Impact of Diabetes, Insulin, and Metformin Use on the Outcome of Patients With Human Epidermal Growth Factor Receptor 2-Positive Primary Breast Cancer: Analysis From the ALTTO Phase III Randomized Trial

Purpose Previous studies have suggested an association between metformin use and improved outcome in patients with diabetes and breast cancer. In the current study, we aimed to explore this association in human epidermal growth factor receptor 2 (HER2 ) -positive primary breast cancer in the context...

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Veröffentlicht in:Journal of clinical oncology 2017-05, Vol.35 (13), p.1421-1429
Hauptverfasser: Sonnenblick, Amir, Agbor-Tarh, Dominique, Bradbury, Ian, Di Cosimo, Serena, Azim, Jr, Hatem A, Fumagalli, Debora, Sarp, Severine, Wolff, Antonio C, Andersson, Michael, Kroep, Judith, Cufer, Tanja, Simon, Sergio D, Salman, Pamela, Toi, Masakazu, Harris, Lyndsay, Gralow, Julie, Keane, Maccon, Moreno-Aspitia, Alvaro, Piccart-Gebhart, Martine, de Azambuja, Evandro
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container_end_page 1429
container_issue 13
container_start_page 1421
container_title Journal of clinical oncology
container_volume 35
creator Sonnenblick, Amir
Agbor-Tarh, Dominique
Bradbury, Ian
Di Cosimo, Serena
Azim, Jr, Hatem A
Fumagalli, Debora
Sarp, Severine
Wolff, Antonio C
Andersson, Michael
Kroep, Judith
Cufer, Tanja
Simon, Sergio D
Salman, Pamela
Toi, Masakazu
Harris, Lyndsay
Gralow, Julie
Keane, Maccon
Moreno-Aspitia, Alvaro
Piccart-Gebhart, Martine
de Azambuja, Evandro
description Purpose Previous studies have suggested an association between metformin use and improved outcome in patients with diabetes and breast cancer. In the current study, we aimed to explore this association in human epidermal growth factor receptor 2 (HER2 ) -positive primary breast cancer in the context of a large, phase III adjuvant trial. Patients and Methods The ALTTO trial randomly assigned patients with HER2-positive breast cancer to receive 1 year of either trastuzumab alone, lapatinib alone, their sequence, or their combination. In this substudy, we evaluated whether patients with diabetes at study entry-with or without metformin treatment-were associated with different disease-free survival (DFS), distant disease-free survival (DDFS), and overall survival (OS) compared with patients without diabetes. Results A total of 8,381 patients were included in the current analysis: 7,935 patients (94.7%) had no history of diabetes at diagnosis, 186 patients (2.2%) had diabetes with no metformin treatment, and 260 patients (3.1%) were diabetic and had been treated with metformin. Median follow-up was 4.5 years (0.16 to 6.31 years), at which 1,205 (14.38%), 929 (11.08%), and 528 (6.3%) patients experienced DFS, DDFS, and OS events, respectively. Patients with diabetes who had not been treated with metformin experienced worse DFS (multivariable hazard ratio [HR], 1.40; 95% CI, 1.01 to 1.94; P = .043), DDFS (multivariable HR, 1.56; 95% CI, 1.10 to 2.22; P = .013), and OS (multivariable HR, 1.87; 95% CI, 1.23 to 2.85; P = .004). This effect was limited to hormone receptor-positive patients. Whereas insulin treatment was associated with a detrimental effect, metformin had a salutary effect in patients with diabetes who had HER2-positive and hormone receptor-positive breast cancer. Conclusion Metformin may improve the worse prognosis that is associated with diabetes and insulin treatment, mainly in patients with primary HER2-positive and hormone receptor-positive breast cancer.
