Fertility Preservation for Patients with Malignant Disease. Guideline of the DGGG, DGU and DGRM (S2k-Level, AWMF Registry No. 015/082, November 2017) – Recommendations and Statements for Girls and Women

Abstract

Aim

The aim of this official guideline published by the German Society of Gynecology and Obstetrics (DGGG) and coordinated with the German Society of Urology (DGU) and the German Society of Reproductive Medicine (DGRM) is to provide consensus-based recommendations, obtained by evaluating the relevant literature, on counseling and fertility preservation for prepubertal girls and boys as well as patients of reproductive age. Statements and recommendations for girls and women are presented below. Statements or recommendations for boys and men are not the focus of this guideline.

Methods

This S2k guideline was developed at the suggestion of the guideline commission of the DGGG, DGU and DGRM and represents the structured consensus of representative members from various professional associations (n = 40).

Recommendations

The guideline provides recommendations on counseling and fertility preservation for women and girls which take account of the patientʼs personal circumstances, the planned oncologic therapy and the individual risk profile as well as the preferred approach for selected tumor entities.

I  Guideline Information

Information on the guidelines program of the DGGG, OEGGG and SGGG is provided at the end of the article.

Citation format

Fertility Preservation for Patients with Malignant Disease. Guideline of the DGGG, DGU and DGRM (S2k-Level, AWMF Registry No. 015/082, November 2017) – Recommendations and Statements for Girls and Women. Geburtsh Frauenheilk 2018; 78: 567–584

Guideline documents

The complete long version of the guideline in German, a PDF slideshow for PowerPoint presentations and a summary of the conflicts of interest of all authors are available on the homepage of the AWMF: http://www.awmf.org/leitlinien/detail/ll/015-082.html

Guideline authors

The following professional and scientific societies/working groups/organizations/associations stated the interest in contributing to the compilation of the guideline text and participating in the consensus conference and nominated representatives to attend the consensus conference ( Table 1 ).

Table 1  Authors and representativity of the guideline group: participation of the target user group.

