Holmes Oliver E, Gratton Julie, Szanto Janos, Vandervoort Eric, Doody Janice, Henderson Elizabeth, Morgan Scott C, O'Sullivan Joseph, Malone Shawn
Division of Radiation Oncology, Dr. H. Bliss Murphy Cancer Centre, St. John's NL, Canada.
Faculty of Medicine, Memorial University of Newfoundland, St. John's NL, Canada.
J Radiosurg SBRT. 2018;5(3):217-227.
Ultra-hypofractionated radiotherapy with SBRT is an established technique for treating localized prostate cancer. CyberKnife based SBRT requires implantation of fiducial markers for soft tissue target tracking by the orthogonal KV X-ray imaging system. The spatial distribution of fiducial markers must allow accurate calculation of a 3D transformation that describes the position of the prostate within the reference frame of the planning CT scan. Accuray provides a fiducial implantation guideline for tracking soft tissue lesions. Despite using the guideline we experienced an unacceptably high rate of rotational tracking failure due to problems with fiducial placement. We adapted the Accuray guideline to prostate SBRT for improved fiducial placement and more reliable target tracking.Methods and materials: 54 patients with prostate adenocarcinoma were treated with ultra-hypofractionated radiotherapy on CyberKnife. Patients had platinum fiducial markers implanted transrectally under ultrasound guidance by a Radiologist. For the first 26 patients, fiducial markers were positioned following the Accuray fiducial placement guidelines for soft tissue lesions (cohort 1). The initial rotational tracking error rate was unacceptably high (23%). On review, inappropriate fiducial placement was identified as the cause of error (especially insufficient spacing between seeds). In October 2016 we developed a seed placement protocol specifically for implanting fiducial markers within the prostate and a second cohort of patients was treated thereafter (cohort 2, 28 patients). The stipulations of the original guideline are maintained while the modified protocol requires that 4 fiducial markers be implanted in the postero-lateral peripheral zone in a single coronal plane.
In cohort 1, patients had a median age of 64 years (50 - 74), PSA of 6.6mcg/L (1.1 - 14.7), and prostate volume of 56 cc (22 - 125), while in cohort 2 they had a mean age of 65 years (53 - 75), PSA of 6.2 mcg/L (1 - 12) and prostate volume of 47 cc (21 - 106). The fiducial markers were easily visualized and there were no cases of urosepsis related to fiducial implantation. In 6 of 26 patients (23%) from cohort 1, only translational mapping without accurate spatial rotations could be calculated. After adopting the prostate specific fiducial implantation protocol, rotational tracking error was eliminated. Accurate 6 degree tracking (accounting for translations and rotations) was achieved in all 28 patients from cohort 2. Using an in-house computer script we analyzed the dose distributions resulting from rotational misalignments of -10, -5, -3, 3, 5, and 10 degrees along all three rotational axes (pitch, roll and yaw). Rotational misalignments result in decreased minimum dose to the PTV and increased maximum dose to OARs.
Implementing a prostate specific fiducial placement protocol for SBRT significantly improved our ability to track prostate motion in 6 degrees 77% to 100% reliability. Failure to track rotations can potentially lead to underdosing and overdosing of portions of the prostate and OARs respectively.
采用立体定向体部放疗(SBRT)的超分割放疗是治疗局限性前列腺癌的成熟技术。基于射波刀的SBRT需要植入基准标记物,以便通过正交千伏X射线成像系统对软组织靶区进行跟踪。基准标记物的空间分布必须能够准确计算出一个三维变换,该变换描述了前列腺在计划CT扫描参考框架内的位置。Accuray提供了用于跟踪软组织病变的基准植入指南。尽管遵循了该指南,但由于基准放置问题,我们仍经历了不可接受的高旋转跟踪失败率。我们对Accuray指南进行了调整,以用于前列腺SBRT,从而改善基准放置并实现更可靠的靶区跟踪。
54例前列腺腺癌患者接受了射波刀超分割放疗。患者在超声引导下由放射科医生经直肠植入铂基准标记物。对于前26例患者,基准标记物按照Accuray软组织病变基准放置指南进行定位(队列1)。初始旋转跟踪误差率高得不可接受(23%)。经检查,发现不合适的基准放置是误差原因(尤其是籽源之间间距不足)。2016年10月,我们制定了专门用于在前列腺内植入基准标记物的籽源放置方案,此后对第二批患者进行了治疗(队列2,28例患者)。在维持原指南规定同时,修改后的方案要求在单个冠状平面的后外侧周边区植入4个基准标记物。
队列1患者的中位年龄为64岁(50 - 74岁),前列腺特异性抗原(PSA)为6.6μg/L(1.1 - 14.7),前列腺体积为56立方厘米(22 - 125);而队列2患者的平均年龄为65岁(53 - 75岁), PSA为6.2μg/L(1 - 12),前列腺体积为47立方厘米(21 - 106)。基准标记物易于显影,且没有与基准植入相关的尿脓毒症病例。队列1的26例患者中有6例(23%)只能计算出无精确空间旋转的平移映射。采用前列腺特异性基准植入方案后,旋转跟踪误差得以消除。队列2的所有28例患者均实现了精确的6度跟踪(包括平移和旋转)。我们使用内部计算机脚本分析了沿所有三个旋转轴(俯仰、横滚和偏航)-10度、-5度、-3度、3度、5度和10度的旋转错位所导致的剂量分布。旋转错位会导致计划靶体积(PTV)的最小剂量降低,危及器官(OARs)的最大剂量增加。
为SBRT实施前列腺特异性基准放置方案显著提高了我们以77%至100%的可靠性跟踪前列腺6度运动的能力。无法跟踪旋转可能分别导致前列腺部分区域剂量不足和OARs剂量过量。