹身标记,代表无图像引导的治疗;(2)通过每日射野图像对准骨性标志;(3)通过每日CT图像对准临床靶区(CTV)。对技术(1)和(3)进行重新模拟,将边缘大小减小至5 mm,以进一步研究剂量增加情况。当给予35次分割的原始临床处方剂量70 Gy时,“CTV配准”技术最常产生最高的肿瘤控制概率(TCP),其次是“骨配准”和“纹身配准”技术。然而,当边缘大小为10 mm时,这三种技术之间的TCP差异很小(≤1.1%)。在五名患者中的两名患者中,将边缘大小减小至5 mm显著降低了“纹身配准”技术的TCP值,与其他技术相比差异很大(≤11.8%)。然而,“CTV配准”技术与10 mm边缘的对应技术相比,确实保持了相似的TCP值。在正常组织保护方面,产生最低NTCP的技术因患者而异。无论采用何种IGART技术,减小边缘大小似乎是显著降低NTCP的唯一可靠方法。在等NTCP约束下增加剂量时,“纹身配准”技术观察到最大的平均剂量增加,其次是“CTV配准”和“骨配准”技术。这归因于在五名患者中的三名患者中,“纹身配准”技术产生了最低的NTCP,因此该技术有更大的剂量增加机会窗口。然而,“纹身配准”技术在五名患者中的变化也最大,在一名患者的情况下,为满足等NTCP约束,所需剂量实际上需要低于原始处方剂量70 Gy。“CTV配准”技术则不然,所有五名患者都允许正向且相似的剂量增加。基于这些数据,一种有吸引力的剂量增加策略可能是实施“CTV配准”技术(用于一致的剂量覆盖)进行每日靶区定位,并结合减小边缘(用于增加正常组织保护)。

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