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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.

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Author(s)
Seock-Ah ImJungsil RoYong Sik JungJung Han YoonMin Hee HurYoon Ji ChoiSoo-Jung LeeJoon JeongSe-Heon ChoSung Yong KimHyun-Ah KimSei Hyun AhnSeok Jin NamSeho ParkMin Hyuk LeeLee Su KimByung-In MoonTae Hyun KimChanheun ParkSei Joong KimSung Hoo JungHeungkyu ParkGeum Hee GwakSun Hee KangJong Gin KimJeryong KimSu Yun ChoiCheol-Wan LimDoyil KimYoungbum YooYoung-Jin SongYoon-Jung KangSang Seol JungHyuk Jai ShinKwan Ju LeeSe-Hwan HanEun Sook LeeWonshik HanHee-Jung KimWoo Chul Noh
Keimyung Author(s)
Kang, Sun Hee
Department
Dept. of Surgery (외과학)
Journal Title
BMC Cancer
Issued Date
2016
Volume
19
Issue
16
Keyword
Ovarian function suppressionGoserelinTamoxifenAdjuvant endocrine therapyPremenopauseBreast cancer
Abstract
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.
Keimyung Author(s)(Kor)
강선희
Publisher
School of Medicine
Citation
Seock-Ah Im et al. (2016). 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. BMC Cancer, 19(16), 319–319. doi: 10.1186/s12885-016-2354-6
Type
Article
ISSN
1471-2407
DOI
10.1186/s12885-016-2354-6
URI
https://kumel.medlib.dsmc.or.kr/handle/2015.oak/33316
Appears in Collections:
1. School of Medicine (의과대학) > Dept. of Surgery (외과학)
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