doi_str_mv 10.1200/JCO.2016.69.7722
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In the current study, we aimed to explore this association in human epidermal growth factor receptor 2 (HER2 ) -positive primary breast cancer in the context of a large, phase III adjuvant trial. Patients and Methods The ALTTO trial randomly assigned patients with HER2-positive breast cancer to receive 1 year of either trastuzumab alone, lapatinib alone, their sequence, or their combination. In this substudy, we evaluated whether patients with diabetes at study entry-with or without metformin treatment-were associated with different disease-free survival (DFS), distant disease-free survival (DDFS), and overall survival (OS) compared with patients without diabetes. Results A total of 8,381 patients were included in the current analysis: 7,935 patients (94.7%) had no history of diabetes at diagnosis, 186 patients (2.2%) had diabetes with no metformin treatment, and 260 patients (3.1%) were diabetic and had been treated with metformin. Median follow-up was 4.5 years (0.16 to 6.31 years), at which 1,205 (14.38%), 929 (11.08%), and 528 (6.3%) patients experienced DFS, DDFS, and OS events, respectively. Patients with diabetes who had not been treated with metformin experienced worse DFS (multivariable hazard ratio [HR], 1.40; 95% CI, 1.01 to 1.94; P = .043), DDFS (multivariable HR, 1.56; 95% CI, 1.10 to 2.22; P = .013), and OS (multivariable HR, 1.87; 95% CI, 1.23 to 2.85; P = .004). This effect was limited to hormone receptor-positive patients. Whereas insulin treatment was associated with a detrimental effect, metformin had a salutary effect in patients with diabetes who had HER2-positive and hormone receptor-positive breast cancer. Conclusion Metformin may improve the worse prognosis that is associated with diabetes and insulin treatment, mainly in patients with primary HER2-positive and hormone receptor-positive breast cancer.</description><identifier>ISSN: 0732-183X</identifier><identifier>EISSN: 1527-7755</identifier><identifier>DOI: 10.1200/JCO.2016.69.7722</identifier><identifier>PMID: 28375706</identifier><language>eng</language><publisher>United States: American Society of Clinical Oncology</publisher><subject>Antineoplastic Agents - administration &amp; dosage ; Breast Neoplasms - drug therapy ; Breast Neoplasms - enzymology ; Breast Neoplasms - metabolism ; Chemotherapy ; Diabetes Mellitus - drug therapy ; Diabetes Mellitus - physiopathology ; Disease-Free Survival ; Female ; Humans ; Hypoglycemic Agents - therapeutic use ; Insulin - therapeutic use ; Lapatinib ; Metformin - therapeutic use ; Middle Aged ; ORIGINAL REPORTS ; Quinazolines - administration &amp; dosage ; Receptor, ErbB-2 ; Trastuzumab - administration &amp; dosage</subject><ispartof>Journal of clinical oncology, 2017-05, Vol.35 (13), p.1421-1429</ispartof><rights>2017 by American Society of Clinical Oncology 2017 American Society of Clinical Oncology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-f4aee4023a0a44550d18cfb1f4792196f1a2a9e50a4c6aa92352577410a7bcba3</citedby><cites>FETCH-LOGICAL-c396t-f4aee4023a0a44550d18cfb1f4792196f1a2a9e50a4c6aa92352577410a7bcba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,3716,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28375706$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sonnenblick, Amir</creatorcontrib><creatorcontrib>Agbor-Tarh, Dominique</creatorcontrib><creatorcontrib>Bradbury, Ian</creatorcontrib><creatorcontrib>Di Cosimo, Serena</creatorcontrib><creatorcontrib>Azim, Jr, Hatem A</creatorcontrib><creatorcontrib>Fumagalli, Debora</creatorcontrib><creatorcontrib>Sarp, Severine</creatorcontrib><creatorcontrib>Wolff, Antonio C</creatorcontrib><creatorcontrib>Andersson, Michael</creatorcontrib><creatorcontrib>Kroep, Judith</creatorcontrib><creatorcontrib>Cufer, Tanja</creatorcontrib><creatorcontrib>Simon, Sergio D</creatorcontrib><creatorcontrib>Salman, Pamela</creatorcontrib><creatorcontrib>Toi, Masakazu</creatorcontrib><creatorcontrib>Harris, Lyndsay</creatorcontrib><creatorcontrib>Gralow, Julie</creatorcontrib><creatorcontrib>Keane, Maccon</creatorcontrib><creatorcontrib>Moreno-Aspitia, Alvaro</creatorcontrib><creatorcontrib>Piccart-Gebhart, Martine</creatorcontrib><creatorcontrib>de Azambuja, Evandro</creatorcontrib><title>Impact of Diabetes, Insulin, and Metformin Use on the Outcome of Patients With Human Epidermal Growth Factor Receptor 2-Positive Primary Breast Cancer: Analysis From the ALTTO Phase III Randomized Trial</title><title>Journal of clinical oncology</title><addtitle>J