Fertility preservation strategies for cancerous women: An updated review.

Oocytes retrieved from IVF/IVM cycles can be cryopreserved using the slow-cooling or vitrification approaches. In theory, there are two methods for immature oocyte cryopreservation before IVM (at GV or MI-stage) or after IVM (MII-stage) ( Table 1 ). The first successful pregnancy and live birth were reported after slow-cooling of immature human oocytes ( 25 ) , but further successful items were from vitrification of MII-stage oocytes after the IVM procedure ( 26 ) .

Cancer incidence in different age groups, especially in adolescents and young women, has shown a slight increase since the 1970s ( 1 ) . Although the survival rates from cancer have improved, cancer is still one of the leading health concerns, especially in young people ( 2 ) . Fertility preservation is an approach used to protect cancer patients from the risk of infertility due to medical treatments, as radiotherapy, chemotherapy, and surgery. Cancer therapies are, in fact, harmful to reproductive function. The treatments used in these patients correlated with a high percentage of losing follicular numbers, especially in young women ( 3 ) . Nowadays, this treatment allows us to maintain the reproductive potential of these patients using methods including, cryopreservation of oocytes, embryos ( 4 ) , and ovarian tissue (OT) ( 5 ) transposition of the ovaries before radiation ( 6 ) , or in vitro culture (IVC) of ovarian follicles ( 7 ) . As recommended by the American Society of Clinical Oncology (ASCO) and the European Society for Medical Oncology, embryo/oocyte cryopreservation a known technique in fertility preservation ( 8 ) . Nevertheless, embryo cryopreservation needs a sperm source, it is not a suitable option for single women. Also, there are other numerous limitations to embryo production, cryopreservation, and storage due to ethical, religious, and social reasons ( 4 ) . However, vitrification of oocytes recovered from stimulated in vitro fertilization (IVF) cycles causes a delay in cancer treatment, due to the time necessary for controlled ovarian hyperstimulation (COH) ( 9 ) . Other fertility preservation techniques, such as ovarian tissue cryopreservation (OTC) and in vitro maturation (IVM) of immature oocytes, can be implemented immediately in cancer therapy, even in underage girls ( 9 ) . The purposes of this review are to explain the up-to-date knowledge about current developments of IVM, the clinical employment of OTC, and transplantation in cancerous women.

Alternative approaches have been introduced for the deletion of malignant cells in certain types of cancer with high metastasis potential, such as leukemia, Burkitt’s lymphoma, neuroblastoma, and ovarian tumors. The artificial ovary technique is one of the new approaches that are known, as primordial follicles isolated from OTs and transferred onto a scaffold-like ovarian organ. The development of human pre-antral follicles was seen after grafting of primordial follicles inside a fibrin scaffold and, respectively, xenografted in nude mice ( 58 ) . Future studies attempt to find a three-dimension-printed artificial ovary to restore both endocrine and reproductive function in animals ( 59 ) . Another approach is to isolate immature oocytes and perform IVM in the ART lab ( 59 ) . The main challenge is maintaining the interaction between the oocytes and the somatic cells that surround them ( 60 ) . The acquisition of meiotic, s developmental conditions, and genome imprinting are important factors that should be considered for this issue. Oocytes differentiated from ovarian stem cells (OSCs) may be another option for the mentioned conditions. Studies have shown that OSCs have been retrieved from mice that it are suitable for fertilization and implantation, as well as embryo development and live births in an animal model ( 61 ) . However, due to the scarcity of OSCs and their ethical issues use of these cells in the clinical application was insufficient, for this reason, this technique is not currently used in clinical practice, especially in cancer patients ( 29 ) . These aforementioned techniques are still in a research setting and can be used for female fertility preservation in the near future.

Nuclear and cytoplasmic maturation are two essential processes for oocyte maturation. The steps of nuclear maturation can be referred to as the meiotic resumption, indicated by the germinal vesicle breakdown, chromatin aggregation, the organization of the meiotic spindle, chromosome separation with the extrusion of the first polar body, progression to MII, and meiotic re-arrest before fertilization ( 13 ) . Cytoplasmic maturation is necessary to obtain a capacity for insemination, and early embryogenesis, subsequently, it provides conditions for implantation, pregnancy, and normal fetal development. This process includes numerous metabolics such as the accumulation of mRNA, proteins and substrates which all are needed to achieve the oocyte developmental competence and structural variations in the organelle typology and distribution for the proper fertilization and early embryo development ( 14 ) .

