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Benchmarking Outcomes for Molecularly Characterized Synchronous Oligometastatic Non–Small-Cell Lung Cancer Reveals EGFR Mutations to Be Associated With Longer Overall Survival

Local consolidative therapy (LCT) for patients with synchronous oligometastatic non–small-cell lung cancer is an evolving treatment strategy, but outcomes following LCT stratified by genetic mutations have not been reported. We sought to identify genomic associations with overall survival (OS) and p...

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Autores principales: De, Brian, Farooqi, Ahsan S., Mitchell, Kyle G., Ludmir, Ethan B., Lewis, Jeff, Rinsurongkawong, Waree, Rinsurongkawong, Vadeerat, Lee, J. Jack, Swisher, Stephen G., Gibbons, Don L., Zhang, Jianjun, Le, Xiuning, Elamin, Yasir Y., Gomez, Daniel R., Ning, Matthew S., Lin, Steven H., Liao, Zhongxing, Chang, Joe Y., Vaporciyan, Ara A., Heymach, John V., Antonoff, Mara B., Gandhi, Saumil J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9928880/
https://www.ncbi.nlm.nih.gov/pubmed/36716413
http://dx.doi.org/10.1200/PO.22.00540
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author De, Brian
Farooqi, Ahsan S.
Mitchell, Kyle G.
Ludmir, Ethan B.
Lewis, Jeff
Rinsurongkawong, Waree
Rinsurongkawong, Vadeerat
Lee, J. Jack
Swisher, Stephen G.
Gibbons, Don L.
Zhang, Jianjun
Le, Xiuning
Elamin, Yasir Y.
Gomez, Daniel R.
Ning, Matthew S.
Lin, Steven H.
Liao, Zhongxing
Chang, Joe Y.
Vaporciyan, Ara A.
Heymach, John V.
Antonoff, Mara B.
Gandhi, Saumil J.
author_facet De, Brian
Farooqi, Ahsan S.
Mitchell, Kyle G.
Ludmir, Ethan B.
Lewis, Jeff
Rinsurongkawong, Waree
Rinsurongkawong, Vadeerat
Lee, J. Jack
Swisher, Stephen G.
Gibbons, Don L.
Zhang, Jianjun
Le, Xiuning
Elamin, Yasir Y.
Gomez, Daniel R.
Ning, Matthew S.
Lin, Steven H.
Liao, Zhongxing
Chang, Joe Y.
Vaporciyan, Ara A.
Heymach, John V.
Antonoff, Mara B.
Gandhi, Saumil J.
author_sort De, Brian
collection PubMed
description Local consolidative therapy (LCT) for patients with synchronous oligometastatic non–small-cell lung cancer is an evolving treatment strategy, but outcomes following LCT stratified by genetic mutations have not been reported. We sought to identify genomic associations with overall survival (OS) and progression-free survival (PFS) for these patients. METHODS: We identified all patients presenting between 2000 and 2017 with stage IV non–small-cell lung cancer and ≤ 3 synchronous metastatic sites. Patients were grouped according to mutational statuses. Primary outcomes included OS and PFS following initial diagnosis. RESULTS: Of 194 included patients, 121 received comprehensive LCT to all sites of disease with either surgery or radiation. TP53 mutations were identified in 40 of 78 (55%), KRAS in 32 of 95 (34%), EGFR in 24 of 109 (22%), and STK11 in nine of 77 (12%). At median follow-up of 96 months, median OS and PFS were 26 (95% CI, 23 to 31) months and 11 (95% CI, 9 to 13) months, respectively. On multivariable analysis, patients with EGFR mutations had lower mortality risk (hazard ratio [HR], 0.53; 95% CI, 0.29 to 0.98; P = .044) compared with wild-type patients, and patients with STK11 mutations had higher risk of progression or mortality (HR, 2.32; 95% CI, 1.12 to 4.79; P = .023) compared with wild-type patients. TP53 and KRAS mutations were not associated with OS or PFS. Among 71 patients with known EGFR mutational status who received comprehensive LCT, EGFR mutations were associated with lower mortality compared with wild-type (HR, 0.45; 95% CI, 0.22 to 0.94; P = .032). CONCLUSION: When compared with wild-type patients, those with EGFR and STK11 mutations had longer OS and shorter PFS, respectively. EGFR mutations were associated with longer OS among oligometastatic patients treated with comprehensive LCT in addition to systemic therapy.