Clin Oncol</addtitle><description>Purpose Previous studies have suggested an association between metformin use and improved outcome in patients with diabetes and breast cancer. In the current study, we aimed to explore this association in human epidermal growth factor receptor 2 (HER2 ) -positive primary breast cancer in the context of a large, phase III adjuvant trial. Patients and Methods The ALTTO trial randomly assigned patients with HER2-positive breast cancer to receive 1 year of either trastuzumab alone, lapatinib alone, their sequence, or their combination. In this substudy, we evaluated whether patients with diabetes at study entry-with or without metformin treatment-were associated with different disease-free survival (DFS), distant disease-free survival (DDFS), and overall survival (OS) compared with patients without diabetes. Results A total of 8,381 patients were included in the current analysis: 7,935 patients (94.7%) had no history of diabetes at diagnosis, 186 patients (2.2%) had diabetes with no metformin treatment, and 260 patients (3.1%) were diabetic and had been treated with metformin. Median follow-up was 4.5 years (0.16 to 6.31 years), at which 1,205 (14.38%), 929 (11.08%), and 528 (6.3%) patients experienced DFS, DDFS, and OS events, respectively. Patients with diabetes who had not been treated with metformin experienced worse DFS (multivariable hazard ratio [HR], 1.40; 95% CI, 1.01 to 1.94; P = .043), DDFS (multivariable HR, 1.56; 95% CI, 1.10 to 2.22; P = .013), and OS (multivariable HR, 1.87; 95% CI, 1.23 to 2.85; P = .004). This effect was limited to hormone receptor-positive patients. Whereas insulin treatment was associated with a detrimental effect, metformin had a salutary effect in patients with diabetes who had HER2-positive and hormone receptor-positive breast cancer. Conclusion Metformin may improve the worse prognosis that is associated with diabetes and insulin treatment, mainly in patients with primary HER2-positive and hormone receptor-positive breast cancer.</description><subject>Antineoplastic Agents - administration &amp; dosage</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - enzymology</subject><subject>Breast Neoplasms - metabolism</subject><subject>Chemotherapy</subject><subject>Diabetes Mellitus - drug therapy</subject><subject>Diabetes Mellitus - physiopathology</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Humans</subject><subject>Hypoglycemic Agents - therapeutic use</subject><subject>Insulin - therapeutic use</subject><subject>Lapatinib</subject><subject>Metformin - therapeutic use</subject><subject>Middle Aged</subject><subject>ORIGINAL REPORTS</subject><subject>Quinazolines - administration &amp; dosage</subject><subject>Receptor, ErbB-2</subject><subject>Trastuzumab - administration &amp; 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Agbor-Tarh, Dominique ; Bradbury, Ian ; Di Cosimo, Serena ; Azim, Jr, Hatem A ; Fumagalli, Debora ; Sarp, Severine ; Wolff, Antonio C ; Andersson, Michael ; Kroep, Judith ; Cufer, Tanja ; Simon, Sergio D ; Salman, Pamela ; Toi, Masakazu ; Harris, Lyndsay ; Gralow, Julie ; Keane, Maccon ; Moreno-Aspitia, Alvaro ; Piccart-Gebhart, Martine ; de Azambuja, Evandro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-f4aee4023a0a44550d18cfb1f4792196f1a2a9e50a4c6aa92352577410a7bcba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Antineoplastic Agents - administration &amp; dosage</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - enzymology</topic><topic>Breast Neoplasms - metabolism</topic><topic>Chemotherapy</topic><topic>Diabetes Mellitus - drug therapy</topic><topic>Diabetes Mellitus - physiopathology</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>Humans</topic><topic>Hypoglycemic Agents - therapeutic use</topic><topic>Insulin - therapeutic use</topic><topic>Lapatinib</topic><topic>Metformin - therapeutic use</topic><topic>Middle Aged</topic><topic>ORIGINAL REPORTS</topic><topic>Quinazolines - administration &amp; dosage</topic><topic>Receptor, ErbB-2</topic><topic>Trastuzumab - administration &amp; dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sonnenblick, Amir</creatorcontrib><creatorcontrib>Agbor-Tarh, Dominique</creatorcontrib><creatorcontrib>Bradbury, Ian</creatorcontrib><creatorcontrib>Di Cosimo, Serena</creatorcontrib><creatorcontrib>Azim, Jr, Hatem A</creatorcontrib><creatorcontrib>Fumagalli, Debora</creatorcontrib><creatorcontrib>Sarp, Severine</creatorcontrib><creatorcontrib>Wolff, Antonio