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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
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.
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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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