There are two standard methodologies that have been introduced for cryopreservation procedure, including conventional slow freezing and vitrification ( 45 ) .

The first successful human live birth from orthotropic transplantation was reported in 2004, and Meirow et al. ( 52 ) reported a second live birth in 2005 ( 53 ) . Up until now, due to the impressive development of the OT freezing technique, specially, the ovarian cortex implantation method, more than 130 healthy babies have been born since, 2017 worldwide ( 54 , 55 ) . This statistic has been mentioned in 200 cases until 2021 ( 56 ) . Andersen et al. ( 43 ) investigated the clinical outcome rate of the 3 largest cohort studies in Belgium, Denmark, and Israel. They reported that pregnancy rates varied from 3.9% to 19.3% and live birth rates from 3.9% to 14% per cycle ( 43 ) . In other studies, the live birth rate was reported from 25.4% to 30.6% ( 56 ) . Also, the cumulative clinical pregnancy and the cumulative live birth and clinical ongoing pregnancy rates were 57.5% and 37.7%, respectively ( 42 ) . The lack of consensus could be due to the timing of initiation of ART from OTT, patient’s age, type of ovarian stimulation protocol, and overall the strategy of centers regarding providing services to these patients. A systematic review showed that clinical outcomes were considerably lower in women undergoing OTT than in IVF cycles ( 43 ) . However, there are few reports on the prevalence of pregnancy in pre-pubertal girls. Recent literature reported only two cases of live births who underwent OTC. One case was 14 years old with sickle cell disease that was underwent autologous tissue transplantation for her at the age of 24 years, and pregnancy was achieved spontaneously. Another case was a girl at the age of 9 years old with beta-thalassemia. After the treatment process, she returned for OTT and achieved a live birth undergoing the IVF program ( 57 ) .

For the cryopreservation of cortical OT, strips of the ovarian cortex removed throughout the menstrual period by laparoscopy or laparotomy. The OT contains many primordial and immature follicles numbers that can be protected by freezing. However, it is more complicated than embryo and oocyte freezing due to different cell types and permeability to water and cell volum ( 40 ) . After removal of the medulla, the cortex is divided into several strips of approximately equal size for grafting (10x5 with 1 mm-thick piece) or slices (4x2 with 1 mm-thick piece) which allow penetrating the cryoprotectant agents (CPAs) into the thin layer of the cortex ( 36 ) . Using larger pieces of the cortex (5x5x1 mm) may prepare better conditions for OTT. It is worth mentioning that too small pieces of the cortex are difficult to fixed to the underlying surface and subsequently oxygenation and normal re-vascularization were disturbed ( 41 ) . Ovarian cortical pieces could be transplanted into patients after treatment of the disease or could be done IVM of obtained follicles from OTs. Almost all the healthy live births were achieved following this method. According to a previous meta-analysis study, the reestablishment of ovarian activity rate was 63.9%, and live birth was reported 57.5% by autotransplantation method in women younger than 30 years at the time of OTT ( 42 ) . A survival rate of 84% was reported in follicles after frozen-thawed OTs. However, up to 72% of the follicles are disrupted due to ischemia and reperfusion injury after OTT ( 43 ) .

