Efficacy of Adjuvant Trastuzumab for Patients With Human Epidermal Growth Factor Receptor 2-Positive Early Breast Cancer and Tumors ≤ 2 cm: A Meta-Analysis of the Randomized Trastuzumab Trials
We compared efficacy of trastuzumab versus no trastuzumab in patients with small (≤ 2 cm) human epidermal growth factor receptor 2 (HER2) -positive breast cancer treated in randomized trials. A meta-analysis was conducted using data from five of the six adjuvant trastuzumab trials. Efficacy end poin...
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Veröffentlicht in: | Journal of clinical oncology 2015-08, Vol.33 (24), p.2600-2608 |
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creator | O'Sullivan, Ciara C Bradbury, Ian Campbell, Christine Spielmann, Marc Perez, Edith A Joensuu, Heikki Costantino, Joseph P Delaloge, Suzette Rastogi, Priya Zardavas, Dimitrios Ballman, Karla V Holmes, Eileen de Azambuja, Evandro Piccart-Gebhart, Martine Zujewski, Jo Anne Gelber, Richard D |
description | We compared efficacy of trastuzumab versus no trastuzumab in patients with small (≤ 2 cm) human epidermal growth factor receptor 2 (HER2) -positive breast cancer treated in randomized trials.
A meta-analysis was conducted using data from five of the six adjuvant trastuzumab trials. Efficacy end points were disease-free survival (DFS) and overall survival (OS). Separate analyses were prospectively planned for hormone receptor (HR) -positive and HR-negative cohorts. Random effect models and Yusuf-Peto fixed effects models assessed the impact of heterogeneity on baseline hazards and treatment effects across studies. Peto-Pike cumulative incidence estimates were stratified by study and nodal status.
Median follow-up time was 8 years. For 2,263 patients with HR-positive disease, 8-year cumulative incidence rates comparing trastuzumab versus no trastuzumab were 17.3% versus 24.3% (P < .001) for DFS and 7.8% versus 11.6% (P = .005) for OS, respectively; for 1,092 HR-positive patients with zero or one positive lymph nodes, results were 12.7% versus 19.4% (P = .005) for DFS and 5.3% versus 7.4% (P = .12) for OS, respectively. For 1,957 patients with HR-negative disease, 8-year cumulative incidence rates were 24.0% versus 33.4% (P < .001) for DFS and 12.4% versus 21.2% (P < .001) for OS, respectively; for 1,040 HR-negative patients with zero or one positive lymph nodes, results were 20.4% versus 26.3% (P = .05) for DFS and 8.2% versus 12.2% (P = .084) for OS, respectively.
Women with HER2-positive tumors ≤ 2 cm in the randomized trastuzumab trials derived substantial DFS and OS benefit from adjuvant trastuzumab. Trastuzumab-treated patients with HR-positive disease and ≤ one positive lymph node may be candidates for trials assessing less aggressive treatment approaches. |
doi_str_mv | 10.1200/JCO.2015.60.8620 |
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A meta-analysis was conducted using data from five of the six adjuvant trastuzumab trials. Efficacy end points were disease-free survival (DFS) and overall survival (OS). Separate analyses were prospectively planned for hormone receptor (HR) -positive and HR-negative cohorts. Random effect models and Yusuf-Peto fixed effects models assessed the impact of heterogeneity on baseline hazards and treatment effects across studies. Peto-Pike cumulative incidence estimates were stratified by study and nodal status.
Median follow-up time was 8 years. For 2,263 patients with HR-positive disease, 8-year cumulative incidence rates comparing trastuzumab versus no trastuzumab were 17.3% versus 24.3% (P < .001) for DFS and 7.8% versus 11.6% (P = .005) for OS, respectively; for 1,092 HR-positive patients with zero or one positive lymph nodes, results were 12.7% versus 19.4% (P = .005) for DFS and 5.3% versus 7.4% (P = .12) for OS, respectively. For 1,957 patients with HR-negative disease, 8-year cumulative incidence rates were 24.0% versus 33.4% (P < .001) for DFS and 12.4% versus 21.2% (P < .001) for OS, respectively; for 1,040 HR-negative patients with zero or one positive lymph nodes, results were 20.4% versus 26.3% (P = .05) for DFS and 8.2% versus 12.2% (P = .084) for OS, respectively.
