Tamoxifen in treatment of intraductal breast cancer: National Surgical Adjuvant Breast and Bowel Project B-24 randomised controlled trial
We have shown previously that lumpectomy with radiation therapy was more effective than lumpectomy alone for the treatment of ductal carcinoma in situ (DCIS). We did a double-blind randomised controlled trial to find out whether lumpectomy, radiation therapy, and tamoxifen was of more benefit than l...
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Veröffentlicht in: | The Lancet (British edition) 1999-06, Vol.353 (9169), p.1993-2000 |
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container_issue | 9169 |
container_start_page | 1993 |
container_title | The Lancet (British edition) |
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creator | Fisher, Bernard Dignam, James Wolmark, Norman Wickerham, D Lawrence Fisher, Edwin R Mamounas, Eleftherios Smith, Roy Begovic, Mirsada Dimitrov, Nikolay V Margolese, Richard G Kardinal, Carl G Kavanah, Maureen T Fehrenbacher, Louis Oishi, Robert H |
description | We have shown previously that lumpectomy with radiation therapy was more effective than lumpectomy alone for the treatment of ductal carcinoma in situ (DCIS). We did a double-blind randomised controlled trial to find out whether lumpectomy, radiation therapy, and tamoxifen was of more benefit than lumpectomy and radiation therapy alone for DCIS.
1804 women with DCIS, including those whose resected sample margins were involved with tumour, were randomly assigned lumpectomy, radiation therapy (50 Gy), and placebo (n=902), or lumpectomy, radiation therapy, and tamoxifen (20 mg daily for 5 years, n=902). Median follow-up was 74 months (range 57–93). We compared annual event rates and cumulative probability of invasive or non-invasive ipsilateral and contralateral tumours over 5 years.
Women in the tamoxifen group had fewer breast-cancer events at 5 years than did those on placebo (8·2 vs 13·4%, p=0·0009). The cumulative incidence of all invasive breast-cancer events in the tamoxifen group was 4·1% at 5 years: 2·1% in the ipsilateral breast, 1·8% in the contralateral breast, and 0·2% at regional or distant sites. The risk of ipsilateral-breast cancer was lower in the tamoxifen group even when sample margins contained tumour and when DCIS was associated with comedonecrosis.
The combination of lumpectomy, radiation therapy, and tamoxifen was effective in the prevention of invasive cancer. |
doi_str_mv | 10.1016/S0140-6736(99)05036-9 |
format | Article |
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1804 women with DCIS, including those whose resected sample margins were involved with tumour, were randomly assigned lumpectomy, radiation therapy (50 Gy), and placebo (n=902), or lumpectomy, radiation therapy, and tamoxifen (20 mg daily for 5 years, n=902). Median follow-up was 74 months (range 57–93). We compared annual event rates and cumulative probability of invasive or non-invasive ipsilateral and contralateral tumours over 5 years.
Women in the tamoxifen group had fewer breast-cancer events at 5 years than did those on placebo (8·2 vs 13·4%, p=0·0009). The cumulative incidence of all invasive breast-cancer events in the tamoxifen group was 4·1% at 5 years: 2·1% in the ipsilateral breast, 1·8% in the contralateral breast, and 0·2% at regional or distant sites. The risk of ipsilateral-breast cancer was lower in the tamoxifen group even when sample margins contained tumour and when DCIS was associated with comedonecrosis.
