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The efficacy of aspirin and metformin combination therapy in patients with rectal aberrant crypt foci: a double-blinded randomized controlled trial
The incidence and mortality rates of colorectal cancer (CRC) continue to increase worldwide. Therefore, new preventive strategies are needed to lower the burden of this disease. Previous studies reported that aspirin could suppress the development of sporadic colorectal adenoma. In addition, metform...
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Published in: | BMC cancer 2020-10, Vol.20 (1), p.1043-7, Article 1043 |
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creator | Higurashi, Takuma Arimoto, Jun Ashikari, Keiichi Takatsu, Tomohiro Misawa, Noboru Yoshihara, Tsutomu Matsuura, Tetsuya Fuyuki, Akiko Ohkubo, Hidenori Nakajima, Atsushi |
description | The incidence and mortality rates of colorectal cancer (CRC) continue to increase worldwide. Therefore, new preventive strategies are needed to lower the burden of this disease. Previous studies reported that aspirin could suppress the development of sporadic colorectal adenoma. In addition, metformin is a biguanide derivative that is long widely used for the treatment of diabetes mellitus and has recently been suggested to have a suppressive effect on carcinogenesis and cancer cell growth. Both drugs exhibit a chemopreventive effect, but their efficacy is limited. Aberrant crypt foci (ACF), defined as lesions containing crypts that are larger in diameter and stain more darkly with methylene blue than normal crypts, are more prevalent in patients with cancer and adenomas, and considered a reliable surrogate biomarker of CRC. Thus, we designed a prospective trial as a preliminary study prior to a CRC chemoprevention trial to evaluate the chemopreventive effect of aspirin combined with metformin on colorectal ACF formation in patients scheduled for polypectomy.
This study is a double-blind randomized controlled trial that will be conducted in patients with both colorectal ACF and colorectal polyps scheduled for polypectomy. Eligible patients will be recruited for the study and the number of ACF in the rectum will be counted at the baseline colonoscopy. Then, the participants will be allocated to one of the following two groups; the aspirin plus placebo group or the aspirin plus metformin group. Patients in the aspirin plus placebo group will receive oral aspirin (100 mg) and placebo for 8 weeks, and those in the aspirin plus metformin group will receive oral aspirin (100 mg) and metformin (250 mg) for 8 weeks. After 8 weeks of administration, polypectomy will be performed to evaluate changes in the number of ACF, and the cell-proliferative activity in the normal colorectal mucosa and colorectal polyps.
This is the first study proposed that will explore the effect of aspirin combined with metformin on the formation of colorectal ACF in humans.
This trial has been registered in the University Hospital Medical Information Network (UMIN) Clinical Trials Registry as UMIN000028259 . Registered 17 July 2017. |
doi_str_mv | 10.1186/s12885-020-07564-z |
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This study is a double-blind randomized controlled trial that will be conducted in patients with both colorectal ACF and colorectal polyps scheduled for polypectomy. Eligible patients will be recruited for the study and the number of ACF in the rectum will be counted at the baseline colonoscopy. Then, the participants will be allocated to one of the following two groups; the aspirin plus placebo group or the aspirin plus metformin group. Patients in the aspirin plus placebo group will receive oral aspirin (100 mg) and placebo for 8 weeks, and those in the aspirin plus metformin group will receive oral aspirin (100 mg) and metformin (250 mg) for 8 weeks. After 8 weeks of administration, polypectomy will be performed to evaluate changes in the number of ACF, and the cell-proliferative activity in the normal colorectal mucosa and colorectal polyps.
This is the first study proposed that will explore the effect of aspirin combined with metformin on the formation of colorectal ACF in humans.
