In vitro fertilization cycles stimulated with follitropin delta result in similar embryo development and quality when compared with cycles stimulated with follitropin alfa or follitropin beta.

A total of 440 IVF/ICSI cycles were identified during the study period: 115 with follitropin delta and 325 with either follitropin alfa or beta used for stimulation. Once exclusion criteria were considered, 106 Delta-1 group cycles and 297 Control-1 group cycles were included ( Fig. 1 ). Demographic characteristics of the 2 groups are listed in Table 2 . The cohorts differed significantly in the proportion of cycles with a diagnosis of male factor infertility (29.2% in Delta-1 vs. 45.1% in Control-1, P =.004) as well as in the incidence of advanced maternal age in each group (52.8% in Delta-1 vs. 41.8% in Control-1, P =.049). More women with cycles in the control group were nulliparous (56.9% in Control-1 vs. 44.3% in Delta-1, P =.026), and more cycles in the control group utilized growth hormone (26.6% in Control-1 vs. 15.1% in Delta-1, P =.017) and menotropin (99.3% in Control-1 vs. 67.0% in Delta-1, P <.001). In the Control-1 group, 31.6% of the women had undergone a previous cycle of IVF compared with 28.3% of women in the Delta-1 group ( P =.521). The mean number of oocytes retrieved was higher in the Control-1 group than in the Delta-1 group (12.3 ± 7.7 vs. 10.4 ± 6.1 [±SD], respectively; P =.033). There were no differences between the groups in the mean length of stimulation; numbers of follicles ≥15 mm, ≥18 mm, and ≥20 mm; mean estradiol level on the trigger day; or proportion of normal fertilization. An equal proportion of fresh transfers occurred on day 3 after fertilization in both the Control-1 and Delta-1 groups ( Table 2 ). Table 2 Demographic characteristics of patients treated with follitropin alfa or beta (Control-1 group) or follitropin delta (Delta-1 group). Characteristic Control-1 Delta-1 P value Number of cycles included a 297 106 Patient characteristics n (%) n (%) Mean age in years 33.91 (SD 4.04) 34.27 (SD 4.59) .409 Nulliparous 169 (56.9) 47 (44.3) .026 Prior IVF 94 (31.6) 30 (28.3) .521 BMI category  Low (<18.5 kg/m 2 ) 2 (0.7) 1 (0.9) .909  Normal (18.5–24.9 kg/m 2 ) 134 (45.1) 44 (41.5)  Overweight (25.0–29.9 kg/m 2 ) 64 (21.5) 23 (21.7)  Obese (≥30.0 kg/m 2 ) 97 (32.7) 38 (35.8) Ovarian reserve category  Low (AFC 0 to 8) 59 (19.9) 19 (17.9) .418  Medium (AFC 9 to 19) 135 (45.5) 56 (52.8)  High (AFC ≥20) 103 (34.7) 31 (29.2) Etiology of infertility  Idiopathic 27 (9.1) 13 (12.3) .348  Tubal factor 32 (10.8) 13 (12.3) .676  Male factor 134 (45.1) 31 (29.2) .004  Endometriosis stage I and II 11 (3.7) 6 (5.7) .403  Endometriosis stage III and IV 20 (6.7) 12 (11.3) .134  Ovulatory disorder 13 (4.4) 2 (1.9) .372  Decreased ovarian reserve 46 (15.5) 23 (21.7) .145  Donor sperm 29 (9.8) 13 (12.3) .470  PCOS 49 (16.5) 10 (9.4) .077  Advanced maternal age 124 (41.8) 56 (52.8) .049  Uterine factor 4 (1.3) 1 (0.9) 1.000 Stimulation cycle characteristics Mean length of stimulation (days) 9.95 (SD 1.70) 9.92 (SD 1.51) .784 Mean total dose follitropin 1951 IU (SD 849) 132 μg (SD 245) — Use of menotropin 295 (99.3) 71 (67.0) <.001 Use of growth hormone 79 (26.6) 16 (15.1) .017 Mean number of follicles ≥15 mm 8.42 (SD 4.64) 7.41 (SD 3.43) .179 Mean number of follicles ≥18 mm 3.94 (SD 2.14) 3.60 (SD 1.87) .209 Mean number of follicles ≥20 mm 1.47 (SD 1.23) 1.41 (SD 1.13) .925 Mean E2 levels at the trigger day (pmol/L) 7520 (SD 4424) 6448 (SD 3507) .050 Mean number of oocytes retrieved 12.3 (SD 7.7) 10.4 (SD 6.1) .033 Proportion of normal fertilization b 0.760 (SD 0.207) 0.732 (SD 0.240) .490 Proportion of fresh transfers on day 3 167 (64.2) 62 (61.4) .614 Note : Data are presented as number (%). AFC = antral follicle count; BMI = body mass index; E 2 = estradiol; IVF = in vitro fertilization; PCOS = polycystic ovary syndrome; SD = standard deviation. a Cycles were excluded from analysis if no oocytes were retrieved or if no fertilization took place. b The proportion of normal fertilization was calculated per injected oocytes for intracytoplasmic sperm injection cycles and per oocytes retrieved for IVF