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Practice Guideline
. 2017 Sep 1;32(9):1802-1811.
doi: 10.1093/humrep/dex218.

Update on fertility preservation from the Barcelona International Society for Fertility Preservation-ESHRE-ASRM 2015 expert meeting: indications, results and future perspectives

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Practice Guideline

Update on fertility preservation from the Barcelona International Society for Fertility Preservation-ESHRE-ASRM 2015 expert meeting: indications, results and future perspectives

Francisca Martinez. Hum Reprod. .

Abstract

Study question: What progress has been made in fertility preservation (FP) over the last decade?

Summary answer: FP techniques have been widely adopted over the last decade and therefore the establishment of international registries on their short- and long-term outcomes is strongly recommended.

What is known already: FP is a fundamental issue for both males and females whose future fertility may be compromised. Reproductive capacity may be seriously affected by age, different medical conditions and also by treatments, especially those with gonadal toxicity. There is general consensus on the need to provide counselling about currently available FP options to all individuals wishing to preserve their fertility.

Study design, size, duration: An international meeting with representatives from expert scientific societies involved in FP was held in Barcelona, Spain, in June 2015.

Participants/materials, setting, methods: Twenty international FP experts belonging to the American Society of Reproductive Medicine, ESHRE and the International Society of Fertility Preservation reviewed the literature up to June 2015 to be discussed at the meeting, and approved the final manuscript. At the time this manuscript was being written, new evidence considered relevant for the debated topics was published, and was consequently included.

Main results and the role of chance: Several oncological and non-oncological diseases may affect current or future fertility, either caused by the disease itself or the gonadotoxic treatment, and need an adequate FP approach. Women wishing to postpone maternity and transgender individuals before starting hormone therapy or undergoing surgery to remove/alter their reproductive organs should also be counselled accordingly. Embryo and oocyte cryopreservation are first-line FP methods in post-pubertal women. Metaphase II oocyte cryopreservation (vitrification) is the preferred option. Cumulative evidence of restoration of ovarian function and spontaneous pregnancies after ART following orthotopic transplantation of cryopreserved ovarian tissue supports its future consideration as an open clinical application. Semen cryopreservation is the only established method for FP in men. Testicular tissue cryopreservation should be recommended in pre-pubertal boys even though fertility restoration strategies by autotransplantation of cryopreserved testicular tissue have not yet been tested for safe clinical use in humans. The establishment of international registries on the short- and long-term outcomes of FP techniques is strongly recommended.

Limitations, reasons for caution: Given the lack of studies in large cohorts or with a randomized design, the level of evidence for most of the evidence reviewed was three or below.

Wider implications of the findings: Further high quality studies are needed to study the long-term outcomes of FP techniques.

Study funding/competing interest(s): None.

Trial registration number: N/A.

Keywords: embryo cryopreservation; fertility preservation; fertoprotection; non-oncological fertility preservation; oncological fertility preservation; oocyte cryopreservation; ovarian tissue cryopreservation; semen cryopreservation; testicular tissue cryopreservation.

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Figures

Figure 1
Figure 1
Algorithm for the cryopreservation of testicular tissue/sperm in pre-pubertal and adolescent patients at high risk of infertility. Clinical assessment for puberty should be carried out by a clinician with experience in pubertal assessment. It must be stressed that no clinical parameter can accurately predict the presence of sperm. The proven treatment option for pubertal and adolescent boys who are considered capable of producing a semen sample is semen collection and cryopreservation. If sufficient sperm are recovered the gametes can be banked using commercial glycerol-based sperm cryomedia. For those young patients who are clinically pre-pubertal and for whom semen cryopreservation is not possible the fertility preservation strategy should include collection of a testicular biopsy by an experienced surgeon. The tissue should be cryopreserved with a protocol optimized for preserving immature germ cells, (immature testis protocol). Patients who are pubertal but are unable to produce a suitable semen sample may proceed to testicular biopsy, with intra-operative analysis. Techniques for intra-operative analysis may vary between institutions but should be aimed at identifying tissue containing (or likely to contain) sperm. This should be carried out by an individual with experience in analysis of testicular tissue (e.g. surgeon, embryologist or andrologist). When sperm are not identified or deemed unlikely the tissue should be frozen with the immature testis protocol used for pre-pubertal patients. For patients in whom sperm are identified or considered likely to be present, tissue should be split into two portions for storage. One portion should be cryopreserved using the immature testis preservation protocol, whilst the second portion should be stored using a protocol aimed at preserving mature sperm cells with glycerol as the main cryoprotectant. As stated in the text at present there are several protocols for cryopreservation of immature testicular tissue and there is no clear evidence at the time of writing to demonstrate which is optimal. Reprinted with permission from Picton et al. (2015).
Figure 2
Figure 2
Fertility preservation techniques in women. Experimental procedures are indicated in discontinuous boxes, while established ones (i.e. those proven to restore fertility, with live births reported) are indicated in shaded boxes. Vitrified-thawed oocytes can be fertilized by IVF/ICSI for embryo transfer. Immature oocytes can be matured in vitro (IVM) for IVF/ICSI. Research is undergoing on the potential use of oogonial stem cells to repopulate follicle-depleted ovaries or differentiating follicle somatic cells and oocytes from embryonic stem cells or induced pluripotent stem cells to assemble de novo follicles for transplantation or IVM and IVF/ICSI. *Cryopreserved. OT, ovarian tissue.

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