Treatment Efficacy, Adherence, and Quality of Life Among Women Younger Than 35 Years in the International Breast Cancer Study Group TEXT and SOFT Adjuvant Endocrine Therapy Trials
Purpose To describe benefits and toxicities of adjuvant endocrine therapies in women younger than 35 years with breast cancer (n = 582) enrolled in the Suppression of Ovarian Function Trial (SOFT) and Tamoxifen and Exemestane Trial (TEXT). Methods In SOFT, women still premenopausal after surgery wit...
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creator | Saha, Poornima Regan, Meredith M Pagani, Olivia Francis, Prudence A Walley, Barbara A Ribi, Karin Bernhard, Jürg Luo, Weixiu Gómez, Henry L Burstein, Harold J Parmar, Vani Torres, Roberto Stewart, Josephine Bellet, Meritxell Perelló, Antonia Dane, Faysal Moreira, Antonio Vorobiof, Daniel Nottage, Michelle Price, Karen N Coates, Alan S Goldhirsch, Aron Gelber, Richard D Colleoni, Marco Fleming, Gini F |
description | Purpose To describe benefits and toxicities of adjuvant endocrine therapies in women younger than 35 years with breast cancer (n = 582) enrolled in the Suppression of Ovarian Function Trial (SOFT) and Tamoxifen and Exemestane Trial (TEXT). Methods In SOFT, women still premenopausal after surgery with or without chemotherapy were randomly assigned to tamoxifen alone, tamoxifen plus ovarian function suppression (OFS), or exemestane plus OFS. In TEXT, all received OFS with or without concomitant chemotherapy and were randomly assigned to exemestane plus OFS or tamoxifen plus OFS. We summarize treatment efficacy, quality of life, and adherence of the cohort of women younger than 35 years in SOFT and TEXT, alongside data from the cohort of older premenopausal women. Results For 240 human epidermal growth factor receptor 2-negative patients younger than 35 years enrolled in SOFT after receiving chemotherapy, the 5-year breast cancer-free interval (BCFI) was 67.1% (95% CI, 54.6% to 76.9%) with tamoxifen alone, 75.9% with tamoxifen plus OFS (95% CI, 64.0% to 84.4%), and 83.2% with exemestane plus OFS (95% CI, 72.7% to 90.0%). For 145 human epidermal growth factor receptor 2-negative patients younger than 35 years in TEXT, 5-year BCFI was 79.2% (95% CI, 66.2% to 87.7%) with tamoxifen plus OFS and 81.6% (95% CI, 69.8% to 89.2%) with exemestane plus OFS. The most prominent quality of life symptom for patients younger than 35 years receiving OFS was vasomotor symptoms, with the greatest worsening from baseline at 6 months (on the order of 30 to 40 points), but loss of sexual interest and difficulties in becoming aroused were also clinically meaningful (≥ 8-point change). The level of symptom burden was similar in older premenopausal women. A total of 19.8% of women younger than 35 years stopped all protocol-assigned endocrine therapy early. Conclusion In women younger than 35 years with hormone receptor-positive breast cancer, adjuvant OFS combined with tamoxifen or exemestane produces large improvements in BCFI compared with tamoxifen alone. Menopausal symptoms are significant but are not worse than those seen in older premenopausal women. |
doi_str_mv | 10.1200/JCO.2016.72.0946 |
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Methods In SOFT, women still premenopausal after surgery with or without chemotherapy were randomly assigned to tamoxifen alone, tamoxifen plus ovarian function suppression (OFS), or exemestane plus OFS. In TEXT, all received OFS with or without concomitant chemotherapy and were randomly assigned to exemestane plus OFS or tamoxifen plus OFS. We summarize treatment efficacy, quality of life, and adherence of the cohort of women younger than 35 years in SOFT and TEXT, alongside data from the cohort of older premenopausal women. Results For 240 human epidermal growth factor receptor 2-negative patients younger than 35 years enrolled in SOFT after receiving chemotherapy, the 5-year breast cancer-free interval (BCFI) was 67.1% (95% CI, 54.6% to 76.9%) with tamoxifen alone, 75.9% with tamoxifen plus