Is There a Need for Luteal Support in Modified Natural Cycle Frozen Embryo Transfer Cycles: a Prospective, Multicenter, Randomized Trial
Is There a Need for Luteal Support in Modified Natural Cycle Frozen Embryo Transfer Cycles: a Prospective, Multicenter, Randomized Trial
Without progesterone there is no pregnancy. Following ovulation, the endocrine function of the follicle changes and progesterone replacing estradiol becomes its main secretory product. In the follicular phase the increasing amount of estradiol secreted by the growing follicle builds up the endometrium, while in the luteal phase progesterone, the main product of the corpus luteum, prepares the endometrium for implantation. This process is called decidualization. If implantation occurs, human chorionic gonadotropin (hCG) secreted by the trophopblasts maintains the function of the corpus luteum. This continued activity is required to be maintained up to week 7-9 of gestation when the hormone secreting activity is taken over by the placenta (luteo-placental shift) and the corpus luteum regresses.
During in vitro fertilization (IVF) gonadotropins are used to induce multifollicular development and therefore following the oocyte retrieval ("ovulation") multiple corpora lutea are formed. At the same time, partly due to the supraphysiologic steroid levels reached during stimulation and partly to the removal of the granulosa cell mass during the retrieval, the activity of these corpora lutea remains insufficient and luteal support, primarily in the form of progesterone, is needed to achieve success.
Embryo cryopreservation has become available soon after the first successful IVF treatment. In some of the IVF treatments cryopreservation is electively planned, while in others surplus embryos are frozen. As a result of the currently available vitrification technology a close to 100% survival can be expected upon thawing.
Frozen embryos can be transferred according to different protocols:
Eligible participants will be randomized to one of the following groups:
Baseline demographic, FET treatment related, and clinical outcomes will be compared in the three different luteal phase management groups.
Aim: The aim of this RCT is to assess whether the use of luteal support improves the outcome of modified natural cycle frozen embryo transfer (FET) treatments.
Background: Without progesterone there is no pregnancy. Following ovulation, the endocrine function of the follicle changes and progesterone replacing estradiol becomes its main secretory product. In the follicular phase the increasing amount of estradiol secreted by the growing follicle builds up the endometrium, while in the luteal phase progesterone, the main product of the corpus luteum, prepares the endometrium for implantation. This process is called decidualization. If implantation occurs, human chorionic gonadotropin (hCG) secreted by the trophopblasts maintains the function of the corpus luteum. This continued activity is required to be maintained up to week 7-9 of gestation when the hormone secreting activity is taken over by the placenta (luteo-placental shift) and the corpus luteum regresses.
During in vitro fertilization (IVF) gonadotropins are used to induce multifollicular development and therefore following the oocyte retrieval ("ovulation") multiple corpora lutea are formed. At the same time, partly due to the supraphysiologic steroid levels reached during stimulation and partly to the removal of the granulosa cell mass during the retrieval, the activity of these copora lutea remains insufficient and luteal support, primarily in the form of progesterone, is needed to achieve success.
Embryo cryopreservation has become available soon after the first successful IVF treatment. In some of the IVF treatments cryopreservation is electively planned, while in others surplus embryos are frozen. As a result of the currently available vitrification technology a close to 100% survival can be expected upon thawing.
Frozen embryos can be transferred according to different protocols:
The common theme in mNC, tNC and sNC FET cycles is that a corpus luteum is formed and its activity is not compromised by supraphysiologic steroid levels and the oocyte retrieval either. Despite this, in most clinics, similarly to the fresh IVF-ETs, luteal support is administered in FET cycles as well. The benefit of luteal support in NC-FET cycles is questionable, however. Various groups have studied the potential advantages of luteal support in the different types on NC-FET cycles.
One study has shown that the chance of live birth was reduced (25.7% vs 41.1%) in tNC FET cycles when the serum progesterone level was below 10 ng/ml. Another study, based on the outcome of close to 400 FET cycles, failed to find a benefit with luteal support. Based on the outcome of different types of FET cycles however, they observed a lower live birth rate when the serum progesterone level was below 7.8 ng/ml. Finally, they also observed suboptimal outcome when the serum progesterone level was over 20.3 ng/ml. Finally, a different group, did not find a difference in the progesterone levels among pregnant and non-pregnant participants not using luteal support in an RCT. They were also unable to identify a progesterone level that could discriminate among pregnant and non-pregnant women.
Several RCTs evaluated the potential benefits of luteal support. One research group has randomly assigned women to luteal support vs no luteal support in an RCT of mNC-FET. Clinical pregnancy, miscarriage and live birth rates were similar in the two groups. Another group, in a study of similar design also failed to show improved clinical outcome with luteal support in mNC-FET cycles. Two larger RCTs of tNC-FET however have reported improved clinical outcome with luteal support. Meta-analyses have reported conflicting results. One has shown improved live birth rate with luteal support in tNC-FET while found no benefit in mNC-FET cycles. Whiel two other meta-analyses have found higher clinical pregnancy rates in cycles with progesterone support. In summary, one can conclude that the literature is conflicting on the benefits of luteal support in mNC-FET cycles and even discuss a potential negative effect of high serum progesterone levels.
