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The value of local consolidative therapy in Osimertinib-treated non-small cell lung cancer with oligo-residual disease

BACKGROUND: There was no study investigating real-world utilization and outcome of LCT in Osimertinib-treated NSCLC with oligo-residual disease. This study was to analyze the clinical value of local consolidative therapy (LCT) in Osimertinib-treated non-small cell lung cancer (NSCLC) patients with o...

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Autores principales: Zeng, Ya, Ni, Jianjiao, Yu, Fan, Zhou, Yue, Zhao, Yang, Li, Shuyan, Guo, Tiantian, Chu, Li, Yang, Xi, Chu, Xiao, Cai, Xuwei, Zhu, Zhengfei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457298/
https://www.ncbi.nlm.nih.gov/pubmed/32854745
http://dx.doi.org/10.1186/s13014-020-01651-y
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author Zeng, Ya
Ni, Jianjiao
Yu, Fan
Zhou, Yue
Zhao, Yang
Li, Shuyan
Guo, Tiantian
Chu, Li
Yang, Xi
Chu, Xiao
Cai, Xuwei
Zhu, Zhengfei
author_facet Zeng, Ya
Ni, Jianjiao
Yu, Fan
Zhou, Yue
Zhao, Yang
Li, Shuyan
Guo, Tiantian
Chu, Li
Yang, Xi
Chu, Xiao
Cai, Xuwei
Zhu, Zhengfei
author_sort Zeng, Ya
collection PubMed
description BACKGROUND: There was no study investigating real-world utilization and outcome of LCT in Osimertinib-treated NSCLC with oligo-residual disease. This study was to analyze the clinical value of local consolidative therapy (LCT) in Osimertinib-treated non-small cell lung cancer (NSCLC) patients with oligo-residual disease. METHODS: Patients receiving standard Osimertinib treatment and developing oligo-residual disease (five or fewer residual metastatic lesions) were retrospectively reviewed. Local therapies performed to the oligo-residual tumor lesions or primary lung site before Osimertinib treatment failure were considered as LCT. RESULTS: Of 108 patients recruited, first-line and second-line Osimertinib were administered in 25 and 83 patients, respectively, while LCT was performed in 14 patients. With a median follow-up of 43.6 months, 69 patients developed progressive disease. LCT significantly improved progression-free survival (PFS) (NR vs 12.8 months, p = 0.01) and was independently associated with prolonged PFS (HR = 0.29, 95%CI 0.12 to 0.68, p = 0.004). Patients receiving LCT had a numerically longer overall survival (OS) (85.8 vs 77.1 months, p = 0.58) and after adjusting for potentially confounding factors, LCT was associated with a non-significantly prolonged OS (HR = 0.37, 95%CI 0.12–1.16, p = 0.089). Pattern of failure analyses indicated that progressive disease developed at the originally existed oligo-residual lesions in 76.2% of the 63 patients who didn’t receive LCT and had Osimertinib treatment failure. Of note, 7 (70%) of the 10 patients who had oligo-residual cranial disease but didn’t receive LCT, developed more than five progressive lesions in the brain, which were no longer suitable for stereotactic radiosurgery. CONCLUSION: Among Osimertinib-treated NSCLC patients having oligo-residual lesions, LCT could improve local control and significantly increase PFS, which need to be verified by further investigations.
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spelling pubmed-74572982020-08-31 The value of local consolidative therapy in Osimertinib-treated non-small cell lung cancer with oligo-residual disease Zeng, Ya Ni, Jianjiao Yu, Fan Zhou, Yue Zhao, Yang Li, Shuyan Guo, Tiantian Chu, Li Yang, Xi Chu, Xiao Cai, Xuwei Zhu, Zhengfei Radiat Oncol Research BACKGROUND: There was no study investigating real-world utilization and outcome of LCT in Osimertinib-treated NSCLC with oligo-residual disease. This study was to analyze the clinical value of local consolidative therapy (LCT) in Osimertinib-treated non-small cell lung cancer (NSCLC) patients with oligo-residual disease. METHODS: Patients receiving standard Osimertinib treatment and developing oligo-residual disease (five or fewer residual metastatic lesions) were retrospectively reviewed. Local therapies performed to the oligo-residual tumor lesions or primary lung site before Osimertinib treatment failure were considered as LCT. RESULTS: Of 108 patients recruited, first-line and second-line Osimertinib were administered in 25 and 83 patients, respectively, while LCT was performed in 14 patients. With a median follow-up of 43.6 months, 69 patients developed progressive disease. LCT significantly improved progression-free survival (PFS) (NR vs 12.8 months, p = 0.01) and was independently associated with prolonged PFS (HR = 0.29, 95%CI 0.12 to 0.68, p = 0.004). Patients receiving LCT had a numerically longer overall survival (OS) (85.8 vs 77.1 months, p = 0.58) and after adjusting for potentially confounding factors, LCT was associated with a non-significantly prolonged OS (HR = 0.37, 95%CI 0.12–1.16, p = 0.089). Pattern of failure analyses indicated that progressive disease developed at the originally existed oligo-residual lesions in 76.2% of the 63 patients who didn’t receive LCT and had Osimertinib treatment failure. Of note, 7 (70%) of the 10 patients who had oligo-residual cranial disease but didn’t receive LCT, developed more than five progressive lesions in the brain, which were no longer suitable for stereotactic radiosurgery. CONCLUSION: Among Osimertinib-treated NSCLC patients having oligo-residual lesions, LCT could improve local control and significantly increase PFS, which need to be verified by further investigations. BioMed Central 2020-08-27 /pmc/articles/PMC7457298/ /pubmed/32854745 http://dx.doi.org/10.1186/s13014-020-01651-y Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Zeng, Ya
Ni, Jianjiao
Yu, Fan
Zhou, Yue
Zhao, Yang
Li, Shuyan
Guo, Tiantian
Chu, Li
Yang, Xi
Chu, Xiao
Cai, Xuwei
Zhu, Zhengfei
The value of local consolidative therapy in Osimertinib-treated non-small cell lung cancer with oligo-residual disease
title The value of local consolidative therapy in Osimertinib-treated non-small cell lung cancer with oligo-residual disease
title_full The value of local consolidative therapy in Osimertinib-treated non-small cell lung cancer with oligo-residual disease
title_fullStr The value of local consolidative therapy in Osimertinib-treated non-small cell lung cancer with oligo-residual disease
title_full_unstemmed The value of local consolidative therapy in Osimertinib-treated non-small cell lung cancer with oligo-residual disease
title_short The value of local consolidative therapy in Osimertinib-treated non-small cell lung cancer with oligo-residual disease
title_sort value of local consolidative therapy in osimertinib-treated non-small cell lung cancer with oligo-residual disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457298/
https://www.ncbi.nlm.nih.gov/pubmed/32854745
http://dx.doi.org/10.1186/s13014-020-01651-y
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