The combination of lumpectomy, radiation therapy, and tamoxifen was effective in the prevention of invasive cancer.</description><identifier>ISSN: 0140-6736</identifier><identifier>EISSN: 1474-547X</identifier><identifier>DOI: 10.1016/S0140-6736(99)05036-9</identifier><identifier>PMID: 10376613</identifier><identifier>CODEN: LANCAO</identifier><language>eng</language><publisher>London: Elsevier Ltd</publisher><subject>Antineoplastic Agents, Hormonal - adverse effects ; Antineoplastic Agents, Hormonal - therapeutic use ; Biological and medical sciences ; Breast Neoplasms - drug therapy ; Breast Neoplasms - mortality ; Breast Neoplasms - pathology ; Breast Neoplasms - therapy ; Cancer ; Carcinoma in Situ - drug therapy ; Carcinoma in Situ - therapy ; Carcinoma, Intraductal, Noninfiltrating - drug therapy ; Carcinoma, Intraductal, Noninfiltrating - mortality ; Carcinoma, Intraductal, Noninfiltrating - secondary ; Carcinoma, Intraductal, Noninfiltrating - therapy ; Carcinoma, Lobular - drug therapy ; Carcinoma, Lobular - therapy ; Clinical trials ; Combined Modality Therapy ; Double-Blind Method ; Drug therapy ; Female ; Gynecology. Andrology. Obstetrics ; Humans ; Mammary gland diseases ; Mastectomy, Segmental ; Medical research ; Medical sciences ; Middle Aged ; Radiation ; Radiation therapy ; Survival Rate ; Tamoxifen - adverse effects ; Tamoxifen - therapeutic use ; Tumors</subject><ispartof>The Lancet (British edition), 1999-06, Vol.353 (9169), p.1993-2000</ispartof><rights>1999 Elsevier Ltd</rights><rights>1999 INIST-CNRS</rights><rights>Copyright Lancet Ltd. Jun 12, 1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c469t-a565b71c56f844d138e65db605239b7bf6984240f3b6b73a8039a0041ebc882c3</citedby><cites>FETCH-LOGICAL-c469t-a565b71c56f844d138e65db605239b7bf6984240f3b6b73a8039a0041ebc882c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0140673699050369$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1845540$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10376613$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fisher, Bernard</creatorcontrib><creatorcontrib>Dignam, James</creatorcontrib><creatorcontrib>Wolmark, Norman</creatorcontrib><creatorcontrib>Wickerham, D Lawrence</creatorcontrib><creatorcontrib>Fisher, Edwin R</creatorcontrib><creatorcontrib>Mamounas, Eleftherios</creatorcontrib><creatorcontrib>Smith, Roy</creatorcontrib><creatorcontrib>Begovic, Mirsada</creatorcontrib><creatorcontrib>Dimitrov, Nikolay V</creatorcontrib><creatorcontrib>Margolese, Richard G</creatorcontrib><creatorcontrib>Kardinal, Carl G</creatorcontrib><creatorcontrib>Kavanah, Maureen T</creatorcontrib><creatorcontrib>Fehrenbacher, Louis</creatorcontrib><creatorcontrib>Oishi, Robert H</creatorcontrib><title>Tamoxifen in treatment of intraductal breast cancer: National Surgical Adjuvant Breast and Bowel Project B-24 randomised controlled trial</title><title>The Lancet (British edition)</title><addtitle>Lancet</addtitle><description>We have shown previously that lumpectomy with radiation therapy was more effective than lumpectomy alone for the treatment of ductal carcinoma in situ (DCIS). We did a double-blind randomised controlled trial to find out whether lumpectomy, radiation therapy, and tamoxifen was of more benefit than lumpectomy and radiation therapy alone for DCIS.
1804 women with DCIS, including those whose resected sample margins were involved with tumour, were randomly assigned lumpectomy, radiation therapy (50 Gy), and placebo (n=902), or lumpectomy, radiation therapy, and tamoxifen (20 mg daily for 5 years, n=902). Median follow-up was 74 months (range 57–93). We compared annual event rates and cumulative probability of invasive or non-invasive ipsilateral and contralateral tumours over 5 years.
Women in the tamoxifen group had fewer breast-cancer events at 5 years than did those on placebo (8·2 vs 13·4%, p=0·0009). The cumulative incidence of all invasive breast-cancer events in the tamoxifen group was 4·1% at 5 years: 2·1% in the ipsilateral breast, 1·8% in the contralateral breast, and 0·2% at regional or distant sites. The risk of ipsilateral-breast cancer was lower in the tamoxifen group even when sample margins contained tumour and when DCIS was associated with comedonecrosis.
