Real-world outcomes of immunotherapy–based regimens in first-line advanced non-small cell lung cancer
•We assessed real-world survival outcomes for 1L I-O in patients with advanced NSCLC.•Survival estimates were generally lower than those reported in pivotal trials.•There is room for improvement of outcomes in patients who receive 1L I-O regimens.•Specific subgroups may have limited treatment benefi...
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Veröffentlicht in: | Lung cancer (Amsterdam, Netherlands) Netherlands), 2021-06, Vol.156, p.41-49 |
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creator | Waterhouse, David Lam, Jenny Betts, Keith A. Yin, Lei Gao, Sophie Yuan, Yong Hartman, John Rao, Sumati Lubinga, Solomon Stenehjem, David |
description | •We assessed real-world survival outcomes for 1L I-O in patients with advanced NSCLC.•Survival estimates were generally lower than those reported in pivotal trials.•There is room for improvement of outcomes in patients who receive 1L I-O regimens.•Specific subgroups may have limited treatment benefit from current I-O therapies.
First-line (1L) immunotherapy (I-O) has improved outcomes in patients with advanced non-small cell lung cancer (NSCLC) in clinical trials and is now routinely used alone or combined with chemotherapy. Although efficacy and safety of I-O therapies have been established in clinical trials, little is known about their performance and long-term efficacy in the real-world setting. We aimed to characterize real-world outcomes for patients with advanced NSCLC treated with 1L I-O therapy in the United States.
Patients aged ≥18 years with confirmed advanced (stage III–IV) NSCLC who received either 1L I-O monotherapy or single-agent I-O combined with chemotherapy on or after January 1, 2016 were identified from the Flatiron Health database. Primary objectives were to examine overall survival (OS) and real-world progression-free survival. Index date was defined as date of 1L treatment initiation; data cut-off date was June 30, 2020.
Among 4271 patients receiving I-O plus chemotherapy, median OS was 10.6 (95 % confidence interval [CI], 9.3–11.8) months in patients with squamous NSCLC (n=814) and 12.0 (95 % CI, 11.3–12.8) months in those with non-squamous disease (n=3457). Regardless of histology, patients with high (≥50 %) tumor programmed death ligand 1 (PD-L1) expression demonstrated longer median OS vs those with low expression. Among 3041 patients receiving I-O monotherapy, median OS was 11.3 (95 % CI, 9.8–12.8) months in patients with squamous NSCLC (n=875) and 14.1 (95 % CI, 12.4–15.8) months in those with non-squamous disease (n=2166). OS benefit appeared to be greatest in the ≥50 % tumor PD-L1 expression group of the non-squamous cohort.
Survival estimates were generally lower than those reported in pivotal clinical trials. These findings indicate that there remains room for improvement of real-world survival outcomes in patients with advanced NSCLC who receive 1L I-O–based regimens and for identification of subgroups of patients not benefitting from treatment with current I-O regimens. |
doi_str_mv | 10.1016/j.lungcan.2021.04.007 |
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First-line (1L) immunotherapy (I-O) has improved outcomes in patients with advanced non-small cell lung cancer (NSCLC) in clinical trials and is now routinely used alone or combined with chemotherapy. Although efficacy and safety of I-O therapies have been established in clinical trials, little is known about their performance and long-term efficacy in the real-world setting. We aimed to characterize real-world outcomes for patients with advanced NSCLC treated with 1L I-O therapy in the United States.
Patients aged ≥18 years with confirmed advanced (stage III–IV) NSCLC who received either 1L I-O monotherapy or single-agent I-O combined with chemotherapy on or after January 1, 2016 were identified from the Flatiron Health database. Primary objectives were to examine overall survival (OS) and real-world progression-free survival. Index date was defined as date of 1L treatment initiation; data cut-off date was June 30, 2020.
