Efficacy of letrozole co-treatment in an antagonist protocol | DDDT

Figure 1 Hormone profiles in women with PCOS undergoing IVF with and without letrozole co-treatment. Hormone levels were measured at the start of ovarian stimulation and on the day of the ovulation trigger. The data are presented using box plots, which visually display the median, interquartile range (representing the middle 50% of the values), and the range (excluding any outliers). Statistical significance is indicated as “***” for P Abbreviations: E2, oestradiol; FSH, follicle-stimulating hormone; GnRH, gonadotropin-releasing hormone; LH, luteinizing hormone; P, progesterone.

Follicle Development and Embryonic Parameters

The follicle recruitment and embryonic parameters were assessed, and the results are depicted in Figure 2. After PSM, there was no significant difference in AFC between the groups (20.9 ± 7.90 vs 21.0 ± 7.57, P = 0.896). However, the total number of follicles was found to be decreased in the letrozole group compared to the antagonist group (15.2 ± 8.71 vs 20.9 ± 8.44, P Figure 2A). Interestingly, there was a significant difference in the percentage of large follicles (>16mm) at oocyte retrieval, with a higher proportion observed in the letrozole group (48% vs 38%, P Figure 2B). Letrozole administration was associated with a reduced number of retrieved oocytes (11.9 ± 9.14 vs 15.5 ± 8.05, P Figure 3), resulting in a subsequent decrease in the number of matured and fertilized oocytes, as well as cleaved embryos (Figure 3). However, this difference did not impact the number of usable embryos (5.11 ± 3.87 vs 5.36 ± 3.54, P = 0.388) or the number of good-quality embryos (4.48 ± 4.02 vs 4.69 ± 3.91, P = 0.485) (Figure 3). While the two groups exhibited comparable oocyte retrieval rate (74% vs 74%, P = 0.874) and maturation rate (78% vs 81%, P = 0.073), the letrozole group demonstrated a higher fertilization rate (82% vs 77%, P = 0.001) and usable embryo rate (74% vs 56%, P P = 0.122; Table 2).

Table 2 IVF Pregnancy Outcomes After PSM

Figure 2 Follicle recruitment in women with PCOS undergoing IVF with and without letrozole co-treatment. (A) Comparison of the number of follicles. The numbers are depicted using purple bars (GnRH antagonist group) and red bars (letrozole co-treatment group). (B) The percentage of follicles categorized by size. Data are represented by a color gradient from light green to dark green, corresponding to the follicle size (>16mm, 14–16mm, 12–14mm, 10–12mm, and

Figure 3 Embryonic parameters in women with PCOS undergoing IVF with and without letrozole co-treatment. Comparison of the numbers of retrieved, matured and fertilized oocytes, as well as the numbers of cleaved, usable, and good-quality embryos. The numbers are depicted using purple bars (GnRH antagonist group) and red bars (letrozole co-treatment group). Statistical significance is indicated as “***” for P

Pregnancy Outcomes

Letrozole co-treatment resulted in a higher rate of fresh ET compared to the antagonist group (58.5% vs 44.5%, P Table 2. The endometrial thickness on the day of transfer was similar between the two groups (P > 0.05; Table 2). There was no significant difference in the stage of embryos transferred (P > 0.05; Table 2). The live birth rates after fresh ET were comparable between the letrozole and control groups (single embryo transfer: 28.9% vs 29.7%, P = 1.000; double embryo transfer: 37.3% vs 45.6%, P = 1.000).

The pregnancy outcomes following FET are presented in Table 2. The letrozole group tended to transfer a higher number of embryos per cycle, resulting in a higher live birth rate per FET cycle (P P = 0.423). The cumulative live birth rate did not differ significantly between the letrozole and control groups (56.9% vs 56.0%, P = 0.884).

Obstetrical and Neonatal Outcomes

Regarding obstetrical and neonatal outcomes (Table 3), no significant associations were found between letrozole co-treatment and twin pregnancy, hypertensive disorders in pregnancy, gestational diabetes, placental previa, preterm premature rupture of the membranes, or cesarean delivery (P > 0.05). Furthermore, there were no significant differences between the two groups in terms of gestational age (preterm birth, very preterm birth), birth weight (low birth weight, macrosomia, large for gestational age, small for gestational age), neonatal death, birth defects, or a composite of neonatal morbidity (including neonatal jaundice, necrotizing enterocolitis, pneumonia, respiratory distress syndrome, sepsis, and hypoxic ischemic encephalopathy) (P > 0.05).