Women with HER2-positive tumors ≤ 2 cm in the randomized trastuzumab trials derived substantial DFS and OS benefit from adjuvant trastuzumab. Trastuzumab-treated patients with HR-positive disease and ≤ one positive lymph node may be candidates for trials assessing less aggressive treatment approaches.</description><identifier>ISSN: 0732-183X</identifier><identifier>EISSN: 1527-7755</identifier><identifier>DOI: 10.1200/JCO.2015.60.8620</identifier><identifier>PMID: 26101239</identifier><language>eng</language><publisher>United States: American Society of Clinical Oncology</publisher><subject>Antibodies, Monoclonal, Humanized - therapeutic use ; Antineoplastic Agents - therapeutic use ; Breast Neoplasms - drug therapy ; Breast Neoplasms - enzymology ; Chemotherapy, Adjuvant ; Disease-Free Survival ; Female ; Humans ; ORIGINAL REPORTS ; Randomized Controlled Trials as Topic ; Receptor, ErbB-2 - biosynthesis ; Trastuzumab</subject><ispartof>Journal of clinical oncology, 2015-08, Vol.33 (24), p.2600-2608</ispartof><rights>2015 by American Society of Clinical Oncology.</rights><rights>2015 by American Society of Clinical Oncology 2015 American Society of Clinical Oncology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-42731ff7247f42d85cc864c1c4cc805f863805629184aec540c017ada4f1e2ba3</citedby><cites>FETCH-LOGICAL-c396t-42731ff7247f42d85cc864c1c4cc805f863805629184aec540c017ada4f1e2ba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,3729,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26101239$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>O'Sullivan, Ciara C</creatorcontrib><creatorcontrib>Bradbury, Ian</creatorcontrib><creatorcontrib>Campbell, Christine</creatorcontrib><creatorcontrib>Spielmann, Marc</creatorcontrib><creatorcontrib>Perez, Edith A</creatorcontrib><creatorcontrib>Joensuu, Heikki</creatorcontrib><creatorcontrib>Costantino, Joseph P</creatorcontrib><creatorcontrib>Delaloge, Suzette</creatorcontrib><creatorcontrib>Rastogi, Priya</creatorcontrib><creatorcontrib>Zardavas, Dimitrios</creatorcontrib><creatorcontrib>Ballman, Karla V</creatorcontrib><creatorcontrib>Holmes, Eileen</creatorcontrib><creatorcontrib>de Azambuja, Evandro</creatorcontrib><creatorcontrib>Piccart-Gebhart, Martine</creatorcontrib><creatorcontrib>Zujewski, Jo Anne</creatorcontrib><creatorcontrib>Gelber, Richard D</creatorcontrib><title>Efficacy of Adjuvant Trastuzumab for Patients With Human Epidermal Growth Factor Receptor 2-Positive Early Breast Cancer and Tumors ≤ 2 cm: A Meta-Analysis of the Randomized Trastuzumab Trials</title><title>Journal of clinical oncology</title><addtitle>J Clin Oncol</addtitle><description>We compared efficacy of trastuzumab versus no trastuzumab in patients with small (≤ 2 cm) human epidermal growth factor receptor 2 (HER2) -positive breast cancer treated in randomized trials.
A meta-analysis was conducted using data from five of the six adjuvant trastuzumab trials. Efficacy end points were disease-free survival (DFS) and overall survival (OS). Separate analyses were prospectively planned for hormone receptor (HR) -positive and HR-negative cohorts. Random effect models and Yusuf-Peto fixed effects models assessed the impact of heterogeneity on baseline hazards and treatment effects across studies. Peto-Pike cumulative incidence estimates were stratified by study and nodal status.
Median follow-up time was 8 years. For 2,263 patients with HR-positive disease, 8-year cumulative incidence rates comparing trastuzumab versus no trastuzumab were 17.3% versus 24.3% (P < .001) for DFS and 7.8% versus 11.6% (P = .005) for OS, respectively; for 1,092 HR-positive patients with zero or one positive lymph nodes, results were 12.7% versus 19.4% (P = .005) for DFS and 5.3% versus 7.4% (P = .12) for OS, respectively. For 1,957 patients with HR-negative disease, 8-year cumulative incidence rates were 24.0% versus 33.4% (P < .001) for DFS and 12.4% versus 21.2% (P < .001) for OS, respectively; for 1,040 HR-negative patients with zero or one positive lymph nodes, results were 20.4% versus 26.3% (P = .05) for DFS and 8.2% versus 12.2% (P = .084) for OS, respectively.
