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Outcomes of ALK positive lung cancer patients treated with crizotinib or second-generation ALK inhibitor: a monoinstitutional experience
Rearrangement in the anaplastic lymphoma kinase (ALK) gene is one of the oncogenic drivers in non-small cell lung cancer (NSCLC) patients. Several ALK inhibitors (ALKis) have been developed and have demonstrated their efficacy, however the best treatment strategy for ALK positive NSCLC patients has...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5880608/ https://www.ncbi.nlm.nih.gov/pubmed/29632648 http://dx.doi.org/10.18632/oncotarget.24573 |
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author | De Carlo, Elisa Del Savio, Maria Chiara Polesel, Jerry Da Ros, Valentina Berto, Eleonora Santarossa, Sandra Chimienti, Emanuela Fratino, Lucia Bearz, Alessandra |
author_facet | De Carlo, Elisa Del Savio, Maria Chiara Polesel, Jerry Da Ros, Valentina Berto, Eleonora Santarossa, Sandra Chimienti, Emanuela Fratino, Lucia Bearz, Alessandra |
author_sort | De Carlo, Elisa |
collection | PubMed |
description | Rearrangement in the anaplastic lymphoma kinase (ALK) gene is one of the oncogenic drivers in non-small cell lung cancer (NSCLC) patients. Several ALK inhibitors (ALKis) have been developed and have demonstrated their efficacy, however the best treatment strategy for ALK positive NSCLC patients has yet to be determined. Our retrospective study has investigated the outcome of 40 ALK-rearranged NSCLC patients treated with two different sequential strategies in our Institute; a “classical group”, treated with crizotinib followed by second or third generation ALKis, and the “experimental group”, treated upfront with a second generation ALK inhibitor. The primary endpoints investigated were Progression-free survival (PFS) and intracranial activity. The analysis has revealed a significant improvement in PFS (p = 0.050) in the experimental group, furthermore none of these patients developed brain metastasis. There was no statistically significant difference in OS, but all patients in the experimental group were still alive after a median follow up of 15 months. Our retrospective analysis suggests that systemic and intracranial efficacy tends to be better in the experimental group; randomized prospective studies could confirm our observations. |
format | Online Article Text |
id | pubmed-5880608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-58806082018-04-09 Outcomes of ALK positive lung cancer patients treated with crizotinib or second-generation ALK inhibitor: a monoinstitutional experience De Carlo, Elisa Del Savio, Maria Chiara Polesel, Jerry Da Ros, Valentina Berto, Eleonora Santarossa, Sandra Chimienti, Emanuela Fratino, Lucia Bearz, Alessandra Oncotarget Research Paper Rearrangement in the anaplastic lymphoma kinase (ALK) gene is one of the oncogenic drivers in non-small cell lung cancer (NSCLC) patients. Several ALK inhibitors (ALKis) have been developed and have demonstrated their efficacy, however the best treatment strategy for ALK positive NSCLC patients has yet to be determined. Our retrospective study has investigated the outcome of 40 ALK-rearranged NSCLC patients treated with two different sequential strategies in our Institute; a “classical group”, treated with crizotinib followed by second or third generation ALKis, and the “experimental group”, treated upfront with a second generation ALK inhibitor. The primary endpoints investigated were Progression-free survival (PFS) and intracranial activity. The analysis has revealed a significant improvement in PFS (p = 0.050) in the experimental group, furthermore none of these patients developed brain metastasis. There was no statistically significant difference in OS, but all patients in the experimental group were still alive after a median follow up of 15 months. Our retrospective analysis suggests that systemic and intracranial efficacy tends to be better in the experimental group; randomized prospective studies could confirm our observations. Impact Journals LLC 2018-02-26 /pmc/articles/PMC5880608/ /pubmed/29632648 http://dx.doi.org/10.18632/oncotarget.24573 Text en Copyright: © 2018 De Carlo et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper De Carlo, Elisa Del Savio, Maria Chiara Polesel, Jerry Da Ros, Valentina Berto, Eleonora Santarossa, Sandra Chimienti, Emanuela Fratino, Lucia Bearz, Alessandra Outcomes of ALK positive lung cancer patients treated with crizotinib or second-generation ALK inhibitor: a monoinstitutional experience |
title | Outcomes of ALK positive lung cancer patients treated with crizotinib or second-generation ALK inhibitor: a monoinstitutional experience |
title_full | Outcomes of ALK positive lung cancer patients treated with crizotinib or second-generation ALK inhibitor: a monoinstitutional experience |
title_fullStr | Outcomes of ALK positive lung cancer patients treated with crizotinib or second-generation ALK inhibitor: a monoinstitutional experience |
title_full_unstemmed | Outcomes of ALK positive lung cancer patients treated with crizotinib or second-generation ALK inhibitor: a monoinstitutional experience |
title_short | Outcomes of ALK positive lung cancer patients treated with crizotinib or second-generation ALK inhibitor: a monoinstitutional experience |
title_sort | outcomes of alk positive lung cancer patients treated with crizotinib or second-generation alk inhibitor: a monoinstitutional experience |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5880608/ https://www.ncbi.nlm.nih.gov/pubmed/29632648 http://dx.doi.org/10.18632/oncotarget.24573 |
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