Table 3 Associations Between Letrozole Co-Treatment and Obstetrical/Neonatal Complications After PSM

Discussion

The present study provides an extensive exploration into the endocrine effects and clinical outcomes of letrozole co-treatment in women with PCOS undergoing IVF treatment. Our findings reveal that letrozole co-treatment induces significant changes in hormonal regulation, leading to an increase in the percentage of large follicles at oocyte retrieval while decreasing the number of retrieved oocytes. Letrozole co-treatment resulted in an elevated fertilization rate and usable embryo rate as well as a higher rate of fresh ET. Despite these changes, we did not observe any statistically significant differences in pregnancy outcomes after ETs.

Hormonal Profiles and Follicular Development

Our analysis of endocrine parameters demonstrated that letrozole effectively suppressed E2 levels on the trigger day in women with PCOS, which is consistent with previous studies investigating letrozole administration.18–20 Moreover, we found that letrozole had an upregulating effect on LH levels during the follicular phase, aligning with the results of two randomized controlled trials.^9,21 Interestingly, our study revealed a significantly lower FSH concentration in the letrozole co-treatment group, contradicting the findings of other studies that reported increased FSH levels following letrozole administration.^9,21 Similar to previous studies, we also observed lower exogenous gonadotropin consumption and shorter stimulation time in women co-treated with letrozole, supporting the notion of increased follicular sensitivity to exogenous FSH.^11,19,22 The observed increase in the percentage of large follicles following letrozole co-treatment is likely a consequence of the altered endocrinology. The finding is consistent with previous studies conducted on both poor- and normo-responders, which have reported an increased number of large follicles in women co-treated with letrozole.^20,23

Potential Mechanisms

Letrozole, functioning as an aromatase inhibitor, inhibits the synthesis of estrogen and reduces negative estrogenic feedback to the hypothalamic/pituitary axis, resulting in the increased secretion of endogenous gonadotrophins.^24,25 Moreover, the elevated levels of LH can facilitate the selection of dominant follicles and promote the growth of the dominant follicle after the initiation of diameter deviation.^26,27 Another possible explanation for the increased follicle diameter in the letrozole group may be attributed to the effects of androgens. Previous studies have indicated that the letrozole group exhibited higher levels of serum testosterone and androstenedione starting from stimulation day 5 onwards.⁹ The accumulation of androgen concentrations could be a result of aromatase inhibition, preventing the conversion of androgens into estrogens. Another plausible mechanism could be the increased activity of the cytochrome p450 CYP17A enzyme in the theca cells, induced by letrozole cotreatment. The elevated levels of LH and inhibin B, caused by letrozole, act synergistically to enhance androgen production by the theca cells.²⁸ Androgens are known to augment follicular sensitivity to FSH and promote early follicular growth by overexpression and sensitization of FSH receptors.²⁹ Furthermore, androgens have been found to attenuate follicular atresia.³⁰

Oocyte Retrieval

Conflicting results have been reported regarding the impact of letrozole co-treatment on the number of aspirated oocytes. A meta-analysis incorporating 26 studies with 3091 women has displayed that letrozole co-treatment has no effect on the number of aspirated oocytes.³¹ We observed a significant decrease in the number of retrieved oocytes during letrozole co-treatment (11.9 ± 9.14 vs 15.5 ± 8.05, P 32 For fresh ET, the live birth rate increases by 12% with each additional oocyte up to a threshold of 11 oocytes, beyond which the rate plateaus. In contrast, for FET, PCOS patients achieve the highest live birth rate when 25 oocytes are retrieved, and the rate stabilizes thereafter. The cumulative live birth rate plateaus at 15 oocytes. It is important to note that retrieving more than 15 oocytes in a fresh ET cycle increases the risk of OHSS, but does not improve the live birth rate.³³ A study has found that PCOS patients with 10–15 retrieved oocytes had a cumulative live birth rate of 81.91%.³⁴ Additionally, when the number of retrieved oocytes exceeds 20, there is a higher likelihood of excess oocytes, increased gonadotropin consumption, longer ovarian stimulation duration, and a significant portion of embryos remaining unused. To optimize IVF outcome, it is crucial to seek a balance between obtaining an optimal number of oocytes through an appropriate ovarian stimulation protocol and enhancing the quality of oocytes and embryos to achieve higher live birth rates. Although a decreased number of retrieved oocytes was noted in the present study, we observed an elevated fertilization rate and usable embryo rate. Importantly, there was no significant difference in the number of usable embryos and good-quality embryos between the groups, indicating a potential improvement in the quality of oocytes and embryos during letrozole co-treatment.