Author Mandate holder	DGGG working group/AWMF/non-AWMF professional society/organization/association
Dr. med. Magdalena Balcerek	Society for Pediatric Oncology and Hematology [Gesellschaft für Pädiatrische Onkologie und Hämatologie e. V.] (GPOH)
Ramona Beck	Self-help Group for Women after Cancer [Frauenselbsthilfe nach Krebs e. V.]
Prof. Dr. med. Matthias W. Beckmann	Expert
Dr. med. Karolin Behringer	Working Group for Internal Oncology [Arbeitsgemeinschaft Internistische Onkologie] (AIO); German Society for Hematology and Medical Oncology [Deutsche Gesellschaft für Hämatologie und Medizinische Onkologie e. V.] (DGHO)
Prof. Dr. med. Anja Borgmann-Sta[udt	German Society for Pediatric and Adolescent Medicine [Deutsche Gesellschaft für Kinder- und Jugendmedizin e. V.] (DGKJ); Society for Pediatric Oncology and Hematology [Gesellschaft für Pädiatrische Onkologie und Hämatologie e. V.] (GPOH)
Dr. rer. nat. Dunja M. Baston-Büst	German Society of Reproductive Medicine [Deutsche Gesellschaft für Reproduktionsmedizin e. V.] (DGRM)
Dr. med. Wolfgang Cremer	Professional Association of Gynecologists [Berufsverband der Frauenärzte e. V.] (BVF)
Dr. med. Christian Denzer	German Society for Pediatric Endocrinology and Diabetes [Deutsche Gesellschaft für Kinderendokrinologie und -diabetologie e. V.] (DGKED)
PD Dr. med. Thorsten Diemer	German Society of Urology [Deutsche Gesellschaft für Urologie e. V.] (DGU)
Prof. Dr. rer. nat. Ralf Dittrich[	German Society of Gynecology and Obstetrics [Deutsche Gesellschaft für Gynäkologie und Geburtshilfe e. V.] (DGGG)
Dipl.-Psych. Dr. phil. Almut Dorn	German Society for Psychiatry, Psychotherapie and Psychosomatics [Deutsche Gesellschaft für Psychiatrie und Psychotherapie, Psychosomatik und Nervenheilkunde e. V.] (DGPPN)
Prof. Dr. med. Tanja Fehm	Gynecologic Oncology Working Group [Arbeitsgemeinschaft Gynäkologische Onkologie e. V.] (AGO)
Dr. med. Rüdiger Gaase	Professional Association of Gynecologists (BVF)
Prof. Dr. med. Ariane Germeyer	German Society for Gynecologic Endocrinology and Reproductive Medicine [Deutsche Gesellschaft für Gynäkologische Endokrinologie und Fortpflanzungsmedizin e. V.] (DGGEF)
Dr. rer. med. Kristina Geue	Psycho-Oncology Working Group [Arbeitsgemeinschaft für Psychoonkologie e. V.] (PSO)
PD Dr. med. Pirus Ghadjar	German Society of Radio-Oncology [Deutsche Gesellschaft für Radioonkologie e. V.] (DEGRO)
Dr. med. Maren Goeckenjan	German Society for Gynecologic Endocrinology and Reproductive Medicine (DGGEF)
Prof. Dr. rer. nat. Martin Götte	German Society for Endocrinology [Deutsche Gesellschaft für Endokrinologie e. V.] (DGE)
Dr. med. Dagmar Guth	Professional Association of Practice-based Gynecologic Oncologists in Germany [Berufsverband Niedergelassener Gynäkologischer Onkologen in Deutschland e. V.] (BNGO)
Prof. Dr. med. Berthold P. Hauffa	German Society for Pediatric Endocrinology and Diabetes (DGKED)
Prof. Dr. med. Ute Hehr	German Society of Human Genetics [Deutsche Gesellschaft für Humangenetik e. V.] (GfH)
Prof. Dr. med. Franc Hetzer	German Society of Coloproctology [Deutsche Gesellschaft für Koloproktologie e. V.] (DGK)
Dr. rer. nat. Jens Hirchenhain	German Society of Human Reproductive Biology [Arbeitsgemeinschaft Reproduktionsbiologie des Menschen e. V.] (AGRBM)
Dr. med. Wilfried Hoffmann	Working Group for Supportive Care in Oncology, Rehabilitation and Social Medicine [Arbeitsgemeinschaft Supportive Maßnahmen in der Onkologie, Rehabilitation und Sozialmedizin e. V.] (ASORS)
Dipl.-Psych. Beate Hornemann	Psycho-Oncology Working Group (PSO)
Dr. med. Andreas Jantke	Federal Association of Reproductive Medicine Centers in Germany [Bundesverband Reproduktionsmedizinischer Zentren Deutschland e. V.] (BRZ)