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spelling pubmed-99288802023-02-16 Benchmarking Outcomes for Molecularly Characterized Synchronous Oligometastatic Non–Small-Cell Lung Cancer Reveals EGFR Mutations to Be Associated With Longer Overall Survival De, Brian Farooqi, Ahsan S. Mitchell, Kyle G. Ludmir, Ethan B. Lewis, Jeff Rinsurongkawong, Waree Rinsurongkawong, Vadeerat Lee, J. Jack Swisher, Stephen G. Gibbons, Don L. Zhang, Jianjun Le, Xiuning Elamin, Yasir Y. Gomez, Daniel R. Ning, Matthew S. Lin, Steven H. Liao, Zhongxing Chang, Joe Y. Vaporciyan, Ara A. Heymach, John V. Antonoff, Mara B. Gandhi, Saumil J. JCO Precis Oncol ORIGINAL REPORTS Local consolidative therapy (LCT) for patients with synchronous oligometastatic non–small-cell lung cancer is an evolving treatment strategy, but outcomes following LCT stratified by genetic mutations have not been reported. We sought to identify genomic associations with overall survival (OS) and progression-free survival (PFS) for these patients. METHODS: We identified all patients presenting between 2000 and 2017 with stage IV non–small-cell lung cancer and ≤ 3 synchronous metastatic sites. Patients were grouped according to mutational statuses. Primary outcomes included OS and PFS following initial diagnosis. RESULTS: Of 194 included patients, 121 received comprehensive LCT to all sites of disease with either surgery or radiation. TP53 mutations were identified in 40 of 78 (55%), KRAS in 32 of 95 (34%), EGFR in 24 of 109 (22%), and STK11 in nine of 77 (12%). At median follow-up of 96 months, median OS and PFS were 26 (95% CI, 23 to 31) months and 11 (95% CI, 9 to 13) months, respectively. On multivariable analysis, patients with EGFR mutations had lower mortality risk (hazard ratio [HR], 0.53; 95% CI, 0.29 to 0.98; P = .044) compared with wild-type patients, and patients with STK11 mutations had higher risk of progression or mortality (HR, 2.32; 95% CI, 1.12 to 4.79; P = .023) compared with wild-type patients. TP53 and KRAS mutations were not associated with OS or PFS. Among 71 patients with known EGFR mutational status who received comprehensive LCT, EGFR mutations were associated with lower mortality compared with wild-type (HR, 0.45; 95% CI, 0.22 to 0.94; P = .032). CONCLUSION: When compared with wild-type patients, those with EGFR and STK11 mutations had longer OS and shorter PFS, respectively. EGFR mutations were associated with longer OS among oligometastatic patients treated with comprehensive LCT in addition to systemic therapy. Wolters Kluwer Health 2023-01-30 /pmc/articles/PMC9928880/ /pubmed/36716413 http://dx.doi.org/10.1200/PO.22.00540 Text en © 2023 by American Society of Clinical Oncology https://creativecommons.org/licenses/by-nc-nd/4.0/Creative Commons Attribution Non-Commercial No Derivatives 4.0 License: https://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle ORIGINAL REPORTS
De, Brian
Farooqi, Ahsan S.
Mitchell, Kyle G.
Ludmir, Ethan B.
Lewis, Jeff
Rinsurongkawong, Waree
Rinsurongkawong, Vadeerat
Lee, J. Jack
Swisher, Stephen G.
Gibbons, Don L.
Zhang, Jianjun
Le, Xiuning
Elamin, Yasir Y.
Gomez, Daniel R.
Ning, Matthew S.
Lin, Steven H.
Liao, Zhongxing
Chang, Joe Y.
Vaporciyan, Ara A.
Heymach, John V.
Antonoff, Mara B.
Gandhi, Saumil J.
Benchmarking Outcomes for Molecularly Characterized Synchronous Oligometastatic Non–Small-Cell Lung Cancer Reveals EGFR Mutations to Be Associated With Longer Overall Survival
title Benchmarking Outcomes for Molecularly Characterized Synchronous Oligometastatic Non–Small-Cell Lung Cancer Reveals EGFR Mutations to Be Associated With Longer Overall Survival
title_full Benchmarking Outcomes for Molecularly Characterized Synchronous Oligometastatic Non–Small-Cell Lung Cancer Reveals EGFR Mutations to Be Associated With Longer Overall Survival
title_fullStr Benchmarking Outcomes for Molecularly Characterized Synchronous Oligometastatic Non–Small-Cell Lung Cancer Reveals EGFR Mutations to Be Associated With Longer Overall Survival
title_full_unstemmed Benchmarking Outcomes for Molecularly Characterized Synchronous Oligometastatic Non–Small-Cell Lung Cancer Reveals EGFR Mutations to Be Associated With Longer Overall Survival
title_short Benchmarking Outcomes for Molecularly Characterized Synchronous Oligometastatic Non–Small-Cell Lung Cancer Reveals EGFR Mutations to Be Associated With Longer Overall Survival
title_sort benchmarking outcomes for molecularly characterized synchronous oligometastatic non–small-cell lung cancer reveals egfr mutations to be associated with longer overall survival
topic ORIGINAL REPORTS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9928880/
https://www.ncbi.nlm.nih.gov/pubmed/36716413
http://dx.doi.org/10.1200/PO.22.00540
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