Actionable Driver Events in Small Cell Lung Cancer
Small cell lung cancer (SCLC) stands out as the most aggressive form of lung cancer, characterized by an extremely high proliferation rate and a very poor prognosis, with a 5-year survival rate that falls below 7%. Approximately two-thirds of patients receive their diagnosis when the disease has alr...
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Published in | International journal of molecular sciences Vol. 25; no. 1; p. 105 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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20.12.2023
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Abstract | Small cell lung cancer (SCLC) stands out as the most aggressive form of lung cancer, characterized by an extremely high proliferation rate and a very poor prognosis, with a 5-year survival rate that falls below 7%. Approximately two-thirds of patients receive their diagnosis when the disease has already reached a metastatic or extensive stage, leaving chemotherapy as the remaining first-line treatment option. Other than the recent advances in immunotherapy, which have shown moderate results, SCLC patients cannot yet benefit from any approved targeted therapy, meaning that this cancer remains treated as a uniform entity, disregarding intra- or inter-tumoral heterogeneity. Continuous efforts and technological improvements have enabled the identification of new potential targets that could be used to implement novel therapeutic strategies. In this review, we provide an overview of the most recent approaches for SCLC treatment, providing an extensive compilation of the targeted therapies that are currently under clinical evaluation and inhibitor molecules with promising results in vitro and in vivo. |
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AbstractList | Small cell lung cancer (SCLC) stands out as the most aggressive form of lung cancer, characterized by an extremely high proliferation rate and a very poor prognosis, with a 5-year survival rate that falls below 7%. Approximately two-thirds of patients receive their diagnosis when the disease has already reached a metastatic or extensive stage, leaving chemotherapy as the remaining first-line treatment option. Other than the recent advances in immunotherapy, which have shown moderate results, SCLC patients cannot yet benefit from any approved targeted therapy, meaning that this cancer remains treated as a uniform entity, disregarding intra- or inter-tumoral heterogeneity. Continuous efforts and technological improvements have enabled the identification of new potential targets that could be used to implement novel therapeutic strategies. In this review, we provide an overview of the most recent approaches for SCLC treatment, providing an extensive compilation of the targeted therapies that are currently under clinical evaluation and inhibitor molecules with promising results in vitro and in vivo.Small cell lung cancer (SCLC) stands out as the most aggressive form of lung cancer, characterized by an extremely high proliferation rate and a very poor prognosis, with a 5-year survival rate that falls below 7%. Approximately two-thirds of patients receive their diagnosis when the disease has already reached a metastatic or extensive stage, leaving chemotherapy as the remaining first-line treatment option. Other than the recent advances in immunotherapy, which have shown moderate results, SCLC patients cannot yet benefit from any approved targeted therapy, meaning that this cancer remains treated as a uniform entity, disregarding intra- or inter-tumoral heterogeneity. Continuous efforts and technological improvements have enabled the identification of new potential targets that could be used to implement novel therapeutic strategies. In this review, we provide an overview of the most recent approaches for SCLC treatment, providing an extensive compilation of the targeted therapies that are currently under clinical evaluation and inhibitor molecules with promising results in vitro and in vivo. Small cell lung cancer (SCLC) stands out as the most aggressive form of lung cancer, characterized by an extremely high proliferation rate and a very poor prognosis, with a 5-year survival rate that falls below 7%. Approximately two-thirds of patients receive their diagnosis when the disease has already reached a metastatic or extensive stage, leaving chemotherapy as the remaining first-line treatment option. Other than the recent advances in immunotherapy, which have shown moderate results, SCLC patients cannot yet benefit from any approved targeted therapy, meaning that this cancer remains treated as a uniform entity, disregarding intra- or inter-tumoral heterogeneity. Continuous efforts and technological improvements have enabled the identification of new potential targets that could be used to implement novel therapeutic strategies. In this review, we provide an overview of the most recent approaches for SCLC treatment, providing an extensive compilation of the targeted therapies that are currently under clinical evaluation and inhibitor molecules with promising results in vitro and in vivo. |
Audience | Academic |
Author | Encío, Ignacio J Freeman, Michael R Gutiérrez, Mirian Zamora, Irene Rotinen, Mirja |
AuthorAffiliation | 4 IdiSNA, Navarre Institute for Health Research, 31006 Pamplona, Spain 2 Departments of Urology and Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA; michael.freeman@cshs.org 1 Department of Health Sciences, Public University of Navarre, 31008 Pamplona, Spain; mirian.gutierrez@unavarra.es (M.G.); zamora.127247@e.unavarra.es (I.Z.) 3 Department of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA |
AuthorAffiliation_xml | – name: 4 IdiSNA, Navarre Institute for Health Research, 31006 Pamplona, Spain – name: 2 Departments of Urology and Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA; michael.freeman@cshs.org – name: 3 Department of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA – name: 1 Department of Health Sciences, Public University of Navarre, 31008 Pamplona, Spain; mirian.gutierrez@unavarra.es (M.G.); zamora.127247@e.unavarra.es (I.Z.) |
Author_xml | – sequence: 1 givenname: Mirian orcidid: 0000-0002-2733-8904 surname: Gutiérrez fullname: Gutiérrez, Mirian organization: Department of Health Sciences, Public University of Navarre, 31008 Pamplona, Spain – sequence: 2 givenname: Irene orcidid: 0009-0004-4723-9403 surname: Zamora fullname: Zamora, Irene organization: Department of Health Sciences, Public University of Navarre, 31008 Pamplona, Spain – sequence: 3 givenname: Michael R surname: Freeman fullname: Freeman, Michael R organization: Department of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA – sequence: 4 givenname: Ignacio J orcidid: 0000-0003-1732-1989 surname: Encío fullname: Encío, Ignacio J organization: IdiSNA, Navarre Institute for Health Research, 31006 Pamplona, Spain – sequence: 5 givenname: Mirja orcidid: 0000-0002-0755-8360 surname: Rotinen fullname: Rotinen, Mirja organization: IdiSNA, Navarre Institute for Health Research, 31006 Pamplona, Spain |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38203275$$D View this record in MEDLINE/PubMed |
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Copyright | COPYRIGHT 2023 MDPI AG 2023 by the authors. 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/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2023 by the authors. 2023 |
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SubjectTerms | Auranofin Cancer Cancer therapies Chemotherapy Clinical trials clinical vulnerability Development and progression Growth factors Health aspects heterogeneity Humans Immune system Immunotherapy inhibitor molecules Kinases Lung cancer Lung cancer, Small cell Lung Neoplasms - drug therapy Medical prognosis Metabolism Metastasis Morphology Mutation Prognosis Proteins Review small cell lung cancer Small Cell Lung Carcinoma - therapy targeted therapy Technology Tobacco Transcription factors Tumors |
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Title | Actionable Driver Events in Small Cell Lung Cancer |
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