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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2018
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.
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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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