A Randomized Comparison of Two Ovarian Stimulation Protocols with Gonadotropin-Releasing Hormone (GnRH) Antagonist Cotreatment for in Vitro Fertilization Commencing Recombinant Follicle-Stimulating Hormone on Cycle Day 2 or 5 with the Standard Long GnRH Agonist Protocol
Femke P. Hohmann,
Nicholas S. Macklon and
Bart C. J. M. Fauser
Division of Reproductive Medicine, Department of Obstetrics and Gynecology (F.P.H., N.S.M., B.C.J.M.F.), Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands
Address all correspondence and requests for reprints to: Prof. B. C. J. M. Fauser, M.D., Ph.D., Division of Reproductive Medicine, Department of Obstetrics and Gynecology, Erasmus Medical Center, Dr. Molewaterplein 40, 3015 GD Rotterdam, The Netherlands. E-mail: fauser{at}gyna.azr.nl.
Extending the FSH window for multifollicular development byadministering FSH from the midfollicular phase onward constitutesa novel mild protocol for ovarian stimulation for in vitro fertilization(IVF) based on the physiology of single dominant follicle selectionin normo-ovulatory women. We compared outcomes from this protocolwith two other stimulation protocols. One hundred and forty-twonormo-ovulatory patients with an indication for IVF (or IVF/ICSI)were randomized to a GnRH agonist long protocol (group A; n= 45) or one of two GnRH antagonist protocols commencing recombinantFSH on cycle d 2 (group B; n = 48) or cycle d 5 (group C; n= 49). A fixed dose (150 IU/d) of rFSH was used for ovarianstimulation, and GnRH antagonist cotreatment was initiated onthe day when the leading follicle reached 14 mm diameter.
Group C showed a shorter duration of stimulation (median duration,11, 9, and 8 d for groups A, B, and C, respectively; P <0.001), reflected in a significantly lower total dose of rFSHused (median amount of rFSH, 1650, 1350, and 1200 IU for groupsA, B, and C, respectively; P < 0.001). In group C more cycleswere cancelled during the stimulation phase due to insufficientresponse, resulting in a lower percentage of oocyte retrievals(84%, 73%, and 63% for groups A, B, and C; P = 0.02). However,women in group C obtained better quality embryos (percentageof embryo score of 1 for best embryo, 29%, 37%, and 61% forgroups A, B, and C, respectively; P = 0.008), resulting in moretransfers per oocyte retrieval (68%, 71%, and 90% for groupsA, B, and C, respectively; P = 0.04). After profound ovarianstimulation (groups A and B) only 7% of the patients who retrievedfour oocytes or less conceived, whereas after mild stimulation(group C) 67% of these patients conceived (P < 0.01). Overall,no differences were found among the three groups comparing pregnancyrate per started IVF cycle.
In conclusion, application of the described mild ovarian stimulationprotocol resulted in pregnancy rates per started IVF cycle similarto those observed after profound stimulation with GnRH agonistcotreatment despite shorter stimulation and a 27% reductionin exogenous FSH. A higher cancellation rate before oocyte retrievalwas compensated by improved embryo quality concomitant witha higher chance of undergoing embryo transfer. A relativelylow number of oocytes retrieved after mild ovarian stimulationdistinctly differs from the pathological reduction in the numberof oocytes retrieved after profound ovarian stimulation (poorresponse) associated with poor IVF outcome. The relatively smallnumber of oocytes obtained after mild ovarian stimulation mayrepresent the best of the cohort in a given cycle.
This work was supported by the Stichting VoortplantingsgeneeskundeRotterdam and an unrestricted research grant from ASTA MedicaB.V. (Amsterdam, The Netherlands).
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B. C. J. M. Fauser and N. S. Macklon Authors' Response: A Randomized Comparison of Two Ovarian Stimulation Protocols with Gonadotropin-Releasing Hormone (GnRH) Antagonist Cotreatment for in Vitro Fertilization Commencing Recombinant Follicle-Stimulating Hormone on Cycle Day 2 or 5 with the Standard Long GnRH Agonist Protocol
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[Full Text]