Prof. Dr. med. Heribert Kentenich	German Society of Psychosomatic Obstetrics and Gynecology [Deutsche Gesellschaft für Psychosomatische Frauenheilkunde und Geburtshilfe e. V.] (DGPFG)
Prof. Dr. med. Frank-Michael Köhn	German Society of Andrology [Deutsche Gesellschaft für Andrologie e. V.] (DGA); German Society for Sexual Medicine, Sexual Therapy and Sexual Science [Deutsche Gesellschaft für Sexualmedizin, Sexualtherapie und Sexualwissenschaft e. V.] (DGSMTW)
Prof. Dr. med. Ludwig Kiesel	German Society for Endocrinology (DGE)
Prof. Dr. med. Sabine Kliesch	German Society of Urology (DGU); Working Group on Urologic Oncology [Arbeitsgemeinschaft Urologische Onkologie e. V.] (AUO)
Prof. Dr. med. Matthias Korell	Gynecologic Endoscopy Working Group [Arbeitsgemeinschaft Gynäkologische Endoskopie e. V.] (AGE)
Prof. Prim. Dr. Sigurd Lax	German Society of Pathology [Deutsche Gesellschaft für Pathologie e. V.] (DGP); Federal Association of German Pathologists [Bundesverband Deutscher Pathologen e.V] (BVDP)
Dr. rer. nat. Jana Liebenthron	FertiPROTEKT Network
Dr. med. Laura Lotz	Guidelines secretary
Prof. Dr. med. Michael Lux	German Society for Senology [Deutsche Gesellschaft für Senologie e. V.] (DGS)
Dr. med. Julia Meißner	Internal Oncology Working Group [Arbeitsgemeinschaft Internistische Onkologie] (AIO); German Society for Hematology and Medical Oncology [Deutsche Gesellschaft für Hämatologie und Medizinische Onkologie e. V.] (DGHO)
Prof. Dr. med. Oliver Micke	AG PRIo of the DKG [German Cancer Society]
Najib Nassar	Federal Association of Reproductive Medicine Centers in Germany (BRZ)
Prof. Dr. med. Frank Nawroth	FertiPROTEKT Network
PD Dr. rer. nat. Verena Nordhoff	Human Reproductive Biology Working Group [Arbeitsgemeinschaft Reproduktionsbiologie des Menschen e. V.] (AGRBM)
Prof. Dr. med. Falk Ochsendorf	German Dermatology Society [Deutsche Dermatologische Gesellschaft e. V.] (DDG)
PD Dr. Patricia G. Oppelt	Pediatric and Adolescent Gynecology Working Group [Arbeitsgemeinschaft Kinder- und Jugendgynäkologie e. V.] (AG)
Prof. Dr. med. Jörg Pelz	German Society for General and Visceral Surgery [Deutsche Gesellschaft für Allgemein- und Viszeralchirurgie e. V.] (DGAV)
Prof. Dr. med. Beate Rau	German Society for General and Visceral Surgery (DGAV)
PD Dr. med. Nicole Reisch	German Society of Internal Medicine [Deutsche Gesellschaft für Innere Medizin e. V.] (DGIM)
Dr. med. Dorothea Riesenbeck	Working Group for Supportive Care in Oncology, Rehabilitation and Social Medicine (ASORS); German Society of Radio-Oncology (DEGRO)
Prof. Dr. rer. nat. Stefan Schlatt	Clinical Research Group for Reproductive Medicine [Klinische Forschergruppe für Reproduktionsmedizin e. V.]
PD Dr. Andreas Schüring	German Society of Reproductive Medicine (DGRM)
Dr. med. Roxana Schwab	Expert
Dip.-Psych. Annekathrin Sender	Expert
PD Dr. med. Friederike Siedentopf	German Society of Psychosomatic Obstetrics and Gynecology (DGPFG)
Dr. phil. Petra Thorn	Infertility Counseling Network Germany [Beratungsnetzwerk Kinderwunsch Deutschland e. V.] (BKiD)
Dr. med. Steffen Wagner	Professional Association of Practice-based Gynecologic Oncologists in Germany (BNGO)
Prof. Dr. med. Ludwig Wildt	German Society for Endocrinology (DGE); Austrian Society of Gynecology and Obstetrics [Österreichische Gesellschaft für Gynäkologie und Geburtshilfe e. V.] (OEGGG)
Prof. Dr. med. Pauline Wimberger	Expert
PD Dr. sc. hum. Tewes Wischmann, Dipl.-Psych.	Infertility Counseling Network Germany (BKiD)
Prof. Dr. med. Michael von Wolff	Swiss Society of Gynecology and Obstetrics [Schweizerische Gesellschaft für Gynäkologie und Geburtshilfe] (SGGG)

