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Implications of pneumonitis after chemoradiation and durvalumab for locally advanced non-small cell lung cancer

BACKGROUND: Consolidation durvalumab improved overall survival (OS) in locally advanced non-small cell lung cancer (LA-NSCLC) treated with chemoradiotherapy (CRT) in the PACIFIC trial; however, pneumonitis was increased with durvalumab. We sought to examine real-world outcomes with the PACIFIC parad...

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Autores principales: Hassanzadeh, Comron, Sita, Timothy, Savoor, Rohan, Samson, Pamela P., Bradley, Jeffrey, Gentile, Michelle, Roach, Michael, Mohindra, Nisha, Waqar, Saiama, Kruser, Timothy J., Robinson, Clifford
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7711405/
https://www.ncbi.nlm.nih.gov/pubmed/33282370
http://dx.doi.org/10.21037/jtd-20-1792
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author Hassanzadeh, Comron
Sita, Timothy
Savoor, Rohan
Samson, Pamela P.
Bradley, Jeffrey
Gentile, Michelle
Roach, Michael
Mohindra, Nisha
Waqar, Saiama
Kruser, Timothy J.
Robinson, Clifford
author_facet Hassanzadeh, Comron
Sita, Timothy
Savoor, Rohan
Samson, Pamela P.
Bradley, Jeffrey
Gentile, Michelle
Roach, Michael
Mohindra, Nisha
Waqar, Saiama
Kruser, Timothy J.
Robinson, Clifford
author_sort Hassanzadeh, Comron
collection PubMed
description BACKGROUND: Consolidation durvalumab improved overall survival (OS) in locally advanced non-small cell lung cancer (LA-NSCLC) treated with chemoradiotherapy (CRT) in the PACIFIC trial; however, pneumonitis was increased with durvalumab. We sought to examine real-world outcomes with the PACIFIC paradigm, especially factors associated with pneumonitis, using a multi-institutional review. METHODS: Patients with LA-NSCLC treated with CRT followed by durvalumab from January 2017–February 2019 were identified at 2 institutions. We characterized demographics, tumor factors, radiotherapy, and duration of durvalumab. We examined pneumonitis outcomes including re-challenge success, with secondary endpoints of progression-free survival (PFS) and OS. RESULTS: Thirty-four patients were included with median follow-up of 12 months (range, 3 to 20 months); 94% had stage III disease. The cumulative grade >2 pneumonitis rate was 26.5% with 2 patients developing grade 3 pneumonitis and no grade 4/5 events. Median time to pneumonitis after RT was 2.4 months (range, 0 to 4.9 months). Pneumonitis management included median prednisone dose of 60 mg for median taper of 6 weeks with durvalumab held for median of 4.5 weeks (range, 2 to 8 weeks); 70% of pneumonitis patients received durvalumab re-challenge, with pneumonitis recurring in 14% of patients. 3-month and 6-month pneumonitis-free-survival were 76.9% and 73.6%, respectively; 9- and 12-month OS were 96% (75.1–99.8%), 86.6% (63.5–95.5%), respectively; 9- and 12-month PFS were 68% (47.5–82.5%), 48.7% (25.3–68.3%). Pneumonitis development did not significantly impact PFS or OS (P>0.05). CONCLUSIONS: Among LA-NSCLC patients treated with CRT followed by consolidation durvalumab, more than 25% developed symptomatic pneumonitis. In this small case series, pneumonitis did not appear to negatively impact survival, and durvalumab re-challenge appeared feasible after pneumonitis treatment with steroids.
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spelling pubmed-77114052020-12-03 Implications of pneumonitis after chemoradiation and durvalumab for locally advanced non-small cell lung cancer Hassanzadeh, Comron Sita, Timothy Savoor, Rohan Samson, Pamela P. Bradley, Jeffrey Gentile, Michelle Roach, Michael Mohindra, Nisha Waqar, Saiama Kruser, Timothy J. Robinson, Clifford J Thorac Dis Original Article BACKGROUND: Consolidation durvalumab improved overall survival (OS) in locally advanced non-small cell lung cancer (LA-NSCLC) treated with chemoradiotherapy (CRT) in the PACIFIC trial; however, pneumonitis was increased with durvalumab. We sought to examine real-world outcomes with the PACIFIC paradigm, especially factors associated with pneumonitis, using a multi-institutional review. METHODS: Patients with LA-NSCLC treated with CRT followed by durvalumab from January 2017–February 2019 were identified at 2 institutions. We characterized demographics, tumor factors, radiotherapy, and duration of durvalumab. We examined pneumonitis outcomes including re-challenge success, with secondary endpoints of progression-free survival (PFS) and OS. RESULTS: Thirty-four patients were included with median follow-up of 12 months (range, 3 to 20 months); 94% had stage III disease. The cumulative grade >2 pneumonitis rate was 26.5% with 2 patients developing grade 3 pneumonitis and no grade 4/5 events. Median time to pneumonitis after RT was 2.4 months (range, 0 to 4.9 months). Pneumonitis management included median prednisone dose of 60 mg for median taper of 6 weeks with durvalumab held for median of 4.5 weeks (range, 2 to 8 weeks); 70% of pneumonitis patients received durvalumab re-challenge, with pneumonitis recurring in 14% of patients. 3-month and 6-month pneumonitis-free-survival were 76.9% and 73.6%, respectively; 9- and 12-month OS were 96% (75.1–99.8%), 86.6% (63.5–95.5%), respectively; 9- and 12-month PFS were 68% (47.5–82.5%), 48.7% (25.3–68.3%). Pneumonitis development did not significantly impact PFS or OS (P>0.05). CONCLUSIONS: Among LA-NSCLC patients treated with CRT followed by consolidation durvalumab, more than 25% developed symptomatic pneumonitis. In this small case series, pneumonitis did not appear to negatively impact survival, and durvalumab re-challenge appeared feasible after pneumonitis treatment with steroids. AME Publishing Company 2020-11 /pmc/articles/PMC7711405/ /pubmed/33282370 http://dx.doi.org/10.21037/jtd-20-1792 Text en 2020 Journal of Thoracic Disease. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Hassanzadeh, Comron
Sita, Timothy
Savoor, Rohan
Samson, Pamela P.
Bradley, Jeffrey
Gentile, Michelle
Roach, Michael
Mohindra, Nisha
Waqar, Saiama
Kruser, Timothy J.
Robinson, Clifford
Implications of pneumonitis after chemoradiation and durvalumab for locally advanced non-small cell lung cancer
title Implications of pneumonitis after chemoradiation and durvalumab for locally advanced non-small cell lung cancer
title_full Implications of pneumonitis after chemoradiation and durvalumab for locally advanced non-small cell lung cancer
title_fullStr Implications of pneumonitis after chemoradiation and durvalumab for locally advanced non-small cell lung cancer
title_full_unstemmed Implications of pneumonitis after chemoradiation and durvalumab for locally advanced non-small cell lung cancer
title_short Implications of pneumonitis after chemoradiation and durvalumab for locally advanced non-small cell lung cancer
title_sort implications of pneumonitis after chemoradiation and durvalumab for locally advanced non-small cell lung cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7711405/
https://www.ncbi.nlm.nih.gov/pubmed/33282370
http://dx.doi.org/10.21037/jtd-20-1792
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