Challenges in Preventing Bone Loss Induced by Aromatase Inhibitors
Abstract Context: Aromatase inhibitors have become a mainstay in the adjuvant treatment regimen in postmenopausal women with hormone receptor–positive breast cancer. While many of these patients have an excellent long-term prognosis, adverse effects on bone represent an emerging complication of arom...
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Veröffentlicht in: | The journal of clinical endocrinology and metabolism 2020-10, Vol.105 (10), p.3122-3133 |
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creator | Rachner, Tilman D Göbel, Andy Jaschke, Nikolai P Hofbauer, Lorenz C |
description | Abstract
Context: Aromatase inhibitors have become a mainstay in the adjuvant treatment regimen in postmenopausal women with hormone receptor–positive breast cancer. While many of these patients have an excellent long-term prognosis, adverse effects on bone represent an emerging complication of aromatase inhibitor treatment, resulting in substantial bone loss and fragility fractures.
Treatment approaches to prevent aromatase inhibitor–induced bone loss typically consist of an antiresorptive approach with bisphosphonates or the RANKL antibody denosumab. However, different guidelines vary with respect to treatment thresholds, duration, and dosing.
The choice of antiresorptive regime is further complicated by comorbidities and potential disease-modifying effects of individual agents.
Objective: This review summarizes the evidence of how aromatase inhibitors affect bone health and provides an update of clinical approaches to preserve bone strength in affected women. (J Clin Endocrinol Metab XX: 0–0, 2020) |
doi_str_mv | 10.1210/clinem/dgaa463 |
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Context: Aromatase inhibitors have become a mainstay in the adjuvant treatment regimen in postmenopausal women with hormone receptor–positive breast cancer. While many of these patients have an excellent long-term prognosis, adverse effects on bone represent an emerging complication of aromatase inhibitor treatment, resulting in substantial bone loss and fragility fractures.
Treatment approaches to prevent aromatase inhibitor–induced bone loss typically consist of an antiresorptive approach with bisphosphonates or the RANKL antibody denosumab. However, different guidelines vary with respect to treatment thresholds, duration, and dosing.
The choice of antiresorptive regime is further complicated by comorbidities and potential disease-modifying effects of individual agents.
Objective: This review summarizes the evidence of how aromatase inhibitors affect bone health and provides an update of clinical approaches to preserve bone strength in affected women. (J Clin Endocrinol Metab XX: 0–0, 2020)</description><identifier>ISSN: 0021-972X</identifier><identifier>EISSN: 1945-7197</identifier><identifier>DOI: 10.1210/clinem/dgaa463</identifier><identifier>PMID: 32674135</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Aromatase ; Aromatase Inhibitors - adverse effects ; Bisphosphonates ; Bone Density - drug effects ; Bone Density Conservation Agents - therapeutic use ; Bone loss ; Bone strength ; Breast cancer ; Breast Neoplasms - drug therapy ; Denosumab - therapeutic use ; Diphosphonates - therapeutic use ; Drug therapy ; Female ; Fractures ; Humans ; Monoclonal antibodies ; Mushrooms ; Osteoporosis ; Osteoporosis - chemically induced ; Osteoporosis - prevention & control ; Post-menopause ; Prevention ; Risk factors ; Targeted cancer therapy ; TRANCE protein</subject><ispartof>The journal of clinical endocrinology and metabolism, 2020-10, Vol.105 (10), p.3122-3133</ispartof><rights>Endocrine Society 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2020</rights><rights>Endocrine Society 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><rights>COPYRIGHT 2020 Oxford University Press</rights><rights>Endocrine Society 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c464t-eeeee5128b1d80c79bb5982aeeceea49e28d194e801c4d244eeae09c1da27c7c3</citedby><cites>FETCH-LOGICAL-c464t-eeeee5128b1d80c79bb5982aeeceea49e28d194e801c4d244eeae09c1da27c7c3</cites><orcidid>0000-0002-8691-8423</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2471031482?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,776,780,21368,21369,27903,27904,33509,33723,43638,43784,64362,64366,72216,72875,72876,72878</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32674135$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rachner, Tilman D</creatorcontrib><creatorcontrib>Göbel, Andy</creatorcontrib><creatorcontrib>Jaschke, Nikolai P</creatorcontrib><creatorcontrib>Hofbauer, Lorenz C</creatorcontrib><title>Challenges in Preventing Bone Loss Induced by Aromatase Inhibitors</title><title>The journal of clinical endocrinology and metabolism</title><addtitle>J Clin Endocrinol Metab</addtitle><description>Abstract
Context: Aromatase inhibitors have become a mainstay in the adjuvant treatment regimen in postmenopausal women with hormone receptor–positive breast cancer. While many of these patients have an excellent long-term prognosis, adverse effects on bone represent an emerging complication of aromatase inhibitor treatment, resulting in substantial bone loss and fragility fractures.
Treatment approaches to prevent aromatase inhibitor–induced bone loss typically consist of an antiresorptive approach with bisphosphonates or the RANKL antibody denosumab. However, different guidelines vary with respect to treatment thresholds, duration, and dosing.
The choice of antiresorptive regime is further complicated by comorbidities and potential disease-modifying effects of individual agents.
