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
Hauptverfasser: 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
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container_end_page 2000
container_issue 9169
container_start_page 1993
container_title The Lancet (British edition)
container_volume 353
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
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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. 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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. 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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. 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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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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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