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Effect of Comorbidity on Outcomes of Patients with Advanced Non-Small Cell Lung Cancer Undergoing Anti-PD1 Immunotherapy
BACKGROUND Comorbidities are reportedly related to the survival of patients with non-small cell lung cancer (NSCLC). The purpose of this study was to explore the impact of comorbidity, assessed by the Charlson comorbidity index (CCI) and the simplified comorbidity scores (SCS) on clinical outcomes o...
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Published in: | Medical science monitor 2020-09, Vol.26, p.e922576-e922576 |
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description | BACKGROUND Comorbidities are reportedly related to the survival of patients with non-small cell lung cancer (NSCLC). The purpose of this study was to explore the impact of comorbidity, assessed by the Charlson comorbidity index (CCI) and the simplified comorbidity scores (SCS) on clinical outcomes of patients with NSCLC treated with immune checkpoint inhibitors. MATERIAL AND METHODS Sixty-six patients with NSCLC who received programmed cell death protein 1 (PD1) inhibitors in our institution in the past 2 years were enrolled in this retrospective study. Data on comorbidity (CCI and SCS) and clinical outcomes, including progression-free survival (PFS), immunotherapy responses, and immunotherapy-related adverse events, were analyzed. RESULTS The disease control rate was obviously higher among patients in the CCI |
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The purpose of this study was to explore the impact of comorbidity, assessed by the Charlson comorbidity index (CCI) and the simplified comorbidity scores (SCS) on clinical outcomes of patients with NSCLC treated with immune checkpoint inhibitors. MATERIAL AND METHODS Sixty-six patients with NSCLC who received programmed cell death protein 1 (PD1) inhibitors in our institution in the past 2 years were enrolled in this retrospective study. Data on comorbidity (CCI and SCS) and clinical outcomes, including progression-free survival (PFS), immunotherapy responses, and immunotherapy-related adverse events, were analyzed. RESULTS The disease control rate was obviously higher among patients in the CCI <1 group than the CCI ≥1 group (P<0.001), but were similar between the SCS <8 group and SCS ≥8 group (P=0.585). The median PFS in the CCI <1 group was 271.0 days (95% CI: 214.3-327.7 days) compared with 232.0 days (95% CI: 66.2-397.8 days) for the CCI ≥1 group (P=0.0084). However, the median PFS showed no difference between the groups with SCS <8 at 271.0 days (95% CI: 138.7-403.3 days) versus SCS ≥8 at 222.0 days (95% CI: 196.2-247.8 days), P=0.2106). The incidence of adverse events was similar among patients with high versus low comorbidity indexes (CCI: 35.8% versus 23.6%, P=0.286, respectively; and SCS: 28.0% versus 29.3%, respectively, P=0.912). CONCLUSIONS The comorbidity burden might be a predictor for survival in patients with NSCLC undergoing PD1 inhibitor immunotherapy.</description><identifier>ISSN: 1643-3750</identifier><identifier>ISSN: 1234-1010</identifier><identifier>EISSN: 1643-3750</identifier><identifier>DOI: 10.12659/MSM.922576</identifier><identifier>PMID: 32893263</identifier><language>eng</language><publisher>United States: International Scientific Literature, Inc</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Clinical Research ; Comorbidity ; Female ; Humans ; Immune Checkpoint Inhibitors - therapeutic use ; Lung Neoplasms - drug therapy ; Male ; Middle Aged ; Progression-Free Survival ; Retrospective Studies ; Treatment Outcome</subject><ispartof>Medical science monitor, 2020-09, Vol.26, p.e922576-e922576</ispartof><rights>Med Sci Monit, 2020 