cycles. Demographic characteristics of patients treated with follitropin alfa or beta (Control-1 group) or follitropin delta (Delta-1 group). Note : Data are presented as number (%). AFC = antral follicle count; BMI = body mass index; E 2 = estradiol; IVF = in vitro fertilization; PCOS = polycystic ovary syndrome; SD = standard deviation. Cycles were excluded from analysis if no oocytes were retrieved or if no fertilization took place. The proportion of normal fertilization was calculated per injected oocytes for intracytoplasmic sperm injection cycles and per oocytes retrieved for IVF cycles. No significant differences were identified between the Delta-1 and Control-1 groups in terms of the proportion of good-, intermediate-, and poor-quality embryos on day 3 after fertilization ( Table 3 ). There were also no significant differences between cohorts in the proportions of poor and arrested blastocysts (day 5 and 6 after fertilization). A significant difference was noted in the proportion of good quality blastocysts, with the Delta-1 group having a lower proportion compared with the Control-1 group (median 0.11 vs. 0.22, respectively; P =.026). This difference persisted even when controlling for potential confounding variables ( Table 3 ). Clinical pregnancy and clinical implantation indices for both day 3 and day 5 fresh embryo transfers did not differ between the Control-1 and Delta-1 groups ( Table 3 ). Table 3 Median proportions of good, intermediate, and poor-quality embryos on day 3 after fertilization and proportions of good, poor, and arrested blastocysts on days 5 and 6 after fertilization. Outcome variable Control-1 Delta-1 P value Analysis of Covariance a Primary analysis day 3 embryo stage B(SE) (95% CI) P value Cycles included 297 106 Good embryos (IQR) 0.54 (0.33–0.75) 0.50 (0.31–0.75) .746 — — Intermediate embryos (IQR) 0.20 (0.00–0.36) 0.25 (0.00–0.40) .338 — — Poor embryos (IQR) 0.14 (0.00–0.33) 0.05 (0.00–0.25) .119 — — Secondary analysis day 3 embryo stage Control-2 Delta-2 Cycles included 109 43 Good embryos (IQR) 0.67 (0.50–0.80) 0.60 (0.44–0.75) .156 — — Intermediate embryos (IQR) 0.20 (0.10–0.31) 0.29 (0.00–0.38) .146 — — Poor embryos (IQR) 0.10 (0.00–0.17) 0.11 (0.00–0.20) .852 — — Primary analysis blastocyst stage Control-1 Delta-1 Cycles included 247 79 Good blastocysts (IQR) 0.22 (0.00–0.50) 0.11 (0.00–0.38) .026 −0.11(0.04) (−0.19, −0.03) .008 Poor blastocysts (IQR) 0.38 (0.13–0.57) 0.40 (0.25–0.67) .137 — — Arrested blastocysts (IQR) 0.25 (0.00–0.50) 0.22 (0.00–0.60) .858 — — Secondary analysis blastocyst stage Control-2 Delta-2 Cycles included b 108 40 Good blastocysts (IQR) 0.33 (0.17–0.56) 0.26 (0.13–0.48) .121 — — Poor blastocysts (IQR) 0.40 (0.26–0.55) 0.40 (0.38–0.60) .127 — — Arrested blastocysts (IQR) 0.17 (0.07–0.35) 0.19 (0.10–0.43) .512 — — Pregnancy outcomes Control Delta Fresh transfer cycles day 3 167 62 Clinical pregnancy (% per fresh transfer) 35.3 38.7 .636 — — Mean clinical implantation (% per embryo transferred) 25.1 (SD 37.1) 26.6 (SD 37.0) .697 — — Fresh transfer cycles day 5 93 39 Clinical pregnancy (% per fresh transfer) 37.6 38.5 .929 — — Mean clinical implantation (% per embryo transferred) 36.6 (SD 47.9) 38.5 (SD 49.3) .859 — — Note : Data are presented as medians with interquartile ranges (IQR). CI = confidence interval; SD = standard deviation; SE = standard error. a Analysis of covariance was performed taking into account the following control variables: etiology of infertility (presence of endometriosis, ovulatory disorder, polycystic ovarian syndrome, advanced maternal age), previous in vitro fertilization attempt, use of growth hormone, use of menotropin, body mass index, and the ovarian reserve category. b Secondary analysis was performed after the exclusion of cycles in which day 3 vitrification or transfer occurred. Median proportions of good, intermediate, and poor-quality embryos on day 3 after fertilization and proportions of good, poor, and arrested blastocysts on days 5 and 6 after fertilization. Note : Data are presented as medians with interquartile ranges (IQR). CI = confidence interval; SD = standard deviation; SE = standard error. Analysis