Women with HER2-positive tumors ≤ 2 cm in the randomized trastuzumab trials derived substantial DFS and OS benefit from adjuvant trastuzumab. Trastuzumab-treated patients with HR-positive disease and ≤ one positive lymph node may be candidates for trials assessing less aggressive treatment approaches.</description><subject>Antibodies, Monoclonal, Humanized - therapeutic use</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - enzymology</subject><subject>Chemotherapy, Adjuvant</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Humans</subject><subject>ORIGINAL REPORTS</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Receptor, ErbB-2 - biosynthesis</subject><subject>Trastuzumab</subject><issn>0732-183X</issn><issn>1527-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUU1vEzEQtRCIhsKdE_KRywZ_rjcckEKUtqCiVlUQ3KyJ1yaudtfB9gal_4D_wS_hp_BLcNRS0dMbzbx58zQPoZeUTCkj5M3HxcWUESqnNZk2NSOP0IRKpiqlpHyMJkRxVtGGfz1Cz1K6JoSKhsun6IjVlFDGZxP0e-mcN2D2ODg8b6_HHQwZryKkPN6MPayxCxFfQvZ2yAl_8XmDz0p_wMutb23socOnMfwo7RMwuXCvrLHbQ8Gqy5B89juLlxC7PX4fbZHFCxiMjRiGFq_GPsSE__z8hRk2_Vs8x59shmo-QLdPPh1M5Y3FV4Ucen9j2wfWVtFDl56jJ66AfXGHx-jzyXK1OKvOL04_LObnleGzOleCKU6dU0woJ1jbSGOaWhhqRCmIdE3NC9RsRhsB1khBDKEKWhCOWrYGfoze3epux3VvW1MeEqHT2-h7iHsdwOuHk8Fv9Lew00JyIRkvAq_vBGL4PtqUde-TsV0Hgw1j0lQRqbhQXBUquaWaGFKK1t2foUQfotclen2IXtdEH6IvK6_-t3e_8C9r_hdD2a4N</recordid><startdate>20150820</startdate><enddate>20150820</enddate><creator>O'Sullivan, Ciara C</creator><creator>Bradbury, Ian</creator><creator>Campbell, Christine</creator><creator>Spielmann, Marc</creator><creator>Perez, Edith A</creator><creator>Joensuu, Heikki</creator><creator>Costantino, Joseph P</creator><creator>Delaloge, Suzette</creator><creator>Rastogi, Priya</creator><creator>Zardavas, Dimitrios</creator><creator>Ballman, Karla V</creator><creator>Holmes, Eileen</creator><creator>de Azambuja, Evandro</creator><creator>Piccart-Gebhart, Martine</creator><creator>Zujewski, Jo Anne</creator><creator>Gelber, Richard D</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150820</creationdate><title>Efficacy of Adjuvant Trastuzumab for Patients With Human Epidermal Growth Factor Receptor 2-Positive Early Breast Cancer and Tumors ≤ 2 cm: A Meta-Analysis of the Randomized Trastuzumab Trials</title><author>O'Sullivan, Ciara C ; Bradbury, Ian ; Campbell, Christine ; Spielmann, Marc ; Perez, Edith A ; Joensuu, Heikki ; Costantino, Joseph P ; Delaloge, Suzette ; Rastogi, Priya ; Zardavas, Dimitrios ; Ballman, Karla V ; Holmes, Eileen ; de Azambuja, Evandro ; Piccart-Gebhart, Martine ; Zujewski, Jo Anne ; Gelber, Richard D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-42731ff7247f42d85cc864c1c4cc805f863805629184aec540c017ada4f1e2ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Antibodies, Monoclonal, Humanized - therapeutic use</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - enzymology</topic><topic>Chemotherapy, Adjuvant</topic><topic>Disease-Free Survival</topic><topic>Female</topic><topic>Humans</topic><topic>ORIGINAL REPORTS</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Receptor, ErbB-2 - biosynthesis</topic><topic>Trastuzumab</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>O'Sullivan, Ciara C</creatorcontrib><creatorcontrib>Bradbury, Ian</creatorcontrib><creatorcontrib>Campbell, Christine</creatorcontrib><creatorcontrib>Spielmann, Marc</creatorcontrib><creatorcontrib>Perez, Edith A</creatorcontrib><creatorcontrib>Joensuu, Heikki</creatorcontrib><creatorcontrib>Costantino, Joseph P</creatorcontrib><creatorcontrib>Delaloge, Suzette</creatorcontrib><creatorcontrib>Rastogi, Priya</creatorcontrib><creatorcontrib>Zardavas, Dimitrios</creatorcontrib><creatorcontrib>Ballman, Karla V</creatorcontrib><creatorcontrib>Holmes, Eileen</creatorcontrib><creatorcontrib>de