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The role of the addition of ovarian suppression to tamoxifen in young women with hormone-sensitive breast cancer who remain premenopausal or regain menstruation after chemotherapy (ASTRRA): study protocol for a randomized controlled trial and progress
BACKGROUND: Ovarian function suppression (OFS) has been shown to be effective as adjuvant endocrine therapy in premenopausal women with hormone receptor-positive breast cancer. However, it is currently unclear if addition of OFS to standard tamoxifen therapy after completion of adjuvant chemotherapy...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872354/ https://www.ncbi.nlm.nih.gov/pubmed/27197523 http://dx.doi.org/10.1186/s12885-016-2354-6 |
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author | Kim, Hyun-Ah Ahn, Sei Hyun Nam, Seok Jin Park, Seho Ro, Jungsil Im, Seock-Ah Jung, Yong Sik Yoon, Jung Han Hur, Min Hee Choi, Yoon Ji Lee, Soo-Jung Jeong, Joon Cho, Se-Heon Kim, Sung Yong Lee, Min Hyuk Kim, Lee Su Moon, Byung-In Kim, Tae Hyun Park, Chanheun Kim, Sei Joong Jung, Sung Hoo Park, Heungkyu Gwak, Geum Hee Kang, Sun Hee Kim, Jong Gin Kim, Jeryong Choi, Su Yun Lim, Cheol-Wan Kim, Doyil Yoo, Youngbum Song, Young-Jin Kang, Yoon-Jung Jung, Sang Seol Shin, Hyuk Jai Lee, Kwan Ju Han, Se-Hwan Lee, Eun Sook Han, Wonshik Kim, Hee-Jung Noh, Woo Chul |
author_facet | Kim, Hyun-Ah Ahn, Sei Hyun Nam, Seok Jin Park, Seho Ro, Jungsil Im, Seock-Ah Jung, Yong Sik Yoon, Jung Han Hur, Min Hee Choi, Yoon Ji Lee, Soo-Jung Jeong, Joon Cho, Se-Heon Kim, Sung Yong Lee, Min Hyuk Kim, Lee Su Moon, Byung-In Kim, Tae Hyun Park, Chanheun Kim, Sei Joong Jung, Sung Hoo Park, Heungkyu Gwak, Geum Hee Kang, Sun Hee Kim, Jong Gin Kim, Jeryong Choi, Su Yun Lim, Cheol-Wan Kim, Doyil Yoo, Youngbum Song, Young-Jin Kang, Yoon-Jung Jung, Sang Seol Shin, Hyuk Jai Lee, Kwan Ju Han, Se-Hwan Lee, Eun Sook Han, Wonshik Kim, Hee-Jung Noh, Woo Chul |
author_sort | Kim, Hyun-Ah |
collection | PubMed |
description | BACKGROUND: Ovarian function suppression (OFS) has been shown to be effective as adjuvant endocrine therapy in premenopausal women with hormone receptor-positive breast cancer. However, it is currently unclear if addition of OFS to standard tamoxifen therapy after completion of adjuvant chemotherapy results in a survival benefit. In 2008, the Korean Breast Cancer Society Study Group initiated the ASTRRA randomized phase III trial to evaluate the efficacy of OFS in addition to standard tamoxifen treatment in hormone receptor-positive breast cancer patients who remain or regain premenopausal status after chemotherapy. METHODS: Premenopausal women with estrogen receptor-positive breast cancer treated with definitive surgery were enrolled after completion of neoadjuvant or adjuvant chemotherapy. Ovarian function was assessed at the time of enrollment and every 6 months for 2 years by follicular-stimulating hormone levels and bleeding history. If ovarian function was confirmed as premenopausal status, the patient was randomized to receive 2 years of goserelin plus 5 years of tamoxifen treatment or 5 years of tamoxifen alone. The primary end point will be the comparison of the 5-year disease-free survival rates between the OFS and tamoxifen alone groups. Patient recruitment was finished on March 2014 with the inclusion of a total of 1483 patients. The interim analysis will be performed at the time of the observation of the 187th event. DISCUSSION: This study will provide evidence of the benefit of OFS plus tamoxifen compared with tamoxifen only in premenopausal patients with estrogen receptor-positive breast cancer treated with chemotherapy. TRIAL REGISTRATION: ClinicalTrials.gov Identifier NCT00912548. Registered May 31 2009. Korean Breast Cancer Society Study Group Register KBCSG005. Registered October 26 2009. |
format | Online Article Text |
id | pubmed-4872354 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48723542016-05-20 The role of the addition of ovarian suppression to tamoxifen in young women with hormone-sensitive breast cancer who remain premenopausal or regain menstruation after chemotherapy (ASTRRA): study protocol for a randomized controlled trial and progress Kim, Hyun-Ah Ahn, Sei Hyun Nam, Seok Jin Park, Seho Ro, Jungsil Im, Seock-Ah Jung, Yong Sik Yoon, Jung Han Hur, Min Hee Choi, Yoon Ji Lee, Soo-Jung Jeong, Joon Cho, Se-Heon Kim, Sung Yong Lee, Min Hyuk Kim, Lee Su Moon, Byung-In Kim, Tae Hyun Park, Chanheun Kim, Sei Joong Jung, Sung Hoo Park, Heungkyu Gwak, Geum Hee Kang, Sun Hee Kim, Jong Gin Kim, Jeryong Choi, Su Yun Lim, Cheol-Wan Kim, Doyil Yoo, Youngbum Song, Young-Jin Kang, Yoon-Jung Jung, Sang Seol Shin, Hyuk Jai Lee, Kwan Ju Han, Se-Hwan