This trial has been registered in the University Hospital Medical Information Network (UMIN) Clinical Trials Registry as UMIN000028259 . Registered 17 July 2017.</description><identifier>ISSN: 1471-2407</identifier><identifier>EISSN: 1471-2407</identifier><identifier>DOI: 10.1186/s12885-020-07564-z</identifier><identifier>PMID: 33121471</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Aberrant crypt foci ; Aberrant Crypt Foci - drug therapy ; Aberrant Crypt Foci - pathology ; Adenoma ; Anti-Inflammatory Agents, Non-Steroidal - therapeutic use ; Anticoagulants ; Antidiabetics ; Aspirin ; Aspirin - therapeutic use ; Cancer research ; Cancer therapies ; Carcinogenesis ; Chemoprevention ; Clinical trials ; Colonoscopy ; Colorectal cancer ; Colorectal carcinoma ; Colorectal Neoplasms - drug therapy ; Colorectal Neoplasms - pathology ; Combination therapy ; Diabetes ; Diabetes mellitus ; Double-Blind Method ; Drug dosages ; Drug Therapy, Combination ; Ethics ; Hospitals ; Humans ; Hypoglycemic Agents - therapeutic use ; Informed consent ; Kinases ; Metformin ; Metformin - therapeutic use ; Methylene blue ; Mucosa ; Patient outcomes ; Patients ; Polyethylene glycol ; Polyps ; Prevention ; Prognosis ; Prospective Studies ; Randomized Controlled Trials as Topic ; Rectum ; Study Protocol ; Tumors</subject><ispartof>BMC cancer, 2020-10, Vol.20 (1), p.1043-7, Article 1043</ispartof><rights>COPYRIGHT 2020 BioMed Central Ltd.</rights><rights>2020. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c628t-8970bdcfd7b44b8b16c378ebdbe81573798b5d1fcd280420396d08d064f67d993</citedby><cites>FETCH-LOGICAL-c628t-8970bdcfd7b44b8b16c378ebdbe81573798b5d1fcd280420396d08d064f67d993</cites><orcidid>0000-0002-1815-4396</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7599108/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2462184990?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33121471$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Higurashi, Takuma</creatorcontrib><creatorcontrib>Arimoto, Jun</creatorcontrib><creatorcontrib>Ashikari, Keiichi</creatorcontrib><creatorcontrib>Takatsu, Tomohiro</creatorcontrib><creatorcontrib>Misawa, Noboru</creatorcontrib><creatorcontrib>Yoshihara, Tsutomu</creatorcontrib><creatorcontrib>Matsuura, Tetsuya</creatorcontrib><creatorcontrib>Fuyuki, Akiko</creatorcontrib><creatorcontrib>Ohkubo, Hidenori</creatorcontrib><creatorcontrib>Nakajima, Atsushi</creatorcontrib><title>The efficacy of aspirin and metformin combination therapy in patients with rectal aberrant crypt foci: a double-blinded randomized controlled trial</title><title>BMC cancer</title><addtitle>BMC Cancer</addtitle><description>The incidence and mortality rates of colorectal cancer (CRC) continue to increase worldwide. Therefore, new preventive strategies are needed to lower the burden of this disease. Previous studies reported that aspirin could suppress the development of sporadic colorectal adenoma. In addition, metformin is a biguanide derivative that is long widely used for the treatment of diabetes mellitus and has recently been suggested to have a suppressive effect on carcinogenesis and cancer cell growth. Both drugs exhibit a chemopreventive effect, but their efficacy is limited. Aberrant crypt foci (ACF), defined as lesions containing crypts that are larger in diameter and stain more darkly with methylene blue than normal crypts, are more prevalent in patients with cancer and adenomas, and considered a reliable surrogate biomarker of CRC. Thus, we designed a prospective trial as a preliminary study prior to a CRC chemoprevention trial to evaluate the chemopreventive effect of aspirin combined with metformin on colorectal ACF formation in patients scheduled for polypectomy.
This study is a double-blind randomized controlled trial that will be conducted in patients with both colorectal ACF and colorectal polyps scheduled for polypectomy. Eligible patients will be recruited for the study and the number of ACF in the rectum will be counted at the baseline colonoscopy. Then, the participants will be allocated to one of the following two groups; the aspirin plus placebo group or the aspirin plus metformin group. Patients in the aspirin plus placebo group will receive oral aspirin (100 mg) and placebo for 8 weeks, and those in the aspirin plus metformin group will receive oral aspirin (100 mg) and metformin (250 mg) for 8 weeks. After 8 weeks of administration, polypectomy will be performed to evaluate changes in the number of ACF, and the cell-proliferative activity in the normal colorectal mucosa and colorectal polyps.
This is the first study proposed that will explore the effect of aspirin combined with metformin on the formation of colorectal ACF in humans.
