Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Diabetologia 2011-07, Vol.54 (7), p.1608-1614
Main Authors: 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.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c443t-5a6dc6460ce758c3cad1455a656d55bcfa6f7deec17aaa6b7c01fe2419a559243
cites cdi_FETCH-LOGICAL-c443t-5a6dc6460ce758c3cad1455a656d55bcfa6f7deec17aaa6b7c01fe2419a559243
container_end_page 1614
container_issue 7
container_start_page 1608
container_title Diabetologia
container_volume 54
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
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_870554777</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2368758671</sourcerecordid><originalsourceid>FETCH-LOGICAL-c443t-5a6dc6460ce758c3cad1455a656d55bcfa6f7deec17aaa6b7c01fe2419a559243</originalsourceid><addsrcrecordid>eNp1kE1PwzAMhiMEYmPwA7igCIljIUmTpjuiiY9JQ1xA4halqTs6trQkKWz_nkwd7MTJkv28tvUgdE7JNSVE3nhCKBMJoTRhlPBkfYCGlKcsIZzlh2i4HSc0z94G6MT7BSEkFTw7RgNGBRlzzofoaWoDWF9_AZ4vO9N4wKaxwTVLrG2JXe0_cFNho60Bh2uLWx1qsMHj7zq847BpATNc1rqAAP4UHVV66eFsV0fo9f7uZfKYzJ4fppPbWWI4T0MidFaajGfEgBS5SY0uKRexK7JSiMJUOqtkCWCo1FpnhTSEVsA4HWshxoynI3TZ721d89mBD2rRdM7GkyqXRAgupYwQ7SHjGu8dVKp19Uq7jaJEbf2p3p-K_tTWn1rHzMVucVesoPxL_AqLwNUO0N7oZeWimNrvOc5kKvM0cqznfBzZObj9h_9f_wHtBog4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>870554777</pqid></control><display><type>article</type><title>Intensive glucose control and risk of cancer in patients with type 2 diabetes</title><source>Springer Link</source><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.</creator><creatorcontrib>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.</creatorcontrib><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><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 &amp; 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&amp;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 &amp; 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 &amp; 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 &amp; 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 &amp; Medical Complete (Alumni)</collection><collection>Health &amp; 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>
fulltext fulltext
identifier ISSN: 0012-186X
ispartof Diabetologia, 2011-07, Vol.54 (7), p.1608-1614
issn 0012-186X
1432-0428
language eng
recordid cdi_proquest_journals_870554777
source Springer Link
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T07%3A59%3A05IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Intensive%20glucose%20control%20and%20risk%20of%20cancer%20in%20patients%20with%20type%202%20diabetes&rft.jtitle=Diabetologia&rft.au=Stefansdottir,%20G.&rft.date=2011-07-01&rft.volume=54&rft.issue=7&rft.spage=1608&rft.epage=1614&rft.pages=1608-1614&rft.issn=0012-186X&rft.eissn=1432-0428&rft_id=info:doi/10.1007/s00125-011-2104-x&rft_dat=%3Cproquest_cross%3E2368758671%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c443t-5a6dc6460ce758c3cad1455a656d55bcfa6f7deec17aaa6b7c01fe2419a559243%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=870554777&rft_id=info:pmid/21509444&rfr_iscdi=true