Based on the above the question arises whether there is a need for luteal support in mNC-FET treatments? Study protocol: In order to answer this question, the investigators plan to perform a prospective, multicenter randomized pilot study.
The investigators plan to enroll women between the ages of 18-40 (at the time of vitrification) who have at least one good morphology blastocyst (BC) frozen (morphology 2AA, 2AB, 2BA, 2BB, 3AA, 3AB, 3BA, 3BB, 4AA, 4AB, 4BA, 4BB, 5AA, 5AB, 5BA, 5BB using the Gardner classification) and who plan to undergo single frozen-thawed blastocyst transfer. In addition, the following inclusion criteria apply:
The following exclusion criteria will apply:
Treatment protocol:
Prior to the start of the FET cycle (latest at the first folliculometry) informed consent is obtained
A first ultrasound is scheduled between days 9-12 of the cycle; the scan is repeated in 2-3 days if the follicle is not large enough or if the endometrium is thin (<7 mm)
Serum progesterone measurement at the time of the last ultrasound. If the value is >1.5 ng/ml, the cycle is cancelled. If the progesterone level is <1.5 ng/ml and the follicle has reached at least 17 mm in diameters hCG (250 mcg recombinant hCG, Ovitrelle) is administered in the evening hours (7-10 PM)
5-6 days after the trigger injection, latest in the AM of the planned FET, serum progesterone is measured again. If the value is under 10 ng/ml (31.8 nmol/l) vaginal luteal support is initiated and while we will proceed with the ET, the patient drops out of the RCT. In these cases, the investigators apply "progesterone rescue" as it has been shown to maintain clinical efficacy when the progesterone levels is low before the transfer.
Those who have a progesterone level >10 ng/ml (31.8 nmol/l) will be randomized to one of the following 3 groups on the day of FET (rHCG + 7):
6-8 days after the ET serum progesterone will be measured
12-13 days after the ET serum beta hCG and progesterone will be measured to check for implantation
3 +/- 0.5 weeks later vaginal ultrasound will be performed to check for clinical pregnancy
Repeat ultrasound will be done at week 10-12 of gestation (by the primary obstetrician provider) to assess for ongoing pregnancy
At the completion of pregnancy data will be collected on outcome parameters (potential hypertensive complications [gestational hypertension, pre-eclampsia, eclampsia] during pregnancy, gestational age at delivery, birthweight, APGAR score) Randomization: randomization will be made according to a computer-generated randomization list (www.randomizer.org). The prepared list will be accessible to all sub-investigators online. Participants who sign an informed consent and reach the trigger hCG injection will be assigned the next treatment option on the randomization list.
Blinding: neither the participants, nor the investigators will be blinded for assignment.
Placebo: the study will not involve the use of placebo. Drop-out: Participants who do not reach the hCG trigger day despite signing a consent form drop out of the study (true dropouts) and will not be randomized. Those who are randomized but do not have an ET for no available embryo to transfer after thawing, or other reasons will be kept in the intent-to-treat analysis but will not be considered in the per protocol analysis.
Sample size calculation: Since it is not known what the expected pregnancy rate without luteal support would be and whether that would be any different compared to treatments involving luteal support as a first step, the investigators plan a pilot study. The goal is to have 180 patients sign informed consent (60 potential patients per arm). 20% of the participants are expected not to reach the ET (lack of follicle development, other complications prior to the day of ET, no available embryos after thawing) that would leave the study with 150 patients treated per protocol.
Data collection: Data will be collected in structured Excel files. No patient identifying parameter (name, ID number) will be included just the randomization number. The name associated with the randomization number will be collected in a separate file by the sub investigator and will not be forwarded to the principal investigator. The principal investigator will only receive the anonymized data, and the combined anonymous dataset will be shared with the statistician. The following parameters will be collected:
Definitions:
Statistical analysis: Baseline demographic, FET treatment related, and clinical outcomes will be compared in the three different luteal phase management groups. Continuous variables will be shown as mean +/- SD, while categorical variable as number and percent. ANOVA and Mann-Whitney U test will be used for the analysis. Subgroups analysis is planned based on progesterone levels both prior to the trigger (31.8-50, 50-100, >100 nmol/l.) and 6-8 days after the trigger (< 31.8, 31.8-50, 50-100, >100 nmol/l). analysis will be performed based on intent-to-treat and per protocol as well. Post hoc comparison of the different treatment groups to each other will be performed.
References:
Inclusion Criteria:
Exclusion Criteria:
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