OFS (95% CI, 64.0% to 84.4%), and 83.2% with exemestane plus OFS (95% CI, 72.7% to 90.0%). For 145 human epidermal growth factor receptor 2-negative patients younger than 35 years in TEXT, 5-year BCFI was 79.2% (95% CI, 66.2% to 87.7%) with tamoxifen plus OFS and 81.6% (95% CI, 69.8% to 89.2%) with exemestane plus OFS. The most prominent quality of life symptom for patients younger than 35 years receiving OFS was vasomotor symptoms, with the greatest worsening from baseline at 6 months (on the order of 30 to 40 points), but loss of sexual interest and difficulties in becoming aroused were also clinically meaningful (≥ 8-point change). The level of symptom burden was similar in older premenopausal women. A total of 19.8% of women younger than 35 years stopped all protocol-assigned endocrine therapy early. Conclusion In women younger than 35 years with hormone receptor-positive breast cancer, adjuvant OFS combined with tamoxifen or exemestane produces large improvements in BCFI compared with tamoxifen alone. Menopausal symptoms are significant but are not worse than those seen in older premenopausal women.</description><identifier>ISSN: 0732-183X</identifier><identifier>EISSN: 1527-7755</identifier><identifier>DOI: 10.1200/JCO.2016.72.0946</identifier><identifier>PMID: 28654365</identifier><language>eng</language><publisher>United States: American Society of Clinical Oncology</publisher><subject>Adult ; Androstadienes - administration & dosage ; Antineoplastic Agents, Hormonal - administration & dosage ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Aromatase Inhibitors - administration & dosage ; Breast Neoplasms - drug therapy ; Breast Neoplasms - surgery ; Chemotherapy, Adjuvant ; Clinical Trials as Topic ; Female ; Hormonal Therapy ; Humans ; ORIGINAL REPORTS ; Premenopause ; Quality of Life ; Receptor, ErbB-2 - analysis ; Tamoxifen - administration & dosage ; Treatment Outcome</subject><ispartof>Journal of clinical oncology, 2017-09, Vol.35 (27), p.3113-3122</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-c509t-45d865baf611ec9c99a0a4867eeed3c9325b7b839efc208c81e2b0dd4eef7a833</citedby><cites>FETCH-LOGICAL-c509t-45d865baf611ec9c99a0a4867eeed3c9325b7b839efc208c81e2b0dd4eef7a833</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/28654365$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Saha, Poornima</creatorcontrib><creatorcontrib>Regan, Meredith M</creatorcontrib><creatorcontrib>Pagani, Olivia</creatorcontrib><creatorcontrib>Francis, Prudence A</creatorcontrib><creatorcontrib>Walley, Barbara A</creatorcontrib><creatorcontrib>Ribi, Karin</creatorcontrib><creatorcontrib>Bernhard, Jürg</creatorcontrib><creatorcontrib>Luo, Weixiu</creatorcontrib><creatorcontrib>Gómez, Henry L</creatorcontrib><creatorcontrib>Burstein, Harold J</creatorcontrib><creatorcontrib>Parmar, Vani</creatorcontrib><creatorcontrib>Torres, Roberto</creatorcontrib><creatorcontrib>Stewart, Josephine</creatorcontrib><creatorcontrib>Bellet, Meritxell</creatorcontrib><creatorcontrib>Perelló, Antonia</creatorcontrib><creatorcontrib>Dane, Faysal</creatorcontrib><creatorcontrib>Moreira, Antonio</creatorcontrib><creatorcontrib>Vorobiof, Daniel</creatorcontrib><creatorcontrib>Nottage, Michelle</creatorcontrib><creatorcontrib>Price, Karen N</creatorcontrib><creatorcontrib>Coates, Alan S</creatorcontrib><creatorcontrib>Goldhirsch, Aron</creatorcontrib><creatorcontrib>Gelber, Richard D</creatorcontrib><creatorcontrib>Colleoni, Marco</creatorcontrib><creatorcontrib>Fleming, Gini F</creatorcontrib><creatorcontrib>International Breast Cancer Study Group</creatorcontrib><creatorcontrib>SOFT</creatorcontrib><creatorcontrib>TEXT Investigators</creatorcontrib><creatorcontrib>the International Breast Cancer Study Group</creatorcontrib><creatorcontrib>for the SOFT</creatorcontrib><title>Treatment Efficacy, Adherence, and Quality of Life Among Women Younger Than 35 Years in the International Breast Cancer Study Group TEXT and SOFT Adjuvant Endocrine Therapy Trials</title><title>Journal of