Department of Oncology, Odense University Hospital, Odense, Denmark;
Department of Nuclear Medicine, Odense University Hospital, Odense, Denmark.
J Nucl Med. 2023 Mar;64(3):355-361. doi: 10.2967/jnumed.121.263358. Epub 2022 Oct 7.
This study aimed to compare contrast-enhanced CT (CE-CT) and F-FDG PET/CT for response monitoring in metastatic breast cancer using the standardized response evaluation criteria RECIST 1.1 and PERCIST. The objective was to examine whether progressive disease was detected systematically earlier by one of the modalities. Women with biopsy-verified metastatic breast cancer were enrolled prospectively and monitored using combined CE-CT and F-FDG PET/CT every 9-12 wk to evaluate response to first-line treatment. CE-CT scans and RECIST 1.1 were used for clinical decision-making without accessing the F-FDG PET/CT scans. At study completion, F-FDG PET/CT scans were unmasked and assessed according to PERCIST. Visual assessment was used if response criteria could not be applied. The modality-specific time to progression was defined as the time from the baseline scan until the first scan demonstrating progression. Paired comparative analyses for CE-CT versus F-FDG PET/CT were applied, and the primary endpoint was earlier detection of progression by one modality. Secondary endpoints were time to detection of progression, response categorization, visualization of changes in response over time, and measurable disease according to RECIST and PERCIST. In total, 87 women were evaluable, with a median of 6 (1-11) follow-up scans. Progression was detected first by F-FDG PET/CT in 43 (49.4%) of 87 patients and first by CE-CT in 1 (1.15%) of 87 patients ( < 0.0001). Excluding patients without progression ( = 32), progression was seen first on F-FDG PET/CT in 78.2% (43/55) of patients. The median time from detection of progression by F-FDG PET/CT to that of CE-CT was 6 mo (95% CI, 4.3-6.4 mo). At baseline, 76 (87.4%) of 87 patients had measurable disease according to PERCIST and 51 (58.6%) of 87 patients had measurable disease according to RECIST 1.1. Moreover, F-FDG PET/CT provided improved visualization of changes in response over time, as seen in the graphical abstract. Disease progression was detected earlier by F-FDG PET/CT than by CE-CT in most patients, with a potentially clinically relevant median 6-mo delay for CE-CT. More patients had measurable disease according to PERCIST than according to RECIST 1.1. The magnitude of the final benefit for patients is a perspective for future research.
本研究旨在比较对比增强 CT(CE-CT)和 F-FDG PET/CT 用于使用 RECIST 1.1 和 PERCIST 标准评估转移性乳腺癌的反应监测。目的是检查一种方法是否系统地更早地检测到进展性疾病。
前瞻性入组经活检证实的转移性乳腺癌患者,每 9-12 周使用联合 CE-CT 和 F-FDG PET/CT 监测,以评估一线治疗的反应。CE-CT 扫描和 RECIST 1.1 用于临床决策,而不访问 F-FDG PET/CT 扫描。在研究结束时,对 F-FDG PET/CT 扫描进行去盲并根据 PERCIST 进行评估。如果无法应用反应标准,则使用视觉评估。特定于模态的进展时间定义为从基线扫描到首次显示进展的扫描的时间。应用 CE-CT 与 F-FDG PET/CT 的配对比较分析,主要终点是一种方法更早地检测到进展。次要终点是进展的检测时间、反应分类、随时间推移的反应变化可视化以及根据 RECIST 和 PERCIST 的可测量疾病。
共有 87 名女性可评估,中位随访 6(1-11)次扫描。43(49.4%)名 87 名患者中的 87 名患者首先通过 F-FDG PET/CT 检测到进展,而 87 名患者中的 1 名(1.15%)患者首先通过 CE-CT 检测到进展(<0.0001)。排除无进展患者( = 32),78.2%(43/55)的患者首先通过 F-FDG PET/CT 检测到进展。从 F-FDG PET/CT 检测到进展到 CE-CT 检测到进展的中位时间为 6 个月(95%CI,4.3-6.4 个月)。基线时,根据 PERCIST,87 名患者中的 76 名(87.4%)有可测量的疾病,根据 RECIST 1.1,87 名患者中的 51 名(58.6%)有可测量的疾病。此外,如图所示,F-FDG PET/CT 提供了随时间推移反应变化的更好可视化。
在大多数患者中,F-FDG PET/CT 比 CE-CT 更早检测到疾病进展,CE-CT 的潜在临床相关中位延迟为 6 个月。根据 PERCIST,更多的患者有可测量的疾病,而根据 RECIST 1.1,则较少的患者有可测量的疾病。对于患者的最终获益程度,是未来研究的一个视角。