New Anticancer Agents in Neuroendocrine Tumors
Abstract
Neuroendocrine tumors (NETs) are a heterogeneous family of neoplasms of increasing incidence and challenging clinical management. Although generally more indolent than carcinomas, they have a widely variable clinical behavior and are on occasions associated with a very aggressive clinical course. For many decades, available medical options for the systemic treatment of advanced disease have been scant and of limited value in the control of disease progression. In this context, sunitinib and everolimus have triggered great enthusiasm in the field as they have proved for the first time in well-designed controlled clinical trials that there are agents able to improve the clinical outcome of this complex disease. In this chapter, we will review emergent data on new drugs for the treatment of G1–2 NETs, including recently approved angiogenesis and mTOR inhibitors, as well as other novel-targeted agents in perspective.
Keywords
Targeted agents Neuroendocrine Gastroenteropancreatic Therapy Everolimus Sunitinib PI3K HER IGFR HDACReferences
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