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Oncologic safety of gonadotropin-releasing hormone agonist for ovarian function protection during breast cancer chemotherapy

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dc.contributor.authorKim, Hee Jeong-
dc.contributor.authorLee, Moo Hyun-
dc.contributor.authorLee, Jeong Eon-
dc.contributor.authorPark, Seho-
dc.contributor.authorLee, Eun Sook-
dc.contributor.authorKang, Yong Joon-
dc.contributor.authorShin, Hae Na-
dc.contributor.authorKim, Seung Il-
dc.contributor.authorLee, Jun Ho-
dc.contributor.authorIm, Seock Ah-
dc.contributor.authorAhn, Sei Hyun-
dc.contributor.authorLee, Keun Seok-
dc.contributor.authorSohn, Joohyuk-
dc.contributor.authorKim, Seonok-
dc.contributor.authorNam, Seok Jin-
dc.contributor.authorHan, Wonshik-
dc.date.accessioned2022-03-22T09:24:06Z-
dc.date.available2022-03-22T09:24:06Z-
dc.date.created2019-06-24-
dc.date.created2019-06-24-
dc.date.created2019-06-24-
dc.date.created2019-06-24-
dc.date.issued2018-10-
dc.identifier.citationClinical Breast Cancer, Vol.18 No.5, pp.e1165-e1172-
dc.identifier.issn1526-8209-
dc.identifier.other76494-
dc.identifier.urihttps://hdl.handle.net/10371/177313-
dc.description.abstractChemotherapy 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.-
dc.language영어-
dc.publisherCancer Information Group-
dc.titleOncologic safety of gonadotropin-releasing hormone agonist for ovarian function protection during breast cancer chemotherapy-
dc.typeArticle-
dc.contributor.AlternativeAuthor임석아-
dc.identifier.doi10.1016/j.clbc.2018.04.008-
dc.citation.journaltitleClinical Breast Cancer-
dc.identifier.wosid000445702400056-
dc.identifier.scopusid2-s2.0-85047392704-
dc.citation.endpagee1172-
dc.citation.number5-
dc.citation.startpagee1165-
dc.citation.volume18-
dc.identifier.sci000445702400056-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorIm, Seock Ah-
dc.contributor.affiliatedAuthorHan, Wonshik-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusADJUVANT CHEMOTHERAPY-
dc.subject.keywordPlusFERTILITY PRESERVATION-
dc.subject.keywordPlusYOUNG-WOMEN-
dc.subject.keywordPlusGNRH AGONIST-
dc.subject.keywordPlusTRIAL-
dc.subject.keywordPlusSUPPRESSION-
dc.subject.keywordPlusAMENORRHEA-
dc.subject.keywordPlusRECOMMENDATIONS-
dc.subject.keywordPlusMETAANALYSIS-
dc.subject.keywordPlusCONSENSUS-
dc.subject.keywordAuthorBreast cancer-
dc.subject.keywordAuthorChemotherapy-
dc.subject.keywordAuthorFertility-
dc.subject.keywordAuthorOvarian suppression-
dc.subject.keywordAuthorPremenopausal-
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  • College of Medicine
  • Department of Medicine
Research Area Clinical Medicine

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