Azambuja, Evandro</creatorcontrib><creatorcontrib>Piccart-Gebhart, Martine</creatorcontrib><creatorcontrib>Zujewski, Jo Anne</creatorcontrib><creatorcontrib>Gelber, Richard D</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>O'Sullivan, Ciara C</au><au>Bradbury, Ian</au><au>Campbell, Christine</au><au>Spielmann, Marc</au><au>Perez, Edith A</au><au>Joensuu, Heikki</au><au>Costantino, Joseph P</au><au>Delaloge, Suzette</au><au>Rastogi, Priya</au><au>Zardavas, Dimitrios</au><au>Ballman, Karla V</au><au>Holmes, Eileen</au><au>de Azambuja, Evandro</au><au>Piccart-Gebhart, Martine</au><au>Zujewski, Jo Anne</au><au>Gelber, Richard D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy of Adjuvant Trastuzumab for Patients With Human Epidermal Growth Factor Receptor 2-Positive Early Breast Cancer and Tumors ≤ 2 cm: A Meta-Analysis of the Randomized Trastuzumab Trials</atitle><jtitle>Journal of clinical oncology</jtitle><addtitle>J Clin Oncol</addtitle><date>2015-08-20</date><risdate>2015</risdate><volume>33</volume><issue>24</issue><spage>2600</spage><epage>2608</epage><pages>2600-2608</pages><issn>0732-183X</issn><eissn>1527-7755</eissn><abstract>We compared efficacy of trastuzumab versus no trastuzumab in patients with small (≤ 2 cm) human epidermal growth factor receptor 2 (HER2) -positive breast cancer treated in randomized trials.
A meta-analysis was conducted using data from five of the six adjuvant trastuzumab trials. Efficacy end points were disease-free survival (DFS) and overall survival (OS). Separate analyses were prospectively planned for hormone receptor (HR) -positive and HR-negative cohorts. Random effect models and Yusuf-Peto fixed effects models assessed the impact of heterogeneity on baseline hazards and treatment effects across studies. Peto-Pike cumulative incidence estimates were stratified by study and nodal status.
Median follow-up time was 8 years. For 2,263 patients with HR-positive disease, 8-year cumulative incidence rates comparing trastuzumab versus no trastuzumab were 17.3% versus 24.3% (P < .001) for DFS and 7.8% versus 11.6% (P = .005) for OS, respectively; for 1,092 HR-positive patients with zero or one positive lymph nodes, results were 12.7% versus 19.4% (P = .005) for DFS and 5.3% versus 7.4% (P = .12) for OS, respectively. For 1,957 patients with HR-negative disease, 8-year cumulative incidence rates were 24.0% versus 33.4% (P < .001) for DFS and 12.4% versus 21.2% (P < .001) for OS, respectively; for 1,040 HR-negative patients with zero or one positive lymph nodes, results were 20.4% versus 26.3% (P = .05) for DFS and 8.2% versus 12.2% (P = .084) for OS, respectively.
Women with HER2-positive tumors ≤ 2 cm in the randomized trastuzumab trials derived substantial DFS and OS benefit from adjuvant trastuzumab. Trastuzumab-treated patients with HR-positive disease and ≤ one positive lymph node may be candidates for trials assessing less aggressive treatment approaches.</abstract><cop>United States</cop><pub>American Society of Clinical Oncology</pub><pmid>26101239</pmid><doi>10.1200/JCO.2015.60.8620</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; American Society of Clinical Oncology Online Journals; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Antibodies, Monoclonal, Humanized - therapeutic use Antineoplastic Agents - therapeutic use Breast Neoplasms - drug therapy Breast Neoplasms - enzymology Chemotherapy, Adjuvant Disease-Free Survival Female Humans ORIGINAL REPORTS Randomized Controlled Trials as Topic Receptor, ErbB-2 - biosynthesis Trastuzumab |
title | Efficacy of Adjuvant Trastuzumab for Patients With Human Epidermal Growth Factor Receptor 2-Positive Early Breast Cancer and Tumors ≤ 2 cm: A Meta-Analysis of the Randomized Trastuzumab Trials |
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