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A Propensity-Matched Retrospective Comparative Study with Historical Control to Determine the Real-World Effectiveness of Durvalumab after Concurrent Chemoradiotherapy in Unresectable Stage III Non-Small Cell Lung Cancer

SIMPLE SUMMARY: The PACIFIC trial demonstrated the survival benefits of durvalumab consolidation (DC) in patients with unresectable stage III non–small cell lung cancer (NSCLC). In this retrospective cohort study, using a propensity score-matched analysis, we investigated the effectiveness of DC aft...

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Autores principales: Park, Cheol-Kyu, Jeon, Nakyung, Park, Hwa-Kyung, Oh, Hyung-Joo, Kim, Young-Chul, Jeon, Ha-Lim, Kim, Yong-Hyub, Ahn, Sung-Ja, Oh, In-Jae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000649/
https://www.ncbi.nlm.nih.gov/pubmed/36900397
http://dx.doi.org/10.3390/cancers15051606
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author Park, Cheol-Kyu
Jeon, Nakyung
Park, Hwa-Kyung
Oh, Hyung-Joo
Kim, Young-Chul
Jeon, Ha-Lim
Kim, Yong-Hyub
Ahn, Sung-Ja
Oh, In-Jae
author_facet Park, Cheol-Kyu
Jeon, Nakyung
Park, Hwa-Kyung
Oh, Hyung-Joo
Kim, Young-Chul
Jeon, Ha-Lim
Kim, Yong-Hyub
Ahn, Sung-Ja
Oh, In-Jae
author_sort Park, Cheol-Kyu
collection PubMed
description SIMPLE SUMMARY: The PACIFIC trial demonstrated the survival benefits of durvalumab consolidation (DC) in patients with unresectable stage III non–small cell lung cancer (NSCLC). In this retrospective cohort study, using a propensity score-matched analysis, we investigated the effectiveness of DC after concurrent chemoradiotherapy (CCRT) and compared DC after CCRT with a historical control in this regard. DC was tolerable and consistently associated with survival benefits (compared with a lack of DC) in real-world contexts. This study suggested that the outcomes of the PACIFIC trial could be successfully translated into real practice and that DC after CCRT could be established as a new standard of care for stage III NSCLC. ABSTRACT: This study aimed to add real-world evidence to the literature regarding the effectiveness and safety of durvalumab consolidation (DC) after concurrent chemoradiotherapy (CCRT) in the treatment of unresectable stage III non-small cell lung cancer (NSCLC). Using a hospital-based NSCLC patient registry and propensity score matching in a 2:1 ratio, we conducted a retrospective cohort study of patients with unresectable stage III NSCLC who completed CCRT with and without DC. The co-primary endpoints were 2-year progression-free survival and overall survival. For the safety evaluation, we evaluated the risk of any adverse events requiring systemic antibiotics or steroids. Of 386 eligible patients, 222 patients—including 74 in the DC group—were included in the analysis after propensity score matching. Compared with CCRT alone, CCRT with DC was associated with increased progression-free survival (median: 13.3 vs. 7.6 months, hazard ratio[HR]: 0.63, 95% confidence interval[CI]: 0.42–0.96) and overall survival (HR: 0.47, 95% CI: 0.27–0.82) without an increased risk of adverse events requiring systemic antibiotics or steroids. While there were differences in patient characteristics between the present real-world study and the pivotal randomized controlled trial, we demonstrated significant survival benefits and tolerable safety with DC after the completion of CCRT.
