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Modern therapies of nonsmall cell lung cancer

Lung cancer (LC), particularly nonsmall cell lung cancer (NSCLC), is one of the most prevalent types of neoplasia worldwide, regardless of gender, with the highest mortality rates in oncology. Over the years, treatment for NSCLC has evolved from conventional surgery, chemotherapy, and radiotherapy t...

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Autores principales: Jachowski, Andrzej, Marcinkowski, Mikołaj, Szydłowski, Jakub, Grabarczyk, Oskar, Nogaj, Zuzanna, Marcin, Łaz, Pławski, Andrzej, Jagodziński, Paweł Piotr, Słowikowski, Bartosz Kazimierz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632224/
https://www.ncbi.nlm.nih.gov/pubmed/37698765
http://dx.doi.org/10.1007/s13353-023-00786-4
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author Jachowski, Andrzej
Marcinkowski, Mikołaj
Szydłowski, Jakub
Grabarczyk, Oskar
Nogaj, Zuzanna
Marcin, Łaz
Pławski, Andrzej
Jagodziński, Paweł Piotr
Słowikowski, Bartosz Kazimierz
author_facet Jachowski, Andrzej
Marcinkowski, Mikołaj
Szydłowski, Jakub
Grabarczyk, Oskar
Nogaj, Zuzanna
Marcin, Łaz
Pławski, Andrzej
Jagodziński, Paweł Piotr
Słowikowski, Bartosz Kazimierz
author_sort Jachowski, Andrzej
collection PubMed
description Lung cancer (LC), particularly nonsmall cell lung cancer (NSCLC), is one of the most prevalent types of neoplasia worldwide, regardless of gender, with the highest mortality rates in oncology. Over the years, treatment for NSCLC has evolved from conventional surgery, chemotherapy, and radiotherapy to more tailored and minimally invasive approaches. The use of personalised therapies has increased the expected efficacy of treatment while simultaneously reducing the frequency of severe adverse effects (AEs). In this review, we discuss established modern approaches, including immunotherapy and targeted therapy, as well as experimental molecular methods like clustered regularly interspaced short palindromic repeat (CRISPR) and nanoparticles. These emerging methods offer promising outcomes and shorten the recovery time for various patients. Recent advances in the diagnostic field, including imaging and genetic profiling, have enabled the implementation of these methods. The versatility of these modern therapies allows for multiple treatment options, such as single-agent use, combination with existing conventional treatments, or incorporation into new regimens. As a result, patients can survive even in the advanced stages of NSCLC, leading to increased survival indicators such as overall survival (OS) and progression-free survival (PFS).
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spelling pubmed-106322242023-11-14 Modern therapies of nonsmall cell lung cancer Jachowski, Andrzej Marcinkowski, Mikołaj Szydłowski, Jakub Grabarczyk, Oskar Nogaj, Zuzanna Marcin, Łaz Pławski, Andrzej Jagodziński, Paweł Piotr Słowikowski, Bartosz Kazimierz J Appl Genet Human Genetics • Review Lung cancer (LC), particularly nonsmall cell lung cancer (NSCLC), is one of the most prevalent types of neoplasia worldwide, regardless of gender, with the highest mortality rates in oncology. Over the years, treatment for NSCLC has evolved from conventional surgery, chemotherapy, and radiotherapy to more tailored and minimally invasive approaches. The use of personalised therapies has increased the expected efficacy of treatment while simultaneously reducing the frequency of severe adverse effects (AEs). In this review, we discuss established modern approaches, including immunotherapy and targeted therapy, as well as experimental molecular methods like clustered regularly interspaced short palindromic repeat (CRISPR) and nanoparticles. These emerging methods offer promising outcomes and shorten the recovery time for various patients. Recent advances in the diagnostic field, including imaging and genetic profiling, have enabled the implementation of these methods. The versatility of these modern therapies allows for multiple treatment options, such as single-agent use, combination with existing conventional treatments, or incorporation into new regimens. As a result, patients can survive even in the advanced stages of NSCLC, leading to increased survival indicators such as overall survival (OS) and progression-free survival (PFS). Springer Berlin Heidelberg 2023-09-12 2023 /pmc/articles/PMC10632224/ /pubmed/37698765 http://dx.doi.org/10.1007/s13353-023-00786-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Human Genetics • Review
Jachowski, Andrzej
Marcinkowski, Mikołaj
Szydłowski, Jakub
Grabarczyk, Oskar
Nogaj, Zuzanna
Marcin, Łaz
Pławski, Andrzej
Jagodziński, Paweł Piotr
Słowikowski, Bartosz Kazimierz
Modern therapies of nonsmall cell lung cancer
title Modern therapies of nonsmall cell lung cancer
title_full Modern therapies of nonsmall cell lung cancer
title_fullStr Modern therapies of nonsmall cell lung cancer
title_full_unstemmed Modern therapies of nonsmall cell lung cancer
title_short Modern therapies of nonsmall cell lung cancer
title_sort modern therapies of nonsmall cell lung cancer
topic Human Genetics • Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632224/
https://www.ncbi.nlm.nih.gov/pubmed/37698765
http://dx.doi.org/10.1007/s13353-023-00786-4
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