Objective: This review summarizes the evidence of how aromatase inhibitors affect bone health and provides an update of clinical approaches to preserve bone strength in affected women. (J Clin Endocrinol Metab XX: 0–0, 2020)</description><subject>Aromatase</subject><subject>Aromatase Inhibitors - adverse effects</subject><subject>Bisphosphonates</subject><subject>Bone Density - drug effects</subject><subject>Bone Density Conservation Agents - therapeutic use</subject><subject>Bone loss</subject><subject>Bone strength</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Denosumab - therapeutic use</subject><subject>Diphosphonates - therapeutic use</subject><subject>Drug therapy</subject><subject>Female</subject><subject>Fractures</subject><subject>Humans</subject><subject>Monoclonal antibodies</subject><subject>Mushrooms</subject><subject>Osteoporosis</subject><subject>Osteoporosis - chemically induced</subject><subject>Osteoporosis - prevention & control</subject><subject>Post-menopause</subject><subject>Prevention</subject><subject>Risk factors</subject><subject>Targeted cancer therapy</subject><subject>TRANCE protein</subject><issn>0021-972X</issn><issn>1945-7197</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqFkc9LwzAUx4Mobk6vHqXgyUO3JE3X5jiHPwYDPSh4C2ny2mW06UxaYf-9GZt6GfhyePDl837kfRG6JnhMKMETVRsLzURXUrJpcoKGhLM0zgjPTtEQY0pintGPAbrwfo0xYSxNztEgodOMkSQdovv5StY12Ap8ZGz06uALbGdsFd23FqJl6320sLpXoKNiG81c28hOegjiyhSma52_RGelrD1cHfIIvT8-vM2f4-XL02I-W8aKTVkXwy5SQvOC6ByrjBdFynMqARSAZBxorsPykGOimKaMBRUwV0RLmqlMJSN0u--7ce1nD74T67Z3NowUlGUEJ4Tl9I-qZA3C2LLtnFSN8UrMpixJE4JzHqjxESo8DY1R4eelCfqxAuXCSRyUYuNMI91WECx2Toi9E-LgRCi4OWzbFw3oX_zn9AG42wNtv_mv2TfIO5Mj</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Rachner, Tilman D</creator><creator>Göbel, Andy</creator><creator>Jaschke, Nikolai P</creator><creator>Hofbauer, Lorenz C</creator><general>Oxford University Press</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>3V.</scope><scope>7QP</scope><scope>7T5</scope><scope>7TM</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>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><orcidid>https://orcid.org/0000-0002-8691-8423</orcidid></search><sort><creationdate>20201001</creationdate><title>Challenges in Preventing Bone Loss Induced by Aromatase Inhibitors</title><author>Rachner, Tilman D ; Göbel, Andy ; Jaschke, Nikolai P ; Hofbauer, Lorenz C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c464t-eeeee5128b1d80c79bb5982aeeceea49e28d194e801c4d244eeae09c1da27c7c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aromatase</topic><topic>Aromatase Inhibitors - adverse effects</topic><topic>Bisphosphonates</topic><topic>Bone Density - drug effects</topic><topic>Bone Density Conservation Agents - therapeutic use</topic><topic>Bone loss</topic><topic>Bone strength</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Denosumab - therapeutic use</topic><topic>Diphosphonates - therapeutic use</topic><topic>Drug therapy</topic><topic>Female</topic><topic>Fractures</topic><topic>Humans</topic><topic>Monoclonal antibodies</topic><topic>Mushrooms</topic><topic>Osteoporosis</topic><topic>Osteoporosis - chemically induced</topic><topic>Osteoporosis - prevention & control</topic><topic>Post-menopause</topic><topic>Prevention</topic><topic>Risk factors</topic><topic>Targeted cancer therapy</topic><topic>TRANCE protein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rachner, Tilman D</creatorcontrib><creatorcontrib>Göbel, Andy</creatorcontrib><creatorcontrib>Jaschke, Nikolai P</creatorcontrib><creatorcontrib>Hofbauer, Lorenz C</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>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>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 Edition)</collection><collection>ProQuest Central UK/Ireland</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>The journal of clinical endocrinology and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rachner, Tilman D</au><au>Göbel, Andy</au><au>Jaschke, Nikolai P</au><au>Hofbauer, Lorenz C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Challenges in Preventing Bone Loss Induced by Aromatase Inhibitors</atitle><jtitle>The journal of clinical endocrinology and metabolism</jtitle><addtitle>J Clin Endocrinol Metab</addtitle><date>2020-10-01</date><risdate>2020</risdate><volume>105</volume><issue>10</issue><spage>3122</spage><epage>3133</epage><pages>3122-3133</pages><issn>0021-972X</issn><eissn>1945-7197</eissn><abstract>Abstract
Context: Aromatase inhibitors have become a mainstay in the adjuvant treatment regimen in postmenopausal women with hormone receptor–positive breast cancer. While many of these patients have an excellent long-term prognosis, adverse effects on bone represent an emerging complication of aromatase inhibitor treatment, resulting in substantial bone loss and fragility fractures.
Treatment approaches to prevent aromatase inhibitor–induced bone loss typically consist of an antiresorptive approach with bisphosphonates or the RANKL antibody denosumab. However, different guidelines vary with respect to treatment thresholds, duration, and dosing.
The choice of antiresorptive regime is further complicated by comorbidities and potential disease-modifying effects of individual agents.
Objective: This review summarizes the evidence of how aromatase inhibitors affect bone health and provides an update of clinical approaches to preserve bone strength in affected women. (J Clin Endocrinol Metab XX: 0–0, 2020)</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>32674135</pmid><doi>10.1210/clinem/dgaa463</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-8691-8423</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aromatase Aromatase Inhibitors - adverse effects Bisphosphonates Bone Density - drug effects Bone Density Conservation Agents - therapeutic use Bone loss Bone strength Breast cancer Breast Neoplasms - drug therapy Denosumab - therapeutic use Diphosphonates - therapeutic use Drug therapy Female Fractures Humans Monoclonal antibodies Mushrooms Osteoporosis Osteoporosis - chemically induced Osteoporosis - prevention & control Post-menopause Prevention Risk factors Targeted cancer therapy TRANCE protein |
title | Challenges in Preventing Bone Loss Induced by Aromatase Inhibitors |
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