Gonadotropin-releasing hormone agonist may minimize premature ovarian failure in young women undergoing autologous stem cell transplantation

Objective To compare the rate of premature ovarian failure (POF) after stem cell transplantation (SCT) in young women receiving GnRH-agonist (GnRH-a) in conjunction with gonadotoxic chemotherapy. Design Prospective, nonrandomized study. Setting Tertiary university hospital. Patient(s) Ninety-five wo...

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Published inFertility and sterility Vol. 98; no. 5; pp. 1266 - 1270.e1
Main Authors Blumenfeld, Zeev, M.D, Patel, Biren, M.D, Leiba, Ronit, M.Sc, Zuckerman, Tsila, M.D
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 01.11.2012
Elsevier
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Summary:Objective To compare the rate of premature ovarian failure (POF) after stem cell transplantation (SCT) in young women receiving GnRH-agonist (GnRH-a) in conjunction with gonadotoxic chemotherapy. Design Prospective, nonrandomized study. Setting Tertiary university hospital. Patient(s) Ninety-five women received conditioning chemotherapy, with or without GnRH-a before SCT. Complete information was available for only 83 patients. Intervention(s) Conditioning chemotherapy, with or without GnRH-a before SCT. Main Outcome Measure(s) Cyclic ovarian function (COF) or POF after SCT. Result(s) There were no significant differences in age, chemotherapy treatment, or diagnoses between the study and control groups. In the GnRH-a group, 38.3% (18/47) patients resumed COF, compared with 11.1% (4/36) for patients who did not receive GnRH-a. Patients who resumed COF were on average 3.7 years (median, 3 years) younger at the time of transplantation than those who experienced POF. GnRH-a had a significant effect on long-term COF in patients with lymphomas (66.7% [14/21] for GnRH-a group vs. 18.2% [2/11] for control) but not for leukemia patients. Conclusion(s) GnRH-a cotreatment in conjunction with conditioning chemotherapy before SCT may significantly decrease the gonadotoxicity and POF from 82% to 33% in lymphoma but not in leukemia patients.
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ISSN:0015-0282
1556-5653
DOI:10.1016/j.fertnstert.2012.07.1144