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Cumulative incidence rates for CNS and non-CNS progression in two phase II studies of alectinib in ALK-positive NSCLC
BACKGROUND: We evaluated the cumulative incidence rate (CIR) of central nervous system (CNS) and non-CNS progression in alectinib-treated patients with anaplastic lymphoma kinase (ALK)-positive non-small-cell lung cancer (NSCLC) to determine the extent to which alectinib may treat or control CNS dis...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765233/ https://www.ncbi.nlm.nih.gov/pubmed/29149104 http://dx.doi.org/10.1038/bjc.2017.395 |
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author | Gadgeel, Shirish Shaw, Alice T Barlesi, Fabrice Crinò, Lucio Yang, James Chih-Hsin Dingemans, Anne-Marie C Kim, Dong-Wan de Marinis, Filippo Schulz, Mathias Liu, Shiyao Gupta, Ravindra Kotb, Ahmed Ou, Sai-Hong Ignatius |
author_facet | Gadgeel, Shirish Shaw, Alice T Barlesi, Fabrice Crinò, Lucio Yang, James Chih-Hsin Dingemans, Anne-Marie C Kim, Dong-Wan de Marinis, Filippo Schulz, Mathias Liu, Shiyao Gupta, Ravindra Kotb, Ahmed Ou, Sai-Hong Ignatius |
author_sort | Gadgeel, Shirish |
collection | PubMed |
description | BACKGROUND: We evaluated the cumulative incidence rate (CIR) of central nervous system (CNS) and non-CNS progression in alectinib-treated patients with anaplastic lymphoma kinase (ALK)-positive non-small-cell lung cancer (NSCLC) to determine the extent to which alectinib may treat or control CNS disease. METHODS: Patients with crizotinib-pretreated locally advanced or metastatic disease received alectinib 600 mg orally twice daily in two phase II trials. All patients underwent baseline imaging and regular centrally reviewed scans. RESULTS: At 24 months, the CIR for CNS progression was lower in patients without vs with baseline CNS metastases (8.0 vs 43.9%). Patients with baseline CNS disease and prior radiotherapy had a higher CIR of CNS progression than radiotherapy-naive patients (50.5 vs 27.4%) and a lower CIR of non-CNS progression (25.8 vs 42.5%). Adverse events leading to withdrawal occurred in 5.9% and 6.7% of patients with and without baseline CNS metastases, respectively. CONCLUSIONS: This analysis indicates a potential role for alectinib in controlling and preventing CNS metastases. |
format | Online Article Text |
id | pubmed-5765233 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-57652332018-01-16 Cumulative incidence rates for CNS and non-CNS progression in two phase II studies of alectinib in ALK-positive NSCLC Gadgeel, Shirish Shaw, Alice T Barlesi, Fabrice Crinò, Lucio Yang, James Chih-Hsin Dingemans, Anne-Marie C Kim, Dong-Wan de Marinis, Filippo Schulz, Mathias Liu, Shiyao Gupta, Ravindra Kotb, Ahmed Ou, Sai-Hong Ignatius Br J Cancer Clinical Study BACKGROUND: We evaluated the cumulative incidence rate (CIR) of central nervous system (CNS) and non-CNS progression in alectinib-treated patients with anaplastic lymphoma kinase (ALK)-positive non-small-cell lung cancer (NSCLC) to determine the extent to which alectinib may treat or control CNS disease. METHODS: Patients with crizotinib-pretreated locally advanced or metastatic disease received alectinib 600 mg orally twice daily in two phase II trials. All patients underwent baseline imaging and regular centrally reviewed scans. RESULTS: At 24 months, the CIR for CNS progression was lower in patients without vs with baseline CNS metastases (8.0 vs 43.9%). Patients with baseline CNS disease and prior radiotherapy had a higher CIR of CNS progression than radiotherapy-naive patients (50.5 vs 27.4%) and a lower CIR of non-CNS progression (25.8 vs 42.5%). Adverse events leading to withdrawal occurred in 5.9% and 6.7% of patients with and without baseline CNS metastases, respectively. CONCLUSIONS: This analysis indicates a potential role for alectinib in controlling and preventing CNS metastases. Nature Publishing Group 2018-01 2017-11-16 /pmc/articles/PMC5765233/ /pubmed/29149104 http://dx.doi.org/10.1038/bjc.2017.395 Text en Copyright © 2018 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Clinical Study Gadgeel, Shirish Shaw, Alice T Barlesi, Fabrice Crinò, Lucio Yang, James Chih-Hsin Dingemans, Anne-Marie C Kim, Dong-Wan de Marinis, Filippo Schulz, Mathias Liu, Shiyao Gupta, Ravindra Kotb, Ahmed Ou, Sai-Hong Ignatius Cumulative incidence rates for CNS and non-CNS progression in two phase II studies of alectinib in ALK-positive NSCLC |
title | Cumulative incidence rates for CNS and non-CNS progression in two phase II studies of alectinib in ALK-positive NSCLC |
title_full | Cumulative incidence rates for CNS and non-CNS progression in two phase II studies of alectinib in ALK-positive NSCLC |
title_fullStr | Cumulative incidence rates for CNS and non-CNS progression in two phase II studies of alectinib in ALK-positive NSCLC |
title_full_unstemmed | Cumulative incidence rates for CNS and non-CNS progression in two phase II studies of alectinib in ALK-positive NSCLC |
title_short | Cumulative incidence rates for CNS and non-CNS progression in two phase II studies of alectinib in ALK-positive NSCLC |
title_sort | cumulative incidence rates for cns and non-cns progression in two phase ii studies of alectinib in alk-positive nsclc |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765233/ https://www.ncbi.nlm.nih.gov/pubmed/29149104 http://dx.doi.org/10.1038/bjc.2017.395 |
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