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Human Reproduction Update Advance Access originally published online on September 26, 2008
Human Reproduction Update 2008 14(6):553-561; doi:10.1093/humupd/dmn041
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© The Author 2008. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

GnRH agonist therapy as ovarian protectants in female patients undergoing chemotherapy: a review of the clinical data

R. Beck-Fruchter1, A. Weiss1 and E. Shalev1,2,3

1 Department of Obstetrics and Gynecology, Ha'Emek Medical Center, Afula, Israel 2 Technion-Israel Institute of Technology, The Rappaport Faculty of Medicine, Haifa, Israel

3 Correspondence address. E-mail: shaleve{at}tx.technion.ac.il

BACKGROUND: Cancer survival rates in young women are improving due to progress in treatment. This includes aggressive chemotherapy, a treatment that often poses a threat to fertility. GnRH agonists were proposed as ovarian protectors during gonadotoxic therapies. This study was undertaken in order to determine the clinical evidence concerning this issue.

METHODS: The medical literature was searched for studies that reported on ovarian function after the administration of GnRH agonists concomitant with chemotherapy. Twelve studies met the predetermined selection criteria.

RESULTS: Data on ovarian function were obtained for 579 women who received chemotherapy. Among 345 women who received GnRH agonist co-treatment, ovarian function was preserved in 91% and 9% had premature ovarian failure. In 234 women who did not receive GnRH agonist co-treatment, ovarian function was preserved in 41% and failed in 59%. Only two of the studies were randomized. The control and the GnRH agonist groups differed in several important characteristics: the follow-up times were not equal, different treatment protocols were utilized and end-points were poorly defined and inconsistent between the studies.

CONCLUSIONS: The effectiveness of GnRH agonists as fertility-preserving agents is debatable. A thorough literature search has found insufficient evidence to show that GnRH agonist co-treatment is effective in protecting the ovary from the damage of chemotherapy. A large randomized controlled trial with adequate follow-up is needed.

Key words: female infertility / GnRH agonist / ovarian function

Received on November 26, 2007; revised June 30, 2008; accepted on August 11, 2008


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