We conducted a prospective observational study between March 2017 to March 2018, including all couple referred to our infertility and IVF clinic with a diagnosis of submucosal fibroid distorting the uterine cavity.
The study was conducted at “Santa Maria alle Scotte” University Hospital, Department of Molecular and Developmental Medicine and it was approved by the ethical committee of the Siena University under the ID 10818 clinical protocol.
Women who met the following inclusion criteria were eligible: age between 20 and 38 years; body mass index (BMI) between 18 and 30 kg/m2; regular menstrual cycles of 25–35 days. Other inclusion criteria were: basal FSH less than 12 IU/L (cycle day 2–5); a total antral follicle count of 10–25 follicles; infertility resulting from tubal factors; unexplained infertility; and presence of both ovaries.
The first selection criterion was the presence of a submucosal fibroid with more than 3 cm diameter [9], which cannot be treated with one step hysteroscopic approach. Only those classified as Type 1 to Type 2, according to the FIGO classification [6] and distorting the uterine cavity were included.
The exclusion criteria were: more than 2 fibroids, other causes of uterine cavity abnormality such as uterine septum or Asherman syndrome, previous surgery for infertility, history of pelvic inflammatory disease, polycystic ovarian syndrome, clinical or ultrasound suspicious for endometriosis, and previous surgery for endometriosis.
Other major comorbidities such as diabetes, hypertension, bowel chronic diseases, rheumatologic diseases or male infertility were also considered as exclusion criteria.
All the women underwent pre-treatment transvaginal ultrasound in which the size of fibroids (the three major diameters) were recorded and a sonohysterography to assess the cavity distortion. After confirming the diagnosis, UPA tablets 5 mg (Esmya, Gedeon Richter, Italy) was prescribed and the patients started therapy at the beginning of the next menstrual cycle (1 tablet/day).
Every patient received a minimum of 1 cycle (84 days), and up to 3 cycle with a full menstrual cycle wash-out, between two consecutive cycles; blood was drawn monthly to assess the liver enzymes profile. This treatment and management is standard in our clinic.
Follow-up visits were carried out at the end of every cycle of UPA therapy: fibroids size was measured by transvaginal ultrasound and a sonohysterography was repeated. A normal uterine cavity at sonohysterography was considered the condition allowing to proceed to ART; otherwise, only if a reduction of the volume was detected, the patient has offered an extra UPA cycle. In case of no change in fibroid volume the patient was withdrawn from the study and referred to surgery.
Medical history was collected from our electronic database and data about previous pregnancy or surgery, ovarian stimulation, oocyte retrieval and ART details were recorded.
Menses were synchronized with combined oral contraception pills and ovarian hyperstimulation was carried out from the second day of the menstruation with a standard start dose of 225 IU of urofollitrophin hormone (uFSH).
The dose was adjusted based on follicle measurements and hormonal evaluation of estradiol (E2) and progesterone (P) at the first ultrasound examination on day 6 of the cycle and subsequently every 2–3 days. When follicles reached a mean diameter of 14 mm, GnRH antagonist was started and continued throughout the stimulation period.
Once at least one follicle reached a diameter of ≥ 18 mm and two additional follicles reached a diameter of ≥ 16 mm, 250 mcg of r-hCG (Ovitrelle; Merck Serono, Germany) was administered to trigger ovulation, and 34–36 h later oocytes were retrieved.
A maximum of two cleaved-embryos or blastocysts were transferred 2–5 days after oocyte retrieval.
Vaginal capsules of micronized 200 mg progesterone (three times/day) were administered from the day of oocyte retrieval and continued for at least 14 days after embryo transfer.
Biochemical pregnancy was defined as transiently positive β-hCG level not associated with the development of an embryo, while ongoing pregnancy was referred as a viable intrauterine pregnancy of at least 12 weeks duration confirmed on ultrasound scan.
Statistical analysis was performed using the Graph Pad Prism 6 software. T Student test for paired data with Welch correction was used and results were reported as mean and standard deviation (SD). A value of P < 0.05 was considered statistically significant. Categorical outcomes were reported as percentages.