NETest in advanced high-grade gastroenteropancreatic neuroendocrine neoplasms

IF 3.3 4区 医学 Q2 ENDOCRINOLOGY & METABOLISM
H. Sorbye, G. O. Hjortland, L. W. Vestermark, A. Sundlov, J. Assmus, A. Couvelard, A. Perren, S. W. Langer
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引用次数: 0

Abstract

Molecular blood biomarkers are lacking for high-grade (HG) gastroenteropancreatic (GEP) neuroendocrine neoplasms (NEN). To histologically distinguish between neuroendocrine carcinoma (NEC), neuroendocrine tumors G3 (NET G3), adenocarcinoma and MINEN is often challenging. The mRNA-based NETest has diagnostic, prognostic and predictive value in neuroendocrine tumors G1-2 but has not been studied in HG GEP-NEN. Patients with advanced HG GEP-NEN were prospectively included in an observational study. A blood sample was collected before the start of chemotherapy and pseudonymised before NETest was performed. NETest results are expressed as an activity index (NETest score) from 0 to 100. The normal score cut-off is 20. Histological sections were pseudonymised before centralized pathological re-evaluation. Samples from 60 patients were evaluable with the NETest. Main primary tumor sites were colon (14), rectum (12), pancreas (11) and esophagus (7). Re-classification: 30 NEC, 12 NET G3, 3 HG-NEN ambiguous morphology, 8 MiNEN, 3 adenocarcinomas with neuroendocrine differentiation (ADNE), 3 adenocarcinomas and 1 NET G2. Elevated NETest (>20) was seen in 38/45 (84%) HG GEP-NEN, all 17 large-cell NEC (100%), 11/13 (85%) small-cell NEC, all ambiguous cases and 7/12 (64%) NET G3. NETest was elevated in 5/8 (63%) MiNEN, 2/3 ADNE, however not in 3 adenocarcinomas. Median survival was 10.2 months (9.6–10.8 95%CI) for evaluable HG GEP-NEN treated with palliative chemotherapy (n = 39), and survival was significantly shorter in patients with NETest >60 with an OS of only 6.5 months. This is the first study to evaluate use of the NETest in advanced HG GEP-NEN. The NETest was almost always elevated in GEP-NEC and in all large-cell NEC. The NETest was also frequently elevated in NET G3 and MiNEN, however cases were limited. Baseline NETest was not predictive for benefit of chemotherapy, however a NETest >60 was prognostic with a shorter survival for patients receiving chemotherapy.

Abstract Image

晚期高级别胃肠胰神经内分泌肿瘤的 NETest。
高级(HG)胃肠胰(GEP)神经内分泌肿瘤(NEN)缺乏分子血液生物标记物。从组织学角度区分神经内分泌癌(NEC)、神经内分泌肿瘤 G3(NET G3)、腺癌和 MINEN 通常具有挑战性。基于 mRNA 的 NETest 对神经内分泌肿瘤 G1-2 具有诊断、预后和预测价值,但尚未对 HG GEP-NEN 进行研究。一项前瞻性观察研究纳入了晚期 HG GEP-NEN 患者。化疗开始前采集血液样本,化名后进行NETest检测。NETest结果以活动指数(NETest得分)表示,从0到100。正常分值为 20 分。组织学切片在集中病理再评估前进行化名。60 名患者的样本可通过 NETest 进行评估。主要原发肿瘤部位为结肠(14 例)、直肠(12 例)、胰腺(11 例)和食道(7 例)。重新分类:30例NEC、12例NET G3、3例HG-NEN形态不清、8例MiNEN、3例神经内分泌分化腺癌(ADNE)、3例腺癌和1例NET G2。38/45(84%)例 HG GEP-NEN、所有 17 例大细胞 NEC(100%)、11/13(85%)例小细胞 NEC、所有不明确病例和 7/12 (64%)例 NET G3 均出现 NETest 升高(>20)。5/8(63%)例 MiNEN 和 2/3 例 ADNE 中的 NETest 升高,但 3 例腺癌中的 NETest 没有升高。接受姑息化疗的可评估 HG GEP-NEN 的中位生存期为 10.2 个月(9.6-10.8 95%CI)(n = 39),NETest >60 的患者生存期明显较短,仅为 6.5 个月。这是第一项评估在晚期 HG GEP-NEN 中使用 NETest 的研究。在 GEP-NEC 和所有大细胞 NEC 中,NETest 几乎总是升高。NETest 在 G3 和 MiNEN 中也经常升高,但病例有限。基线NETest不能预测化疗的疗效,但NETest>60则预示接受化疗的患者生存期缩短。
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来源期刊
Journal of Neuroendocrinology
Journal of Neuroendocrinology 医学-内分泌学与代谢
CiteScore
6.40
自引率
6.20%
发文量
137
审稿时长
4-8 weeks
期刊介绍: Journal of Neuroendocrinology provides the principal international focus for the newest ideas in classical neuroendocrinology and its expanding interface with the regulation of behavioural, cognitive, developmental, degenerative and metabolic processes. Through the rapid publication of original manuscripts and provocative review articles, it provides essential reading for basic scientists and clinicians researching in this rapidly expanding field. In determining content, the primary considerations are excellence, relevance and novelty. While Journal of Neuroendocrinology reflects the broad scientific and clinical interests of the BSN membership, the editorial team, led by Professor Julian Mercer, ensures that the journal’s ethos, authorship, content and purpose are those expected of a leading international publication.
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