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DOI 10.1007/s11154-017-9431-2

Медицинская библиотека · Reviews in endocrine & metabolic disorders · 2017

Liver transarterial embolizations in metastatic neuroendocrine tumors.

de Mestier Louis, Zappa Magaly, Hentic Olivia, Vilgrain Valérie, Ruszniewski Philippe

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Аннотация

The management of patients with well-differentiated neuroendocrine tumors (NET) and non-resectable liver metastases is challenging. Liver-directed transarterial embolization (TAE), transarterial chemo-embolization (TACE) and selective internal radiation therapy (SIRT) have a place of choice among other treatment modalities. However, their utilization relies on a low level of proof, due to the lack of prospective data, the absence of comparative studies and considerable heterogeneity between local practices. TAE and TACE generally achieve average symptomatic, biological and radiological responses of 75%, 56% and 50%, with progression-free survival of 12-18 months, with acceptable tolerance. Although not clearly demonstrated, TACE may be more effective than TAE in pancreatic NET, but not in small-intestine NET. SIRT has been developed more recently and may achieve similar results, with improved tolerance, but decreased cost-effectiveness, although no prospective comparison has been published to date. There is currently no strong argument to choose between TAE, TACE and SIRT, and they have not been compared to other treatment modalities. The evaluation of their efficacy has mostly relied on criteria based on size variations, which do not take into account tumor viability and metabolism, and thus may not be relevant. These techniques may be especially effective when performed as first-line therapies, in patients with non-major liver involvement (<75%) and with hypervascular metastases. Finally, studies exploring their combination with systemic therapies are ongoing.

Для цитирования: de Mestier Louis, Zappa Magaly, Hentic Olivia, Vilgrain Valérie, Ruszniewski Philippe. Liver transarterial embolizations in metastatic neuroendocrine tumors.. Reviews in endocrine & metabolic disorders. 2017. DOI: 10.1007/s11154-017-9431-2.

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