Adiposity and cancer survival: a systematic review and meta-analysis

Purpose The increasing availability of clinical imaging tests (especially CT and MRI) that directly quantify adipose tissue has led to a rapid increase in studies examining the relationship of visceral, subcutaneous, and overall adiposity to cancer survival. To summarize this emerging body of litera...

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Veröffentlicht in:Cancer causes & control 2022-10, Vol.33 (10), p.1219-1246
Hauptverfasser: Cheng, En, Kirley, Jocelyn, Cespedes Feliciano, Elizabeth M., Caan, Bette J.
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container_end_page 1246
container_issue 10
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container_title Cancer causes & control
container_volume 33
creator Cheng, En
Kirley, Jocelyn
Cespedes Feliciano, Elizabeth M.
Caan, Bette J.
description Purpose The increasing availability of clinical imaging tests (especially CT and MRI) that directly quantify adipose tissue has led to a rapid increase in studies examining the relationship of visceral, subcutaneous, and overall adiposity to cancer survival. To summarize this emerging body of literature, we conducted a systematic review and meta-analysis of imaging-measured as well as anthropometric proxies for adipose tissue distribution and cancer survival across a wide range of cancer types. Methods Using keywords related to adiposity, cancer, and survival, we conducted a systematic search of the literature in PubMed and MEDLINE, Embase, and Web of Science Core Collection databases from database inception to 30 June 2021. We used a random-effect method to calculate pooled hazard ratios (HR) and corresponding 95% confidence intervals (CI) within each cancer type and tested for heterogeneity using Cochran’s Q test and the I 2 test. Results We included 203 records for this review, of which 128 records were utilized for quantitative analysis among 10 cancer types: breast, colorectal, gastroesophageal, head and neck, hepatocellular carcinoma, lung, ovarian, pancreatic, prostate, and renal cancer. We found that imaging-measured visceral, subcutaneous, and total adiposity were not significantly associated with increased risk of overall mortality, death from primary cancer, or cancer progression among patients diagnosed with these 10 cancer types; however, we found significant or high heterogeneity for many cancer types. For example, heterogeneity was similarly high when the pooled HRs (95% CI) for overall mortality associated with visceral adiposity were essentially null as in 1.03 (0.55, 1.92; I 2  = 58%) for breast, 0.99 (0.81, 1.21; I 2  = 71%) for colorectal, versus when they demonstrated a potential increased risk 1.17 (0.85, 1.60; I 2  = 78%) for hepatocellular carcinoma and 1.62 (0.90, 2.95; I 2  = 84%) for renal cancer. Conclusion Greater adiposity at diagnosis (directly measured by imaging) is not associated with worse survival among cancer survivors. However, heterogeneity and other potential limitations were noted across studies, suggesting differences in study design and adiposity measurement approaches, making interpretation of meta-analyses challenging. Future work to standardize imaging measurements and data analyses will strengthen research on the role of adiposity in cancer survival.
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To summarize this emerging body of literature, we conducted a systematic review and meta-analysis of imaging-measured as well as anthropometric proxies for adipose tissue distribution and cancer survival across a wide range of cancer types. Methods Using keywords related to adiposity, cancer, and survival, we conducted a systematic search of the literature in PubMed and MEDLINE, Embase, and Web of Science Core Collection databases from database inception to 30 June 2021. We used a random-effect method to calculate pooled hazard ratios (HR) and corresponding 95% confidence intervals (CI) within each cancer type and tested for heterogeneity using Cochran’s Q test and the I 2 test. Results We included 203 records for this review, of which 128 records were utilized for quantitative analysis among 10 cancer types: breast, colorectal, gastroesophageal, head and neck, hepatocellular carcinoma, lung, ovarian, pancreatic, prostate, and renal cancer. We found that imaging-measured visceral, subcutaneous, and total adiposity were not significantly associated with increased risk of overall mortality, death from primary cancer, or cancer progression among patients diagnosed with these 10 cancer types; however, we found significant or high heterogeneity for many cancer types. For example, heterogeneity was similarly high when the pooled HRs (95% CI) for overall mortality associated with visceral adiposity were essentially null as in 1.03 (0.55, 1.92; I 2  = 58%) for breast, 0.99 (0.81, 1.21; I 2  = 71%) for colorectal, versus when they demonstrated a potential increased risk 1.17 (0.85, 1.60; I 2  = 78%) for hepatocellular carcinoma and 1.62 (0.90, 2.95; I 2  = 84%) for renal cancer. Conclusion Greater adiposity at diagnosis (directly measured by imaging) is not associated with worse survival among cancer survivors. However, heterogeneity and other potential limitations were noted across studies, suggesting differences in study design and adiposity measurement approaches, making interpretation of meta-analyses challenging. Future work to standardize imaging measurements and data analyses will strengthen research on the role of adiposity in cancer survival.