Among 4271 patients receiving I-O plus chemotherapy, median OS was 10.6 (95 % confidence interval [CI], 9.3–11.8) months in patients with squamous NSCLC (n=814) and 12.0 (95 % CI, 11.3–12.8) months in those with non-squamous disease (n=3457). Regardless of histology, patients with high (≥50 %) tumor programmed death ligand 1 (PD-L1) expression demonstrated longer median OS vs those with low expression. Among 3041 patients receiving I-O monotherapy, median OS was 11.3 (95 % CI, 9.8–12.8) months in patients with squamous NSCLC (n=875) and 14.1 (95 % CI, 12.4–15.8) months in those with non-squamous disease (n=2166). OS benefit appeared to be greatest in the ≥50 % tumor PD-L1 expression group of the non-squamous cohort.
Survival estimates were generally lower than those reported in pivotal clinical trials. These findings indicate that there remains room for improvement of real-world survival outcomes in patients with advanced NSCLC who receive 1L I-O–based regimens and for identification of subgroups of patients not benefitting from treatment with current I-O regimens.</description><identifier>ISSN: 0169-5002</identifier><identifier>EISSN: 1872-8332</identifier><identifier>DOI: 10.1016/j.lungcan.2021.04.007</identifier><identifier>PMID: 33894493</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>Immune checkpoint inhibitors ; Immunotherapy ; Non-small cell lung cancer ; Real-world outcomes</subject><ispartof>Lung cancer (Amsterdam, Netherlands), 2021-06, Vol.156, p.41-49</ispartof><rights>2021 Bristol Myers Squibb</rights><rights>Copyright © 2021 Bristol Myers Squibb. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-4ea34209319532d77b5798f922cd71e6f905fb666942daa03f69d321912e1aff3</citedby><cites>FETCH-LOGICAL-c412t-4ea34209319532d77b5798f922cd71e6f905fb666942daa03f69d321912e1aff3</cites><orcidid>0000-0002-9741-7376 ; 0000-0003-0539-9156 ; 0000-0001-5589-9939 ; 0000-0002-1831-285X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0169500221001355$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33894493$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Waterhouse, David</creatorcontrib><creatorcontrib>Lam, Jenny</creatorcontrib><creatorcontrib>Betts, Keith A.</creatorcontrib><creatorcontrib>Yin, Lei</creatorcontrib><creatorcontrib>Gao, Sophie</creatorcontrib><creatorcontrib>Yuan, Yong</creatorcontrib><creatorcontrib>Hartman, John</creatorcontrib><creatorcontrib>Rao, Sumati</creatorcontrib><creatorcontrib>Lubinga, Solomon</creatorcontrib><creatorcontrib>Stenehjem, David</creatorcontrib><title>Real-world outcomes of immunotherapy–based regimens in first-line advanced non-small cell lung cancer</title><title>Lung cancer (Amsterdam, Netherlands)</title><addtitle>Lung Cancer</addtitle><description>•We assessed real-world survival outcomes for 1L I-O in patients with advanced NSCLC.•Survival estimates were generally lower than those reported in pivotal trials.•There is room for improvement of outcomes in patients who receive 1L I-O regimens.•Specific subgroups may have limited treatment benefit from current I-O therapies.
First-line (1L) immunotherapy (I-O) has improved outcomes in patients with advanced non-small cell lung cancer (NSCLC) in clinical trials and is now routinely used alone or combined with chemotherapy. Although efficacy and safety of I-O therapies have been established in clinical trials, little is known about their performance and long-term efficacy in the real-world setting. We aimed to characterize real-world outcomes for patients with advanced NSCLC treated with 1L I-O therapy in the United States.
Patients aged ≥18 years with confirmed advanced (stage III–IV) NSCLC who received either 1L I-O monotherapy or single-agent I-O combined with chemotherapy on or after January 1, 2016 were identified from the Flatiron Health database. Primary objectives were to examine overall survival (OS) and real-world progression-free survival. Index date was defined as date of 1L treatment initiation; data cut-off date was June 30, 2020.
