Xu Huijun, Gordon J James, Siebers Jeffrey V
Department of Radiation Oncology, Virginia Commonwealth University, Richmond, Virginia 23298 and Department of Radiation Oncology, University of Maryland, Baltimore, Maryland 21201.
Department of Radiation Oncology, Henry Ford Health System, Detroit, Michigan 48202.
Med Phys. 2015 Sep;42(9):5435-43. doi: 10.1118/1.4928490.
To compare two coverage-based planning (CP) techniques with fixed margin-based (FM) planning for high-risk prostate cancer treatments, with the exclusive consideration of the dosimetric impact of delineation uncertainties of target structures and normal tissues.
In this work, 19-patient data sets were involved. To estimate structure dose for each delineated contour under the influence of interobserver contour variability and CT image quality limitations, 1000 alternative structures were simulated by an average-surface-of-standard-deviation model, which utilized the patient-specific information of delineated structure and CT image contrast. An IMRT plan with zero planning-target-volume (PTV) margin on the delineated prostate and seminal vesicles [clinical-target-volume (CTV prostate) and CTVSV] was created and dose degradation due to contour variability was quantified by the dosimetric consequences of 1000 alternative structures. When D98 failed to achieve a 95% coverage probability objective D98,95 ≥ 78 Gy (CTV prostate) or D98,95 ≥ 66 Gy (CTVSV), replanning was performed using three planning techniques: (1) FM (PTV prostate margin = 4,5,6 mm and PTVSV margin = 4,5,7 mm for RL, PA, and SI directions, respectively), (2) CPOM which optimized uniform PTV margins for CTV prostate and CTVSV to meet the D98,95 objectives, and (3) CPCOP which directly optimized coverage-based objectives for all the structures. These plans were intercompared by computing percentile dose-volume histograms and tumor-control probability/normal tissue complication probability (TCP/NTCP) distributions.
Inherent contour variability resulted in unacceptable CTV coverage for the zero-PTV-margin plans for all patients. For plans designed to accommodate contour variability, 18/19 CP plans were most favored by achieving desirable D98,95 and TCP/NTCP values. The average improvement of probability of complication free control was 9.3% for CPCOP plans and 3.4% for CPOM plans.
When the delineation uncertainties need to be considered for prostate patients, CP techniques can produce more desirable plans than FM plans for most patients. The relative advantages between CPCOP and CPOM techniques are patient specific.
比较两种基于覆盖范围的计划(CP)技术与基于固定边界的(FM)计划在高危前列腺癌治疗中的应用,仅考虑靶区结构和正常组织轮廓勾画不确定性的剂量学影响。
本研究纳入了19例患者的数据集。为了在观察者间轮廓变异性和CT图像质量限制的影响下估计每个勾画轮廓的结构剂量,采用标准差平均表面模型模拟了1000个替代结构,该模型利用了勾画结构的患者特定信息和CT图像对比度。在勾画的前列腺和精囊(临床靶区体积[CTV前列腺]和CTV精囊)上创建了零计划靶区体积(PTV)边界的调强放疗计划,并通过1000个替代结构的剂量学结果量化轮廓变异性导致的剂量下降。当D98未能达到95%覆盖概率目标D98,95≥78 Gy(CTV前列腺)或D98,95≥66 Gy(CTV精囊)时,使用三种计划技术进行重新计划:(1)FM(RL、PA和SI方向的PTV前列腺边界分别为4、5、6 mm,PTV精囊边界分别为4、5、7 mm),(2)CPOM,为CTV前列腺和CTV精囊优化均匀的PTV边界以满足D98,95目标,(3)CPCOP,直接为所有结构优化基于覆盖范围的目标。通过计算百分位数剂量体积直方图和肿瘤控制概率/正常组织并发症概率(TCP/NTCP)分布对这些计划进行相互比较。
对于所有患者,固有轮廓变异性导致零PTV边界计划的CTV覆盖不可接受。对于旨在适应轮廓变异性的计划,18/19个CP计划通过实现理想的D98,95和TCP/NTCP值而最受青睐。CPCOP计划无并发症控制概率的平均改善为9.3%,CPOM计划为3.4%。
当需要考虑前列腺患者的轮廓勾画不确定性时,对于大多数患者,CP技术比FM计划能产生更理想的计划。CPCOP和CPOM技术之间的相对优势因患者而异。