Oocyte maturation in vivo is an intricate mechanism regulated through hormonal pathways, interactions with circumambient somatic cells, and gene expression, which is regulated by transcription factors. The elevation of cyclic adenosine 3’, 5’-monophosphate (cAMP) levels can prevent oocyte maturation. The high intra-oocyte cAMP concentration inactivates the meiosis promoting factor (MPF), thus blocking meiotic development. A drop in the cAMP levels stimulates the luteinizing hormone (LH) surge, resulting in the oocytes being released from the inhibitory milieu of the follicle, and maturation occurs. There are three sources of high cAMP levels within the oocyte. It includes the oocyte itself via G-protein coupled receptors on the oolemma ( 15 ) , cumulus cells (CCs) through the gap junctions, which is necessary for connecting cytoplasm and nuclear maturation ( 10 ) , and guanosine 3,5-cyclic monophosphate (cGMP), which is produced in the mural and CCs, crosses through gap junctions into the oocyte and inhibits cAMP hydrolysis by the oocyte-specific phosphodiesterase 3A ( 16 ) . Is mentioned that cAMP and cGMP, are the main molecules that play a key role in controlling mammalian oocyte meiosis. After the LH surge, another factor induced by mural granulosa cells is the epidermal growth factor (EGF). LH activation of mural granulosa cells induces the expression of the EGFs binding to their receptors in CCs; thus, mitogen-activated protein kinase (MAPK) is activated. The increased activation of MAPK may lead to the synthesis of meiosis resumption-inducing factor (s) and the blocking of gap junctions via a gap junction protein ( 17 ) . Also, hyaluronan is synthesized by hyaluronan synthase (HAS2) in the plasma membrane and directly extends into the mucous-elastic extracellular matrix (ECM). After that, the COCs are interrupted, which cessation the transportation of cAMP and resulting in the activation of MPF. Furthermore, oocytes secret soluble factors, such as growth differentiation factor-9 (GDF-9), bone morphogenetic protein 15 (BMP-15), and BMP-6. These growth factors stimulate the HAS2 gene expression and cumulus expansion in the presence of the follicle-stimulating hormone (FSH) ( 18 ) . In standard IVM cycles, the immature COCs are isolated from antral follicles and subsequently saturated in a culture medium without cAMP-modulating agents. Standard IVM mediums typically include FSH or other additives such as EGF, EGF-p, and/or LH/hCG. In this system, FSH significantly improves MII rates, intra-oocyte cAMP levels decrease, and stimulation of the meiotic process begins.

Due to the impressive clinical development of OTC in cancerous patients, it is recommended as a standard treatment in cryopreservation strategies. However, OTC was a useful procedure that allows for restore ovarian function and natural pregnancy. However, IVM treatment does not require high gonadotropin stimulation and it is not necessary to take more than 48 h for the decision to perform. Therefore, when patients are unable to delay the chemotherapy, retrieving immature oocytes from the antral follicles and the IVM method may be a good approach. A combination of IVC of isolated OSCs, small follicles, and an artificial ovary technique could eliminate the risk of malignant cell transmission. These approaches could be a good fertility preservation strategy for cancer patients in future studies.

Heterotopic transplantation refers to the grafting of cortical OT into extra-pelvic sites such as the forearm, abdominal, and chest wall. The transplanted tissue can easily removed or replaced when necessary. Contrary to the orthotropic method, it avoids major abdominal surgery and, has no limit to the number of grafted fragments. Although this technique is less invasive than orthotropic, although, spontaneous pregnancy is impossible; therefore, subsequent ovarian stimulation and IVF must be performed ( 44 ) .

OTC and ovarian tissue transplantation (OTT) is the best choice for women undergoing chemoradiotherapy who cannot delay the start of these therapies or are ineligible for ovarian stimulation ( 29 ) . Also, it could be used by women in postponing their first pregnancy and menopause ( 30 ) . This approach described some diseases, including genetic abnormalities such as Turner’s syndrome ( 31 ) , gynecological diseases ( 32 ) , systemic and endocrine disorders, autoimmune disease ( 33 ) , and endometriosis leading to premature ovarian insufficiency ( 34 ) . It is the only option available for pre-pubertal girls and women with estrogen-sensitive malignancies ( 35 , 36 ) . However, OTC is a useful procedure that allows for restoring ovarian function and natural pregnancy ( 37 ) . It is an important evaluation of cumulative factors, such as adequate ovarian reservation, level of AMH hormone, age of patients, and previous treatment regimens for performing this technique ( 38 ) . This approach was suggested in some guidelines, such as ASCO 2018, which mentioned OTC as a standard treatment for these cases, due to the rapid improvement of the OT freezing technique ( 39 ) .

MEDLINE-PubMed (http://www.ncbi.nlm.nih.gov/PubMed), Google Scholar (https://scholar.google.com/), Scopus (https://www.scopus.com) and ISI web of science (http://apps.lib.wosg.ir/WOS) databases were applied for extracting available human original and review studies, from 2010-August 2021. The keywords were used: “fertility preservation,” “in vitro maturation,” “ovarian cryopreservation” and “ovarian transplantation.” We mentioned 75 pieces of scientific literature consisting of reviews, original, guidelines, and recommendations, which have addressed the issue of fertility cryopreservation recently.