Lee, Eun Sook Han, Wonshik Kim, Hee-Jung Noh, Woo Chul BMC Cancer Study Protocol BACKGROUND: Ovarian function suppression (OFS) has been shown to be effective as adjuvant endocrine therapy in premenopausal women with hormone receptor-positive breast cancer. However, it is currently unclear if addition of OFS to standard tamoxifen therapy after completion of adjuvant chemotherapy results in a survival benefit. In 2008, the Korean Breast Cancer Society Study Group initiated the ASTRRA randomized phase III trial to evaluate the efficacy of OFS in addition to standard tamoxifen treatment in hormone receptor-positive breast cancer patients who remain or regain premenopausal status after chemotherapy. METHODS: Premenopausal women with estrogen receptor-positive breast cancer treated with definitive surgery were enrolled after completion of neoadjuvant or adjuvant chemotherapy. Ovarian function was assessed at the time of enrollment and every 6 months for 2 years by follicular-stimulating hormone levels and bleeding history. If ovarian function was confirmed as premenopausal status, the patient was randomized to receive 2 years of goserelin plus 5 years of tamoxifen treatment or 5 years of tamoxifen alone. The primary end point will be the comparison of the 5-year disease-free survival rates between the OFS and tamoxifen alone groups. Patient recruitment was finished on March 2014 with the inclusion of a total of 1483 patients. The interim analysis will be performed at the time of the observation of the 187th event. DISCUSSION: This study will provide evidence of the benefit of OFS plus tamoxifen compared with tamoxifen only in premenopausal patients with estrogen receptor-positive breast cancer treated with chemotherapy. TRIAL REGISTRATION: ClinicalTrials.gov Identifier NCT00912548. Registered May 31 2009. Korean Breast Cancer Society Study Group Register KBCSG005. Registered October 26 2009. BioMed Central 2016-05-19 /pmc/articles/PMC4872354/ /pubmed/27197523 http://dx.doi.org/10.1186/s12885-016-2354-6 Text en © Kim et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Study Protocol Kim, Hyun-Ah Ahn, Sei Hyun Nam, Seok Jin Park, Seho Ro, Jungsil Im, Seock-Ah Jung, Yong Sik Yoon, Jung Han Hur, Min Hee Choi, Yoon Ji Lee, Soo-Jung Jeong, Joon Cho, Se-Heon Kim, Sung Yong Lee, Min Hyuk Kim, Lee Su Moon, Byung-In Kim, Tae Hyun Park, Chanheun Kim, Sei Joong Jung, Sung Hoo Park, Heungkyu Gwak, Geum Hee Kang, Sun Hee Kim, Jong Gin Kim, Jeryong Choi, Su Yun Lim, Cheol-Wan Kim, Doyil Yoo, Youngbum Song, Young-Jin Kang, Yoon-Jung Jung, Sang Seol Shin, Hyuk Jai Lee, Kwan Ju Han, Se-Hwan Lee, Eun Sook Han, Wonshik Kim, Hee-Jung Noh, Woo Chul The role of the addition of ovarian suppression to tamoxifen in young women with hormone-sensitive breast cancer who remain premenopausal or regain menstruation after chemotherapy (ASTRRA): study protocol for a randomized controlled trial and progress |
title | The role of the addition of ovarian suppression to tamoxifen in young women with hormone-sensitive breast cancer who remain premenopausal or regain menstruation after chemotherapy (ASTRRA): study protocol for a randomized controlled trial and progress |
title_full | The role of the addition of ovarian suppression to tamoxifen in young women with hormone-sensitive breast cancer who remain premenopausal or regain menstruation after chemotherapy (ASTRRA): study protocol for a randomized controlled trial and progress |
title_fullStr | The role of the addition of ovarian suppression to tamoxifen in young women with hormone-sensitive breast cancer who remain premenopausal or regain menstruation after chemotherapy (ASTRRA): study protocol for a randomized controlled trial and progress |
title_full_unstemmed | The role of the addition of ovarian suppression to tamoxifen in young women with hormone-sensitive breast cancer who remain premenopausal or regain menstruation after chemotherapy (ASTRRA): study protocol for a randomized controlled trial and progress |
title_short | The role of the addition of ovarian suppression to tamoxifen in young women with hormone-sensitive breast cancer who remain premenopausal or regain menstruation after chemotherapy (ASTRRA): study protocol for a randomized controlled trial and progress |
title_sort | role of the addition of ovarian suppression to tamoxifen in young women with hormone-sensitive breast cancer who remain premenopausal or regain menstruation after chemotherapy (astrra): study protocol for a randomized controlled trial and progress |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872354/ https://www.ncbi.nlm.nih.gov/pubmed/27197523 http://dx.doi.org/10.1186/s12885-016-2354-6 |
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