The combination of lumpectomy, radiation therapy, and tamoxifen was effective in the prevention of invasive cancer.</description><subject>Antineoplastic Agents, Hormonal - adverse effects</subject><subject>Antineoplastic Agents, Hormonal - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - mortality</subject><subject>Breast Neoplasms - pathology</subject><subject>Breast Neoplasms - therapy</subject><subject>Cancer</subject><subject>Carcinoma in Situ - drug therapy</subject><subject>Carcinoma in Situ - therapy</subject><subject>Carcinoma, Intraductal, Noninfiltrating - drug therapy</subject><subject>Carcinoma, Intraductal, Noninfiltrating - mortality</subject><subject>Carcinoma, Intraductal, Noninfiltrating - secondary</subject><subject>Carcinoma, Intraductal, Noninfiltrating - therapy</subject><subject>Carcinoma, Lobular - drug therapy</subject><subject>Carcinoma, Lobular - therapy</subject><subject>Clinical trials</subject><subject>Combined Modality Therapy</subject><subject>Double-Blind Method</subject><subject>Drug therapy</subject><subject>Female</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Mammary gland diseases</subject><subject>Mastectomy, Segmental</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Radiation</subject><subject>Radiation therapy</subject><subject>Survival Rate</subject><subject>Tamoxifen - adverse effects</subject><subject>Tamoxifen - therapeutic use</subject><subject>Tumors</subject><issn>0140-6736</issn><issn>1474-547X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkFtrFTEQgIMo9lj9CUoQH-rDanJy2cQXaYs3KCq0gm8ht5Ucdjc1ybb6E_zXTrsH9c2nTGa-GWY-hB5T8oISKl-eE8pJJ3smj7R-TgRhstN30IbynneC91_vos0f5AA9qHVHCOGSiPvogBLWS0nZBv26sFP-kYY44zTjVqJtU5wbzgP8W7Fh8c2O2EGhNuzt7GN5hT_alvIM-fOlfEseguOwW64sNJ6spJ0DPsnXccSfS95FD4Vuy3GBfJ5SjQH7DPPzOELYSrLjQ3RvsGONj_bvIfry9s3F6fvu7NO7D6fHZ53nUrfOCilcT72Qg-I8UKaiFMHBXVumXe8GqRXfcjIwJ13PrCJMWzicRueV2np2iJ6ucy9L_r7E2swuLwWOqYZqpZVgPQdIrJAvudYSB3NZ0mTLT0OJufFvbv2bG7lGa3Pr32joe7Ifvrgphn-6VuEAPNsDtoK3AYT4VP9yigvBCWCvVyyCiasUi6k-RZAfUgGZJuT0n01-A9_9oj0</recordid><startdate>19990612</startdate><enddate>19990612</enddate><creator>Fisher, Bernard</creator><creator>Dignam, James</creator><creator>Wolmark, Norman</creator><creator>Wickerham, D Lawrence</creator><creator>Fisher, Edwin R</creator><creator>Mamounas, Eleftherios</creator><creator>Smith, Roy</creator><creator>Begovic, Mirsada</creator><creator>Dimitrov, Nikolay V</creator><creator>Margolese, Richard G</creator><creator>Kardinal, Carl G</creator><creator>Kavanah, Maureen T</creator><creator>Fehrenbacher, Louis</creator><creator>Oishi, Robert H</creator><general>Elsevier Ltd</general><general>Lancet</general><general>Elsevier Limited</general><scope>IQODW</scope><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>0TT</scope><scope>0TZ</scope><scope>0U~</scope><scope>3V.</scope><scope>7QL</scope><scope>7QP</scope><scope>7RV</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88C</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8C2</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AN0</scope><scope>ASE</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FPQ</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K6X</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>KB~</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>S0X</scope></search><sort><creationdate>19990612</creationdate><title>Tamoxifen in treatment of intraductal breast cancer: National Surgical Adjuvant Breast and Bowel Project B-24 randomised controlled trial</title><author>Fisher, Bernard ; Dignam, James ; Wolmark, Norman ; Wickerham, D Lawrence ; Fisher, Edwin R ; Mamounas, Eleftherios ; Smith, Roy ; Begovic, Mirsada ; Dimitrov, Nikolay V ; Margolese, Richard G ; Kardinal, Carl G ; Kavanah, Maureen T ; Fehrenbacher, Louis ; Oishi, Robert H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c469t-a565b71c56f844d138e65db605239b7bf6984240f3b6b73a8039a0041ebc882c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Antineoplastic Agents, Hormonal - adverse effects</topic><topic>Antineoplastic Agents, Hormonal - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - mortality</topic><topic>Breast Neoplasms - pathology</topic><topic>Breast Neoplasms - therapy</topic><topic>Cancer</topic><topic>Carcinoma in Situ - drug therapy</topic><topic>Carcinoma in Situ - therapy</topic><topic>Carcinoma, Intraductal, Noninfiltrating - drug therapy</topic><topic>Carcinoma, Intraductal, Noninfiltrating - mortality</topic><topic>Carcinoma, Intraductal, Noninfiltrating - secondary</topic><topic>Carcinoma, Intraductal, Noninfiltrating - therapy</topic><topic>Carcinoma, Lobular - drug therapy</topic><topic>Carcinoma, Lobular - therapy</topic><topic>Clinical trials</topic><topic>Combined Modality Therapy</topic><topic>Double-Blind Method</topic><topic>Drug therapy</topic><topic>Female</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Mammary gland diseases</topic><topic>Mastectomy, Segmental</topic><topic>Medical research</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Radiation</topic><topic>Radiation therapy</topic><topic>Survival Rate</topic><topic>Tamoxifen - adverse effects</topic><topic>Tamoxifen - therapeutic use</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fisher, Bernard</creatorcontrib><creatorcontrib>Dignam, James</creatorcontrib><creatorcontrib>Wolmark, Norman</creatorcontrib><creatorcontrib>Wickerham, D Lawrence</creatorcontrib><creatorcontrib>Fisher, Edwin R</creatorcontrib><creatorcontrib>Mamounas, Eleftherios</creatorcontrib><creatorcontrib>Smith, Roy</creatorcontrib><creatorcontrib>Begovic, Mirsada</creatorcontrib><creatorcontrib>Dimitrov, Nikolay V</creatorcontrib><creatorcontrib>Margolese, Richard G</creatorcontrib><creatorcontrib>Kardinal, Carl 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Adjuvant Breast and Bowel Project B-24 randomised controlled trial</atitle><jtitle>The Lancet (British edition)</jtitle><addtitle>Lancet</addtitle><date>1999-06-12</date><risdate>1999</risdate><volume>353</volume><issue>9169</issue><spage>1993</spage><epage>2000</epage><pages>1993-2000</pages><issn>0140-6736</issn><eissn>1474-547X</eissn><coden>LANCAO</coden><abstract>We have shown previously that lumpectomy with radiation therapy was more effective than lumpectomy alone for the treatment of ductal carcinoma in situ (DCIS). We did a double-blind randomised controlled trial to find out whether lumpectomy, radiation therapy, and tamoxifen was of more benefit than lumpectomy and radiation therapy alone for DCIS.
1804 women with DCIS, including those whose resected sample margins were involved with tumour, were randomly assigned lumpectomy, radiation therapy (50 Gy), and placebo (n=902), or lumpectomy, radiation therapy, and tamoxifen (20 mg daily for 5 years, n=902). Median follow-up was 74 months (range 57–93). We compared annual event rates and cumulative probability of invasive or non-invasive ipsilateral and contralateral tumours over 5 years.
Women in the tamoxifen group had fewer breast-cancer events at 5 years than did those on placebo (8·2 vs 13·4%, p=0·0009). The cumulative incidence of all invasive breast-cancer events in the tamoxifen group was 4·1% at 5 years: 2·1% in the ipsilateral breast, 1·8% in the contralateral breast, and 0·2% at regional or distant sites. The risk of ipsilateral-breast cancer was lower in the tamoxifen group even when sample margins contained tumour and when DCIS was associated with comedonecrosis.
The combination of lumpectomy, radiation therapy, and tamoxifen was effective in the prevention of invasive cancer.</abstract><cop>London</cop><pub>Elsevier Ltd</pub><pmid>10376613</pmid><doi>10.1016/S0140-6736(99)05036-9</doi><tpages>8</tpages></addata></record> |
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ispartof | The Lancet (British edition), 1999-06, Vol.353 (9169), p.1993-2000 |
issn | 0140-6736 1474-547X |
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source | MEDLINE; Elsevier ScienceDirect Journals Complete; EBSCOhost Business Source Complete |
subjects | Antineoplastic Agents, Hormonal - adverse effects Antineoplastic Agents, Hormonal - therapeutic use Biological and medical sciences Breast Neoplasms - drug therapy Breast Neoplasms - mortality Breast Neoplasms - pathology Breast Neoplasms - therapy Cancer Carcinoma in Situ - drug therapy Carcinoma in Situ - therapy Carcinoma, Intraductal, Noninfiltrating - drug therapy Carcinoma, Intraductal, Noninfiltrating - mortality Carcinoma, Intraductal, Noninfiltrating - secondary Carcinoma, Intraductal, Noninfiltrating - therapy Carcinoma, Lobular - drug therapy Carcinoma, Lobular - therapy Clinical trials Combined Modality Therapy Double-Blind Method Drug therapy Female Gynecology. Andrology. Obstetrics Humans Mammary gland diseases Mastectomy, Segmental Medical research Medical sciences Middle Aged Radiation Radiation therapy Survival Rate Tamoxifen - adverse effects Tamoxifen - therapeutic use Tumors |
title | Tamoxifen in treatment of intraductal breast cancer: National Surgical Adjuvant Breast and Bowel Project B-24 randomised controlled trial |
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