Gondi Vinai, Cui Yunfeng, Mehta Minesh P, Manfredi Denise, Xiao Ying, Galvin James M, Rowley Howard, Tome Wolfgang A
Cadence Brain Tumor Center and CDH Proton Center, Warrenville, Illinois; University of Wisconsin School of Medicine & Public Health, Madison, Wisconsin.
Duke University School of Medicine, Durham, North Carolina.
Int J Radiat Oncol Biol Phys. 2015 Mar 1;91(3):564-70. doi: 10.1016/j.ijrobp.2014.10.054. Epub 2015 Jan 10.
RTOG 0933 was a phase II trial of hippocampal avoidance during whole brain radiation therapy for patients with brain metastases. The results demonstrated improvement in short-term memory decline, as compared with historical control individuals, and preservation of quality of life. Integral to the conduct of this trial were quality assurance processes inclusive of pre-enrollment credentialing and pretreatment centralized review of enrolled patients.
Before enrolling patients, all treating physicians and sites were required to successfully complete a "dry-run" credentialing test. The treating physicians were credentialed based on accuracy of magnetic resonance imaging-computed tomography image fusion and hippocampal and normal tissue contouring, and the sites were credentialed based on protocol-specified dosimetric criteria. Using the same criteria, pretreatment centralized review of enrolled patients was conducted. Physicians enrolling 3 consecutive patients without unacceptable deviations were permitted to enroll further patients without pretreatment review, although their cases were reviewed after treatment.
In all, 113 physicians and 84 sites were credentialed. Eight physicians (6.8%) failed hippocampal contouring on the first attempt; 3 were approved on the second attempt. Eight sites (9.5%) failed intensity modulated radiation therapy planning on the first attempt; all were approved on the second attempt. One hundred thirteen patients were enrolled in RTOG 0933; 100 were analyzable. Eighty-seven cases were reviewed before treatment; 5 (5.7%) violated the eligibility criteria, and 21 (24%) had unacceptable deviations. With feedback, 18 cases were approved on the second attempt and 2 cases on the third attempt. One patient was treated off protocol. Twenty-two cases were reviewed after treatment; 1 (4.5%) violated the eligibility criteria, and 5 (23%) had unacceptable deviations.
Although >95% of the cases passed the pre-enrollment credentialing, the pretreatment centralized review disqualified 5.7% of reviewed cases, prevented unacceptable deviations in 24% of reviewed cases, and limited the final unacceptable deviation rate to 5%. Thus, pretreatment review is deemed necessary in future hippocampal avoidance trials and is potentially useful in other similarly challenging radiation therapy technique trials.
RTOG 0933是一项针对脑转移瘤患者在全脑放射治疗期间进行海马回避的II期试验。结果表明,与历史对照个体相比,短期记忆衰退有所改善,且生活质量得以保留。该试验的实施不可或缺的是质量保证流程,包括入组前资格认定和对入组患者的治疗前集中审查。
在入组患者之前,所有治疗医师和治疗地点都必须成功完成一次“预演”资格认定测试。治疗医师根据磁共振成像 - 计算机断层扫描图像融合的准确性以及海马和正常组织轮廓的勾画情况进行资格认定,治疗地点则根据方案规定的剂量学标准进行资格认定。使用相同标准对入组患者进行治疗前集中审查。连续纳入3例无不可接受偏差的患者的医师,在未经治疗前审查的情况下可进一步纳入患者,不过他们的病例在治疗后会进行审查。
共有113名医师和84个治疗地点获得资格认定。8名医师(6.8%)首次尝试时海马轮廓勾画失败;3名在第二次尝试时获得批准。8个治疗地点(9.5%)首次尝试时调强放射治疗计划失败;均在第二次尝试时获得批准。113例患者入组RTOG 0933;100例可进行分析。87例病例在治疗前进行了审查;5例(5.7%)不符合入选标准,21例(24%)存在不可接受的偏差。经过反馈,18例在第二次尝试时获得批准,2例在第三次尝试时获得批准。1例患者未按方案治疗。22例病例在治疗后进行了审查;1例(4.5%)不符合入选标准,5例(23%)存在不可接受的偏差。
尽管超过95%的病例通过了入组前资格认定,但治疗前集中审查使5.7%的审查病例不合格,在24%的审查病例中防止了不可接受的偏差,并将最终不可接受偏差率限制在5%。因此,治疗前审查在未来的海马回避试验中被认为是必要的,并且可能在其他同样具有挑战性的放射治疗技术试验中有用。