Abbreviations

ABVD

doxorubicin, bleomycin, vinblastine, dacarbazine

AC

doxorubicin, cyclophosphamide

ALL

acute lymphoblastic leukemia

AMH

anti-Müllerian hormone

AML

acute myeloid leukemia

ART

assisted reproductive technologies

BEACOPP

bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, prednisone

BOT

borderline tumor

CAF

cyclophosphamide, adriamycin, fluorouracil

CEF

cyclophosphamide, epirubicin, 5-flourouracil

ChlVPP/EVA hybrid COPP

chlorambucil, vinblastine, procarbazine, prednisone/ etoposide, vincristine, doxorubicin

CHOP

cyclophosphamide, doxorubicin, vincristine, prednisolone

CI

confidence interval

CMF

cyclophosphamide, methotrexate, 5-fluorouracil

CML

chronic myelogenous leukemia

CVP

cyclophosphamide, vincristine, prednisone

DMSO

dimethyl sulfoxide

EC

epirubicin, cyclophosphamide

ESD

effective sterilizing dose

FOLFOX

folinic acid (leucovorin), 5-fluorouracil, oxaliplatin

GnRH

gonadotropin-releasing hormone

GnRHa

gonadotropin-releasing hormone agonist

Gy

Gray

HL

Hodgkinʼs lymphoma

MVPP

mustine, vinblastine, procarbazine, prednisolone

NHL

non-Hodgkinʼs lymphoma

OR

odds ratio

POI

premature ovarian insufficiency

RR

relative risk

SCT

stem cell transplantation

TAC

paclitaxel (taxol), doxorubicin (adriamycin), cyclophosphamide

TKI

tyrosine kinase inhibitors  

II  Guideline Application

Purpose and Objectives

The purpose of this guideline is to provide recommendations for action with regard to counseling and fertility preservation for prepubertal girls and women of reproductive age with oncologic disease which take account of the patientsʼ personal circumstances and risk profile. The aim is to increase the rate of successful pregnancies after completing oncologic therapy and to improve the patientsʼ quality of life.

Targeted areas of patient care

• Outpatient care

• Inpatient care

• Semi-residential care

Target patient groups

The guideline is aimed at all prepubertal girls and patients of reproductive age who require gonadotoxic treatment for malignant disease.

Target user group/target audience

This guideline is aimed at all physicians and medical professionals involved in the care of patients who require gonadotoxic therapy.

The principal among these are: gynecologists, reproductive medicine physicians, andrologists, urologists, oncologists, radio-oncologists, general practitioners, pediatricians, pathologists, psycho-oncologists.

Adoption of the guideline and period of validity

This guideline is valid from November 1, 2017 to October 31, 2020. Because of the contents of the guideline, this period of validity is only an estimate. If there are important changes to the evidence, then amendments to the guideline will be published before the period of validity has expired, once the new evidence has been carefully reviewed in accordance with the methodology of the AWMF.

III  Methodology

Basic principles

The methodology used to prepare this guideline is determined by the class to which the guideline is assigned. The AWMF Guidance Manual (version 1.0) has set out the respective rules and regulations for the classification of guidelines. Guidelines are differentiated into lowest (S1), intermediate (S2) and highest (S3) class. The lowest class is defined as a summary of recommendations for action compiled by a non-representative group of experts. In 2004 the S2 class was divided into two subclasses: a systematic evidence-based subclass (S2e) and a structural consensus-based subclass (S2k). The highest S3 class combines both approaches.

This guideline is classified as: S2k

Grading of recommendations

While the description of the quality of the evidence (strength of evidence) serves as an indication for the robustness of the publicized data and therefore expresses the extent of certainty/uncertainty about the data, the classification of the level of recommendation reflects the result of weighing up the desirable and adverse consequences of alternative approaches.

A grading of the evidence and of the recommendations is not envisaged for S2k-level guidelines. The level of recommendation is differentiated by syntax, not by symbols. The syntax used to grade the level of recommendation is described in the background text ( Table 2 ).

Table 2  Grading of recommendations.

Description of level of recommendation	Syntax
Strong recommendation, highly binding	must/must not
Recommendation, moderately binding	should/should not
Open recommendation, not binding	may/may not

Statements

Expert statements included in this guideline which are not recommendations for action but simple statements of fact are referred to as Statements. It is not possible to provide a level of evidence for these statements.

Achieving consensus and strength of consensus

As part of structured consensus-based decision-making (S2k/S3 level), authorized participants present at consensus sessions vote on draft Statements and Recommendations. Discussions at the sessions can lead to significant changes in the wording of Statements and Recommendations. The extent of agreement, which depends on the number of participants, is then determined at the end of the session ( Table 3 ).

Table 3  Classification on extent of agreement following consensus-based decision-making.

Symbol	Strength of consensus	Extent of agreement in percent
+++	Strong consensus	> 95% of participants agree
++	Consensus	> 75 – 95% of participants agree
+	Majority agreement	> 50 – 75% of participants agree
–	No consensus	< 50% of participants agree

Expert consensus

As the name implies, this term refers to consensus decisions taken with regard to specific Recommendations/Statements without a previous systematic search of the literature (S2k) or when evidence is lacking (S2e/S3). The term “expert consensus” (EC) used here is synonymous with terms used in other guidelines such as “good clinical practice” (GCP) or “clinical consensus point” (CCP). The strength of the recommendation is graded as previously described in the chapter “Grading of recommendations”; the strength of consensus is only indicated semantically (“must”/“must not” or “should”/“should not” or “may”/“may not”) with no use of symbols.