2020</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-f83e431bc5427e6dd1834a389bcc3f9d227a451e8b1ba435a6473cddc81a0f423</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496511/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496511/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32893263$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zeng, Xianghua</creatorcontrib><creatorcontrib>Zhu, Shicong</creatorcontrib><creatorcontrib>Xu, Cheng</creatorcontrib><creatorcontrib>Wang, Zhongyu</creatorcontrib><creatorcontrib>Su, Xingxing</creatorcontrib><creatorcontrib>Zeng, Dong</creatorcontrib><creatorcontrib>Long, Haixia</creatorcontrib><creatorcontrib>Zhu, Bo</creatorcontrib><title>Effect of Comorbidity on Outcomes of Patients with Advanced Non-Small Cell Lung Cancer Undergoing Anti-PD1 Immunotherapy</title><title>Medical science monitor</title><addtitle>Med Sci Monit</addtitle><description>BACKGROUND Comorbidities are reportedly related to the survival of patients with non-small cell lung cancer (NSCLC). The purpose of this study was to explore the impact of comorbidity, assessed by the Charlson comorbidity index (CCI) and the simplified comorbidity scores (SCS) on clinical outcomes of patients with NSCLC treated with immune checkpoint inhibitors. MATERIAL AND METHODS Sixty-six patients with NSCLC who received programmed cell death protein 1 (PD1) inhibitors in our institution in the past 2 years were enrolled in this retrospective study. Data on comorbidity (CCI and SCS) and clinical outcomes, including progression-free survival (PFS), immunotherapy responses, and immunotherapy-related adverse events, were analyzed. RESULTS The disease control rate was obviously higher among patients in the CCI <1 group than the CCI ≥1 group (P<0.001), but were similar between the SCS <8 group and SCS ≥8 group (P=0.585). The median PFS in the CCI <1 group was 271.0 days (95% CI: 214.3-327.7 days) compared with 232.0 days (95% CI: 66.2-397.8 days) for the CCI ≥1 group (P=0.0084). However, the median PFS showed no difference between the groups with SCS <8 at 271.0 days (95% CI: 138.7-403.3 days) versus SCS ≥8 at 222.0 days (95% CI: 196.2-247.8 days), P=0.2106). The incidence of adverse events was similar among patients with high versus low comorbidity indexes (CCI: 35.8% versus 23.6%, P=0.286, respectively; and SCS: 28.0% versus 29.3%, respectively, P=0.912). CONCLUSIONS The comorbidity burden might be a predictor for survival in patients with NSCLC undergoing PD1 inhibitor immunotherapy.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Clinical Research</subject><subject>Comorbidity</subject><subject>Female</subject><subject>Humans</subject><subject>Immune Checkpoint Inhibitors - therapeutic use</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Progression-Free Survival</subject><subject>Retrospective Studies</subject><subject>Treatment Outcome</subject><issn>1643-3750</issn><issn>1234-1010</issn><issn>1643-3750</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNpVUclOwzAQtRCIpXDijnxEQgFvcZILUhVWqSwScLYc22mNGrvYDtC_J1BAcJkZzXt6szwA9jE6xoTn1cnNw81xRUhe8DWwjTmjGS1ytP6n3gI7MT4jREqO8k2wRUlZUcLpNng_b1ujEvQtrH3nQ2O1TUvoHbzrk_KdiZ_QvUzWuBThm00zONav0imj4a132UMn53NYmyFMejeF9ScU4JPTJky9HTpjl2x2f4bhddf1zqeZCXKx3AUbrZxHs_edR-Dp4vyxvsomd5fX9XiSKVrilLUlNYziRuWMFIZrjUvKJC2rRinaVpqQQrIcm7LBjWQ0l5wVVGmtSixRywgdgdOV7qJvOqPVcEaQc7EItpNhKby04j_i7ExM_asoWMVzjAeBw2-B4F96E5PobFTDvdIZ30dBGEOcczS8cwSOVlQVfIzBtL9jMBJfXonBK7HyamAf_N3sl_tjDv0AKXmQvQ</recordid><startdate>20200907</startdate><enddate>20200907</enddate><creator>Zeng, Xianghua</creator><creator>Zhu, Shicong</creator><creator>Xu, Cheng</creator><creator>Wang, Zhongyu</creator><creator>Su, Xingxing</creator><creator>Zeng, Dong</creator><creator>Long, Haixia</creator><creator>Zhu, Bo</creator><general>International Scientific Literature, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20200907</creationdate><title>Effect of Comorbidity on Outcomes of Patients with Advanced Non-Small Cell Lung Cancer Undergoing Anti-PD1 Immunotherapy</title><author>Zeng, Xianghua ; Zhu, Shicong ; Xu, Cheng ; Wang, Zhongyu ; Su, Xingxing ; Zeng, Dong ; Long, Haixia ; Zhu, Bo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c381t-f83e431bc5427e6dd1834a389bcc3f9d227a451e8b1ba435a6473cddc81a0f423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Clinical Research</topic><topic>Comorbidity</topic><topic>Female</topic><topic>Humans</topic><topic>Immune Checkpoint Inhibitors - therapeutic use</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Progression-Free Survival</topic><topic>Retrospective Studies</topic><topic>Treatment Outcome</topic><toplevel>online_resources</toplevel><creatorcontrib>Zeng, Xianghua</creatorcontrib><creatorcontrib>Zhu, Shicong</creatorcontrib><creatorcontrib>Xu, Cheng</creatorcontrib><creatorcontrib>Wang, Zhongyu</creatorcontrib><creatorcontrib>Su, Xingxing</creatorcontrib><creatorcontrib>Zeng, Dong</creatorcontrib><creatorcontrib>Long, Haixia</creatorcontrib><creatorcontrib>Zhu, Bo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Medical science monitor</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zeng, Xianghua</au><au>Zhu, Shicong</au><au>Xu, Cheng</au><au>Wang, Zhongyu</au><au>Su, Xingxing</au><au>Zeng, Dong</au><au>Long, Haixia</au><au>Zhu, Bo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Comorbidity on Outcomes of Patients with Advanced Non-Small Cell Lung Cancer Undergoing Anti-PD1 Immunotherapy</atitle><jtitle>Medical science monitor</jtitle><addtitle>Med Sci Monit</addtitle><date>2020-09-07</date><risdate>2020</risdate><volume>26</volume><spage>e922576</spage><epage>e922576</epage><pages>e922576-e922576</pages><issn>1643-3750</issn><issn>1234-1010</issn><eissn>1643-3750</eissn><abstract>BACKGROUND Comorbidities are reportedly related to the survival of patients with non-small cell lung cancer (NSCLC). The purpose of this study was to explore the impact of comorbidity, assessed by the Charlson comorbidity index (CCI) and the simplified comorbidity scores (SCS) on clinical outcomes of patients with NSCLC treated with immune checkpoint inhibitors. MATERIAL AND METHODS Sixty-six patients with NSCLC who received programmed cell death protein 1 (PD1) inhibitors in our institution in the past 2 years were enrolled in this retrospective study. Data on comorbidity (CCI and SCS) and clinical outcomes, including progression-free survival (PFS), immunotherapy responses, and immunotherapy-related adverse events, were analyzed. RESULTS The disease control rate was obviously higher among patients in the CCI <1 group than the CCI ≥1 group (P<0.001), but were similar between the SCS <8 group and SCS ≥8 group (P=0.585). The median PFS in the CCI <1 group was 271.0 days (95% CI: 214.3-327.7 days) compared with 232.0 days (95% CI: 66.2-397.8 days) for the CCI ≥1 group (P=0.0084). However, the median PFS showed no difference between the groups with SCS <8 at 271.0 days (95% CI: 138.7-403.3 days) versus SCS ≥8 at 222.0 days (95% CI: 196.2-247.8 days), P=0.2106). The incidence of adverse events was similar among patients with high versus low comorbidity indexes (CCI: 35.8% versus 23.6%, P=0.286, respectively; and SCS: 28.0% versus 29.3%, respectively, P=0.912). CONCLUSIONS The comorbidity burden might be a predictor for survival in patients with NSCLC undergoing PD1 inhibitor immunotherapy.</abstract><cop>United States</cop><pub>International Scientific Literature, Inc</pub><pmid>32893263</pmid><doi>10.12659/MSM.922576</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Aged, 80 and over Carcinoma, Non-Small-Cell Lung - drug therapy Clinical Research Comorbidity Female Humans Immune Checkpoint Inhibitors - therapeutic use Lung Neoplasms - drug therapy Male Middle Aged Progression-Free Survival Retrospective Studies Treatment Outcome |
title | Effect of Comorbidity on Outcomes of Patients with Advanced Non-Small Cell Lung Cancer Undergoing Anti-PD1 Immunotherapy |
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