clinical oncology</title><addtitle>J Clin Oncol</addtitle><description>Purpose To describe benefits and toxicities of adjuvant endocrine therapies in women younger than 35 years with breast cancer (n = 582) enrolled in the Suppression of Ovarian Function Trial (SOFT) and Tamoxifen and Exemestane Trial (TEXT). Methods In SOFT, women still premenopausal after surgery with or without chemotherapy were randomly assigned to tamoxifen alone, tamoxifen plus ovarian function suppression (OFS), or exemestane plus OFS. In TEXT, all received OFS with or without concomitant chemotherapy and were randomly assigned to exemestane plus OFS or tamoxifen plus OFS. We summarize treatment efficacy, quality of life, and adherence of the cohort of women younger than 35 years in SOFT and TEXT, alongside data from the cohort of older premenopausal women. Results For 240 human epidermal growth factor receptor 2-negative patients younger than 35 years enrolled in SOFT after receiving chemotherapy, the 5-year breast cancer-free interval (BCFI) was 67.1% (95% CI, 54.6% to 76.9%) with tamoxifen alone, 75.9% with tamoxifen plus OFS (95% CI, 64.0% to 84.4%), and 83.2% with exemestane plus OFS (95% CI, 72.7% to 90.0%). For 145 human epidermal growth factor receptor 2-negative patients younger than 35 years in TEXT, 5-year BCFI was 79.2% (95% CI, 66.2% to 87.7%) with tamoxifen plus OFS and 81.6% (95% CI, 69.8% to 89.2%) with exemestane plus OFS. The most prominent quality of life symptom for patients younger than 35 years receiving OFS was vasomotor symptoms, with the greatest worsening from baseline at 6 months (on the order of 30 to 40 points), but loss of sexual interest and difficulties in becoming aroused were also clinically meaningful (≥ 8-point change). The level of symptom burden was similar in older premenopausal women. A total of 19.8% of women younger than 35 years stopped all protocol-assigned endocrine therapy early. Conclusion In women younger than 35 years with hormone receptor-positive breast cancer, adjuvant OFS combined with tamoxifen or exemestane produces large improvements in BCFI compared with tamoxifen alone. Menopausal symptoms are significant but are not worse than those seen in older premenopausal women.</description><subject>Adult</subject><subject>Androstadienes - administration & dosage</subject><subject>Antineoplastic Agents, Hormonal - administration & dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Aromatase Inhibitors - administration & dosage</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - surgery</subject><subject>Chemotherapy, Adjuvant</subject><subject>Clinical Trials as Topic</subject><subject>Female</subject><subject>Hormonal Therapy</subject><subject>Humans</subject><subject>ORIGINAL REPORTS</subject><subject>Premenopause</subject><subject>Quality of Life</subject><subject>Receptor, ErbB-2 - analysis</subject><subject>Tamoxifen - administration & dosage</subject><subject>Treatment Outcome</subject><issn>0732-183X</issn><issn>1527-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkV1v0zAUhi0EYmVwzxU6P2Dp_BHHyQ1SqboxVKlCC2K7slznpPXU2pWTTMrv4g_ibDDB1bmw3uc9xw8hHxmdM07p5bflZs4pK-aKz2mVF6_IjEmuMqWkfE1mVAmesVLcnZF3XfdAKctLId-SM14WMheFnJFfdUTTH9H3sGpbZ40dL2DR7DGit3gBxjfwfTAH148QWli7FmFxDH4HP0NKwX0Y_A4j1HvjQUi4RxM7cB76PcKN7zF607vgzQG-pKauh6VJ4Ai3_dCMcB3DcIJ6dVc_Nd1ururU_jA8mmkh3wQbncdEx2hOI9TRmUP3nrxp08APf-Y5-XG1qpdfs_Xm-ma5WGdW0qrPctmkM7emLRhDW9mqMtTkZaEQsRG2Elxu1bYUFbaW09KWDPmWNk2O2CpTCnFOPj9zT8P2iI1NnxTNQZ-iO5o46mCc_v_Fu73ehUctZaW4nAD0GWBj6LqI7UuWUT0J1EmgngRqxfUkMEU-_dv5EvhrTPwGsAiaHg</recordid><startdate>20170920</startdate><enddate>20170920</enddate><creator>Saha, Poornima</creator><creator>Regan, Meredith M</creator><creator>Pagani, Olivia</creator><creator>Francis, Prudence A</creator><creator>Walley, Barbara A</creator><creator>Ribi, Karin</creator><creator>Bernhard, Jürg</creator><creator>Luo, Weixiu</creator><creator>Gómez, Henry L</creator><creator>Burstein, Harold