</description><identifier>ISSN: 0957-5243</identifier><identifier>EISSN: 1573-7225</identifier><identifier>DOI: 10.1007/s10552-022-01613-7</identifier><identifier>PMID: 35971021</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Adipose tissue ; Adiposity ; Biomedical and Life Sciences ; Biomedicine ; Body fat ; Breast cancer ; Cancer ; Cancer Research ; Carcinoma, Hepatocellular ; Colorectal cancer ; Colorectal carcinoma ; Colorectal Neoplasms ; Computed tomography ; Epidemiology ; Head and neck carcinoma ; Hematology ; Hepatocellular carcinoma ; Heterogeneity ; Humans ; Kidney cancer ; Kidney Neoplasms ; Liver cancer ; Liver Neoplasms ; Lung cancer ; Lung carcinoma ; Male ; Medical imaging ; Meta-analysis ; Mortality ; Obesity ; Oncology ; Pancreatic cancer ; Pancreatic carcinoma ; Prostate cancer ; Public Health ; Review Article ; Survival ; Systematic review</subject><ispartof>Cancer causes &amp; control, 2022-10, Vol.33 (10), p.1219-1246</ispartof><rights>The Author(s), under exclusive licence to Springer Nature Switzerland AG 2022. 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The Author(s), under exclusive licence to Springer Nature Switzerland AG.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-d8cc16567bf8af61a86fce59b613f4e59a8095a85c61fe135447140df9cc5f693</citedby><cites>FETCH-LOGICAL-c475t-d8cc16567bf8af61a86fce59b613f4e59a8095a85c61fe135447140df9cc5f693</cites><orcidid>0000-0002-5803-310X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10552-022-01613-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10552-022-01613-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,780,784,885,27922,27923,41486,42555,51317</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35971021$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cheng, En</creatorcontrib><creatorcontrib>Kirley, Jocelyn</creatorcontrib><creatorcontrib>Cespedes Feliciano, Elizabeth M.</creatorcontrib><creatorcontrib>Caan, Bette J.</creatorcontrib><title>Adiposity and cancer survival: a systematic review and meta-analysis</title><title>Cancer causes &amp; control</title><addtitle>Cancer Causes Control</addtitle><addtitle>Cancer Causes Control</addtitle><description>Purpose The increasing availability of clinical imaging tests (especially CT and MRI) that directly quantify adipose tissue has led to a rapid increase in studies examining the relationship of visceral, subcutaneous, and overall adiposity to cancer survival. To summarize this emerging body of literature, we conducted a systematic review and meta-analysis of imaging-measured as well as anthropometric proxies for adipose tissue distribution and cancer survival across a wide range of cancer types. Methods Using keywords related to adiposity, cancer, and survival, we conducted a systematic search of the literature in PubMed and MEDLINE, Embase, and Web of Science Core Collection databases from database inception to 30 June 2021. We used a random-effect method to calculate pooled hazard ratios (HR) and corresponding 95% confidence intervals (CI) within each cancer type and tested for heterogeneity using Cochran’s Q test and the I 2 test. Results We included 203 records for this review, of which 128 records were utilized for quantitative analysis among 10 cancer types: breast, colorectal, gastroesophageal, head and neck, hepatocellular carcinoma, lung, ovarian, pancreatic, prostate, and renal cancer. We found that imaging-measured visceral, subcutaneous, and total adiposity were not significantly associated with increased risk of overall mortality, death from primary cancer, or cancer progression among patients diagnosed with these 10 cancer types; however, we found significant or high heterogeneity for many cancer types. For example, heterogeneity was similarly high when the pooled HRs (95% CI) for overall mortality associated with visceral adiposity were essentially null as in 1.03 (0.55, 1.92; I 2  = 58%) for breast, 0.99 (0.81, 1.21; I 2  = 71%) for colorectal, versus when they demonstrated a potential increased risk 1.17 (0.85, 1.60; I 2  = 78%) for hepatocellular carcinoma and 1.62 (0.90, 2.95; I 2  = 84%) for renal cancer. Conclusion Greater adiposity at diagnosis (directly measured by imaging) is not associated with worse survival among cancer survivors. However, heterogeneity and other potential limitations were noted across studies, suggesting differences in study design and adiposity measurement approaches, making interpretation of meta-analyses challenging. 