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Intensive glucose control and risk of cancer in patients with type 2 diabetes
Aims/hypothesis Type 2 diabetes has been associated with an increased risk of cancer. This study examines the effect of more vs less intensive glucose control on the risk of cancer in patients with type 2 diabetes. Methods All 11,140 participants from the Action in Diabetes and Vascular Disease: Pre...
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Published in: | Diabetologia 2011-07, Vol.54 (7), p.1608-1614 |
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creator | Stefansdottir, G. Zoungas, S. Chalmers, J. Kengne, A. P. Knol, M. J. Leufkens, H. G. M. Patel, A. Woodward, M. Grobbee, D. E. De Bruin, M. L. |
description | Aims/hypothesis
Type 2 diabetes has been associated with an increased risk of cancer. This study examines the effect of more vs less intensive glucose control on the risk of cancer in patients with type 2 diabetes.
Methods
All 11,140 participants from the Action in Diabetes and Vascular Disease: Preterax and Diamicron-MR Controlled Evaluation (ADVANCE) trial (ClinicalTrials.gov NCT00145925) were studied. Cancer incidence and cancer mortality was compared in groups randomised to intensive or standard glucose control. Information on events during follow-up was obtained from serious adverse event reports and death certificates. HRs (95% CI) were calculated for all cancers, all solid cancers, cancer deaths and site-specific cancers.
Results
After a median follow-up of 5 years, 363 and 337 cancer events were reported in the intensive and standard control groups, respectively (incidence 1.39/100 person-years [PY] and 1.28/100 PY; HR 1.08 [95% CI 0.93–1.26]). The incidences of all solid cancers and cancer deaths were 1.25/100 PY and 0.15/100 PY in the intensive group and 1.15/100 PY and 0.13/100 PY in the standard group (HR 1.09 [95% CI 0.93–1.27] for solid cancers, and 1.17 [0.75–1.84] for cancer death). Across all the major organ systems studied, no significant differences in the cancer incidences were observed in the intensive and standard control groups.
Conclusions/interpretations
More intensive glucose control achieved with a regimen that included greater use of gliclazide, insulin, metformin and other agents, did not affect the risk of cancer events or death in patients with type 2 diabetes. |
doi_str_mv | 10.1007/s00125-011-2104-x |
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Type 2 diabetes has been associated with an increased risk of cancer. This study examines the effect of more vs less intensive glucose control on the risk of cancer in patients with type 2 diabetes.
Methods
All 11,140 participants from the Action in Diabetes and Vascular Disease: Preterax and Diamicron-MR Controlled Evaluation (ADVANCE) trial (ClinicalTrials.gov NCT00145925) were studied. Cancer incidence and cancer mortality was compared in groups randomised to intensive or standard glucose control. Information on events during follow-up was obtained from serious adverse event reports and death certificates. HRs (95% CI) were calculated for all cancers, all solid cancers, cancer deaths and site-specific cancers.
Results
After a median follow-up of 5 years, 363 and 337 cancer events were reported in the intensive and standard control groups, respectively (incidence 1.39/100 person-years [PY] and 1.28/100 PY; HR 1.08 [95% CI 0.93–1.26]). The incidences of all solid cancers and cancer deaths were 1.25/100 PY and 0.15/100 PY in the intensive group and 1.15/100 PY and 0.13/100 PY in the standard group (HR 1.09 [95% CI 0.93–1.27] for solid cancers, and 1.17 [0.75–1.84] for cancer death). Across all the major organ systems studied, no significant differences in the cancer incidences were observed in the intensive and standard control groups.
