Oncologic Safety of Gonadotropin-Releasing Hormone Agonist for Ovarian Function Protection During Breast Cancer Chemotherapy

被引:1
|
作者
Kim, Hee Jeong [1 ]
Lee, Moo Hyun [3 ]
Lee, Jeong Eon [4 ]
Park, Seho [6 ]
Lee, Eun Sook [3 ]
Kang, Yong Joon [8 ]
Shin, Hae Na [1 ]
Kim, Seung Il [6 ]
Lee, Jun Ho [5 ]
Im, Seock Ah [9 ]
Ahn, Sei Hyun [1 ]
Lee, Keun Seok [3 ]
Sohn, Joohyuk [7 ]
Kim, Seonok [2 ]
Nam, Seok Jin [4 ]
Han, Wonshik [10 ,11 ]
机构
[1] Univ Ulsan, Coll Med, Dept Surg, Div Breast, Seoul, South Korea
[2] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Clin Epidemiol & Biostat, Seoul, South Korea
[3] Natl Canc Ctr, Res Inst & Hosp, Res Inst Natl Canc Control & Evaluat, Canc Biostat Branch, Goyang, South Korea
[4] Sungkyunkwan Univ, Samsung Med Ctr, Sch Med, Div Breast & Endocrine Surg,Dept Surg, Seoul, South Korea
[5] Sungkyunkwan Univ, Samsung Changwon Hosp, Dept Surg, Sch Med, Chang Won, South Korea
[6] Yonsei Univ, Coll Med, Dept Surg, Seoul, South Korea
[7] Yonsei Univ, Coll Med, Div Med Oncol, Dept Internal Med, Seoul, South Korea
[8] Seoul Natl Univ Hosp, Canc Res Inst, Dept Surg, Seoul, South Korea
[9] Seoul Natl Univ Hosp, Canc Res Inst, Dept Internal Med, Seoul, South Korea
[10] Seoul Natl Univ, Coll Med, Dept Surg, Seoul, South Korea
[11] Seoul Natl Univ, Coll Med, Canc Res Inst, Seoul, South Korea
关键词
Breast cancer; Chemotherapy; Fertility; Ovarian suppression; Premenopausal; ADJUVANT CHEMOTHERAPY; FERTILITY PRESERVATION; YOUNG-WOMEN; GNRH AGONIST; TRIAL; SUPPRESSION; AMENORRHEA; RECOMMENDATIONS; METAANALYSIS; CONSENSUS;
D O I
10.1016/j.clbc.2018.04.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chemotherapy with a gonadotropin-releasing hormone (GnRH) agonist has been reported to protect against ovarian failure. This retrospective, individual matching study from 5 large institutes in Korea found that disease-free survival and distant metastasis-free survival were better in a GnRH agonist group than in a chemotherapy-alone group. Background: Receipt of a gonadotropin-releasing hormone (GnRH) agonist has been reported to protect against ovarian failure. We sought to determine the oncologic effect of a GnRH agonist with chemotherapy for breast cancer patients. Patients and Methods: Data from 1160 patients aged 20 to 40 years with stage I to III breast cancer who received chemotherapy from 5 hospitals in Korea from 2002 to 2012 were reviewed. A GnRH agonist was provided to 406 patients for ovarian protection during chemotherapy, and 754 patients received chemotherapy without ovarian protection. An individual score-matching strategy was used to create sets matched by age, tumor stage, hormone receptor status, neoadjuvant or adjuvant chemotherapy, and institute. Results: Survival analysis by Cox regression showed that the GnRH agonist group had better distant metastasis-free survival (hazard ratio [HR], 0.59; 95% confidence interval [CI], 0.39-0.89) and disease-free survival (HR, 0.72; 95% CI, 0.52-0.99) than the chemotherapy-alone group. Among patients with hormone receptor-positive breast cancer, the benefit was significant for distant metastasis-free survival (HR, 0.53; 95% CI, 0.29-0.99) and disease-free survival (HR, 0.58; 95% CI, 0.35-0.96). Conclusion: Ovarian protection using a GnRH agonist can be safely considered for premenopausal breast cancer patients for whom chemotherapy is planned.
引用
收藏
页码:E1165 / E1172
页数:8
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