IV  Guideline

Statements and Recommendations on fertility preservation for girls and women with oncologic disease are presented below.

1  Introduction to Fertility Protection for Persons Diagnosed with Oncologic Disease

1.2  Importance and problems of fertility protection for persons diagnosed with cancer

Oncologic therapies often lead to partial or complete impairment of gonadal function in both men and women along with the potential loss of germ cells. Faced by the impact of a life-threatening disease, subsequent infertility may appear to be a minor issue for non-affected persons. For many of the patients themselves, however, premature ovarian insufficiency or sterility is a very stressful situation for both the affected patient and their partner 2 ,  3 .

Consensus-based Recommendation 1.R1
Expert consensus	Strength of consensus ++
Assessing the risk of possible infertility and the choice of method(s) for fertility preservation must be done by an interdisciplinary panel and discussed with the patient in good time before the start of oncologic therapy.

Consensus-based Statement 1.S1
Expert consensus	Strength of consensus +++
Counseling about concepts to preserve fertility must be an integral part of every patientʼs oncologic treatment and must take account of the patientʼs personal circumstances, recommended oncologic therapy and individual risk profile.

2  Causes of Gonadal Toxicity in Women

2.1  Gonadal damage from surgery

Depending on the extent of radical surgery, gynecologic oncologic disease can result in sterility following complete or partial removal of the uterus and/or ovaries. Fertility-preserving surgery for various tumor entities is discussed in Chapter 4.1 of the long version of the guideline.

2.2  Gonadal toxicity from chemotherapy

The gonadal toxicity of individual chemotherapeutic drugs depends on their mechanism of action, the administered dose, the duration of therapy, the way in which therapy is administered, concomitant therapeutic treatments such as simultaneous radiotherapy or ovary-removal surgery, the patientʼs age, and the patientʼs individual disposition ( Table 4 ).

Table 4  Ovarian toxicity of different chemotherapeutic drugs (modified from 4 ,  5 ).

Risk	Regimen/Substance
High risk (> 80% risk of permanent amenorrhea)	CMF, CEF, CAF, TAC × 6 for women aged ≥ 40 years Conditioning for stem cell transplantation (particularly alkylating agent-based myeloablative conditioning with busulfan, cyclophosphamide, melphalan) BEACOPP × 6 – 8 for women aged > 35 years
Intermediate risk (40 – 60% risk of permanent amenorrhea)	CMF, CEF, CAF, TAC × 6 for women aged 30 – 39 years AC × 4 for women aged ≥ 40 years AC or EC × 4 → taxane BEACOPP × 6 – 8 for women aged 25 – 35 years CHOP × 6 for women aged ≥ 35 years Standard therapies for bone and soft tissue sarcomas
Low risk (< 20% risk of permanent amenorrhea)	CMF, CEF, CAF, TAC × 6 for women aged ≤ 30 years AC × 4 for women aged ≤ 40 years BEACOPP × 6 – 8 for women aged < 25 years ABVD × 2 – 4 CHOP × 6 for women aged < 35 years CVP AML-type therapy (anthracyclines/ cytarabine) ALL-type therapy (multi-agent) FOLFOX for women aged ≤ 40 years
Very low or no risk of permanent amenorrhea	Methotrexate Fluorouracil Vincristine

Consensus-based Statement 2.R2
Expert consensus	Strength of consensus +++
Women scheduled to receive a potentially gonadotoxic dose of chemotherapeutic drugs must be informed about the risk of ovarian insufficiency and about methods to preserve fertility.

Consensus-based Statement 2.S3
Expert consensus	Strength of consensus +++
The negative impact of the gonadal toxicity of chemotherapies increases with patient age. Not all patients in a specific age group who receive therapy according to a defined regimen will develop the same fertility disorder.

2.3  Gonadal toxicity from radiotherapy

2.3.1  Ovarian radiation damage

( Table 5 )

Table 5  Radiotoxicity and ovarian insufficiency (modified from 6 ).