Conclusions/interpretations
More intensive glucose control achieved with a regimen that included greater use of gliclazide, insulin, metformin and other agents, did not affect the risk of cancer events or death in patients with type 2 diabetes.</description><identifier>ISSN: 0012-186X</identifier><identifier>EISSN: 1432-0428</identifier><identifier>DOI: 10.1007/s00125-011-2104-x</identifier><identifier>PMID: 21509444</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Aged ; Biological and medical sciences ; Blood Glucose - drug effects ; Cancer therapies ; Diabetes ; Diabetes Mellitus, Type 2 - drug therapy ; Diabetes Mellitus, Type 2 - mortality ; Diabetes. Impaired glucose tolerance ; Disease ; Endocrine pancreas. Apud cells (diseases) ; Endocrinopathies ; Etiopathogenesis. Screening. Investigations. Target tissue resistance ; Female ; Gliclazide - adverse effects ; Gliclazide - therapeutic use ; Glucose ; Human Physiology ; Humans ; Hypoglycemic Agents - adverse effects ; Hypoglycemic Agents - therapeutic use ; Insulin - adverse effects ; Insulin - therapeutic use ; Insulin resistance ; Internal Medicine ; Male ; Medical sciences ; Medicine ; Medicine & Public Health ; Metabolic Diseases ; Metformin - adverse effects ; Metformin - therapeutic use ; Middle Aged ; Mortality ; Neoplasms - epidemiology ; Neoplasms - etiology ; Observational studies ; Tumors ; Urogenital system</subject><ispartof>Diabetologia, 2011-07, Vol.54 (7), p.1608-1614</ispartof><rights>Springer-Verlag 2011</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-5a6dc6460ce758c3cad1455a656d55bcfa6f7deec17aaa6b7c01fe2419a559243</citedby><cites>FETCH-LOGICAL-c443t-5a6dc6460ce758c3cad1455a656d55bcfa6f7deec17aaa6b7c01fe2419a559243</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24273783$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21509444$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stefansdottir, G.</creatorcontrib><creatorcontrib>Zoungas, S.</creatorcontrib><creatorcontrib>Chalmers, J.</creatorcontrib><creatorcontrib>Kengne, A. P.</creatorcontrib><creatorcontrib>Knol, M. J.</creatorcontrib><creatorcontrib>Leufkens, H. G. M.</creatorcontrib><creatorcontrib>Patel, A.</creatorcontrib><creatorcontrib>Woodward, M.</creatorcontrib><creatorcontrib>Grobbee, D. E.</creatorcontrib><creatorcontrib>De Bruin, M. L.</creatorcontrib><title>Intensive glucose control and risk of cancer in patients with type 2 diabetes</title><title>Diabetologia</title><addtitle>Diabetologia</addtitle><addtitle>Diabetologia</addtitle><description>Aims/hypothesis
Type 2 diabetes has been associated with an increased risk of cancer. This study examines the effect of more vs less intensive glucose control on the risk of cancer in patients with type 2 diabetes.
Methods
All 11,140 participants from the Action in Diabetes and Vascular Disease: Preterax and Diamicron-MR Controlled Evaluation (ADVANCE) trial (ClinicalTrials.gov NCT00145925) were studied. Cancer incidence and cancer mortality was compared in groups randomised to intensive or standard glucose control. Information on events during follow-up was obtained from serious adverse event reports and death certificates. HRs (95% CI) were calculated for all cancers, all solid cancers, cancer deaths and site-specific cancers.
Results
After a median follow-up of 5 years, 363 and 337 cancer events were reported in the intensive and standard control groups, respectively (incidence 1.39/100 person-years [PY] and 1.28/100 PY; HR 1.08 [95% CI 0.93–1.26]). The incidences of all solid cancers and cancer deaths were 1.25/100 PY and 0.15/100 PY in the intensive group and 1.15/100 PY and 0.13/100 PY in the standard group (HR 1.09 [95% CI 0.93–1.27] for solid cancers, and 1.17 [0.75–1.84] for cancer death). Across all the major organ systems studied, no significant differences in the cancer incidences were observed in the intensive and standard control groups.