C</creatorcontrib><creatorcontrib>Andersson, Michael</creatorcontrib><creatorcontrib>Kroep, Judith</creatorcontrib><creatorcontrib>Cufer, Tanja</creatorcontrib><creatorcontrib>Simon, Sergio D</creatorcontrib><creatorcontrib>Salman, Pamela</creatorcontrib><creatorcontrib>Toi, Masakazu</creatorcontrib><creatorcontrib>Harris, Lyndsay</creatorcontrib><creatorcontrib>Gralow, Julie</creatorcontrib><creatorcontrib>Keane, Maccon</creatorcontrib><creatorcontrib>Moreno-Aspitia, Alvaro</creatorcontrib><creatorcontrib>Piccart-Gebhart, Martine</creatorcontrib><creatorcontrib>de Azambuja, Evandro</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>Journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sonnenblick, Amir</au><au>Agbor-Tarh, Dominique</au><au>Bradbury, Ian</au><au>Di Cosimo, Serena</au><au>Azim, Jr, Hatem A</au><au>Fumagalli, Debora</au><au>Sarp, Severine</au><au>Wolff, Antonio C</au><au>Andersson, Michael</au><au>Kroep, Judith</au><au>Cufer, Tanja</au><au>Simon, Sergio D</au><au>Salman, Pamela</au><au>Toi, Masakazu</au><au>Harris, Lyndsay</au><au>Gralow, Julie</au><au>Keane, Maccon</au><au>Moreno-Aspitia, Alvaro</au><au>Piccart-Gebhart, Martine</au><au>de Azambuja, Evandro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of Diabetes, Insulin, and Metformin Use on the Outcome of Patients With Human Epidermal Growth Factor Receptor 2-Positive Primary Breast Cancer: Analysis From the ALTTO Phase III Randomized Trial</atitle><jtitle>Journal of clinical oncology</jtitle><addtitle>J Clin Oncol</addtitle><date>2017-05-01</date><risdate>2017</risdate><volume>35</volume><issue>13</issue><spage>1421</spage><epage>1429</epage><pages>1421-1429</pages><issn>0732-183X</issn><eissn>1527-7755</eissn><abstract>Purpose Previous studies have suggested an association between metformin use and improved outcome in patients with diabetes and breast cancer. In the current study, we aimed to explore this association in human epidermal growth factor receptor 2 (HER2 ) -positive primary breast cancer in the context of a large, phase III adjuvant trial. Patients and Methods The ALTTO trial randomly assigned patients with HER2-positive breast cancer to receive 1 year of either trastuzumab alone, lapatinib alone, their sequence, or their combination. In this substudy, we evaluated whether patients with diabetes at study entry-with or without metformin treatment-were associated with different disease-free survival (DFS), distant disease-free survival (DDFS), and overall survival (OS) compared with patients without diabetes. Results A total of 8,381 patients were included in the current analysis: 7,935 patients (94.7%) had no history of diabetes at diagnosis, 186 patients (2.2%) had diabetes with no metformin treatment, and 260 patients (3.1%) were diabetic and had been treated with metformin. Median follow-up was 4.5 years (0.16 to 6.31 years), at which 1,205 (14.38%), 929 (11.08%), and 528 (6.3%) patients experienced DFS, DDFS, and OS events, respectively. Patients with diabetes who had not been treated with metformin experienced worse DFS (multivariable hazard ratio [HR], 1.40; 95% CI, 1.01 to 1.94; P = .043), DDFS (multivariable HR, 1.56; 95% CI, 1.10 to 2.22; P = .013), and OS (multivariable HR, 1.87; 95% CI, 1.23 to 2.85; P = .004). This effect was limited to hormone receptor-positive patients. Whereas insulin treatment was associated with a detrimental effect, metformin had a salutary effect in patients with diabetes who had HER2-positive and hormone receptor-positive breast cancer. Conclusion Metformin may improve the worse prognosis that is associated with diabetes and insulin treatment, mainly in patients with primary HER2-positive and hormone receptor-positive breast cancer.</abstract><cop>United States</cop><pub>American Society of Clinical Oncology</pub><pmid>28375706</pmid><doi>10.1200/JCO.2016.69.7722</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Antineoplastic Agents - administration & dosage
Breast Neoplasms - drug therapy
Breast Neoplasms - enzymology
Breast Neoplasms - metabolism
Chemotherapy
Diabetes Mellitus - drug therapy
Diabetes Mellitus - physiopathology
Disease-Free Survival
Female
Humans
Hypoglycemic Agents - therapeutic use
Insulin - therapeutic use
Lapatinib
Metformin - therapeutic use
Middle Aged
ORIGINAL REPORTS
Quinazolines - administration & dosage
Receptor, ErbB-2
Trastuzumab - administration & dosage
title Impact of Diabetes, Insulin, and Metformin Use on the Outcome of Patients With Human Epidermal Growth Factor Receptor 2-Positive Primary Breast Cancer: Analysis From the ALTTO Phase III Randomized Trial
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