J</creator><creator>Parmar, Vani</creator><creator>Torres, Roberto</creator><creator>Stewart, Josephine</creator><creator>Bellet, Meritxell</creator><creator>Perelló, Antonia</creator><creator>Dane, Faysal</creator><creator>Moreira, Antonio</creator><creator>Vorobiof, Daniel</creator><creator>Nottage, Michelle</creator><creator>Price, Karen N</creator><creator>Coates, Alan S</creator><creator>Goldhirsch, Aron</creator><creator>Gelber, Richard D</creator><creator>Colleoni, Marco</creator><creator>Fleming, Gini F</creator><general>American Society of Clinical Oncology</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>5PM</scope></search><sort><creationdate>20170920</creationdate><title>Treatment Efficacy, Adherence, and Quality of Life Among Women Younger Than 35 Years in the International Breast Cancer Study Group TEXT and SOFT Adjuvant Endocrine Therapy Trials</title><author>Saha, Poornima ; Regan, Meredith M ; Pagani, Olivia ; Francis, Prudence A ; Walley, Barbara A ; Ribi, Karin ; Bernhard, Jürg ; Luo, Weixiu ; Gómez, Henry L ; Burstein, Harold J ; Parmar, Vani ; Torres, Roberto ; Stewart, Josephine ; Bellet, Meritxell ; Perelló, Antonia ; Dane, Faysal ; Moreira, Antonio ; Vorobiof, Daniel ; Nottage, Michelle ; Price, Karen N ; Coates, Alan S ; Goldhirsch, Aron ; Gelber, Richard D ; Colleoni, Marco ; Fleming, Gini F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c509t-45d865baf611ec9c99a0a4867eeed3c9325b7b839efc208c81e2b0dd4eef7a833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Androstadienes - administration & dosage</topic><topic>Antineoplastic Agents, Hormonal - administration & dosage</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Aromatase Inhibitors - administration & dosage</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - surgery</topic><topic>Chemotherapy, Adjuvant</topic><topic>Clinical Trials as Topic</topic><topic>Female</topic><topic>Hormonal Therapy</topic><topic>Humans</topic><topic>ORIGINAL REPORTS</topic><topic>Premenopause</topic><topic>Quality of Life</topic><topic>Receptor, ErbB-2 - analysis</topic><topic>Tamoxifen - administration & dosage</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Saha, Poornima</creatorcontrib><creatorcontrib>Regan, Meredith M</creatorcontrib><creatorcontrib>Pagani, Olivia</creatorcontrib><creatorcontrib>Francis, Prudence A</creatorcontrib><creatorcontrib>Walley, Barbara A</creatorcontrib><creatorcontrib>Ribi, Karin</creatorcontrib><creatorcontrib>Bernhard, Jürg</creatorcontrib><creatorcontrib>Luo, Weixiu</creatorcontrib><creatorcontrib>Gómez, Henry L</creatorcontrib><creatorcontrib>Burstein, Harold J</creatorcontrib><creatorcontrib>Parmar, Vani</creatorcontrib><creatorcontrib>Torres, Roberto</creatorcontrib><creatorcontrib>Stewart, Josephine</creatorcontrib><creatorcontrib>Bellet, Meritxell</creatorcontrib><creatorcontrib>Perelló, Antonia</creatorcontrib><creatorcontrib>Dane, Faysal</creatorcontrib><creatorcontrib>Moreira, Antonio</creatorcontrib><creatorcontrib>Vorobiof, Daniel</creatorcontrib><creatorcontrib>Nottage, Michelle</creatorcontrib><creatorcontrib>Price, Karen N</creatorcontrib><creatorcontrib>Coates, Alan S</creatorcontrib><creatorcontrib>Goldhirsch, Aron</creatorcontrib><creatorcontrib>Gelber, Richard D</creatorcontrib><creatorcontrib>Colleoni, Marco</creatorcontrib><creatorcontrib>Fleming, Gini F</creatorcontrib><creatorcontrib>International Breast Cancer Study Group</creatorcontrib><creatorcontrib>SOFT</creatorcontrib><creatorcontrib>TEXT Investigators</creatorcontrib><creatorcontrib>the International Breast Cancer Study Group</creatorcontrib><creatorcontrib>for the SOFT</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</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>Saha, Poornima</au><au>Regan, Meredith M</au><au>Pagani, Olivia</au><au>Francis, Prudence A</au><au>Walley, Barbara A</au><au>Ribi, Karin</au><au>Bernhard, Jürg</au><au>Luo, Weixiu</au><au>Gómez, Henry L</au><au>Burstein, Harold J</au><au>Parmar, Vani</au><au>Torres, Roberto</au><au>Stewart, Josephine</au><au>Bellet, Meritxell</au><au>Perelló, Antonia</au><au>Dane, Faysal</au><au>Moreira, Antonio</au><au>Vorobiof, Daniel</au><au>Nottage, Michelle</au><au>Price, Karen