This trial has been registered in the University Hospital Medical Information Network (UMIN) Clinical Trials Registry as UMIN000028259 . Registered 17 July 2017.</description><subject>Aberrant crypt foci</subject><subject>Aberrant Crypt Foci - drug therapy</subject><subject>Aberrant Crypt Foci - pathology</subject><subject>Adenoma</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</subject><subject>Anticoagulants</subject><subject>Antidiabetics</subject><subject>Aspirin</subject><subject>Aspirin - therapeutic use</subject><subject>Cancer research</subject><subject>Cancer therapies</subject><subject>Carcinogenesis</subject><subject>Chemoprevention</subject><subject>Clinical trials</subject><subject>Colonoscopy</subject><subject>Colorectal cancer</subject><subject>Colorectal carcinoma</subject><subject>Colorectal Neoplasms - drug therapy</subject><subject>Colorectal Neoplasms - pathology</subject><subject>Combination therapy</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Double-Blind Method</subject><subject>Drug dosages</subject><subject>Drug Therapy, Combination</subject><subject>Ethics</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Hypoglycemic Agents - therapeutic use</subject><subject>Informed consent</subject><subject>Kinases</subject><subject>Metformin</subject><subject>Metformin - therapeutic use</subject><subject>Methylene blue</subject><subject>Mucosa</subject><subject>Patient outcomes</subject><subject>Patients</subject><subject>Polyethylene glycol</subject><subject>Polyps</subject><subject>Prevention</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Rectum</subject><subject>Study Protocol</subject><subject>Tumors</subject><issn>1471-2407</issn><issn>1471-2407</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkl2L1DAUhoso7rr6B7yQgCB40TVp0jT1QlgWPwYWBF2vQz6nGdqmJqk68zf8w2Zm1nUKkoucnLznSXLyFsVzBC8RYvRNRBVjdQkrWMKmpqTcPSjOEWlQWRHYPDyJz4onMW4gRA2D7HFxhjGq9pvnxe_bzgBjrVNCbYG3QMTJBTcCMWowmGR9GPJK-UG6USTnR5A6E8S0BTk95YwZUwQ_XepAMCqJHghpQhBjAipspwSsV-4tEED7WfamlL0btdEgK7Qf3C6Hyo8p-L7PYQpO9E-LR1b00Ty7my-Kbx_e315_Km8-f1xdX92UilYslaxtoNTK6kYSIplEVOGGGamlYahucNMyWWtkla4YJBXELdWQaUiJpY1uW3xRrI5c7cWGT8ENImy5F44fEj6suQjJqd5wDDOCIQpxrQhqa1nhfBCixKi6oZZm1rsja5rlYLTKXQmiX0CXO6Pr-Nr_4E3dtgiyDHh5Bwj--2xi4hs_hzG_n1eEVoiRtoX_VGuRb-VG6zNMDS4qfkUJxBCzA-vyP6o8tBlc7raxLucXBa8XBfsfMb_SWswx8tXXL0vtqxNtZ0Sfuuj7ee-NuBRWR6EKPsZg7H03EOR7A_OjgXk2MD8YmO9y0YvTPt6X_HUs_gNp5OuX</recordid><startdate>20201029</startdate><enddate>20201029</enddate><creator>Higurashi, Takuma</creator><creator>Arimoto, Jun</creator><creator>Ashikari, Keiichi</creator><creator>Takatsu, Tomohiro</creator><creator>Misawa, Noboru</creator><creator>Yoshihara, Tsutomu</creator><creator>Matsuura, Tetsuya</creator><creator>Fuyuki, Akiko</creator><creator>Ohkubo, Hidenori</creator><creator>Nakajima, Atsushi</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</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>ISR</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-1815-4396</orcidid></search><sort><creationdate>20201029</creationdate><title>The efficacy of aspirin and metformin combination therapy in patients with rectal aberrant crypt foci: a double-blinded randomized controlled trial</title><author>Higurashi, Takuma ; Arimoto, Jun ; Ashikari, Keiichi ; Takatsu, Tomohiro ; Misawa, Noboru ; Yoshihara, Tsutomu ; Matsuura, Tetsuya ; Fuyuki, Akiko ; Ohkubo, Hidenori ; Nakajima, Atsushi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c628t-8970bdcfd7b44b8b16c378ebdbe81573798b5d1fcd280420396d08d064f67d993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aberrant crypt foci</topic><topic>Aberrant Crypt Foci - drug therapy</topic><topic>Aberrant Crypt Foci - pathology</topic><topic>Adenoma</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</topic><topic>Anticoagulants</topic><topic>Antidiabetics</topic><topic>Aspirin</topic><topic>Aspirin - therapeutic use</topic><topic>Cancer research</topic><topic>Cancer therapies</topic><topic>Carcinogenesis</topic><topic>Chemoprevention</topic><topic>Clinical trials</topic><topic>Colonoscopy</topic><topic>Colorectal cancer</topic><topic>Colorectal carcinoma</topic><topic>Colorectal Neoplasms - drug therapy</topic><topic>Colorectal Neoplasms - pathology</topic><topic>Combination therapy</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Double-Blind Method</topic><topic>Drug dosages</topic><topic>Drug Therapy, Combination</topic><topic>Ethics</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Hypoglycemic Agents - therapeutic use</topic><topic>Informed consent</topic><topic>Kinases</topic><topic>Metformin</topic><topic>Metformin - therapeutic use</topic><topic>Methylene blue</topic><topic>Mucosa</topic><topic>Patient outcomes</topic><topic>Patients</topic><topic>Polyethylene glycol</topic><topic>Polyps</topic><topic>Prevention</topic><topic>Prognosis</topic><topic>Prospective Studies</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Rectum</topic><topic>Study