Brief report: Impact of consolidation durvalumab on unresectable non-small lung cancer with driver mutations
Unresectable stage III non-small cell lung cancer (NSCLC) carries a poor prognosis. The PACIFIC trial established consolidation durvalumab after chemoradiation as a standard treatment; however, its efficacy in patients with driver mutations remains uncertain. This retrospective cohort study analyzed...
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Veröffentlicht in: | Cancer treatment and research communications 2024, Vol.42, p.100863, Article 100863 |
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description | Unresectable stage III non-small cell lung cancer (NSCLC) carries a poor prognosis. The PACIFIC trial established consolidation durvalumab after chemoradiation as a standard treatment; however, its efficacy in patients with driver mutations remains uncertain. This retrospective cohort study analyzed data from three oncology centers in Hong Kong, covering the period from January 2019 to December 2022. Among the 118 patients who underwent definitive chemoradiation, 33 had common driver mutations, including EGFR mutations, ALK rearrangements, ROS1 rearrangements, and RET fusions. The addition of durvalumab did not improve real-world recurrence-free survival (rwRFS) in patients with these mutations (hazard ratio [HR] 0.852, 95 % confidence interval [CI] 0.394 – 1.843, p= 0.683). In contrast, rwRFS significantly improved for patients without common mutations (HR 0.342, 95 % CI 0.203 – 0.577, p< 0.001). These findings suggest that consolidation durvalumab may not be beneficial for patients with common driver mutations, underscoring the need for personalized treatment strategies in this population. |
doi_str_mv | 10.1016/j.ctarc.2025.100863 |
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The PACIFIC trial established consolidation durvalumab after chemoradiation as a standard treatment; however, its efficacy in patients with driver mutations remains uncertain. This retrospective cohort study analyzed data from three oncology centers in Hong Kong, covering the period from January 2019 to December 2022. Among the 118 patients who underwent definitive chemoradiation, 33 had common driver mutations, including EGFR mutations, ALK rearrangements, ROS1 rearrangements, and RET fusions. The addition of durvalumab did not improve real-world recurrence-free survival (rwRFS) in patients with these mutations (hazard ratio [HR] 0.852, 95 % confidence interval [CI] 0.394 – 1.843, p= 0.683). In contrast, rwRFS significantly improved for patients without common mutations (HR 0.342, 95 % CI 0.203 – 0.577, p< 0.001). 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The PACIFIC trial established consolidation durvalumab after chemoradiation as a standard treatment; however, its efficacy in patients with driver mutations remains uncertain. This retrospective cohort study analyzed data from three oncology centers in Hong Kong, covering the period from January 2019 to December 2022. Among the 118 patients who underwent definitive chemoradiation, 33 had common driver mutations, including EGFR mutations, ALK rearrangements, ROS1 rearrangements, and RET fusions. The addition of durvalumab did not improve real-world recurrence-free survival (rwRFS) in patients with these mutations (hazard ratio [HR] 0.852, 95 % confidence interval [CI] 0.394 – 1.843, p= 0.683). In contrast, rwRFS significantly improved for patients without common mutations (HR 0.342, 95 % CI 0.203 – 0.577, p< 0.001). These findings suggest that consolidation durvalumab may not be beneficial for patients with common driver mutations, underscoring the need for personalized treatment strategies in this population.</description><subject>Chemoradiotherapy</subject><subject>Durvalumab</subject><subject>Immunotherapy</subject><subject>Non-small cell lung cancer</subject><subject>Real-world data</subject><issn>2468-2942</issn><issn>2468-2942</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kUtv1TAQhSMEolXpL0BCXrLJxY_4ESQWUPG4UiU2sLac8aT4yokvdnIR_x73plSsWHk8OnOOPV_TvGR0xyhTbw47WFyGHadc1g41SjxpLnmnTMv7jj_9p75orks5UEqZ4Ux3_fPmQvSGGmPkZRM_5IAjyXhMeXlL9tPRwULSSCDNJcXg3RLSTPyaTy6ukxtIva1zxoL1AUNEMqe5LZOLkcR1viPgZsBMfoXlB_E5nGo9rcvZpbxono0uFrx-OK-a758-frv50t5-_by_eX_bAudUtmoA36muQzNw7TonwUlu3Ci1F4OTsgcGkkmPA2hQI_cjdANHPYyKyk734qrZb74-uYM95jC5_NsmF-y5kfKddXkJENGiElJroTyDvmMKe-kE-L43I3dIQVSv15vXMaefK5bFTqEAxuhmTGuxgkmpmeZCVanYpJBTKRnHx2hG7T01e7Bnavaemt2o1alXDwHrMKF_nPnLqArebQKsKzsFzLZAwLplH3KFUP8U_hvwB4qnqro</recordid><startdate>2024</startdate><enddate>2024</enddate><creator>Ho, Jason C.S.</creator><creator>Cheung, K.M.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>DOA</scope><orcidid>https://orcid.org/0009-0006-4397-2135</orcidid></search><sort><creationdate>2024</creationdate><title>Brief report: Impact of consolidation durvalumab on unresectable non-small lung cancer with driver mutations</title><author>Ho, Jason C.S. ; Cheung, K.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2205-6bcd4644e8b27a4a5ca528af57d3ba559c1c515debc7c6f2dfc4b2e7bf6054793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Chemoradiotherapy</topic><topic>Durvalumab</topic><topic>Immunotherapy</topic><topic>Non-small cell lung cancer</topic><topic>Real-world data</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ho, Jason C.S.</creatorcontrib><creatorcontrib>Cheung, K.M.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Cancer treatment and research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ho, Jason C.S.</au><au>Cheung, K.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Brief report: Impact of consolidation durvalumab on unresectable non-small lung cancer with driver mutations</atitle><jtitle>Cancer treatment and research communications</jtitle><addtitle>Cancer Treat Res Commun</addtitle><date>2024</date><risdate>2024</risdate><volume>42</volume><spage>100863</spage><pages>100863-</pages><artnum>100863</artnum><issn>2468-2942</issn><eissn>2468-2942</eissn><abstract>Unresectable stage III non-small cell lung cancer (NSCLC) carries a poor prognosis. The PACIFIC trial established consolidation durvalumab after chemoradiation as a standard treatment; however, its efficacy in patients with driver mutations remains uncertain. This retrospective cohort study analyzed data from three oncology centers in Hong Kong, covering the period from January 2019 to December 2022. Among the 118 patients who underwent definitive chemoradiation, 33 had common driver mutations, including EGFR mutations, ALK rearrangements, ROS1 rearrangements, and RET fusions. The addition of durvalumab did not improve real-world recurrence-free survival (rwRFS) in patients with these mutations (hazard ratio [HR] 0.852, 95 % confidence interval [CI] 0.394 – 1.843, p= 0.683). In contrast, rwRFS significantly improved for patients without common mutations (HR 0.342, 95 % CI 0.203 – 0.577, p< 0.001). 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subjects | Chemoradiotherapy Durvalumab Immunotherapy Non-small cell lung cancer Real-world data |
title | Brief report: Impact of consolidation durvalumab on unresectable non-small lung cancer with driver mutations |
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