Effective sterilizing dose (ESD)	Ovarian radiation dose (Gy)
No relevant effect	0.6
No relevant effect at < 40 years	1.5
0 years	20.3
10 years	18.4
20 years	16.5
30 years	14.3
40 years	6

Consensus-based Statement 2.S4
Expert consensus	Strength of consensus +++
Whether women develop ovarian insufficiency depends on the radiation dose, the age when the patient was exposed to radiation and the volume of irradiated ovarian tissue.

Consensus-based Recommendation 2.R3
Expert consensus	Strength of consensus +++
Patients who are scheduled to receive radiotherapy which will also irradiate the anatomical area of the ovaries must be informed about the risk of ovarian damage and must be made aware of methods which could preserve their fertility.

2.3.2  Tubal radiation damage

Radiogenic tubal changes can lead to a loss of function, resulting in limited fertility. Extrauterine pregnancies and their associated subsequent complications can occur, even if ovarian and uterine function have been preserved. Nothing is known about tubal tolerance doses.

2.3.3  Uterine radiation damage

In contrast to chemotherapy, radiotherapy can affect uterine function in addition to affecting the ovaries. Here again, the effect depends on the dose; the dose-response relationship has not yet been clearly defined 7 .

Consensus-based Statement 2.S5
Expert consensus	Strength of consensus +++
Irradiation of the uterus can lead to uterine and tubal sterility and to increased pregnancy risks such as preterm birth, miscarriage and lower birth weight of the infant.

2.3.4  Radiation damage to the hypothalamic/hypophyseal axis

Consensus-based Recommendation 2.R4
Expert consensus	Strength of consensus +++
Before undergoing radiotherapy of the head region, patients must be informed about the risk of damaging the hypothalamic/hypophyseal axis and the consequences of this damage.

2.4  Gonadal toxicity through immunotherapy or targeted therapies

Consensus-based Recommendation 2.R5
Expert consensus	Strength of consensus +++
Women receiving therapy with bevacizumab should be informed about the risk of ovarian insufficiency and about methods to preserve fertility.

Consensus-based Recommendation 2.R2
Expert consensus	Strength of consensus +++
Patients who receive immunotherapy or targeted therapy should be informed about the unclear risk of ovarian insufficiency and about methods to preserve fertility.

2.5  Gonadal toxicity from endocrine therapies

Consensus-based Statement 2.S6
Expert consensus	Strength of consensus +++
Data on gonadal toxicity of tamoxifen are limited and inconsistent; there are no data on the possible effects of aromatase inhibitors combined with GnRH agonists. A gonadotoxic effect is unlikely.

Consensus-based Statement 2.S7
Expert consensus	Strength of consensus +++
The most important fertility-reducing effect of endocrine therapy used to treat breast cancer is the length of the treatment, as it postpones the time when the patient can have children to a stage in life when patient has reduced ovarian reserve.

Consensus-based Recommendation 2.R7
Expert consensus	Strength of consensus ++
Ways of protecting fertility such as cryopreservation of fertilized and/or unfertilized oocytes or ovarian tissue should be discussed with women receiving endocrine therapy alone (5 – 10 years) to treat breast cancer.

Consensus-based Recommendation 2.R8
Expert consensus	Strength of consensus ++
The possibility of postponing or interrupting endocrine therapy may be discussed with the patient if this would allow her to have children early.

4  Methods of Fertility Protection for Girls and Women

( Figs. 1 and 2 )

Fig. 1.

 Flow diagram of potential approaches to protect the fertility of girls and women after the onset of menarche before they start gonadotoxic therapy.

Fig. 2.

 Fertility protection for women based on oncologic therapy and the available timeframe (modified from 1 ).

4.1  Organ-preserving surgery

There are a number of S3 guidelines on the treatment of patients with malignant ovarian tumors, cervical cancer und endometrial cancer. To prevent discrepancies between guidelines, the guideline coordinators of the S3 guidelines and the coordinators of the S2k guideline on fertility preservation unanimously agreed to incorporate the relevant Statements, Recommendations and background texts from the S3 guidelines into the S2k guideline. The relevant Recommendations and Statements are available in the long version of the guideline.

4.2  Ovariopexy and gonadal protection for radiotherapy

Consensus-based Statement 4.S25
Expert consensus	Strength of consensus +++
Transposition of the ovaries out of the area which will be irradiated may reduce the risk of radiogenic ovarian insufficiency.

