首页> 外文期刊>EJNMMI Research >The role of [ 68?Ga]Ga-DOTATATE PET/CT in wild-type KIT/ PDGFRA gastrointestinal stromal tumours (GIST)
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The role of [ 68?Ga]Ga-DOTATATE PET/CT in wild-type KIT/ PDGFRA gastrointestinal stromal tumours (GIST)

机译:[ 68 pe] ga-dotatate pET / ct在野生型 kit / <斜体> pdgfra 胃肠道基质肿瘤(GIST)中的作用

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Background [ ~(68)?Ga]Ga-DOTATATE PET/CT is now recognised as the most sensitive functional imaging modality for the diagnosis of well-differentiated neuroendocrine tumours (NET) and can inform treatment with peptide receptor radionuclide therapy with [ ~(177)Lu]Lu-DOTATATE. However, somatostatin receptor (SSTR) expression is not unique to NET, and therefore, [ ~(68)?Ga]Ga-DOTATATE PET/CT may have oncological application in other tumours. Molecular profiling of gastrointestinal stromal tumours that lack activating somatic mutations in KIT or PDGFRA or so-called ‘wild-type’ GIST (wtGIST) has demonstrated that wtGIST and NET have overlapping molecular features and has encouraged exploration of shared therapeutic targets, due to a lack of effective therapies currently available for metastatic wtGIST. Aims To investigate (i) the diagnostic role of [ ~(68)?Ga]Ga-DOTATATE PET/CT; and, (ii) to investigate the potential of this imaging modality to guide treatment with [ ~(177)Lu]Lu-DOTATATE in patients with wtGIST. Methods [ ~(68)?Ga]Ga-DOTATATE PET/CT was performed on 11 patients with confirmed or metastatic wtGIST and one patient with a history of wtGIST and a mediastinal mass suspicious for metastatic wtGIST, who was subsequently diagnosed with a metachronous mediastinal paraganglioma. Tumour expression of somatostatin receptor subtype 2 (SSTR2) using immunohistochemistry was performed on 54 tumour samples including samples from 8/12 (66.6%) patients who took part in the imaging study and 46 tumour samples from individuals not included in the imaging study. Results [ ~(68)?Ga]Ga-DOTATATE PET/CT imaging was negative, demonstrating that liver metastases had lower uptake than background liver for nine cases (9/12 cases, 75%) and heterogeneous uptake of somatostatin tracer was noted for two cases (16.6%) of wtGIST. However, [ ~(68)?Ga]Ga-DOTATATE PET/CT demonstrated intense tracer uptake in a synchronous paraganglioma in one case and a metachronous paraganglioma in another case with wtGIST. Conclusions Our data suggest that SSTR2 is not a diagnostic or therapeutic target in wtGIST. [ ~(68)?Ga]Ga-DOTATATE PET/CT may have specific diagnostic utility in differentiating wtGIST from other primary tumours such as paraganglioma in patients with sporadic and hereditary forms of wtGIST.
机译:背景[〜(68)?Ga-dotatate PET / CT现在被认为是用于诊断良好分化的神经内分泌肿瘤(净)的最敏感的功能成像模型,并且可以通过肽受体放射性核素治疗( 177)Lu] Lu-Dotatate。然而,生长抑素受体(SSTR)表达不是净独特的,因此,[〜(68)α-Ga-dotatate PET / CT可能在其他肿瘤中具有肿瘤学应用。缺乏激活试剂盒或PDGFRA或所谓的“野生型”或者WTGIST)缺乏激活体细胞突变的胃肠突变的分子分析已经证明了WTGIST和NET具有重叠的分子特征,并鼓励由于A的共用治疗目标探索缺乏目前可用于转移性WTGIST的有效疗法。旨在调查(i)[〜(68)〜ga] ga-dotatate pet / ct的诊断作用; (ii)探讨该成像模型的潜力,以指导WTGIST患者的[〜(177)Lu] Lu-dotatate治疗。方法[〜(68)吗?Ga-dotatate PET / CT在11例确诊或转移性WTGIST和一个患有WTGIST病史的患者和转移性WTGIST的患者进行,随后被诊断出了同学纵隔Paraganglioma。使用免疫组织化学的生长抑素受体亚型2(SSTR2)的肿瘤表达在54个肿瘤样品上进行,包括来自8/12(66.6%)患者的样品,其中参加成像研究和来自成像研究中未包含的个体的46个肿瘤样本。结果[〜(68)吗?Ga-Dotatate PET / CT成像是阴性的,表明肝转移比背景肝脏较低,九种病例(9/12例,75%)和生长抑制素示踪剂的异质摄取两种案例(16.6%)WTGIST。然而,[〜(68)吗?Ga-dotatate PET / CT在一种情况下在一个病例中显示出在同步的伞状脑膜瘤中的强烈示踪剂吸收,并且在另一个案例中具有与WTGIST的另一个案例。结论我们的数据表明SSTR2不是WTGIST中的诊断或治疗目标。 [〜(68)吗?Ga-dotatate PET / CT可以具有特异性诊断效用,用于区分WTGIST与散发性和遗传形式的WTGIST患者的患者中的其他原发性肿瘤等原发性肿瘤。
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