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首页> 外文期刊>Tumour biology : >Everolimus-based combination for the treatment of advanced gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs): biological rationale and critical review of published data
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Everolimus-based combination for the treatment of advanced gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs): biological rationale and critical review of published data

机译:基于依维莫司的组合治疗晚期胃肠道胰腺神经内分泌肿瘤(GEP-NENs):生物学原理和已发表数据的重要评论

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摘要

Gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs) comprise a heterogeneous group of diseases. Advanced GEP-NENs are considered distinct disease entity with limited treatments. In this review, we will explore the biological rationale and clinical data of everolimus-based combinations for advanced GEP-NENs. PubMed/Medline, the Cochrane Library, and Google Scholar were searched using the terms "GEP-NENs" and "everolimus" and "systemic therapy" and selecting English literature only. Outcomes of interest included progression-free survival and overall survival (PFS and OS), toxicities, and tumor response. A total of 14 potentially relevant trials were initially identified, of which five studies were excluded. Hence, nine trials including 699 patients were included. Median PFS was reported in four out of the nine studies ranging from 14.6 to 16.4 months. The disease control rate was reported in all studies, and it ranged from 75 to 93 %. Frequently reported grade 3/4 toxicities were elevated transaminases, hyperglycemia, and hematologic toxicities. The presence of clinical and statistical heterogeneity of the primary studies precludes reliable evidence-based conclusions. Further well-conducted randomized controlled trials are awaited to better evaluate the treatment of GEP-NENs.
机译:胃肠道胰腺神经内分泌肿瘤(GEP-NENs)包括一组异质性疾病。晚期GEP-NENs被认为是治疗方法有限的独特疾病。在这篇综述中,我们将探讨基于依维莫司的联合治疗晚期GEP-NENs的生物学原理和临床数据。使用“ GEP-NENs”,“ everolimus”和“全身疗法”这两个词搜索PubMed / Medline,Cochrane图书馆和Google Scholar,并且仅选择英语文献。感兴趣的结果包括无进展生存期和总生存期(PFS和OS),毒性和肿瘤反应。最初确定了总共14项潜在相关的试验,其中5项研究被排除在外。因此,纳入了包括699名患者在内的9个试验。 9项研究中有4项报道了PFS的中位数,范围为14.6到16.4个月。在所有研究中均报告了疾病控制率,范围为75%至93%。经常报告的3/4级毒性是转氨酶升高,高血糖症和血液学毒性。主要研究的临床和统计异质性的存在排除了可靠的基于证据的结论。有待进行更完善的随机对照试验,以更好地评估GEP-NENs的治疗。

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