Orthotropic transplantation involves transplanting strips of OT into the remaining portion of the ovary or the peritoneum of the ovarian fossa. The advantage of this procedure becomes possible by natural conception and has provided a suitable environment for follicular development ( 44 ) . However, the number of grafted fragments limited by the remaining ovarian size, also, it may increase ischemia and follicle atresia after grafting due to avascular condition. However, the first pregnancy was reported in 2004 using this method, and so far most live births have been from this transplantation ( 44 ) .

In this technique, a controlled cooling machine is used to OT slowly until -140 ˚C at low rates (~1 ˚C/min) before plunging it into liquid nitrogen (LN2) ( 46 ) . Ovarian sample as a complex tissue has different types of cell and ECM. The slow freezing method can prepare a higher equilibration period to allow the release CPA release into the inner complex tissue areas. Slow freezing helps osmotic adjustments between extra and intracellular fluids with CPAs during freezing/thawing procedures. Most times the combination of permeating CPAs, such as glycerol, dimethyl sulfoxide, ethylene glycol, and 1,2-propanediol, and non-permeating CPAs as sucrose, trehalose, and raffinose, was used to protect against cell damage caused by the production of ice crystals and hypertonicity during cryopreservation ( 47 ) . More than 130 live birth was reported from this method; however, its disadvantages are time-consuming and require costly equipment ( 48 ) .

The vitrification procedure was introduced with an ultrafast cooling rate (~20,000 ˚C/min) by direct plunging into LN2 and a high concentration of CPAs. The concentration of CPA was the most critical cause of cell damage; however, it is recommended to use a combination of two or more CPAs ( 47 ) . Vitrification is a considerable method due to its quickness, ease, and cost-effectiveness without using special and expensive equipment ( 30 ) . It has been reported in a low risk of ice crystal formation in the vitrification method ( 29 ) . Nevertheless, there is still no optimal protocol for vitrification. As a result, data about the vitrification technique in human OT is still limited, and some centers may prefer to perform slow freezing for OTC. Thus, the superiority between vitrification and slow freezing for OTC remains unresolved. Some studies showed a lower percentage of apoptotic cells and higher viability of primordial follicles after the slow freezing procedure. Additionally, the frozen-thawed cortical tissue could produce a higher number of hormones AMH in tissue culture after the slow freezing method ( 49 ) . However, others found no differences in the percentage of apoptotic cells and follicle viability and density between these procedures ( 21 , 50 ) . The viability rate of primordial follicles should be assessed after different cryopreservation methods. This assessment is performed using staining assays such as hematoxylin-eosin and trypan blue solution. By staining, the state of primordial follicle quality, including intact nucleolus, clear cytoplasm, and round shape, density, and viability, can be examined ( 50 ) . A meta-analysis of 14 studies in 2017 suggested that less primordial follicular DNA damage and better conditions for the preservation of stromal cells after vitrification ( 51 ) . A disadvantage of vitrification is the direct contact of the sample with nitrogen, therefore, it can lead to viral cross-contamination. Sugishita et al. ( 20 ) recently introduced a new closed vitrification system. According to this study, none of the cryopreservation methods, including slow freezing, conventional vitrification, and closed vitrification didn’t show any significant difference in terms of DNA damage and apoptosis pathway in both primordial and primary follicles compared with a fresh baseline control group ( 21 ) . Nevertheless, only three live births have been reported from the vitrification procedure. A summary of the main properties and outcomes regarding the comparison of vitrification and slow freezing are presented in Table 2 .

In theory, the transplantation of thawed whole ovaries can lead to vascular anastomosis in the ovarian pedicle, however, the ischemia and follicle atresia is reduced due to vascular grafting. As a result, it may provide a more significant follicular reserve and a longer lifetime for an organ transplant. Although, it had some problems, such as a large mass of OT, creating a non-homogeneous cooling rate between different layers of OT. Problems associated with mass and cold transfer eventually increase the probability of ice formation. The multi-thermal gradient technique provides a possible way to overcome the ischemic damage to the whole ovary ( 45 ) .