Preventive therapy for breast cancer: a consensus statement
Summary In March, 2010, a group of breast cancer experts met to develop a consensus statement on breast cancer prevention, with a focus on medical and therapeutic interventions. We present the conclusions in this Review. First we agreed that the term chemoprevention is inappropriate and suggested th...
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Veröffentlicht in: | The lancet oncology 2011-05, Vol.12 (5), p.496-503 |
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creator | Cuzick, Jack, Prof DeCensi, Andrea, MD Arun, Banu, Prof Brown, Powel H, Prof Castiglione, Monica, Prof Dunn, Barbara, MD Forbes, John F, Prof Glaus, Agnes, PhD Howell, Anthony, Prof von Minckwitz, Gunter, Prof Vogel, Victor, MD Zwierzina, Heinz, Prof |
description | Summary In March, 2010, a group of breast cancer experts met to develop a consensus statement on breast cancer prevention, with a focus on medical and therapeutic interventions. We present the conclusions in this Review. First we agreed that the term chemoprevention is inappropriate and suggested that the term preventive therapy better represents this feature of management. Two selective oestrogen-receptor modulators—tamoxifen and raloxifene—are so far the only medical options approved by the US Food and Drug Administration for preventive therapy. Of these tamoxifen has greater efficacy and can be used in premenopausal women, but raloxifene has fewer side-effects. Two newer drugs in this class, lasofoxifene and arzoxifene, also show efficacy and possibly a better overall risk-benefit profile, but need further assessment. Aromatase inhibitors might be more efficacious, and results of prevention trials are eagerly awaited. Newer agents, notably bisphosphonates and metformin, have shown promise in observational studies and need to be assessed in randomised prevention trials. Other agents, such as aspirin, other non-steroidal anti-inflammatory drugs, COX-2 inhibitors, retinoids, rexinoids, and dietary components have limited effects or are in the early phases of investigation. New contralateral tumours in women with breast cancer might be generally useful as a model for prevention, as has been seen for tamoxifen. If valid such a model would facilitate the design of simpler, cheaper, and better-focused trials for assessing new agents. |
doi_str_mv | 10.1016/S1470-2045(11)70030-4 |
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We present the conclusions in this Review. First we agreed that the term chemoprevention is inappropriate and suggested that the term preventive therapy better represents this feature of management. Two selective oestrogen-receptor modulators—tamoxifen and raloxifene—are so far the only medical options approved by the US Food and Drug Administration for preventive therapy. Of these tamoxifen has greater efficacy and can be used in premenopausal women, but raloxifene has fewer side-effects. Two newer drugs in this class, lasofoxifene and arzoxifene, also show efficacy and possibly a better overall risk-benefit profile, but need further assessment. Aromatase inhibitors might be more efficacious, and results of prevention trials are eagerly awaited. Newer agents, notably bisphosphonates and metformin, have shown promise in observational studies and need to be assessed in randomised prevention trials. Other agents, such as aspirin, other non-steroidal anti-inflammatory drugs, COX-2 inhibitors, retinoids, rexinoids, and dietary components have limited effects or are in the early phases of investigation. New contralateral tumours in women with breast cancer might be generally useful as a model for prevention, as has been seen for tamoxifen. If valid such a model would facilitate the design of simpler, cheaper, and better-focused trials for assessing new agents.</description><identifier>ISSN: 1470-2045</identifier><identifier>EISSN: 1474-5488</identifier><identifier>DOI: 10.1016/S1470-2045(11)70030-4</identifier><identifier>PMID: 21441069</identifier><identifier>CODEN: LANCAO</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Anastrozole ; Androstadienes - therapeutic use ; Anti-Inflammatory Agents, Non-Steroidal - therapeutic use ; Anticarcinogenic Agents - therapeutic use ; Antineoplastic Agents, Hormonal - adverse effects ; Antineoplastic Agents, Hormonal - therapeutic use ; Aromatase Inhibitors - adverse effects ; Aromatase Inhibitors - therapeutic use ; Breast cancer ; Breast Neoplasms - prevention & control ; Consensus Development Conferences as Topic ; Diphosphonates - therapeutic use ; Estrogen Receptor Modulators - adverse effects ; Estrogen Receptor Modulators - therapeutic use ; Expert Testimony ; Female ; Fenretinide - therapeutic use ; Hematology, Oncology and Palliative Medicine ; Humans ; Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use ; Metformin - therapeutic use ; Nitriles - therapeutic use ; Norpregnenes - therapeutic use ; Piperidines - therapeutic use ; Premenopause ; Pyrrolidines - therapeutic use ; Raloxifene Hydrochloride - therapeutic use ; Retinoids - therapeutic use ; Selective Estrogen Receptor Modulators - adverse effects ; Selective Estrogen Receptor Modulators - therapeutic use ; Tamoxifen - therapeutic use ; Tetrahydronaphthalenes - therapeutic use ; Thiophenes - therapeutic use ; Triazoles - therapeutic use</subject><ispartof>The lancet oncology, 2011-05, Vol.12 (5), p.496-503</ispartof><rights>Elsevier Ltd</rights><rights>2011 Elsevier Ltd</rights><rights>Copyright © 2011 Elsevier Ltd. All rights reserved.