Literature DB >> 24557872

[Management of metabolic disorders induced by everolimus in patients with differentiated neuroendocrine tumors: expert proposals].

Catherine Lombard-Bohas1, Bertrand Cariou2, Bruno Vergès3, Romain Coriat4, Thierry N'guyen5, Eric François6, Pascal Hammel7, Patricia Niccoli8, Olivia Hentic7.   

Abstract

Medical management of pancreatic neuroendocrine tumors has recently been improved by new molecules of which the mTOR inhibitor everolimus. If digestive neuroendocrine tumors are rare, the incidence is in constant increase and the prevalence in digestive cancers put them right behind colorectal cancers. Everolimus has demonstrated efficacy in unresectable and progressive pancreatic neuroendocrine tumors, by doubling the median progression free survival (11 versus 4.6 months), with a median time of exposure to everolimus of nine months. Everolimus is generally maintained until progression or intolerance and some patients are treated during several years. Potential metabolic disorders induced by everolimus (dyslipidemia, hyperglycemia) in patients with life expectancy of several years, justify monitoring of these parameters and accurate treatment management algorithm. These will avoid worsening patient's prognostic, but also prematurely discontinue potentially effective treatment or contraindicate other therapeutic weapons, in a pathology in which there are multiple therapeutic options in metastatic phase. We propose a standard practice in terms of initial assessment, monitoring, care threshold, and therapeutic objectives to manage metabolic disorders, fitted to our patients with advanced pancreatic neuroendocrine tumors.

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Keywords:  dyslipidemia; everolimus; hyperglycemia; mTOR inhibitor; metabolic disorders; neuroendocrine tumors

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Year:  2014        PMID: 24557872     DOI: 10.1684/bdc.2014.1887

Source DB:  PubMed          Journal:  Bull Cancer        ISSN: 0007-4551            Impact factor:   1.276


  1 in total

1.  Prediction of response to everolimus in neuroendocrine tumors: evaluation of clinical, biological and histological factors.

Authors:  Noura Benslama; Julien Bollard; Cécile Vercherat; Patrick Massoma; Colette Roche; Valérie Hervieu; Julien Peron; Catherine Lombard-Bohas; Jean-Yves Scoazec; Thomas Walter
Journal:  Invest New Drugs       Date:  2016-05-26       Impact factor: 3.850

  1 in total

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