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Kirley, Jocelyn ; Cespedes Feliciano, Elizabeth M. ; Caan, Bette J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-d8cc16567bf8af61a86fce59b613f4e59a8095a85c61fe135447140df9cc5f693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adipose tissue</topic><topic>Adiposity</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Body fat</topic><topic>Breast cancer</topic><topic>Cancer</topic><topic>Cancer Research</topic><topic>Carcinoma, Hepatocellular</topic><topic>Colorectal cancer</topic><topic>Colorectal carcinoma</topic><topic>Colorectal Neoplasms</topic><topic>Computed tomography</topic><topic>Epidemiology</topic><topic>Head and neck carcinoma</topic><topic>Hematology</topic><topic>Hepatocellular carcinoma</topic><topic>Heterogeneity</topic><topic>Humans</topic><topic>Kidney cancer</topic><topic>Kidney Neoplasms</topic><topic>Liver cancer</topic><topic>Liver Neoplasms</topic><topic>Lung cancer</topic><topic>Lung carcinoma</topic><topic>Male</topic><topic>Medical imaging</topic><topic>Meta-analysis</topic><topic>Mortality</topic><topic>Obesity</topic><topic>Oncology</topic><topic>Pancreatic cancer</topic><topic>Pancreatic carcinoma</topic><topic>Prostate cancer</topic><topic>Public Health</topic><topic>Review Article</topic><topic>Survival</topic><topic>Systematic review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cheng, En</creatorcontrib><creatorcontrib>Kirley, Jocelyn</creatorcontrib><creatorcontrib>Cespedes Feliciano, Elizabeth M.</creatorcontrib><creatorcontrib>Caan, Bette J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; 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control</jtitle><stitle>Cancer Causes Control</stitle><addtitle>Cancer Causes Control</addtitle><date>2022-10-01</date><risdate>2022</risdate><volume>33</volume><issue>10</issue><spage>1219</spage><epage>1246</epage><pages>1219-1246</pages><issn>0957-5243</issn><eissn>1573-7225</eissn><abstract>Purpose The increasing availability of clinical imaging tests (especially CT and MRI) that directly quantify adipose tissue has led to a rapid increase in studies examining the relationship of visceral, subcutaneous, and overall adiposity to cancer survival. To summarize this emerging body of literature, we conducted a systematic review and meta-analysis of imaging-measured as well as anthropometric proxies for adipose tissue distribution and cancer survival across a wide range of cancer types. Methods Using keywords related to adiposity, cancer, and survival, we conducted a systematic search of the literature in PubMed and MEDLINE, Embase, and Web of Science Core Collection databases from database inception to 30 June 2021. We used a random-effect method to calculate pooled hazard ratios (HR) and corresponding 95% confidence intervals (CI) within each cancer type and tested for heterogeneity using Cochran’s Q test and the I 2 test. Results We included 203 records for this review, of which 128 records were utilized for quantitative analysis among 10 cancer types: breast, colorectal, gastroesophageal, head and neck, hepatocellular carcinoma, lung, ovarian, pancreatic, prostate, and renal cancer. We found that imaging-measured visceral, subcutaneous, and total adiposity were not significantly associated with increased risk of overall mortality, death from primary cancer, or cancer progression among patients diagnosed with these 10 cancer types; however, we found significant or high heterogeneity for many cancer types. For example, heterogeneity was similarly high when the pooled HRs (95% CI) for overall mortality associated with visceral adiposity were essentially null as in 1.03 (0.55, 1.92; I 2  = 58%) for breast, 0.99 (0.81, 1.21; I 2  = 71%) for colorectal, versus when they demonstrated a potential increased risk 1.17 (0.85, 1.60; I 2  = 78%) for hepatocellular carcinoma and 1.62 (0.90, 2.95; I 2  = 84%) for renal cancer. Conclusion Greater adiposity at diagnosis (directly measured by imaging) is not associated with worse survival among cancer survivors. However, heterogeneity and other potential limitations were noted across studies, suggesting differences in study design and adiposity measurement approaches, making interpretation of meta-analyses challenging. Future work to standardize imaging measurements and data analyses will strengthen research on the role of adiposity in cancer survival.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>35971021</pmid><doi>10.1007/s10552-022-01613-7</doi><tpages>28</tpages><orcidid>https://orcid.org/0000-0002-5803-310X</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adipose tissue
Adiposity
Biomedical and Life Sciences
Biomedicine
Body fat
Breast cancer
Cancer
Cancer Research
Carcinoma, Hepatocellular
Colorectal cancer
Colorectal carcinoma
Colorectal Neoplasms
Computed tomography
Epidemiology
Head and neck carcinoma
Hematology
Hepatocellular carcinoma
Heterogeneity
Humans
Kidney cancer
Kidney Neoplasms
Liver cancer
Liver Neoplasms
Lung cancer
Lung carcinoma
Male
Medical imaging
Meta-analysis
Mortality
Obesity
Oncology
Pancreatic cancer
Pancreatic carcinoma
Prostate cancer
Public Health
Review Article
Survival
Systematic review
title Adiposity and cancer survival: a systematic review and meta-analysis
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