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Real-World Management and Outcomes of Crizotinib-Treated ROS1-Rearranged NSCLC: A Retrospective Canadian Cohort

The use, safety and effectiveness of crizotinib as part of the management of ROS1-rearranged NSCLC patients in a real-world Canadian clinical cohort was the focus of this retrospective review. Twenty-one ROS1-rearranged patients with advanced/metastatic disease receiving crizotinib between 2014–2020...

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Autores principales: Gibson, Amanda J. W., Box, Adrian, Cheung, Winson Y., Dean, Michelle L., Elegbede, Anifat A., Hao, Desiree, Pabani, Aliyah, Sangha, Randeep, Bebb, Dafydd Gwyn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947433/
https://www.ncbi.nlm.nih.gov/pubmed/35323360
http://dx.doi.org/10.3390/curroncol29030160
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author Gibson, Amanda J. W.
Box, Adrian
Cheung, Winson Y.
Dean, Michelle L.
Elegbede, Anifat A.
Hao, Desiree
Pabani, Aliyah
Sangha, Randeep
Bebb, Dafydd Gwyn
author_facet Gibson, Amanda J. W.
Box, Adrian
Cheung, Winson Y.
Dean, Michelle L.
Elegbede, Anifat A.
Hao, Desiree
Pabani, Aliyah
Sangha, Randeep
Bebb, Dafydd Gwyn
author_sort Gibson, Amanda J. W.
collection PubMed
description The use, safety and effectiveness of crizotinib as part of the management of ROS1-rearranged NSCLC patients in a real-world Canadian clinical cohort was the focus of this retrospective review. Twenty-one ROS1-rearranged patients with advanced/metastatic disease receiving crizotinib between 2014–2020 were identified; crizotinib demonstrated tolerability and effectiveness in this population where outcomes were similar to those described in other crizotinib-treated real-world cohorts, but lower than those of the PROFILE 1001 clinical trial population. Systemic anti-cancer therapy prior to crizotinib initiation occurred in half of the study cohort, with platin-pemetrexed and immune checkpoint inhibitors being most common. Platin-pemetrexed showed good effectiveness in this cohort, but despite high prevalence of upregulated PD-L1 expression, immune checkpoint inhibitors showed poor effectiveness in his cohort. Among all systemic therapies received, crizotinib showed the most effective disease control, although longer intervals between diagnosis and crizotinib initiation were more common among those showing a lack of clinical response to crizotinib, and patients with brain metastases at the time of crizotinib initiation also showed increased diagnosis to crizotinib initiation intervals and decreased clinical response to crizotinib. This study reveals crizotinib has clinical benefit, but timely identification of ROS1-rearrangements and initiation targeted therapies appears important to maximize outcome in this population.
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spelling pubmed-89474332022-03-25 Real-World Management and Outcomes of Crizotinib-Treated ROS1-Rearranged NSCLC: A Retrospective Canadian Cohort Gibson, Amanda J. W. Box, Adrian Cheung, Winson Y. Dean, Michelle L. Elegbede, Anifat A. Hao, Desiree Pabani, Aliyah Sangha, Randeep Bebb, Dafydd Gwyn Curr Oncol Article The use, safety and effectiveness of crizotinib as part of the management of ROS1-rearranged NSCLC patients in a real-world Canadian clinical cohort was the focus of this retrospective review. Twenty-one ROS1-rearranged patients with advanced/metastatic disease receiving crizotinib between 2014–2020 were identified; crizotinib demonstrated tolerability and effectiveness in this population where outcomes were similar to those described in other crizotinib-treated real-world cohorts, but lower than those of the PROFILE 1001 clinical trial population. Systemic anti-cancer therapy prior to crizotinib initiation occurred in half of the study cohort, with platin-pemetrexed and immune checkpoint inhibitors being most common. Platin-pemetrexed showed good effectiveness in this cohort, but despite high prevalence of upregulated PD-L1 expression, immune checkpoint inhibitors showed poor effectiveness in his cohort. Among all systemic therapies received, crizotinib showed the most effective disease control, although longer intervals between diagnosis and crizotinib initiation were more common among those showing a lack of clinical response to crizotinib, and patients with brain metastases at the time of crizotinib initiation also showed increased diagnosis to crizotinib initiation intervals and decreased clinical response to crizotinib. This study reveals crizotinib has clinical benefit, but timely identification of ROS1-rearrangements and initiation targeted therapies appears important to maximize outcome in this population. MDPI 2022-03-14 /pmc/articles/PMC8947433/ /pubmed/35323360 http://dx.doi.org/10.3390/curroncol29030160 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gibson, Amanda J. W.
Box, Adrian
Cheung, Winson Y.
Dean, Michelle L.
Elegbede, Anifat A.
Hao, Desiree
Pabani, Aliyah
Sangha, Randeep
Bebb, Dafydd Gwyn
Real-World Management and Outcomes of Crizotinib-Treated ROS1-Rearranged NSCLC: A Retrospective Canadian Cohort
title Real-World Management and Outcomes of Crizotinib-Treated ROS1-Rearranged NSCLC: A Retrospective Canadian Cohort
title_full Real-World Management and Outcomes of Crizotinib-Treated ROS1-Rearranged NSCLC: A Retrospective Canadian Cohort
title_fullStr Real-World Management and Outcomes of Crizotinib-Treated ROS1-Rearranged NSCLC: A Retrospective Canadian Cohort
title_full_unstemmed Real-World Management and Outcomes of Crizotinib-Treated ROS1-Rearranged NSCLC: A Retrospective Canadian Cohort
title_short Real-World Management and Outcomes of Crizotinib-Treated ROS1-Rearranged NSCLC: A Retrospective Canadian Cohort
title_sort real-world management and outcomes of crizotinib-treated ros1-rearranged nsclc: a retrospective canadian cohort
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947433/
https://www.ncbi.nlm.nih.gov/pubmed/35323360
http://dx.doi.org/10.3390/curroncol29030160
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