Department of Nuclear Medicine, Odense University Hospital, Odense, Denmark.
Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
Mol Imaging Biol. 2020 Feb;22(1):33-46. doi: 10.1007/s11307-019-01351-4.
Positron emission tomography/x-ray computed tomography (PET/CT) has long been discussed as a promising modality for response evaluation in cancer. When designing respective clinical trials, several design issues have to be addressed, especially the number/timing of PET/CT scans, the approach for quantifying metabolic activity, and the final translation of measurements into a rule. It is unclear how well these issues have been tackled in quest of an optimised use of PET/CT in response evaluation. Medline via Ovid and Science Citation Index via Web of Science were systematically searched for articles from 2015 on cancer patients scanned with PET/CT before and during/after treatment. Reports were categorised as being either developmental or evaluative, i.e. focusing on either the establishment or the evaluation of a rule discriminating responders from non-responders. Of 124 included papers, 112 (90 %) were accuracy and/or prognostic studies; the remainder were response-curve studies. No randomised controlled trials were found. Most studies were prospective (62 %) and from single centres (85 %); median number of patients was 38.5 (range 5-354). Most (69 %) of the studies employed only one post-baseline scan. Quantification was mainly based on SUVmax (91 %), while change over time was most frequently used to combine measurements into a rule (79 %). Half of the reports were categorised as developmental, the other half evaluative. Most development studies assessed only one element (35/62, 56 %), most frequently the choice of cut-off points (25/62, 40 %). In summary, the majority of studies did not address the essential open issues in establishing PET/CT for response evaluation. Reasonably sized multicentre studies are needed to systematically compare the many different options when using PET/CT for response evaluation.
正电子发射断层扫描/计算机断层扫描(PET/CT)长期以来一直被认为是评估癌症疗效的一种很有前途的方法。在设计相应的临床试验时,必须解决几个设计问题,尤其是 PET/CT 扫描的次数/时间、量化代谢活性的方法以及最终将测量结果转化为规则的方法。目前尚不清楚在寻求优化 PET/CT 在疗效评估中的应用时,这些问题解决得如何。通过 Ovid 平台的 Medline 和 Web of Science 平台的 Science Citation Index 系统地检索了 2015 年以来癌症患者在治疗前后接受 PET/CT 扫描的文章。报告分为发展性或评价性,即关注建立或评价区分应答者和非应答者的规则。在纳入的 124 篇论文中,112 篇(90%)为准确性和/或预后研究;其余为反应曲线研究。未发现随机对照试验。大多数研究为前瞻性(62%),来自单一中心(85%);中位数患者人数为 38.5 人(范围为 5-354 人)。大多数(69%)研究仅使用一次基线后扫描。定量主要基于 SUVmax(91%),而时间变化最常用于将测量结果组合成规则(79%)。一半的报告被归类为发展性,另一半为评价性。大多数发展研究仅评估了一个元素(35/62,56%),最常评估的是截止值的选择(25/62,40%)。总之,大多数研究没有解决在建立用于疗效评估的 PET/CT 方面的关键开放性问题。需要进行合理规模的多中心研究,以系统比较在使用 PET/CT 进行疗效评估时的许多不同选择。