</rights><rights>Copyright Elsevier Limited May 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c446t-18283d294a05afe178b3ce208392f3446a77cd34392515e4d923332b2531feb33</citedby><cites>FETCH-LOGICAL-c446t-18283d294a05afe178b3ce208392f3446a77cd34392515e4d923332b2531feb33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1470204511700304$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21441069$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cuzick, Jack, Prof</creatorcontrib><creatorcontrib>DeCensi, Andrea, MD</creatorcontrib><creatorcontrib>Arun, Banu, Prof</creatorcontrib><creatorcontrib>Brown, Powel H, Prof</creatorcontrib><creatorcontrib>Castiglione, Monica, Prof</creatorcontrib><creatorcontrib>Dunn, Barbara, MD</creatorcontrib><creatorcontrib>Forbes, John F, Prof</creatorcontrib><creatorcontrib>Glaus, Agnes, PhD</creatorcontrib><creatorcontrib>Howell, Anthony, Prof</creatorcontrib><creatorcontrib>von Minckwitz, Gunter, Prof</creatorcontrib><creatorcontrib>Vogel, Victor, MD</creatorcontrib><creatorcontrib>Zwierzina, Heinz, Prof</creatorcontrib><title>Preventive therapy for breast cancer: a consensus statement</title><title>The lancet oncology</title><addtitle>Lancet Oncol</addtitle><description>Summary In March, 2010, a group of breast cancer experts met to develop a consensus statement on breast cancer prevention, with a focus on medical and therapeutic interventions. We present the conclusions in this Review. First we agreed that the term chemoprevention is inappropriate and suggested that the term preventive therapy better represents this feature of management. Two selective oestrogen-receptor modulators—tamoxifen and raloxifene—are so far the only medical options approved by the US Food and Drug Administration for preventive therapy. Of these tamoxifen has greater efficacy and can be used in premenopausal women, but raloxifene has fewer side-effects. Two newer drugs in this class, lasofoxifene and arzoxifene, also show efficacy and possibly a better overall risk-benefit profile, but need further assessment. Aromatase inhibitors might be more efficacious, and results of prevention trials are eagerly awaited. Newer agents, notably bisphosphonates and metformin, have shown promise in observational studies and need to be assessed in randomised prevention trials. Other agents, such as aspirin, other non-steroidal anti-inflammatory drugs, COX-2 inhibitors, retinoids, rexinoids, and dietary components have limited effects or are in the early phases of investigation. New contralateral tumours in women with breast cancer might be generally useful as a model for prevention, as has been seen for tamoxifen. If valid such a model would facilitate the design of simpler, cheaper, and better-focused trials for assessing new agents.</description><subject>Anastrozole</subject><subject>Androstadienes - therapeutic use</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</subject><subject>Anticarcinogenic Agents - therapeutic use</subject><subject>Antineoplastic Agents, Hormonal - adverse effects</subject><subject>Antineoplastic Agents, Hormonal - therapeutic use</subject><subject>Aromatase Inhibitors - adverse effects</subject><subject>Aromatase Inhibitors - therapeutic use</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - prevention & control</subject><subject>Consensus Development Conferences as Topic</subject><subject>Diphosphonates - therapeutic use</subject><subject>Estrogen Receptor Modulators - adverse effects</subject><subject>Estrogen Receptor Modulators - therapeutic use</subject><subject>Expert Testimony</subject><subject>Female</subject><subject>Fenretinide - therapeutic use</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use</subject><subject>Metformin - therapeutic use</subject><subject>Nitriles - therapeutic use</subject><subject>Norpregnenes - therapeutic use</subject><subject>Piperidines - therapeutic use</subject><subject>Premenopause</subject><subject>Pyrrolidines - therapeutic use</subject><subject>Raloxifene Hydrochloride - therapeutic use</subject><subject>Retinoids - therapeutic use</subject><subject>Selective Estrogen Receptor Modulators - adverse effects</subject><subject>Selective Estrogen Receptor Modulators - therapeutic use</subject><subject>Tamoxifen - therapeutic use</subject><subject>Tetrahydronaphthalenes - therapeutic use</subject><subject>Thiophenes - therapeutic use</subject><subject>Triazoles - therapeutic use</subject><issn>1470-2045</issn><issn>1474-5488</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkMtKxDAUQIMovj9BKW7URTU3j7ajoMjgCwQFdR3S9BajnXZM2oH5ezPtOAs3rpKUc0-aQ8gB0DOgkJy_gkhpzKiQJwCnKaWcxmKNbIfPIpYiy9b7_YBskR3vPymFFKjcJFsMhACajLbJ5YvDGdatnWHUfqDT03lUNi7KHWrfRkbXBt1FpCPT1B5r3_nIt7rFSZjZIxulrjzuL9dd8n53-zZ-iJ-e7x_HN0-xESJpY8hYxgs2EppKXSKkWc4NMprxESt5QHSamoKLcJQgURQjxjlnOZMcSsw53yXHg3fqmu8Ofasm1husKl1j03mVJSLNZMJZII_-kJ9N5-rwcz3EBciFTg6QcY33Dks1dXai3VwBVYu2qm-rFuEUgOrbKhHmDpfyLp9gsZr6jRmA6wHAEGNm0SlvLIaAhXVoWlU09t8rrv4YTGVra3T1hXP0q8eA8kzRQbJwAPQGwX8AeX2axA</recordid><startdate>20110501</startdate><enddate>20110501</enddate><creator>Cuzick, Jack, Prof</creator><creator>DeCensi, Andrea, MD</creator><creator>Arun, Banu, Prof</creator><creator>Brown, Powel H, Prof</creator><creator>Castiglione, Monica, Prof</creator><creator>Dunn, Barbara, MD</creator><creator>Forbes, John F, Prof</creator><creator>Glaus, Agnes, PhD</creator><creator>Howell, Anthony, Prof</creator><creator>von Minckwitz, Gunter, Prof</creator><creator>Vogel, Victor, MD</creator><creator>Zwierzina, Heinz, Prof</creator><general>Elsevier Ltd</general><general>Elsevier Limited</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>0TZ</scope><scope>3V.</scope><scope>7RV</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8C2</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>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20110501</creationdate><title>Preventive therapy for breast cancer: a consensus statement</title><author>Cuzick, Jack, Prof ; DeCensi, Andrea, MD ; Arun, Banu, Prof ; Brown, Powel H, Prof ; Castiglione, Monica, Prof ; Dunn, Barbara, MD ; Forbes, John F, Prof ; Glaus, Agnes, PhD ; Howell, Anthony, Prof ; von Minckwitz, Gunter, Prof ; Vogel, Victor, MD ; Zwierzina, Heinz, Prof</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c446t-18283d294a05afe178b3ce208392f3446a77cd34392515e4d923332b2531feb33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Anastrozole</topic><topic>Androstadienes - 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We present the conclusions in this Review. First we agreed that the term chemoprevention is inappropriate and suggested that the term preventive therapy better represents this feature of management. Two selective oestrogen-receptor modulators—tamoxifen and raloxifene—are so far the only medical options approved by the US Food and Drug Administration for preventive therapy. Of these tamoxifen has greater efficacy and can be used in premenopausal women, but raloxifene has fewer side-effects. Two newer drugs in this class, lasofoxifene and arzoxifene, also show efficacy and possibly a better overall risk-benefit profile, but need further assessment. Aromatase inhibitors might be more efficacious, and results of prevention trials are eagerly awaited. Newer agents, notably bisphosphonates and metformin, have shown promise in observational studies and need to be assessed in randomised prevention trials. Other agents, such as aspirin, other non-steroidal anti-inflammatory drugs, COX-2 inhibitors, retinoids, rexinoids, and dietary components have limited effects or are in the early phases of investigation. New contralateral tumours in women with breast cancer might be generally useful as a model for prevention, as has been seen for tamoxifen. If valid such a model would facilitate the design of simpler, cheaper, and better-focused trials for assessing new agents.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>21441069</pmid><doi>10.1016/S1470-2045(11)70030-4</doi><tpages>8</tpages></addata></record> |
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subjects | Anastrozole Androstadienes - therapeutic use Anti-Inflammatory Agents, Non-Steroidal - therapeutic use Anticarcinogenic Agents - therapeutic use Antineoplastic Agents, Hormonal - adverse effects Antineoplastic Agents, Hormonal - therapeutic use Aromatase Inhibitors - adverse effects Aromatase Inhibitors - therapeutic use Breast cancer Breast Neoplasms - prevention & control Consensus Development Conferences as Topic Diphosphonates - therapeutic use Estrogen Receptor Modulators - adverse effects Estrogen Receptor Modulators - therapeutic use Expert Testimony Female Fenretinide - therapeutic use Hematology, Oncology and Palliative Medicine Humans Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use Metformin - therapeutic use Nitriles - therapeutic use Norpregnenes - therapeutic use Piperidines - therapeutic use Premenopause Pyrrolidines - therapeutic use Raloxifene Hydrochloride - therapeutic use Retinoids - therapeutic use Selective Estrogen Receptor Modulators - adverse effects Selective Estrogen Receptor Modulators - therapeutic use Tamoxifen - therapeutic use Tetrahydronaphthalenes - therapeutic use Thiophenes - therapeutic use Triazoles - therapeutic use |
title | Preventive therapy for breast cancer: a consensus statement |
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