School of Biomedical Engineering and Imaging Sciences, King's College London and Guy's and St. Thomas' PET Centre, King's College London, King's Health Partners, London, United Kingdom;
Department of Haematology, Royal Marsden NHS Foundation Trust, London, United Kingdom.
J Nucl Med. 2022 Aug;63(8):1149-1154. doi: 10.2967/jnumed.121.262869. Epub 2021 Dec 2.
Complete metabolic response (CMR) on PET/CT was the sole independent predictor of overall survival in the PET substudy of the phase III GALLIUM trial (NCT01332968) in first-line treatment of high-tumor-burden follicular lymphoma. The aim of this analysis was to further investigate the outcome of patients not achieving CMR. Two international experts rereviewed PET/CT scans from patients failing to achieve CMR assessed by the Independent Review Committee masked otherwise to committee results. Metabolic response category and Deauville score were assigned. Progression-free survival (PFS) was investigator-assessed with contrast-enhanced CT. Kaplan-Meier methodology was used to estimate landmark PFS and time to next treatment from end of induction by Deauville score. Patients who experienced CT-based progressive disease at the end of induction were excluded. Fifty-four patients were reviewed. Six had CMR, 37 had a partial metabolic response, 2 had no metabolic response, and 9 had progressive metabolic disease. Patients were reassigned to CMR because F-FDG uptake was considered inflammatory ( = 2), was considered incidental neoplasia ( = 2), or was visually close to liver uptake but quantitatively lower ( = 2). There was a trend for shorter PFS and time to next treatment for patients with a Deauville score of 5 than a score of 4. High-grade mesenteric uptake at the end of induction was common, occurring in 20 patients with non-CMR, 14 of whom achieved CMR at all other sites. Only 3 of 14 (21%) patients with mesenteric uptake as the only site of disease experienced progression or death within 24 mo, whereas 4 of 6 patients (67%) with mesenteric and additional sites of F-FDG-avid disease experienced progression or death within 24 mo. All patients with early progression had measurable disease on contrast-enhanced CT at F-FDG-avid sites at the end of induction. After induction immunochemotherapy, CMR was assigned after reassessment in some patients, in whom increased F-FDG uptake was considered due to inflammation or incidental neoplasia rather than to lymphoma. Quantitative assessment to confirm the visual impression of residual uptake in lesions is suggested. Isolated mesenteric F-FDG uptake is likely a common false-positive finding at the end of induction and does not warrant changes in clinical management or disease surveillance unless there is measurable disease on contrast-enhanced CT or clinical suspicion of active disease.
在 III 期 GALLIUM 试验的 PET 子研究中(NCT01332968),PET/CT 上的完全代谢反应(CMR)是一线治疗高肿瘤负荷滤泡淋巴瘤患者总生存的唯一独立预测因素。本分析的目的是进一步研究未达到 CMR 的患者的结果。两名国际专家重新审查了未能达到 CMR 的患者的 PET/CT 扫描,这些患者的 CMR 由独立审查委员会评估,但结果对委员会保密。分配代谢反应类别和 Deauville 评分。无进展生存期(PFS)由研究者使用对比增强 CT 评估。Kaplan-Meier 方法用于根据 Deauville 评分从诱导结束时估计 landmark PFS 和下一次治疗的时间。在诱导结束时经历基于 CT 的疾病进展的患者被排除在外。54 名患者接受了审查。6 名患者达到 CMR,37 名患者达到部分代谢反应,2 名患者无代谢反应,9 名患者出现进展性代谢疾病。由于 F-FDG 摄取被认为是炎症( = 2)、被认为是偶然肿瘤( = 2)或在视觉上接近肝脏摄取但在定量上较低( = 2),患者被重新分配到 CMR。与 Deauville 评分为 4 的患者相比,评分为 5 的患者的 PFS 和下一次治疗时间有缩短的趋势。高等级肠系膜摄取在诱导结束时很常见,在非 CMR 的 20 名患者中发生,其中 14 名在所有其他部位均达到 CMR。只有 14 名肠系膜摄取为唯一疾病部位的患者中有 3 名(21%)在 24 个月内发生进展或死亡,而 6 名肠系膜和其他部位有 F-FDG 摄取的疾病患者中有 4 名(67%)在 24 个月内发生进展或死亡。所有在 F-FDG 摄取部位有可测量疾病的早期进展患者在诱导结束时均在对比增强 CT 上有可见病灶。在诱导免疫化疗后,一些患者在重新评估后被分配 CMR,其中增加的 F-FDG 摄取被认为是由于炎症或偶然肿瘤,而不是淋巴瘤。建议进行定量评估以确认病变中残留摄取的视觉印象。孤立的肠系膜 F-FDG 摄取很可能是诱导结束时常见的假阳性发现,除非在对比增强 CT 上有可测量的疾病或有活动性疾病的临床怀疑,否则不需要改变临床管理或疾病监测。