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Targeted Cancer Therapy: What’s New in the Field of Neuroendocrine Neoplasms?
SIMPLE SUMMARY: Neuroendocrine neoplasms are highly heterogeneous tumors in terms of primary origin, molecular landscape, clinical presentation and behavior. To date, several drugs have been approved and many ongoing trials are testing new agents or new combinations. In this work we aim to provide a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8038369/ https://www.ncbi.nlm.nih.gov/pubmed/33916707 http://dx.doi.org/10.3390/cancers13071701 |
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author | La Salvia, Anna Espinosa-Olarte, Paula Riesco-Martinez, Maria Del Carmen Anton-Pascual, Beatriz Garcia-Carbonero, Rocío |
author_facet | La Salvia, Anna Espinosa-Olarte, Paula Riesco-Martinez, Maria Del Carmen Anton-Pascual, Beatriz Garcia-Carbonero, Rocío |
author_sort | La Salvia, Anna |
collection | PubMed |
description | SIMPLE SUMMARY: Neuroendocrine neoplasms are highly heterogeneous tumors in terms of primary origin, molecular landscape, clinical presentation and behavior. To date, several drugs have been approved and many ongoing trials are testing new agents or new combinations. In this work we aim to provide a comprehensive review of approved agents and promising novel drugs in clinical development for the treatment of neuroendocrine neoplasms. Our manuscript could be a useful review and guidance for neuroendocrine neoplasms-dedicated clinicians. ABSTRACT: Neuroendocrine tumors (NETs) are a heterogeneous family of neoplasms of increasing incidence and high prevalence due to their relatively indolent nature. Their wide anatomic distribution and their characteristic ability to secrete hormonally active substances pose unique challenges for clinical management. They are also characterized by the common expression of somatostatin receptors, a target that has been extremely useful for diagnosis and treatment (i.e., somatostatin analogues (SSAs) and peptide-receptor radionuclide therapy (PRRT)). Chemotherapy is of limited use for NETs of non-pancreatic origin, and the only approved targeted agents for advanced progressive NETs are sunitinib for those of pancreatic origin, and everolimus for lung, gastrointestinal and pancreatic primaries. Despite recent therapeutic achievements, thus, systemic treatment options remain limited. In this review we will discuss the state-of-the-art targeted therapies in the field of NETs, and also future perspectives of novel therapeutic drugs or strategies in clinical development, including recently presented results from randomized trials of yet unapproved antiangiogenic agents (i.e., pazopanib, surufatinib and axitinib), PRRT including both approved radiopharmaceuticals (177Lu-Oxodotreotide) and others in development (177Lu-Edotreotide, 177Lu-Satoreotide Tetraxetan), immunotherapy and other innovative targeted strategies (antibody-drug conjugates, bites,…) that shall soon improve the landscape of personalized treatment options in NET patients. |
format | Online Article Text |
id | pubmed-8038369 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80383692021-04-12 Targeted Cancer Therapy: What’s New in the Field of Neuroendocrine Neoplasms? La Salvia, Anna Espinosa-Olarte, Paula Riesco-Martinez, Maria Del Carmen Anton-Pascual, Beatriz Garcia-Carbonero, Rocío Cancers (Basel) Review SIMPLE SUMMARY: Neuroendocrine neoplasms are highly heterogeneous tumors in terms of primary origin, molecular landscape, clinical presentation and behavior. To date, several drugs have been approved and many ongoing trials are testing new agents or new combinations. In this work we aim to provide a comprehensive review of approved agents and promising novel drugs in clinical development for the treatment of neuroendocrine neoplasms. Our manuscript could be a useful review and guidance for neuroendocrine neoplasms-dedicated clinicians. ABSTRACT: Neuroendocrine tumors (NETs) are a heterogeneous family of neoplasms of increasing incidence and high prevalence due to their relatively indolent nature. Their wide anatomic distribution and their characteristic ability to secrete hormonally active substances pose unique challenges for clinical management. They are also characterized by the common expression of somatostatin receptors, a target that has been extremely useful for diagnosis and treatment (i.e., somatostatin analogues (SSAs) and peptide-receptor radionuclide therapy (PRRT)). Chemotherapy is of limited use for NETs of non-pancreatic origin, and the only approved targeted agents for advanced progressive NETs are sunitinib for those of pancreatic origin, and everolimus for lung, gastrointestinal and pancreatic primaries. Despite recent therapeutic achievements, thus, systemic treatment options remain limited. In this review we will discuss the state-of-the-art targeted therapies in the field of NETs, and also future perspectives of novel therapeutic drugs or strategies in clinical development, including recently presented results from randomized trials of yet unapproved antiangiogenic agents (i.e., pazopanib, surufatinib and axitinib), PRRT including both approved radiopharmaceuticals (177Lu-Oxodotreotide) and others in development (177Lu-Edotreotide, 177Lu-Satoreotide Tetraxetan), immunotherapy and other innovative targeted strategies (antibody-drug conjugates, bites,…) that shall soon improve the landscape of personalized treatment options in NET patients. MDPI 2021-04-03 /pmc/articles/PMC8038369/ /pubmed/33916707 http://dx.doi.org/10.3390/cancers13071701 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review La Salvia, Anna Espinosa-Olarte, Paula Riesco-Martinez, Maria Del Carmen Anton-Pascual, Beatriz Garcia-Carbonero, Rocío Targeted Cancer Therapy: What’s New in the Field of Neuroendocrine Neoplasms? |
title | Targeted Cancer Therapy: What’s New in the Field of Neuroendocrine Neoplasms? |
title_full | Targeted Cancer Therapy: What’s New in the Field of Neuroendocrine Neoplasms? |
title_fullStr | Targeted Cancer Therapy: What’s New in the Field of Neuroendocrine Neoplasms? |
title_full_unstemmed | Targeted Cancer Therapy: What’s New in the Field of Neuroendocrine Neoplasms? |
title_short | Targeted Cancer Therapy: What’s New in the Field of Neuroendocrine Neoplasms? |
title_sort | targeted cancer therapy: what’s new in the field of neuroendocrine neoplasms? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8038369/ https://www.ncbi.nlm.nih.gov/pubmed/33916707 http://dx.doi.org/10.3390/cancers13071701 |
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