Pregnancy and Live Birth Rates

The available data for letrozole co-treatment in PCOS patients or high responders are limited.³¹ A randomized parallel controlled study involving 130 individuals has revealed a negative impact on clinical pregnancy rate following the administration of letrozole in antagonist protocol for high responders, defined as those with an AFC of at least 15.³⁵ It may be attributed to the premature rise in progesterone levels during the late follicular phase. Another retrospective study with 125 non-obese PCOS participants has demonstrated a slightly favorable effect of letrozole on cumulative clinical pregnancy rate, but the evidence is not fulfilled the criteria as a high-quality study.³⁶ A recent retrospective study has shown that letrozole co-treatment with the progestin-primed ovarian stimulation protocol in PCOS patients resulted in a higher implantation rate, including all FET cycles associated with the IVF cycle.³⁷ According to previous studies, the fully developed preovulatory-stage follicles promoted by letrozole are more likely to yield high-quality oocytes and embryos and lead to improved implantation potential.³⁸ It is important to note that prior studies have been limited by factors such as differences in patient populations, small sample sizes, variations in treatment protocols, and the use of different outcome measures not focused on live birth rates. In contrast, our study specifically examined the effects of letrozole co-treatment in women with PCOS undergoing IVF antagonist protocols, showing no significant differences between the letrozole and control groups in live birth outcomes after fresh and frozen-thawed ET cycles for women with PCOS. Nevertheless, future randomized controlled trials are needed to validate these findings.

OHSS Risks

PCOS patients are at a higher risk of developing OHSS during IVF. Lowering E2 levels with letrozole may have a potential clinical benefit in reducing the risk of OHSS.^11,39 A prior investigation has explored the dose-dependent reduction of serum E2 levels through the administration of letrozole, commencing on the day of oocyte retrieval in patients with high-risk OHSS.⁴⁰ It is proposed that continuing letrozole treatment after triggering, to stabilize E2 levels, may be a strategy to prevent or reduce the risk of OHSS.^40,41 Our study found a significantly lower level of E2 and a decreased number of follicles during letrozole cotreatment, as well as a higher rate of fresh ET, highlighting its potential application in lowering the risk of OHSS in women with PCOS. However, no conclusive evidence has been provided in such an effect, as most studies had limitations in sample size and power to assess OHSS as an outcome. In a previous meta-analysis of three studies, including 303 women (all normal responders), a non-significant tendency was observed towards a reduction of OHSS risk favoring letrozole.³¹

Obstetrical and Neonatal Complications

Letrozole co-treatment did not appear to be associated with any significant obstetrical or neonatal complications. Previous studies have also suggested that letrozole during IVF does not pose an elevated risk of major congenital anomalies or compromise neonatal outcomes compared to natural cycles, supporting the safety profile of letrozole.^42,43 This is reassuring and suggests that letrozole co-treatment may be a safe option for women with PCOS undergoing IVF/ICSI. However, further studies with larger sample sizes are needed to verify this notion.

Strengths and Limitations

This study was subject to several limitations that could potentially affect the generalizability and validity of its findings. The retrospective study design, for instance, might introduce selection bias due to its reliance on existing data rather than random assignment to treatment groups. Secondly, participants retrospective self-reporting of certain variables or outcomes might be subject to recall bias, potentially compromising the data accuracy. Despite statistical adjustments, residual confounding factors that were not accounted for in the analysis could still influence the results. Additionally, the study’s constraints, such as a limited sample size for live births, lack of strict control over gonadotropin dosages, and failure to assess androgen levels, luteal phase hormone profiles, and endometrial receptivity, should be considered when interpreting the study findings.

Despite these limitations, the study made efforts to enhance its methodological robustness by utilizing high-quality data gathered from a single IVF center to ensure accurate outcome assessments and comprehensive collection of confounding variables, as well as employing a PSM model to reduce bias from confounding variables by mimicking randomization. Our study contributed to the literature by evaluating the endocrinological characteristics and clinical outcomes of letrozole co-administration in an IVF antagonist protocol for women with PCOS, filling a gap in the current research landscape.

Conclusion

Our study provides evidence that letrozole co-treatment in PCOS patients undergoing IVF/ICSI treatment is associated with a reduction in the number of retrieved oocytes but does not impact the number of embryos. Letrozole co-treatment results in a higher rate of fresh ET and does not have any significant adverse effects on pregnancy outcomes. The findings highlight the complex hormonal changes induced by letrozole and their impact on follicular development and oocyte retrieval. This information may guide clinicians in making informed decisions for patients with PCOS to reduce the risks of OHSS and potentially enhance the likelihood of a successful fresh embryo transfer. Further research is warranted to fully elucidate the mechanisms underlying these effects and to optimize the use of letrozole co-treatment in IVF protocols for women with PCOS.