of covariance was performed taking into account the following control variables: etiology of infertility (presence of endometriosis, ovulatory disorder, polycystic ovarian syndrome, advanced maternal age), previous in vitro fertilization attempt, use of growth hormone, use of menotropin, body mass index, and the ovarian reserve category. Secondary analysis was performed after the exclusion of cycles in which day 3 vitrification or transfer occurred. For the secondary analysis, once day 3 after fertilization embryo transfer and vitrification cycles were excluded, the Delta-2 group included 43 cycles and the Control-2 group included 109 cycles ( Fig. 1 ). There were no significant differences between the groups in the quality of embryos on day 3 after fertilization as well as at the blastocyst level ( Table 3 ).

A retrospective cohort study was performed at The Fertility Clinic in London, Ontario, Canada, a hospital-based, university-affiliated fertility clinic. The study included all IVF/ICSI cycles from September 1, 2018 to December 31, 2019. Ethics approval was provided by the Western University Health Sciences Research Ethics board under project ID number 115800. All IVF/ICSI cycles in which follitropin delta (Rekovelle, FE 999049; Ferring Pharmaceuticals, St. Prex, Switzerland) was used for ovarian stimulation were identified as the exposure cohort (Delta-1). The start date of follitropin delta use in our center was September 1, 2018; all remaining IVF/ICSI cycles from September 1, 2018 to December 31, 2019 were then identified as the control cohort (Control-1), including cycles stimulated with follitropin alfa (Gonal-F; Merck KgaA, Darmstadt, Germany) and follitropin beta (Puregon; MSD, Darmstadt, Germany). Cycles that did not result in embryos were excluded ( Fig. 1 ). Figure 1 Flow chart of the cycles excluded from the initial sample to form the study and control cohorts. IVF/ICSI = in vitro fertilization/intracytoplasmic sperm injection; OPU = oocyte pick-up. Flow chart of the cycles excluded from the initial sample to form the study and control cohorts. IVF/ICSI = in vitro fertilization/intracytoplasmic sperm injection; OPU = oocyte pick-up. All cycles involved controlled ovarian stimulation using recombinant FSH with gonadotropin-releasing hormone (GnRH) antagonist, long GnRH agonist, or flare GnRH agonist protocols. Growth hormone 3.33 mg daily for 9 days was used during stimulation as an adjunct treatment for patients with a history of prior inadequate ovarian response. The follitropin preparation used in the cycle was based on health care provider preference. Menotropin was added in certain cycles on the basis of patient history, recombinant FSH used, and practitioner preference. Follitropin alfa and beta were dosed taking into account the patient’s age, weight, baseline FSH level, and prior history. Follitropin delta was dosed using the patient’s weight in kilograms and the AMH level. Ultrasound monitoring was started on day 4 or 5 of stimulation until the lead follicles reached 17–18 mm in diameter. Final oocyte maturation was triggered with recombinant human chorionic gonadotropin or GnRH agonist, and oocyte retrieval was performed 36–37 hours later. Conventional IVF or ICSI were performed according to standard protocols. The method of oocyte fertilization used was based on practitioner preference and previous patient history, with only a small number of cycles using insemination through standard IVF (4 in the Delta-1 group and 15 in the Control-1 group). The criteria for the extended culture of embryos consisted of the presence of ≥4 good quality embryos on day 3. Embryo transfers were performed on day 3 or day 5 under ultrasound guidance. Generally, only embryos that reached the blastocyst stage by day 5 or 6 were cryopreserved. The demographic data were collected from paper-based patient treatment records. For the purposes of analysis, the patient’s body mass index was categorized as underweight (<18.5 kg/m 2 ), normal weight (18.5–24.9 kg/m 2 ), overweight (25.0–29.9 kg/m 2 ), and obese (≥30.0 kg/m 2 ). An ovarian reserve category was assigned on the basis of the total number of