Conclusions/interpretations
More intensive glucose control achieved with a regimen that included greater use of gliclazide, insulin, metformin and other agents, did not affect the risk of cancer events or death in patients with type 2 diabetes.</description><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Blood Glucose - drug effects</subject><subject>Cancer therapies</subject><subject>Diabetes</subject><subject>Diabetes Mellitus, Type 2 - drug therapy</subject><subject>Diabetes Mellitus, Type 2 - mortality</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Disease</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Female</subject><subject>Gliclazide - adverse effects</subject><subject>Gliclazide - therapeutic use</subject><subject>Glucose</subject><subject>Human Physiology</subject><subject>Humans</subject><subject>Hypoglycemic Agents - adverse effects</subject><subject>Hypoglycemic Agents - therapeutic use</subject><subject>Insulin - adverse effects</subject><subject>Insulin - therapeutic use</subject><subject>Insulin resistance</subject><subject>Internal Medicine</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metabolic Diseases</subject><subject>Metformin - adverse effects</subject><subject>Metformin - therapeutic use</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Neoplasms - epidemiology</subject><subject>Neoplasms - etiology</subject><subject>Observational studies</subject><subject>Tumors</subject><subject>Urogenital system</subject><issn>0012-186X</issn><issn>1432-0428</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp1kE1PwzAMhiMEYmPwA7igCIljIUmTpjuiiY9JQ1xA4halqTs6trQkKWz_nkwd7MTJkv28tvUgdE7JNSVE3nhCKBMJoTRhlPBkfYCGlKcsIZzlh2i4HSc0z94G6MT7BSEkFTw7RgNGBRlzzofoaWoDWF9_AZ4vO9N4wKaxwTVLrG2JXe0_cFNho60Bh2uLWx1qsMHj7zq847BpATNc1rqAAP4UHVV66eFsV0fo9f7uZfKYzJ4fppPbWWI4T0MidFaajGfEgBS5SY0uKRexK7JSiMJUOqtkCWCo1FpnhTSEVsA4HWshxoynI3TZ721d89mBD2rRdM7GkyqXRAgupYwQ7SHjGu8dVKp19Uq7jaJEbf2p3p-K_tTWn1rHzMVucVesoPxL_AqLwNUO0N7oZeWimNrvOc5kKvM0cqznfBzZObj9h_9f_wHtBog4</recordid><startdate>20110701</startdate><enddate>20110701</enddate><creator>Stefansdottir, G.</creator><creator>Zoungas, S.</creator><creator>Chalmers, J.</creator><creator>Kengne, A. P.</creator><creator>Knol, M. J.</creator><creator>Leufkens, H. G. M.</creator><creator>Patel, A.</creator><creator>Woodward, M.</creator><creator>Grobbee, D. E.</creator><creator>De Bruin, M. L.</creator><general>Springer-Verlag</general><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</scope><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>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20110701</creationdate><title>Intensive glucose control and risk of cancer in patients with type 2 diabetes</title><author>Stefansdottir, G. ; Zoungas, S. ; Chalmers, J. ; Kengne, A. P. ; Knol, M. J. ; Leufkens, H. G. M. ; Patel, A. ; Woodward, M. ; Grobbee, D. E. ; De Bruin, M. L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-5a6dc6460ce758c3cad1455a656d55bcfa6f7deec17aaa6b7c01fe2419a559243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Blood Glucose - drug effects</topic><topic>Cancer therapies</topic><topic>Diabetes</topic><topic>Diabetes Mellitus, Type 2 - drug therapy</topic><topic>Diabetes Mellitus, Type 2 - mortality</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Disease</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Female</topic><topic>Gliclazide - adverse effects</topic><topic>Gliclazide - therapeutic use</topic><topic>Glucose</topic><topic>Human Physiology</topic><topic>Humans</topic><topic>Hypoglycemic Agents - adverse effects</topic><topic>Hypoglycemic Agents - therapeutic use</topic><topic>Insulin - adverse effects</topic><topic>Insulin - therapeutic use</topic><topic>Insulin resistance</topic><topic>Internal Medicine</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metabolic Diseases</topic><topic>Metformin - adverse effects</topic><topic>Metformin - therapeutic use</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Neoplasms - epidemiology</topic><topic>Neoplasms - etiology</topic><topic>Observational studies</topic><topic>Tumors</topic><topic>Urogenital system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stefansdottir, G.