N</au><au>Coates, Alan S</au><au>Goldhirsch, Aron</au><au>Gelber, Richard D</au><au>Colleoni, Marco</au><au>Fleming, Gini F</au><aucorp>International Breast Cancer Study Group</aucorp><aucorp>SOFT</aucorp><aucorp>TEXT Investigators</aucorp><aucorp>the International Breast Cancer Study Group</aucorp><aucorp>for the SOFT</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Treatment Efficacy, Adherence, and Quality of Life Among Women Younger Than 35 Years in the International Breast Cancer Study Group TEXT and SOFT Adjuvant Endocrine Therapy Trials</atitle><jtitle>Journal of clinical oncology</jtitle><addtitle>J Clin Oncol</addtitle><date>2017-09-20</date><risdate>2017</risdate><volume>35</volume><issue>27</issue><spage>3113</spage><epage>3122</epage><pages>3113-3122</pages><issn>0732-183X</issn><eissn>1527-7755</eissn><abstract>Purpose To describe benefits and toxicities of adjuvant endocrine therapies in women younger than 35 years with breast cancer (n = 582) enrolled in the Suppression of Ovarian Function Trial (SOFT) and Tamoxifen and Exemestane Trial (TEXT). Methods In SOFT, women still premenopausal after surgery with or without chemotherapy were randomly assigned to tamoxifen alone, tamoxifen plus ovarian function suppression (OFS), or exemestane plus OFS. In TEXT, all received OFS with or without concomitant chemotherapy and were randomly assigned to exemestane plus OFS or tamoxifen plus OFS. We summarize treatment efficacy, quality of life, and adherence of the cohort of women younger than 35 years in SOFT and TEXT, alongside data from the cohort of older premenopausal women. Results For 240 human epidermal growth factor receptor 2-negative patients younger than 35 years enrolled in SOFT after receiving chemotherapy, the 5-year breast cancer-free interval (BCFI) was 67.1% (95% CI, 54.6% to 76.9%) with tamoxifen alone, 75.9% with tamoxifen plus OFS (95% CI, 64.0% to 84.4%), and 83.2% with exemestane plus OFS (95% CI, 72.7% to 90.0%). For 145 human epidermal growth factor receptor 2-negative patients younger than 35 years in TEXT, 5-year BCFI was 79.2% (95% CI, 66.2% to 87.7%) with tamoxifen plus OFS and 81.6% (95% CI, 69.8% to 89.2%) with exemestane plus OFS. The most prominent quality of life symptom for patients younger than 35 years receiving OFS was vasomotor symptoms, with the greatest worsening from baseline at 6 months (on the order of 30 to 40 points), but loss of sexual interest and difficulties in becoming aroused were also clinically meaningful (≥ 8-point change). The level of symptom burden was similar in older premenopausal women. A total of 19.8% of women younger than 35 years stopped all protocol-assigned endocrine therapy early. Conclusion In women younger than 35 years with hormone receptor-positive breast cancer, adjuvant OFS combined with tamoxifen or exemestane produces large improvements in BCFI compared with tamoxifen alone. Menopausal symptoms are significant but are not worse than those seen in older premenopausal women.</abstract><cop>United States</cop><pub>American Society of Clinical Oncology</pub><pmid>28654365</pmid><doi>10.1200/JCO.2016.72.0946</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Androstadienes - administration & dosage Antineoplastic Agents, Hormonal - administration & dosage Antineoplastic Combined Chemotherapy Protocols - therapeutic use Aromatase Inhibitors - administration & dosage Breast Neoplasms - drug therapy Breast Neoplasms - surgery Chemotherapy, Adjuvant Clinical Trials as Topic Female Hormonal Therapy Humans ORIGINAL REPORTS Premenopause Quality of Life Receptor, ErbB-2 - analysis Tamoxifen - administration & dosage Treatment Outcome |
title | Treatment Efficacy, Adherence, and Quality of Life Among Women Younger Than 35 Years in the International Breast Cancer Study Group TEXT and SOFT Adjuvant Endocrine Therapy Trials |
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