Wang Rang, Guo Linlin, Pan Lili, Tian Rong, Shen Guohua
Department of Nuclear Medicine, West China Hospital, Sichuan University, Chengdu, China.
Quant Imaging Med Surg. 2023 Oct 1;13(10):6814-6826. doi: 10.21037/qims-23-477. Epub 2023 Aug 31.
The imaging of somatostatin receptors (SSTRs) plays a significant role in imaging neuroendocrine tumors (NETs). However, there has been no clear definition on whether it is necessary to withdraw somatostatin analogs (SSAs) before SSTRs imaging. We aimed to assess whether nonradioactive SSAs affect the uptake of radiolabeled SSAs on imaging for NETs patients.
The databases of PubMed, Embase, and Web of Science (WoS) were searched until March 12, 2022 to identify eligible studies. Maximum standardized uptake values (SUVmax) in tumor and normal tissues were extracted, pooled, and compared before and after SSAs treatment. The change of tumor-to-background/liver ratio was also described. The quality of each study was assessed using the revised Quality Assessment of Diagnostic Accuracy Studies-2 tool.
A total of 9 articles involving 285 patients were included and 5 studies using Gallium-68-labeled [1,4,7,10-tetraazacyclododecane-N,N',N'',N'''-tetraacetic acid]-D-Phe-Tyr-Thr-octreotide (Ga-DOTATATE) were used for pooled evaluation. We found a significantly decreased SUVmax in the liver (9.56±2.47 7.62±2.12, P=0.001) and spleen (25.74±7.14 20.39±6.07, P=0.006) after SSAs treatment whereas no significant differences were observed in the uptake of thyroid, adrenal, and pituitary gland. For either primary tumor sites or metastases, the SUVmax did not change significantly before and after SSAs treatment. The tumor-to-liver/background ratio increased following SSAs therapy. High heterogeneity was observed across the studies, mainly due to inherent diversity of study design, sample size, and scanning technique.
Based on current evidence, long-acting SSAs therapy before imaging has no effect on the uptake of radiolabeled SSAs at tumor primary sites and metastatic lesions, but results in a significant reduction of uptake in the liver and spleen. These findings may implicate the unnecessary discontinuation of SSAs before radiolabeled SSAs imaging.
生长抑素受体(SSTRs)成像在神经内分泌肿瘤(NETs)成像中发挥着重要作用。然而,对于在SSTRs成像前是否有必要停用生长抑素类似物(SSAs),目前尚无明确的定义。我们旨在评估非放射性SSAs是否会影响NETs患者成像时放射性标记的SSAs的摄取。
检索PubMed、Embase和Web of Science(WoS)数据库至2022年3月12日,以确定符合条件的研究。提取、汇总并比较SSAs治疗前后肿瘤组织和正常组织中的最大标准化摄取值(SUVmax)。还描述了肿瘤与背景/肝脏比值的变化。使用修订后的诊断准确性研究质量评估-2工具评估每项研究的质量。
共纳入9篇涉及285例患者的文章,5项使用镓-68标记的[1,4,7,10-四氮杂环十二烷-N,N',N'',N'''-四乙酸]-D-苯丙氨酸-酪氨酸-苏氨酸-奥曲肽(Ga-DOTATATE)的研究用于汇总评估。我们发现SSAs治疗后肝脏(9.56±2.47对7.62±2.12,P = 0.001)和脾脏(25.74±7.14对20.39±6.07,P = 0.006)的SUVmax显著降低,而甲状腺、肾上腺和垂体的摄取未观察到显著差异。对于原发肿瘤部位或转移灶,SSAs治疗前后SUVmax均无显著变化。SSAs治疗后肿瘤与肝脏/背景比值增加。各研究间观察到高度异质性,主要是由于研究设计、样本量和扫描技术的固有差异。
基于目前的证据,成像前的长效SSAs治疗对肿瘤原发部位和转移病灶处放射性标记的SSAs摄取没有影响,但会导致肝脏和脾脏摄取显著降低。这些发现可能意味着在放射性标记的SSAs成像前无需停用SSAs。