</creatorcontrib><creatorcontrib>Zoungas, S.</creatorcontrib><creatorcontrib>Chalmers, J.</creatorcontrib><creatorcontrib>Kengne, A. P.</creatorcontrib><creatorcontrib>Knol, M. J.</creatorcontrib><creatorcontrib>Leufkens, H. G. M.</creatorcontrib><creatorcontrib>Patel, A.</creatorcontrib><creatorcontrib>Woodward, M.</creatorcontrib><creatorcontrib>Grobbee, D. E.</creatorcontrib><creatorcontrib>De Bruin, M. L.</creatorcontrib><collection>Pascal-Francis</collection><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>Immunology Abstracts</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database (Proquest)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Diabetologia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stefansdottir, G.</au><au>Zoungas, S.</au><au>Chalmers, J.</au><au>Kengne, A. P.</au><au>Knol, M. J.</au><au>Leufkens, H. G. M.</au><au>Patel, A.</au><au>Woodward, M.</au><au>Grobbee, D. E.</au><au>De Bruin, M. L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intensive glucose control and risk of cancer in patients with type 2 diabetes</atitle><jtitle>Diabetologia</jtitle><stitle>Diabetologia</stitle><addtitle>Diabetologia</addtitle><date>2011-07-01</date><risdate>2011</risdate><volume>54</volume><issue>7</issue><spage>1608</spage><epage>1614</epage><pages>1608-1614</pages><issn>0012-186X</issn><eissn>1432-0428</eissn><abstract>Aims/hypothesis
Type 2 diabetes has been associated with an increased risk of cancer. This study examines the effect of more vs less intensive glucose control on the risk of cancer in patients with type 2 diabetes.
Methods
All 11,140 participants from the Action in Diabetes and Vascular Disease: Preterax and Diamicron-MR Controlled Evaluation (ADVANCE) trial (ClinicalTrials.gov NCT00145925) were studied. Cancer incidence and cancer mortality was compared in groups randomised to intensive or standard glucose control. Information on events during follow-up was obtained from serious adverse event reports and death certificates. HRs (95% CI) were calculated for all cancers, all solid cancers, cancer deaths and site-specific cancers.
Results
After a median follow-up of 5 years, 363 and 337 cancer events were reported in the intensive and standard control groups, respectively (incidence 1.39/100 person-years [PY] and 1.28/100 PY; HR 1.08 [95% CI 0.93–1.26]). The incidences of all solid cancers and cancer deaths were 1.25/100 PY and 0.15/100 PY in the intensive group and 1.15/100 PY and 0.13/100 PY in the standard group (HR 1.09 [95% CI 0.93–1.27] for solid cancers, and 1.17 [0.75–1.84] for cancer death). Across all the major organ systems studied, no significant differences in the cancer incidences were observed in the intensive and standard control groups.
Conclusions/interpretations
More intensive glucose control achieved with a regimen that included greater use of gliclazide, insulin, metformin and other agents, did not affect the risk of cancer events or death in patients with type 2 diabetes.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>21509444</pmid><doi>10.1007/s00125-011-2104-x</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Biological and medical sciences Blood Glucose - drug effects Cancer therapies Diabetes Diabetes Mellitus, Type 2 - drug therapy Diabetes Mellitus, Type 2 - mortality Diabetes. Impaired glucose tolerance Disease Endocrine pancreas. Apud cells (diseases) Endocrinopathies Etiopathogenesis. Screening. Investigations. Target tissue resistance Female Gliclazide - adverse effects Gliclazide - therapeutic use Glucose Human Physiology Humans Hypoglycemic Agents - adverse effects Hypoglycemic Agents - therapeutic use Insulin - adverse effects Insulin - therapeutic use Insulin resistance Internal Medicine Male Medical sciences Medicine Medicine & Public Health Metabolic Diseases Metformin - adverse effects Metformin - therapeutic use Middle Aged Mortality Neoplasms - epidemiology Neoplasms - etiology Observational studies Tumors Urogenital system |
title | Intensive glucose control and risk of cancer in patients with type 2 diabetes |
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