antral follicles measured by ultrasound on day 2 or 3 of the cycle as follows: low (0–8 antral follicles), medium (9–19 antral follicles), and high (≥20 antral follicles). The outcome data were collected from paper-based embryology laboratory records. The primary outcome was embryo quality. The quality of embryos on day 3 after fertilization and of blastocysts on days 5 and 6 were categorized according to the system used in our clinic, largely on the basis of the Istanbul consensus recommendations ( 12 ), taking into account the cell number and grade of each embryo on days 2 and 3 after fertilization and the Gardner grade ( 13 ) of each blastocyst on day 5 and 6 ( Table 1 ). Secondary outcomes included the clinical pregnancy rates and clinical implantation rates. Clinical pregnancy was defined as the presence of a gestational sac on transvaginal ultrasound on luteal day 40. The clinical pregnancy rate was calculated per fresh transfer on day 3 or day 5 after fertilization. The clinical implantation rate was defined as the number of clinical pregnancies per total number of fresh embryos transferred on either day 3 or day 5. Live birth rates were not a part of the study objective. Table 1 Ranking of the embryo quality on day 3 after fertilization and ranking of the blastocyst quality on day 5/6 after fertilization. Day 3 embryo quality ranking Embryo characteristic Good Intermediate Poor Day 2 cell number 3–5 2, >5 Non-division Day 3 cell number 6–10 6–10, >10 <6 cells Embryo grade (fragmentation) G1–G2 G1–G2 G3–G6 Cleavage rate a Appropriate Appropriate Too slow/fast Arrested Too slow/fast Day 5/6 blastocyst quality ranking Embryo characteristic Good Poor Arrested Day 5 (ET) stage b ≥ early blastocysts Morula Cleavage Day 5/6 stage ≥3 blastocysts ≤2 blastocysts Morula Cleavage ICM grade A/B C — TE grade A/B/C A/B/C — ET = embryo transfer. a An appropriate cleavage rate was defined as an increase of ≥3 cells and ≤7 cells from day 2 to 3. An increase of <3 cells from day 2 to 3 was considered too slow. Embryos that had the same cell number on day 2 and 3 were classified as “Arrested.” b Only embryos that were transferred on day 5 were subjected to the day 5 (ET) stage quality categories. All other embryos were either frozen or discarded on day 5 or 6 and follow the day 5/6 stage grading scheme. Ranking of the embryo quality on day 3 after fertilization and ranking of the blastocyst quality on day 5/6 after fertilization. ET = embryo transfer. An appropriate cleavage rate was defined as an increase of ≥3 cells and ≤7 cells from day 2 to 3. An increase of <3 cells from day 2 to 3 was considered too slow. Embryos that had the same cell number on day 2 and 3 were classified as “Arrested.” Only embryos that were transferred on day 5 were subjected to the day 5 (ET) stage quality categories. All other embryos were either frozen or discarded on day 5 or 6 and follow the day 5/6 stage grading scheme. Continuous variables were summarized using medians (interquartile ranges [IQRs]), and group comparisons were examined using Mann-Whitney U tests. Categorical variables were summarized using frequencies (%), and group comparisons were examined using chi-square tests (or exact chi-square tests, when appropriate). Analyses of covariance and logistic regression models were conducted to examine group differences for continuous and dichotomous outcomes, respectively, while also controlling for potential confounding variables, including etiology of infertility (with advanced maternal age included), use of growth hormone, use of menotropin, body mass index, ovarian reserve, as well as whether a previous treatment cycle had taken place. The initial analysis included both the full study cohort (Delta-1) and the full control cohort (Control-1). A secondary analysis was performed excluding cycles where embryos were transferred or vitrified on day 3 after fertilization. This was done to accurately assess the blastocyst development quality in both the study group (Delta-2) and the control group (Control-2). All analyses were conducted using SPSS v26 (IBM Corp., Armonk, NY), and P values <.05 were considered statistically significant.