Among 4271 patients receiving I-O plus chemotherapy, median OS was 10.6 (95 % confidence interval [CI], 9.3–11.8) months in patients with squamous NSCLC (n=814) and 12.0 (95 % CI, 11.3–12.8) months in those with non-squamous disease (n=3457). Regardless of histology, patients with high (≥50 %) tumor programmed death ligand 1 (PD-L1) expression demonstrated longer median OS vs those with low expression. Among 3041 patients receiving I-O monotherapy, median OS was 11.3 (95 % CI, 9.8–12.8) months in patients with squamous NSCLC (n=875) and 14.1 (95 % CI, 12.4–15.8) months in those with non-squamous disease (n=2166). OS benefit appeared to be greatest in the ≥50 % tumor PD-L1 expression group of the non-squamous cohort.
Survival estimates were generally lower than those reported in pivotal clinical trials. These findings indicate that there remains room for improvement of real-world survival outcomes in patients with advanced NSCLC who receive 1L I-O–based regimens and for identification of subgroups of patients not benefitting from treatment with current I-O regimens.</description><subject>Immune checkpoint inhibitors</subject><subject>Immunotherapy</subject><subject>Non-small cell lung cancer</subject><subject>Real-world outcomes</subject><issn>0169-5002</issn><issn>1872-8332</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkM1O3DAQgK2qqGyhjwDysZcE_yRxfKqqFdBKKyEhOFuOPd56ldhbO6Hi1nfgDXkSEu2Way8zh_nm70PogpKSEtpc7cp-ClujQ8kIoyWpSkLEB7SirWBFyzn7iFYzJ4uaEHaKPue8I4QKSuQndMp5K6tK8hXa3oPuiz8x9RbHaTRxgIyjw34YphDHX5D0_vn170unM1icYOsHCBn7gJ1PeSx6HwBr-6SDmeshhiIPuu-xgTksF2KzlNI5OnG6z_DlmM_Q4831w_pHsbm7_bn-vilMRdlYVKB5xYjkVNacWSG6WsjWScaMFRQaJ0ntuqZpZMWs1oS7RlrOqKQMqHaOn6Gvh7n7FH9PkEc1-LwcowPEKStW05axRtRiRusDalLMOYFT--QHnZ4VJWpxrHbq6FgtjhWp1Ox47rs8rpi6Aex71z-pM_DtAMD86JOHpLLxsAjyCcyobPT_WfEG6L-Rlg</recordid><startdate>202106</startdate><enddate>202106</enddate><creator>Waterhouse, David</creator><creator>Lam, Jenny</creator><creator>Betts, Keith A.</creator><creator>Yin, Lei</creator><creator>Gao, Sophie</creator><creator>Yuan, Yong</creator><creator>Hartman, John</creator><creator>Rao, Sumati</creator><creator>Lubinga, Solomon</creator><creator>Stenehjem, David</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9741-7376</orcidid><orcidid>https://orcid.org/0000-0003-0539-9156</orcidid><orcidid>https://orcid.org/0000-0001-5589-9939</orcidid><orcidid>https://orcid.org/0000-0002-1831-285X</orcidid></search><sort><creationdate>202106</creationdate><title>Real-world outcomes of immunotherapy–based regimens in first-line advanced non-small cell lung cancer</title><author>Waterhouse, David ; Lam, Jenny ; Betts, Keith A. ; Yin, Lei ; Gao, Sophie ; Yuan, Yong ; Hartman, John ; Rao, Sumati ; Lubinga, Solomon ; Stenehjem, David</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c412t-4ea34209319532d77b5798f922cd71e6f905fb666942daa03f69d321912e1aff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Immune checkpoint inhibitors</topic><topic>Immunotherapy</topic><topic>Non-small cell lung cancer</topic><topic>Real-world outcomes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Waterhouse, David</creatorcontrib><creatorcontrib>Lam, Jenny</creatorcontrib><creatorcontrib>Betts, Keith A.</creatorcontrib><creatorcontrib>Yin, Lei</creatorcontrib><creatorcontrib>Gao, Sophie</creatorcontrib><creatorcontrib>Yuan, Yong</creatorcontrib><creatorcontrib>Hartman, John</creatorcontrib><creatorcontrib>Rao, Sumati</creatorcontrib><creatorcontrib>Lubinga, Solomon</creatorcontrib><creatorcontrib>Stenehjem, David</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Lung cancer (Amsterdam, Netherlands)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Waterhouse, David</au><au>Lam, Jenny</au><au>Betts, Keith A.