Shieh Chun-Chien, Caillet Vincent, Dunbar Michelle, Keall Paul J, Booth Jeremy T, Hardcastle Nicholas, Haddad Carol, Eade Thomas, Feain Ilana
Sydney Medical School, The University of Sydney, NSW 2006, Australia.
Phys Med Biol. 2017 Apr 21;62(8):3065-3080. doi: 10.1088/1361-6560/aa6393. Epub 2017 Mar 21.
The ability to monitor tumor motion without implanted markers can potentially enable broad access to more accurate and precise lung radiotherapy. A major challenge is that kilovoltage (kV) imaging based methods are rarely able to continuously track the tumor due to the inferior tumor visibility on 2D kV images. Another challenge is the estimation of 3D tumor position based on only 2D imaging information. The aim of this work is to address both challenges by proposing a Bayesian approach for markerless tumor tracking for the first time. The proposed approach adopts the framework of the extended Kalman filter, which combines a prediction and measurement steps to make the optimal tumor position update. For each imaging frame, the tumor position is first predicted by a respiratory-correlated model. The 2D tumor position on the kV image is then measured by template matching. Finally, the prediction and 2D measurement are combined based on the 3D distribution of tumor positions in the past 10 s and the estimated uncertainty of template matching. To investigate the clinical feasibility of the proposed method, a total of 13 lung cancer patient datasets were used for retrospective validation, including 11 cone-beam CT scan pairs and two stereotactic ablative body radiotherapy cases. The ground truths for tumor motion were generated from the the 3D trajectories of implanted markers or beacons. The mean, standard deviation, and 95th percentile of the 3D tracking error were found to range from 1.6-2.9 mm, 0.6-1.5 mm, and 2.6-5.8 mm, respectively. Markerless tumor tracking always resulted in smaller errors compared to the standard of care. The improvement was the most pronounced in the superior-inferior (SI) direction, with up to 9.5 mm reduction in the 95th-percentile SI error for patients with >10 mm 5th-to-95th percentile SI tumor motion. The percentage of errors with 3D magnitude <5 mm was 96.5% for markerless tumor tracking and 84.1% for the standard of care. The feasibility of 3D markerless tumor tracking has been demonstrated on realistic clinical scenarios for the first time. The clinical implementation of the proposed method will enable more accurate and precise lung radiotherapy using existing hardware and workflow. Future work is focused on the clinical and real-time implementation of this method.
无需植入标记物就能监测肿瘤运动,这有可能使更多人能够获得更准确、精确的肺癌放疗。一个主要挑战是,基于千伏(kV)成像的方法由于二维kV图像上肿瘤可见性较差,很少能够连续跟踪肿瘤。另一个挑战是仅基于二维成像信息估计三维肿瘤位置。这项工作的目的是首次提出一种贝叶斯方法用于无标记肿瘤跟踪,以应对这两个挑战。所提出的方法采用扩展卡尔曼滤波器的框架,该框架结合预测和测量步骤来进行最佳肿瘤位置更新。对于每个成像帧,首先通过呼吸相关模型预测肿瘤位置。然后通过模板匹配测量kV图像上的二维肿瘤位置。最后,根据过去10秒内肿瘤位置的三维分布以及模板匹配的估计不确定性,将预测值和二维测量值相结合。为了研究所提出方法的临床可行性,总共使用了13个肺癌患者数据集进行回顾性验证,包括11对锥形束CT扫描以及两个立体定向消融体部放疗病例。肿瘤运动的真实情况是根据植入标记物或信标的三维轨迹生成的。发现三维跟踪误差的平均值、标准差和第95百分位数分别在1.6 - 2.9毫米、0.6 - 1.5毫米和2.6 - 5.8毫米范围内。与护理标准相比,无标记肿瘤跟踪始终产生较小的误差。在上下(SI)方向上改善最为明显,对于第5至第95百分位数SI肿瘤运动大于10毫米的患者,第95百分位数SI误差最多减少9.5毫米。无标记肿瘤跟踪三维误差幅度<5毫米的百分比为96.5%,护理标准为84.1%。首次在实际临床场景中证明了三维无标记肿瘤跟踪的可行性。所提出方法的临床应用将能够使用现有硬件和工作流程实现更准确、精确的肺癌放疗。未来的工作重点是该方法的临床和实时应用。