OTO-IVM is a method of fertility preservation for patients with ovarian tumors

Author:

Lavrinovich O. E.1ORCID,Tatischeva Yu. A.2ORCID,Berlev I. V.3ORCID,Yakovleva M. G.1ORCID,Karitski A. P.1ORCID,Kalugina A. S.4ORCID

Affiliation:

1. N.N. Petrov National Medical Oncology Research Center of the Ministry of Health of Russia

2. N.N. Petrov National Medical Oncology Research Center of the Ministry of Health of Russia; Clinic of Reproductive Medicine “Skyfert”

3. N.N. Petrov National Medical Oncology Research Center of the Ministry of Health of Russia; I.I. Mechnikov North-Western State Medical University of the Ministry of Health of Russia

4. Clinic of Reproductive Medicine “Skyfert”; I.P. Pavlov First Saint Petersburg State Medical University of the Ministry of Health of Russia

Abstract

Introduction. An increasing number of patients of reproductive age get cancer and are highly interested in preserving fertility. Survival rates for cancer patients are improving. Methods of reproductive technologies are being improved to preserve the ability to bear children. Rehabilitation aimed to ensure a satisfactory quality of life takes on a new meaning, and with the development of new technologies, the level of possible assistance also changes. Today, rehabilitation measures for cancer patients of reproductive age should undoubtedly include all possible ways to preserve and restore fertility. Aim: preservation of fertility in patients with ovarian tumors. Material and Methods. After ovariectomy, the ovaries were transported to the embryology laboratory, where oocyte-cumulus complexes were extracted and subsequently matured using the OTO-IVM (ovarian tissue oocyte in vitro maturation) method. The resulting mature oocytes (Metaphase II) were cryopreserved by vitrification or, if a partner was available, fertilized by ICSI (intracytoplasmic sperm injection), the embryos were cultured to the blastocyst stage and also cryopreserved by vitrification. Cryopreserved oocytes and embryos can be used by patients after cancer treatment in assisted reproductive technology programs. Results. A total of 218 OCCs were recovered, 29.8 % were degraded oocytes (n=65). The proportion of OCC suitable for ripening was 153 (70.2 %). After 36 or 48 hours, 65 oocytes matured in 13 patients, which amounted to 42.5 % of oocytes without signs of degradation. In 11 patients the OCC was removed from the tumor-affected ovary. 149 oocytes were obtained, of which 50 (33.6 %) were oocytes with signs of degradation. The remaining 99 (66.4 %) of OCCs had satisfactory quality; after maturation, the Metaphase II stage reached in 49 (49.5 %) of oocytes. As a result, biological material was cryopreserved in 13 of 15 patients: 5 embryos and 60 oocytes.

Publisher

Tomsk Cancer Research Institute

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