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Controlled Ovarian Stimulation in Cancer Patients Under 18 Years Old; a Case Series

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Abstract

Background: Fertility preservation for adolescent pubescent girls is a concern of the healthcare system and parents. Oocyte cryopreservation is regarded as a standard medical intervention for patients with a minimum age of 18 years. Evidence suggests that mature oocyte cryopreservation is possible for adolescent pubescent girls, although, ovarian stimulation for these patients remains a challenge.

Cases Presentation: This case series is the first report regarding ovarian stimulation with oocyte cryopreservation in younger than 18 years cancerous girls, who refer to ROYAN institute, Tehran, Iran, prior to the start of the treatment of cancer (November 2015 to February 2021). The oocyte cryopreservation was carried out in the 7 patients (five patients with Hodgkin lymphoma, one patient with Ewing sarcoma, and one patient with osteogenic tumor), the embryo cryopreservation in one patient with dysgerminoma, and the oocyte and embryo cryopreservation in one patient with germ cell tumor. No oocytes were retrieved after ovarian stimulation in the patient with medulloblastoma. For one of the patients with Hodgkin lymphoma, half of the tissues of one ovary were cryopreserved prior to ovarian stimulation.

Conclusions: Oocyte cryopreservation is a feasible option of fertility preservation in the adolescent's patients with cancer. However, only if reported acceptable fertilization rates, as well as the successful cases of live birth from oocyte cryopreservation at the ages under 18, this option of preserving fertility can be applied to this age range.

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References
1.
Moffat R, Pirtea P, Gayet V, Wolf J, Chapron C, de Ziegler D . Dual ovarian stimulation is a new viable option for enhancing the oocyte yield when the time for assisted reproductive technnology is limited. Reprod Biomed Online. 2014; 29(6):659-61. DOI: 10.1016/j.rbmo.2014.08.010. View

2.
Stoop D, Ermini B, Polyzos N, Haentjens P, De Vos M, Verheyen G . Reproductive potential of a metaphase II oocyte retrieved after ovarian stimulation: an analysis of 23 354 ICSI cycles. Hum Reprod. 2012; 27(7):2030-5. DOI: 10.1093/humrep/des131. View

3.
Shapiro B, Daneshmand S, Restrepo H, Garner F, Aguirre M, Hudson C . Efficacy of induced luteinizing hormone surge after "trigger" with gonadotropin-releasing hormone agonist. Fertil Steril. 2010; 95(2):826-8. DOI: 10.1016/j.fertnstert.2010.09.009. View

4.
Nagashima T, Muroi K, Kawano-Yamamoto C, Miyoshi T, Ohmine K, Toshima M . Autologous gamete cryopreservation before hemopoietic stem cell transplantation. Med Sci Monit. 2005; 11(3):CR91-4. View

5.
Reichman D, Davis O, Zaninovic N, Rosenwaks Z, Goldschlag D . Fertility preservation using controlled ovarian hyperstimulation and oocyte cryopreservation in a premenarcheal female with myelodysplastic syndrome. Fertil Steril. 2012; 98(5):1225-8. DOI: 10.1016/j.fertnstert.2012.07.1056. View