Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Med Phys. 2017 Oct;44(10):5089-5095. doi: 10.1002/mp.12334. Epub 2017 Jul 12.
The purpose of this study is to quantify tumor displacement during real-time PET/CT guided biopsy and to investigate correlations between tumor displacement and false-negative results.
19 patients who underwent real-time F-FDG PET-guided biopsy and were found positive for malignancy were included in this study under IRB approval. PET/CT images were acquired for all patients within minutes prior to biopsy to visualize the FDG-avid region and plan the needle insertion. The biopsy needle was inserted and a post-insertion CT scan was acquired. The two CT scans acquired before and after needle insertion were registered using a deformable image registration (DIR) algorithm. The DIR deformation vector field (DVF) was used to calculate the mean displacement between the pre-insertion and post-insertion CT scans for a region around the tip of the biopsy needle. For 12 patients one biopsy core from each was tracked during histopathological testing to investigate correlations of the mean displacement between the two CT scans and false-negative or true-positive biopsy results. For 11 patients, two PET scans were acquired; one at the beginning of the procedure, pre-needle insertion, and an additional one with the needle in place. The pre-insertion PET scan was corrected for intraprocedural motion by applying the DVF. The corrected PET was compared with the post-needle insertion PET to validate the correction method.
The mean displacement of tissue around the needle between the pre-biopsy CT and the postneedle insertion CT was 5.1 mm (min = 1.1 mm, max = 10.9 mm and SD = 3.0 mm). For mean displacements larger than 7.2 mm, the biopsy cores gave false-negative results. Correcting pre-biopsy PET using the DVF improved the PET/CT registration in 8 of 11 cases.
The DVF obtained from DIR of the CT scans can be used for evaluation and correction of the error in needle placement with respect to the FDG-avid area. Misregistration between the pre-biopsy PET and the CT acquired with the needle in place was shown to correlate with false negative biopsy results.
本研究旨在量化实时 PET/CT 引导活检过程中的肿瘤移位,并探讨肿瘤移位与假阴性结果之间的相关性。
本研究经机构审查委员会批准,共纳入 19 例在实时 F-FDG PET 引导活检中发现恶性肿瘤的患者。所有患者均在活检前数分钟内进行 PET/CT 扫描,以可视化 FDG 摄取区域并规划穿刺针插入路径。插入活检针后,立即进行 CT 扫描。使用可变形图像配准(DIR)算法对插入前后的两次 CT 扫描进行配准。使用 DIR 变形向量场(DVF)计算活检针尖端周围区域的预插入和后插入 CT 扫描之间的平均位移。对 12 例患者,在组织病理学检查中对每个活检样本的一个核心进行了跟踪,以研究两次 CT 扫描之间的平均位移与假阴性或真阳性活检结果的相关性。对 11 例患者,进行了两次 PET 扫描;一次在手术开始前,即针插入前,另一次在针插入后。通过应用 DVF 对术中运动进行校正,对针插入前的 PET 进行校正。将校正后的 PET 与针插入后的 PET 进行比较,以验证校正方法。
活检前 CT 和针插入后 CT 之间针周围组织的平均位移为 5.1mm(最小值为 1.1mm,最大值为 10.9mm,标准差为 3.0mm)。对于大于 7.2mm 的平均位移,活检样本的结果为假阴性。使用 DVF 校正针插入前的 PET 可改善 11 例中的 8 例 PET/CT 配准。
从 CT 扫描的 DIR 获得的 DVF 可用于评估和校正 FDG 摄取区域的针放置误差。在针插入后的 CT 与针插入前的 PET 之间的配准错误与假阴性活检结果相关。