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Evolution of Systemic Treatment Uptake and Survival in Advanced Non-Small Cell Lung Cancer
Background: Non-small cell lung cancer (NSCLC) commonly presents at advanced stage. We previously reported systemic treatment uptake in stage IV NSCLC climbing from 55% (2009–2012) to 62% (2015–2017). Since then, first-line immunotherapy and 2nd/3rd generation tyrosine kinase inhibitors (TKIs) have...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7816185/ https://www.ncbi.nlm.nih.gov/pubmed/33704175 http://dx.doi.org/10.3390/curroncol28010008 |
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author | Stock-Martineau, Sophie Laurie, Katie McKinnon, Mathieu Zhang, Tinghua Wheatley-Price, Paul |
author_facet | Stock-Martineau, Sophie Laurie, Katie McKinnon, Mathieu Zhang, Tinghua Wheatley-Price, Paul |
author_sort | Stock-Martineau, Sophie |
collection | PubMed |
description | Background: Non-small cell lung cancer (NSCLC) commonly presents at advanced stage. We previously reported systemic treatment uptake in stage IV NSCLC climbing from 55% (2009–2012) to 62% (2015–2017). Since then, first-line immunotherapy and 2nd/3rd generation tyrosine kinase inhibitors (TKIs) have emerged as standards of care. We explored whether treatment rates continued to rise and studied outcomes. Methods: We reviewed all cases of de novo stage IIIB/IIIC/IV NSCLC seen in out-patient medical oncology consultation at our institution between 2009–2012 (cohort A), 2015–2017 (cohort B), and June–December 2018 (cohort C). We compared rates of systemic treatment, molecular testing, targeted therapy, and immune checkpoint inhibitor (ICI) use. We compared survival in the overall, treated/untreated, younger and elderly population in cohort A vs. cohort B + C (=cohort D). Results: Cohorts A, B, and C included 528, 463, and 93 patients, respectively. Overall, 66% received any systemic therapy in cohort C, compared to 62% in cohort B and 55% in cohort A. Across three time periods, first-line chemotherapy rates fell (93, 76, 46%) while rates of first-line targeted therapy (5, 16, 15%) and ICI (0, 2, 36%) rose. Among molecular subtypes, first-line targeted treatment in EGFR-positive patients (63, 94, 100%) and anaplastic lymphoma kinase (ALK)-positive patients (0, 91, 100%) rose. Survival improved in all subgroups in cohort D vs. cohort A, except for patients ≥ 70 years and the untreated population. Conclusions: Systemic treatment rose across three time periods, reflecting the introduction of rapid diagnostic pathways, reflex molecular testing, ICI, and targeted therapies. Survival outcomes of advanced NSCLC patients have significantly improved. |
format | Online Article Text |
id | pubmed-7816185 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78161852021-01-27 Evolution of Systemic Treatment Uptake and Survival in Advanced Non-Small Cell Lung Cancer Stock-Martineau, Sophie Laurie, Katie McKinnon, Mathieu Zhang, Tinghua Wheatley-Price, Paul Curr Oncol Article Background: Non-small cell lung cancer (NSCLC) commonly presents at advanced stage. We previously reported systemic treatment uptake in stage IV NSCLC climbing from 55% (2009–2012) to 62% (2015–2017). Since then, first-line immunotherapy and 2nd/3rd generation tyrosine kinase inhibitors (TKIs) have emerged as standards of care. We explored whether treatment rates continued to rise and studied outcomes. Methods: We reviewed all cases of de novo stage IIIB/IIIC/IV NSCLC seen in out-patient medical oncology consultation at our institution between 2009–2012 (cohort A), 2015–2017 (cohort B), and June–December 2018 (cohort C). We compared rates of systemic treatment, molecular testing, targeted therapy, and immune checkpoint inhibitor (ICI) use. We compared survival in the overall, treated/untreated, younger and elderly population in cohort A vs. cohort B + C (=cohort D). Results: Cohorts A, B, and C included 528, 463, and 93 patients, respectively. Overall, 66% received any systemic therapy in cohort C, compared to 62% in cohort B and 55% in cohort A. Across three time periods, first-line chemotherapy rates fell (93, 76, 46%) while rates of first-line targeted therapy (5, 16, 15%) and ICI (0, 2, 36%) rose. Among molecular subtypes, first-line targeted treatment in EGFR-positive patients (63, 94, 100%) and anaplastic lymphoma kinase (ALK)-positive patients (0, 91, 100%) rose. Survival improved in all subgroups in cohort D vs. cohort A, except for patients ≥ 70 years and the untreated population. Conclusions: Systemic treatment rose across three time periods, reflecting the introduction of rapid diagnostic pathways, reflex molecular testing, ICI, and targeted therapies. Survival outcomes of advanced NSCLC patients have significantly improved. MDPI 2020-12-04 /pmc/articles/PMC7816185/ /pubmed/33704175 http://dx.doi.org/10.3390/curroncol28010008 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Stock-Martineau, Sophie Laurie, Katie McKinnon, Mathieu Zhang, Tinghua Wheatley-Price, Paul Evolution of Systemic Treatment Uptake and Survival in Advanced Non-Small Cell Lung Cancer |
title | Evolution of Systemic Treatment Uptake and Survival in Advanced Non-Small Cell Lung Cancer |
title_full | Evolution of Systemic Treatment Uptake and Survival in Advanced Non-Small Cell Lung Cancer |
title_fullStr | Evolution of Systemic Treatment Uptake and Survival in Advanced Non-Small Cell Lung Cancer |
title_full_unstemmed | Evolution of Systemic Treatment Uptake and Survival in Advanced Non-Small Cell Lung Cancer |
title_short | Evolution of Systemic Treatment Uptake and Survival in Advanced Non-Small Cell Lung Cancer |
title_sort | evolution of systemic treatment uptake and survival in advanced non-small cell lung cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7816185/ https://www.ncbi.nlm.nih.gov/pubmed/33704175 http://dx.doi.org/10.3390/curroncol28010008 |
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