Fischell Department of Bioengineering, University of Maryland, College Park, MD, USA.
Med Phys. 2012 Apr;39(4):2042-8. doi: 10.1118/1.3676690.
To evaluate Hotelling's T(2) statistic and the input variable squared prediction error (Q((X))) for detecting large respiratory surrogate-based tumor displacement prediction errors without directly measuring the tumor's position.
Tumor and external marker positions from a database of 188 Cyberknife Synchrony™ lung, liver, and pancreas treatment fractions were analyzed. The first ten measurements of tumor position in each fraction were used to create fraction-specific models of tumor displacement using external surrogates as input; the models were used to predict tumor position from subsequent external marker measurements. A partial least squares (PLS) model with four scores was developed for each fraction to determine T(2) and Q((X)) confidence limits based on the first ten measurements in a fraction. The T(2) and Q((X)) statistics were then calculated for every set of external marker measurements. Correlations between model error and both T(2) and Q((X)) were determined. Receiver operating characteristic analysis was applied to evaluate sensitivities and specificities of T(2), Q((X)), and T(2)∪Q((X)) for predicting real-time tumor localization errors >3 mm over a range of T(2) and Q((X)) confidence limits.
Sensitivity and specificity of detecting errors >3 mm varied with confidence limit selection. At 95% sensitivity, T(2)∪Q((X)) specificity was 15%, 2% higher than either T(2) or Q((X)) alone. The mean time to alarm for T(2)∪Q((X)) at 95% sensitivity was 5.3 min but varied with a standard deviation of 8.2 min. Results did not differ significantly by tumor site.
The results of this study establish the feasibility of respiratory surrogate-based online monitoring of real-time respiration-induced tumor motion model accuracy for lung, liver, and pancreas tumors. The T(2) and Q((X)) statistics were able to indicate whether inferential model errors exceeded 3 mm with high sensitivity. Modest improvements in specificity were achieved by combining T(2) and Q((X)) results.
评估 Hotelling 的 T(2)统计量和输入变量平方预测误差 (Q((X))),以便在不直接测量肿瘤位置的情况下检测大的基于呼吸的肿瘤位移预测误差。
分析了来自 188 例 Cyberknife Synchrony™肺部、肝脏和胰腺治疗部分的数据库中的肿瘤和外部标记位置。每个部分的前十个肿瘤位置测量值用于使用外部替代物作为输入创建部分特定的肿瘤位移模型;该模型用于从后续的外部标记测量值预测肿瘤位置。为每个部分开发了一个具有四个得分的偏最小二乘 (PLS) 模型,以基于部分中的前十个测量值确定 T(2)和 Q((X))置信限。然后为每组外部标记测量值计算 T(2)和 Q((X))统计量。确定模型误差与 T(2)和 Q((X))之间的相关性。应用接收者操作特征分析评估 T(2)、Q((X))和 T(2)∪Q((X))预测实时肿瘤定位误差>3 毫米的灵敏度和特异性,T(2)和 Q((X))置信限范围。
检测>3 毫米误差的灵敏度和特异性随置信限选择而变化。在 95%灵敏度下,T(2)∪Q((X))特异性为 15%,比 T(2)或 Q((X))单独高 2%。在 95%灵敏度下,T(2)∪Q((X))的平均报警时间为 5.3 分钟,但变化范围为 8.2 分钟。结果不因肿瘤部位而异。
这项研究的结果确立了基于呼吸的在线监测实时呼吸诱导肿瘤运动模型准确性的可行性,用于肺部、肝脏和胰腺肿瘤。T(2)和 Q((X))统计量能够以高灵敏度指示推断模型误差是否超过 3 毫米。通过结合 T(2)和 Q((X))的结果,可以适度提高特异性。