</au><au>Yin, Lei</au><au>Gao, Sophie</au><au>Yuan, Yong</au><au>Hartman, John</au><au>Rao, Sumati</au><au>Lubinga, Solomon</au><au>Stenehjem, David</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Real-world outcomes of immunotherapy–based regimens in first-line advanced non-small cell lung cancer</atitle><jtitle>Lung cancer (Amsterdam, Netherlands)</jtitle><addtitle>Lung Cancer</addtitle><date>2021-06</date><risdate>2021</risdate><volume>156</volume><spage>41</spage><epage>49</epage><pages>41-49</pages><issn>0169-5002</issn><eissn>1872-8332</eissn><abstract>•We assessed real-world survival outcomes for 1L I-O in patients with advanced NSCLC.•Survival estimates were generally lower than those reported in pivotal trials.•There is room for improvement of outcomes in patients who receive 1L I-O regimens.•Specific subgroups may have limited treatment benefit from current I-O therapies.
First-line (1L) immunotherapy (I-O) has improved outcomes in patients with advanced non-small cell lung cancer (NSCLC) in clinical trials and is now routinely used alone or combined with chemotherapy. Although efficacy and safety of I-O therapies have been established in clinical trials, little is known about their performance and long-term efficacy in the real-world setting. We aimed to characterize real-world outcomes for patients with advanced NSCLC treated with 1L I-O therapy in the United States.
Patients aged ≥18 years with confirmed advanced (stage III–IV) NSCLC who received either 1L I-O monotherapy or single-agent I-O combined with chemotherapy on or after January 1, 2016 were identified from the Flatiron Health database. Primary objectives were to examine overall survival (OS) and real-world progression-free survival. Index date was defined as date of 1L treatment initiation; data cut-off date was June 30, 2020.
Among 4271 patients receiving I-O plus chemotherapy, median OS was 10.6 (95 % confidence interval [CI], 9.3–11.8) months in patients with squamous NSCLC (n=814) and 12.0 (95 % CI, 11.3–12.8) months in those with non-squamous disease (n=3457). Regardless of histology, patients with high (≥50 %) tumor programmed death ligand 1 (PD-L1) expression demonstrated longer median OS vs those with low expression. Among 3041 patients receiving I-O monotherapy, median OS was 11.3 (95 % CI, 9.8–12.8) months in patients with squamous NSCLC (n=875) and 14.1 (95 % CI, 12.4–15.8) months in those with non-squamous disease (n=2166). OS benefit appeared to be greatest in the ≥50 % tumor PD-L1 expression group of the non-squamous cohort.
Survival estimates were generally lower than those reported in pivotal clinical trials. These findings indicate that there remains room for improvement of real-world survival outcomes in patients with advanced NSCLC who receive 1L I-O–based regimens and for identification of subgroups of patients not benefitting from treatment with current I-O regimens.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>33894493</pmid><doi>10.1016/j.lungcan.2021.04.007</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-9741-7376</orcidid><orcidid>https://orcid.org/0000-0003-0539-9156</orcidid><orcidid>https://orcid.org/0000-0001-5589-9939</orcidid><orcidid>https://orcid.org/0000-0002-1831-285X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Immune checkpoint inhibitors Immunotherapy Non-small cell lung cancer Real-world outcomes |
title | Real-world outcomes of immunotherapy–based regimens in first-line advanced non-small cell lung cancer |
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