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spelling pubmed-100006492023-03-11 A Propensity-Matched Retrospective Comparative Study with Historical Control to Determine the Real-World Effectiveness of Durvalumab after Concurrent Chemoradiotherapy in Unresectable Stage III Non-Small Cell Lung Cancer Park, Cheol-Kyu Jeon, Nakyung Park, Hwa-Kyung Oh, Hyung-Joo Kim, Young-Chul Jeon, Ha-Lim Kim, Yong-Hyub Ahn, Sung-Ja Oh, In-Jae Cancers (Basel) Article SIMPLE SUMMARY: The PACIFIC trial demonstrated the survival benefits of durvalumab consolidation (DC) in patients with unresectable stage III non–small cell lung cancer (NSCLC). In this retrospective cohort study, using a propensity score-matched analysis, we investigated the effectiveness of DC after concurrent chemoradiotherapy (CCRT) and compared DC after CCRT with a historical control in this regard. DC was tolerable and consistently associated with survival benefits (compared with a lack of DC) in real-world contexts. This study suggested that the outcomes of the PACIFIC trial could be successfully translated into real practice and that DC after CCRT could be established as a new standard of care for stage III NSCLC. ABSTRACT: This study aimed to add real-world evidence to the literature regarding the effectiveness and safety of durvalumab consolidation (DC) after concurrent chemoradiotherapy (CCRT) in the treatment of unresectable stage III non-small cell lung cancer (NSCLC). Using a hospital-based NSCLC patient registry and propensity score matching in a 2:1 ratio, we conducted a retrospective cohort study of patients with unresectable stage III NSCLC who completed CCRT with and without DC. The co-primary endpoints were 2-year progression-free survival and overall survival. For the safety evaluation, we evaluated the risk of any adverse events requiring systemic antibiotics or steroids. Of 386 eligible patients, 222 patients—including 74 in the DC group—were included in the analysis after propensity score matching. Compared with CCRT alone, CCRT with DC was associated with increased progression-free survival (median: 13.3 vs. 7.6 months, hazard ratio[HR]: 0.63, 95% confidence interval[CI]: 0.42–0.96) and overall survival (HR: 0.47, 95% CI: 0.27–0.82) without an increased risk of adverse events requiring systemic antibiotics or steroids. While there were differences in patient characteristics between the present real-world study and the pivotal randomized controlled trial, we demonstrated significant survival benefits and tolerable safety with DC after the completion of CCRT. MDPI 2023-03-05 /pmc/articles/PMC10000649/ /pubmed/36900397 http://dx.doi.org/10.3390/cancers15051606 Text en © 2023 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
Park, Cheol-Kyu
Jeon, Nakyung
Park, Hwa-Kyung
Oh, Hyung-Joo
Kim, Young-Chul
Jeon, Ha-Lim
Kim, Yong-Hyub
Ahn, Sung-Ja
Oh, In-Jae
A Propensity-Matched Retrospective Comparative Study with Historical Control to Determine the Real-World Effectiveness of Durvalumab after Concurrent Chemoradiotherapy in Unresectable Stage III Non-Small Cell Lung Cancer
title A Propensity-Matched Retrospective Comparative Study with Historical Control to Determine the Real-World Effectiveness of Durvalumab after Concurrent Chemoradiotherapy in Unresectable Stage III Non-Small Cell Lung Cancer
title_full A Propensity-Matched Retrospective Comparative Study with Historical Control to Determine the Real-World Effectiveness of Durvalumab after Concurrent Chemoradiotherapy in Unresectable Stage III Non-Small Cell Lung Cancer
title_fullStr A Propensity-Matched Retrospective Comparative Study with Historical Control to Determine the Real-World Effectiveness of Durvalumab after Concurrent Chemoradiotherapy in Unresectable Stage III Non-Small Cell Lung Cancer
title_full_unstemmed A Propensity-Matched Retrospective Comparative Study with Historical Control to Determine the Real-World Effectiveness of Durvalumab after Concurrent Chemoradiotherapy in Unresectable Stage III Non-Small Cell Lung Cancer
title_short A Propensity-Matched Retrospective Comparative Study with Historical Control to Determine the Real-World Effectiveness of Durvalumab after Concurrent Chemoradiotherapy in Unresectable Stage III Non-Small Cell Lung Cancer
title_sort propensity-matched retrospective comparative study with historical control to determine the real-world effectiveness of durvalumab after concurrent chemoradiotherapy in unresectable stage iii non-small cell lung cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000649/
https://www.ncbi.nlm.nih.gov/pubmed/36900397
http://dx.doi.org/10.3390/cancers15051606
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