Evidence map›Paper›PMID 41114338›Full record

ArticleFrontiers in oncology2025

Comparative study on bone mineral density in premenopausal patients with estrogen receptor-positive breast cancer in ASTRRA Study: a 5-year follow-up study.

Eunju Shin, Seung Il Kim, Min-Ho Park, Hyun-Ah Kim, Yongsik Jung, Jai Min Ryu, Eun Hwa Park, Sung Yong Kim, Eun-Gyeong Lee, Min Hyuk Lee and 18 more

Erratum issuedAbstract read
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Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors.

Eunju ShinDivision of Breast Surgery, Department of Surgery, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea.
Seung Il KimDepartment of Surgery, Yonsei University College of Medicine, Seoul, Republic of Korea.
Min-Ho ParkDepartment of Surgery, Chonnam National University Medical School, Chonnam National University Hwasun Hospital, Jeollanam-do, Republic of Korea.
Hyun-Ah KimDepartment of Surgery, Korea Cancer Center Hospital, Korea Institute of Radiological and Medical Sciences, Seoul, Republic of Korea.
Yongsik JungDepartment of Surgery, Ajou University School of Medicine, Suwon, Republic of Korea.
Jai Min RyuDivision of Breast Surgery, Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Eun Hwa ParkDepartment of Surgery, Dong-A University College of Medicine, Busan, Republic of Korea.
Sung Yong KimDepartment of Surgery, Soonchunhyang University, College of Medicine, Cheonan Hospital, Chungnam, Republic of Korea.
Eun-Gyeong LeeDepartment of Surgery, Research Institute and Hospital, National Cancer Center, Goyang, Republic of Korea.
Min Hyuk LeeDepartment of Surgery, Soon Chun Hyang University Hospital, Seoul, Republic of Korea.
Jung Ho ParkDivision of Breast and Endocrine Surgery, Hallym University Sacred Heart Hospital, Anyang, Republic of Korea.
Seock-Ah ImSeoul National University Hospital, Cancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.
Soong June BaeDepartment of Surgery, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Su Hwan KangDepartment of Surgery, Yeungnam University College of Medicine, Daegu, Republic of Korea.
Woo Sung LimDepartment of Surgery, Ewha Womans University Mokdong Hospital, Seoul, Republic of Korea.
Hyun Jo YounDepartment of Surgery, Research Institute of Clinical Medicine, Jeonbuk National University Hospital, Jeonbuk National University and Biomedical Research Institute, Jeonju, Republic of Korea.
Heung Kyu ParkDepartment of Surgery, Gachon University Gil Hospital, Incheon, Republic of Korea.
Kyong Hwa ParkDepartment of Internal Medicine, Division of Oncology/Hematology, Korea University College of Medicine, Seoul, Republic of Korea.
Tae Hyun KimDepartment of General Surgery, Busan Paik Hospital, Inje University Surgery, Busan, Republic of Korea.
Shin Young ParkDepartment of Surgery, Inha University Hospital, Inha University School of Medicine, Incheon, Republic of Korea.
Cheol Wan LimDepartment of Surgery, Soonchunhyang University Bucheon Hospital, Bucheon, Republic of Korea.
Geum Hee KwakDepartment of Surgery, Inje University Sanggye Paik Hospital, Seoul, Republic of Korea.
Chanheun ParkDepartment of Surgery, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Hyuk Jae ShinDepartment of Surgery, Myongji Hospital, Goyang, Republic of Korea.
Young Bum YooDepartment of Surgery, Konkuk University Medical Center, Konkuk University School of Medicine, Seoul, Republic of Korea.
Sun Hee KangDepartment of General Surgery, Keimyung University School of Medicine, Daegu, Republic of Korea.
Bong Kyun KimDepartment of Surgery, Daejeon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Hee Jeong KimDivision of Breast Surgery, Department of Surgery, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: We compared the impact of tamoxifen alone or with ovarian function suppression (OFS) on bone mineral density (BMD) in premenopausal patients after chemotherapy. Methods: Of 1483 premenopausal women enrolled in the ASTRRA study, we included 522 who underwent BMD examinations at diagnosis and 3 and 5 years after diagnosis. All BMD measurements were performed using the same scanner in each center across different time points. Patients were stratified into three groups: within the expected range for age (A, Z-score>-1.0), below the expected range (B,-2.0≤ Z-score ≤-1.0), and low bone mineral density for chronological age (C, Z-score< -2.0) groups. We examined changes in groups from baseline to >3-year and 5-year periods to identify any deterioration in BMD. We conducted a subset analysis using the Asan Medical Center (AMC; n=141) data, focusing on the absolute value of bone density (in g/cm Results: The 522 included patients (median age, 41.1 years) had a higher bone loss incidence in the OFS addition group at baseline (p=0.028). The tamoxifen-only and tamoxifen+OFS groups did not differ significantly in terms of changes in BMD categories from baseline to 3 (p=0.567) or 5 years (p=0.600). The OFS addition group had a significantly increased risk of BMD deterioration when randomized at the first visit (odds ratio=2.970, p=0.008). Within the AMC subset, the OFS addition group exhibited significantly decreased BMD in the spine (p=0.023) and femur (p=0.040) from the baseline to 3-year period. A non-significantly decreased BMD occurred from the baseline to 5 years in the spine and femur. Conclusion: Our findings highlighted the deleterious impact on BMD following OFS addition, compared with tamoxifen only treatment. Early OFS exerted an even more detrimental influence on bone health in premenopausal patients with estrogen receptor-positive breast cancer and recovered ovarian function. Abbreviations: ANOVA, analysis of variance; BMD, one mineral density; CTIBL, Cancer treatment-induced bone loss; DXA, dual-energy X-ray absorptiometry; HER2 human epidermal growth factor receptor 2; L-spin, lumbar spine; OFS, ovarian function suppression; TAM, tamoxifen.

Indexed as

bone healthbreast cancerchemotherapyovarian functionpremenopausal women

Identifiers

PMID41114338
PMCPMC12529552

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