Future Options of Molecular-Targeted Therapy in Small Cell Lung Cancer

Lung cancer is the leading cause of cancer-related deaths worldwide. With a focus on histology, there are two major subtypes: Non-small cell lung cancer (NSCLC) (the more frequent subtype), and small cell lung cancer (SCLC) (the more aggressive one). Even though SCLC, in general, is a chemosensitive...

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Main Authors: Arik Bernard Schulze, Georg Evers, Andrea Kerkhoff, Michael Mohr, Christoph Schliemann, Wolfgang E. Berdel, Lars Henning Schmidt
Format: Article
Language:English
Published: MDPI AG 2019-05-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/11/5/690
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spelling doaj-4f28fe7f4485479592053e1b484b3eda2020-11-25T01:31:32ZengMDPI AGCancers2072-66942019-05-0111569010.3390/cancers11050690cancers11050690Future Options of Molecular-Targeted Therapy in Small Cell Lung CancerArik Bernard Schulze0Georg Evers1Andrea Kerkhoff2Michael Mohr3Christoph Schliemann4Wolfgang E. Berdel5Lars Henning Schmidt6Department of Medicine A, Hematology, Oncology and Pulmonary Medicine, University Hospital Muenster, 48149 Muenster, GermanyDepartment of Medicine A, Hematology, Oncology and Pulmonary Medicine, University Hospital Muenster, 48149 Muenster, GermanyDepartment of Medicine A, Hematology, Oncology and Pulmonary Medicine, University Hospital Muenster, 48149 Muenster, GermanyDepartment of Medicine A, Hematology, Oncology and Pulmonary Medicine, University Hospital Muenster, 48149 Muenster, GermanyDepartment of Medicine A, Hematology, Oncology and Pulmonary Medicine, University Hospital Muenster, 48149 Muenster, GermanyDepartment of Medicine A, Hematology, Oncology and Pulmonary Medicine, University Hospital Muenster, 48149 Muenster, GermanyDepartment of Medicine A, Hematology, Oncology and Pulmonary Medicine, University Hospital Muenster, 48149 Muenster, GermanyLung cancer is the leading cause of cancer-related deaths worldwide. With a focus on histology, there are two major subtypes: Non-small cell lung cancer (NSCLC) (the more frequent subtype), and small cell lung cancer (SCLC) (the more aggressive one). Even though SCLC, in general, is a chemosensitive malignancy, relapses following induction therapy are frequent. The standard of care treatment of SCLC consists of platinum-based chemotherapy in combination with etoposide that is subsequently enhanced by PD-L1-inhibiting atezolizumab in the extensive-stage disease, as the addition of immune-checkpoint inhibition yielded improved overall survival. Although there are promising molecular pathways with potential therapeutic impacts, targeted therapies are still not an integral part of routine treatment. Against this background, we evaluated current literature for potential new molecular candidates such as surface markers (e.g., DLL3, TROP-2 or CD56), apoptotic factors (e.g., BCL-2, BET), genetic alterations (e.g., CREBBP, NOTCH or PTEN) or vascular markers (e.g., VEGF, FGFR1 or CD13). Apart from these factors, the application of so-called ‘poly-(ADP)-ribose polymerases’ (PARP) inhibitors can influence tumor repair mechanisms and thus offer new perspectives for future treatment. Another promising therapeutic concept is the inhibition of ‘enhancer of zeste homolog 2’ (EZH2) in the loss of function of tumor suppressors or amplification of (proto-) oncogenes. Considering the poor prognosis of SCLC patients, new molecular pathways require further investigation to augment our therapeutic armamentarium in the future.https://www.mdpi.com/2072-6694/11/5/690SCLCanti-angiogenesisapoptosisepigeneticstargeted therapy
collection DOAJ
language English
format Article
sources DOAJ
author Arik Bernard Schulze
Georg Evers
Andrea Kerkhoff
Michael Mohr
Christoph Schliemann
Wolfgang E. Berdel
Lars Henning Schmidt
spellingShingle Arik Bernard Schulze
Georg Evers
Andrea Kerkhoff
Michael Mohr
Christoph Schliemann
Wolfgang E. Berdel
Lars Henning Schmidt
Future Options of Molecular-Targeted Therapy in Small Cell Lung Cancer
Cancers
SCLC
anti-angiogenesis
apoptosis
epigenetics
targeted therapy
author_facet Arik Bernard Schulze
Georg Evers
Andrea Kerkhoff
Michael Mohr
Christoph Schliemann
Wolfgang E. Berdel
Lars Henning Schmidt
author_sort Arik Bernard Schulze
title Future Options of Molecular-Targeted Therapy in Small Cell Lung Cancer
title_short Future Options of Molecular-Targeted Therapy in Small Cell Lung Cancer
title_full Future Options of Molecular-Targeted Therapy in Small Cell Lung Cancer
title_fullStr Future Options of Molecular-Targeted Therapy in Small Cell Lung Cancer
title_full_unstemmed Future Options of Molecular-Targeted Therapy in Small Cell Lung Cancer
title_sort future options of molecular-targeted therapy in small cell lung cancer
publisher MDPI AG
series Cancers
issn 2072-6694
publishDate 2019-05-01
description Lung cancer is the leading cause of cancer-related deaths worldwide. With a focus on histology, there are two major subtypes: Non-small cell lung cancer (NSCLC) (the more frequent subtype), and small cell lung cancer (SCLC) (the more aggressive one). Even though SCLC, in general, is a chemosensitive malignancy, relapses following induction therapy are frequent. The standard of care treatment of SCLC consists of platinum-based chemotherapy in combination with etoposide that is subsequently enhanced by PD-L1-inhibiting atezolizumab in the extensive-stage disease, as the addition of immune-checkpoint inhibition yielded improved overall survival. Although there are promising molecular pathways with potential therapeutic impacts, targeted therapies are still not an integral part of routine treatment. Against this background, we evaluated current literature for potential new molecular candidates such as surface markers (e.g., DLL3, TROP-2 or CD56), apoptotic factors (e.g., BCL-2, BET), genetic alterations (e.g., CREBBP, NOTCH or PTEN) or vascular markers (e.g., VEGF, FGFR1 or CD13). Apart from these factors, the application of so-called ‘poly-(ADP)-ribose polymerases’ (PARP) inhibitors can influence tumor repair mechanisms and thus offer new perspectives for future treatment. Another promising therapeutic concept is the inhibition of ‘enhancer of zeste homolog 2’ (EZH2) in the loss of function of tumor suppressors or amplification of (proto-) oncogenes. Considering the poor prognosis of SCLC patients, new molecular pathways require further investigation to augment our therapeutic armamentarium in the future.
topic SCLC
anti-angiogenesis
apoptosis
epigenetics
targeted therapy
url https://www.mdpi.com/2072-6694/11/5/690
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