Rachinger Walter, Stoecklein Veit M, Terpolilli Nicole A, Haug Alexander R, Ertl Lorenz, Pöschl Julia, Schüller Ulrich, Schichor Christian, Thon Niklas, Tonn Jörg-Christian
Department of Neurosurgery, University of Munich, Munich, Germany
Department of Neurosurgery, University of Munich, Munich, Germany.
J Nucl Med. 2015 Mar;56(3):347-53. doi: 10.2967/jnumed.114.149120. Epub 2015 Jan 29.
Meningiomas are known to express somatostatin receptor 2 (SSTR2). PET using the SSTR2 analog (68)Ga-DOTATATE has recently been introduced for imaging of meningiomas. However, a systematic correlation between (68)Ga-DOTATATE uptake, SSTR2 expression, and histology (including tumor-free scar tissue) is still lacking. For elucidation, we conducted this prospective study.
Twenty-one adult patients with primary (n = 12) or recurrent (n = 9) meningiomas were prospectively enrolled. Preoperative MR imaging and (68)Ga-DOTATATE PET scans were fused and used for a spatially precise neuronavigated tissue-sampling procedure during tumor resection. Histopathologic diagnosis included immunohistochemical determination of SSTR2 expression. At each individual sampling site, the maximum standardized uptake value (SUVmax) of (68)Ga-DOTATATE was correlated with MR imaging findings, histology, and semiquantitative SSTR2 expression.
One hundred fifteen samples (81 tumor, 34 tumor-free) were obtained. There was a significant positive correlation between SUVmax and SSTR2 expression. Receiver-operating characteristic analysis revealed a threshold of 2.3 for SUVmax to discriminate between tumor and nontumoral tissue. Regarding the detection of tumor tissue, PET imaging showed a higher sensitivity (90% vs. 79%; P = 0.049), with specificity and positive predictive values similar to MR imaging, for both de novo and recurrent tumors.
(68)Ga-DOTATATE uptake correlates with SSTR2 expression and offers high diagnostic accuracy to delineate meningioma from tumor-free tissue even in recurrent tumors after previous therapy. Our findings substantiate an important role for (68)Ga-DOTATATE PET in meningioma management.
已知脑膜瘤表达生长抑素受体2(SSTR2)。最近已引入使用SSTR2类似物(68)Ga - DOTATATE的PET用于脑膜瘤成像。然而,(68)Ga - DOTATATE摄取、SSTR2表达与组织学(包括无肿瘤瘢痕组织)之间仍缺乏系统的相关性。为了阐明这一点,我们进行了这项前瞻性研究。
前瞻性纳入21例患有原发性(n = 12)或复发性(n = 9)脑膜瘤的成年患者。术前将MR成像和(68)Ga - DOTATATE PET扫描融合,并用于肿瘤切除期间在空间上精确的神经导航组织采样程序。组织病理学诊断包括SSTR2表达的免疫组化测定。在每个单独的采样部位,(68)Ga - DOTATATE的最大标准化摄取值(SUVmax)与MR成像结果、组织学和半定量SSTR2表达相关。
共获得115个样本(81个肿瘤样本,34个无肿瘤样本)。SUVmax与SSTR2表达之间存在显著正相关。受试者操作特征分析显示,SUVmax区分肿瘤组织和非肿瘤组织的阈值为2.3。对于肿瘤组织的检测,PET成像显示出更高的灵敏度(90%对79%;P = 0.049),对于初发和复发性肿瘤,其特异性和阳性预测值与MR成像相似。
(68)Ga - DOTATATE摄取与SSTR2表达相关,即使对于先前接受过治疗的复发性肿瘤,也能提供高诊断准确性以区分脑膜瘤与无肿瘤组织。我们的研究结果证实了(68)Ga - DOTATATE PET在脑膜瘤管理中的重要作用。