Protocol</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Higurashi, Takuma</creatorcontrib><creatorcontrib>Arimoto, Jun</creatorcontrib><creatorcontrib>Ashikari, Keiichi</creatorcontrib><creatorcontrib>Takatsu, Tomohiro</creatorcontrib><creatorcontrib>Misawa, Noboru</creatorcontrib><creatorcontrib>Yoshihara, Tsutomu</creatorcontrib><creatorcontrib>Matsuura, Tetsuya</creatorcontrib><creatorcontrib>Fuyuki, Akiko</creatorcontrib><creatorcontrib>Ohkubo, Hidenori</creatorcontrib><creatorcontrib>Nakajima, Atsushi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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 Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</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>Publicly Available Content (ProQuest)</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><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>BMC cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Higurashi, Takuma</au><au>Arimoto, Jun</au><au>Ashikari, Keiichi</au><au>Takatsu, Tomohiro</au><au>Misawa, Noboru</au><au>Yoshihara, Tsutomu</au><au>Matsuura, Tetsuya</au><au>Fuyuki, Akiko</au><au>Ohkubo, Hidenori</au><au>Nakajima, Atsushi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The efficacy of aspirin and metformin combination therapy in patients with rectal aberrant crypt foci: a double-blinded randomized controlled trial</atitle><jtitle>BMC cancer</jtitle><addtitle>BMC Cancer</addtitle><date>2020-10-29</date><risdate>2020</risdate><volume>20</volume><issue>1</issue><spage>1043</spage><epage>7</epage><pages>1043-7</pages><artnum>1043</artnum><issn>1471-2407</issn><eissn>1471-2407</eissn><abstract>The incidence and mortality rates of colorectal cancer (CRC) continue to increase worldwide. Therefore, new preventive strategies are needed to lower the burden of this disease. Previous studies reported that aspirin could suppress the development of sporadic colorectal adenoma. In addition, metformin is a biguanide derivative that is long widely used for the treatment of diabetes mellitus and has recently been suggested to have a suppressive effect on carcinogenesis and cancer cell growth. Both drugs exhibit a chemopreventive effect, but their efficacy is limited. Aberrant crypt foci (ACF), defined as lesions containing crypts that are larger in diameter and stain more darkly with methylene blue than normal crypts, are more prevalent in patients with cancer and adenomas, and considered a reliable surrogate biomarker of CRC. Thus, we designed a prospective trial as a preliminary study prior to a CRC chemoprevention trial to evaluate the chemopreventive effect of aspirin combined with metformin on colorectal ACF formation in patients scheduled for polypectomy.
This study is a double-blind randomized controlled trial that will be conducted in patients with both colorectal ACF and colorectal polyps scheduled for polypectomy. Eligible patients will be recruited for the study and the number of ACF in the rectum will be counted at the baseline colonoscopy. Then, the participants will be allocated to one of the following two groups; the aspirin plus placebo group or the aspirin plus metformin group. Patients in the aspirin plus placebo group will receive oral aspirin (100 mg) and placebo for 8 weeks, and those in the aspirin plus metformin group will receive oral aspirin (100 mg) and metformin (250 mg) for 8 weeks. After 8 weeks of administration, polypectomy will be performed to evaluate changes in the number of ACF, and the cell-proliferative activity in the normal colorectal mucosa and colorectal polyps.
This is the first study proposed that will explore the effect of aspirin combined with metformin on the formation of colorectal ACF in humans.
This trial has been registered in the University Hospital Medical Information Network (UMIN) Clinical Trials Registry as UMIN000028259 . Registered 17 July 2017.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>33121471</pmid><doi>10.1186/s12885-020-07564-z</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-1815-4396</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aberrant crypt foci Aberrant Crypt Foci - drug therapy Aberrant Crypt Foci - pathology Adenoma Anti-Inflammatory Agents, Non-Steroidal - therapeutic use Anticoagulants Antidiabetics Aspirin Aspirin - therapeutic use Cancer research Cancer therapies Carcinogenesis Chemoprevention Clinical trials Colonoscopy Colorectal cancer Colorectal carcinoma Colorectal Neoplasms - drug therapy Colorectal Neoplasms - pathology Combination therapy Diabetes Diabetes mellitus Double-Blind Method Drug dosages Drug Therapy, Combination Ethics Hospitals Humans Hypoglycemic Agents - therapeutic use Informed consent Kinases Metformin Metformin - therapeutic use Methylene blue Mucosa Patient outcomes Patients Polyethylene glycol Polyps Prevention Prognosis Prospective Studies Randomized Controlled Trials as Topic Rectum Study Protocol Tumors |
title | The efficacy of aspirin and metformin combination therapy in patients with rectal aberrant crypt foci: a double-blinded randomized controlled trial |
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