Our results suggest there was no difference in the embryo quality associated with IVF/ICSI cycles in which follitropin delta was used for stimulation as compared with cycles in which follitropins alfa or beta were used. The clinical pregnancy indices with fresh transfer were comparable. The ESTHER-1 trial showed an improved safety profile with follitropin delta, with fewer excessive stimulation responses and fewer measures taken to prevent ovarian hyperstimulation syndrome ( 1 , 10 , 11 ). Our findings of equivalent cycle outcomes contribute to the evidence on follitropin delta and support its position as an important alternative stimulation medication. The findings of equivalent clinical implantation and clinical pregnancy indices between the 2 groups are consistent with the findings of ESTHER-1, where similar efficacy was reported between follitropin delta and follitropin alfa in ongoing implantation rates, ongoing pregnancy rates, and live birth rates. In that study, however, oocyte yield was equivalent between the groups under comparison ( 1 ). A randomized, controlled, multicenter trial in 2014 found that although a positive relationship existed between the dose of follitropin delta administered and the number of oocytes retrieved, this did not translate into an increase in the number of blastocysts ( 3 ). Oocyte yield is, therefore, not necessarily a useful parameter for evaluating the performance of follitropin delta. The difference between the 2 groups in the number of oocytes retrieved was not reflective of the sample as cycles in which no oocytes were retrieved were excluded. The wide variation between groups in the use of menotropin was explained largely by possible differences in physician preference. Menotropin was not routinely used in cycles stimulated with follitropin delta. Follitropin delta has a lower clearance compared with that of follitropin alfa, which is likely related to differences in glycosylation patterns, but a similar absolute bioavailability ( 4 , 14 ). In addition, its in vitro potency at the human FSH receptor was the same as that of follitropin alfa ( 14 ). These pharmacodynamic traits may explain why the outcome parameters associated with the use of this medication have been equivalent to those of follitropin alfa, whereas the lower clearance and individualized dosing may contribute to the improved safety profile. Our study was retrospective in design and consisted of a relatively small sample size. The study cohorts differed significantly in their demographic characteristics, and efforts were made to control for these differences when a difference in outcomes was observed. The ovarian reserve categories were based on antral follicle counts at the start of each stimulation cycle as AMH serum levels were unfortunately not available for all patients in the study. This could be considered a limitation because AMH is a better predictor of ovarian response ( 15 , 16 ), and it is used in the formal dosing of follitropin delta ( 1 ). The significant proportion of embryos that were either transferred or vitrified on day 3 after fertilization affected the evaluation of resulting blastocyst number and quality; secondary analysis was performed to account for this, albeit with a smaller sample size. A significant strength of our study was that it contributed important information on the quality of embryos and blastocysts associated with the use of follitropin delta for stimulation, a parameter that has not previously been reported. In conclusion, stimulation with follitropin delta in IVF/ICSI cycles was associated with comparable embryo quality, clinical implantation, and clinical pregnancy incidence as compared to stimulation with follitropin alfa or beta. Further study of this association, with a greater number of cycles, in the future would be interesting to determine whether these results can be reproduced.