Consensus-based Recommendation 4.R33
Expert consensus	Strength of consensus +++
The possibility of an ovariopexy to preserve ovarian function must be discussed before commencing radiotherapy/radiochemotherapy of the lesser pelvis.

Consensus-based Statement 4.S36
Expert consensus	Strength of consensus +++
If ovariopexy is performed, ovarian tissue may be harvested at the same time for cryopreservation.

4.3  GnRH agonists

Consensus-based Statement 4.S47
Expert consensus	Strength of consensus ++
The data is still contradictory, so administering GnRH agonists as the only method for fertility protection is not sufficient.

Consensus-based Statement 4.S58
Expert consensus	Strength of consensus +++
Because of the contradictory study results, it is currently not possible to evaluate the benefit of administering a GnRH agonist.

Consensus-based Recommendation 4.R34
Expert consensus	Strength of consensus +++
Depending on the underlying tumor entity, GnRH agonists may be offered as a fertility protection measure if the patient has been informed in detail.

4.4  Cryopreservation of fertilized or unfertilized oocytes

Consensus-based Statement 4.S19
Expert consensus	Strength of consensus +++
Cryopreservation of fertilized and unfertilized oocytes is an established technique in reproductive medicine which can be used before starting gonadotoxic therapy.

4.4.1  Controlled ovarian stimulation to harvest oocytes in cancer patients

Consensus-based Statement 4.S20
Expert consensus	Strength of consensus +++
A protocol with the lowest possible risk of ovarian hyperstimulation syndrome should be used for ovarian stimulation treatment to protect fertility.

4.4.2  Cryopreservation of unfertilized oocytes

( Table 6 )

Table 6  Outcomes for unfertilized oocytes after slow freezing or vitrification (modified from 8 and 9 ).

	Slow freezing	Vitrification
Survival rate per unfertilized oocyte after cryopreservation/thawing	45 – 67%	80 – 90%
Fertilization rate per unfertilized oocyte after cryopreservation/thawing	54 – 68%	76 – 83%
Clinical pregnancy rate/transfers	11.6%	44.9% (p = 0.002)
Congenital malformation rate	0.5%	1.3%

Consensus-based Statement 4.S21
Expert consensus	Strength of consensus ++
In contrast to the cryopreservation of fertilized oocytes, the cryopreservation of unfertilized oocytes is not associated with a significantly increased rate of malformations or developmental deficits in children.

4.4.3  Cryopreservation of fertilized oocytes

( Tables 7 and 8 )

Table 7  Survival rate and development of embryos after slow freezing or vitrification (open/closed) (modified from 10 ).

	Slow freezing	Vitrification (open/closed)
* p < 0,001
Survival rate per embryo after cryopreservation/thawing	63.8%	89.4%*/87.6%*
Rate of intact morphology of all blastomeres per embryo after cryopreservation/thawing	44.3%	80.1%*/76.1%*

Table 8  Pregnancy outcomes for blastocysts after slow freezing or vitrification (modified from 11 and 8 ).

	Slow freezing	Vitrification
* p = significant, ** ARR: 1.38, 95% CI: 1.32–1.45, *** ARR: 1.41, 95% CI: 1.34–1.49
Rate of transferred blastocysts per cryopreservation/thawing	71.4%	84.5%*
Rate of clinical pregnancies per transferred blastocyst	23.8%	32.7%**
Rate of live births per transferred blastocyst	17.7%	24.8%***

Consensus-based Recommendation 4.R35
Expert consensus	Strength of consensus +++
The cryopreservation of unfertilized oocytes must be additionally offered, even if the patient has a partner.

4.5  Cryopreservation of ovarian tissue

Consensus-based Statement 4.S22
Expert consensus	Strength of consensus ++
Cryopreservation of ovarian tissue is an established method to restore fertility after receiving treatment for cancer.

Consensus-based Statement 4.S23
Expert consensus	Strength of consensus ++
Cryopreservation of ovarian tissue may be carried out at any time of the menstrual cycle and does not lead to any relevant delay in oncologic therapy.

4.5.1  Harvesting and transport of ovarian tissue

Consensus-based Recommendation 4.R36
Expert consensus	Strength of consensus +++
The harvested tissue must be cooled (4 – 8 °C) during its transportation to a center which specializes in cryopreservation. The harvested tissue must be processed promptly, at the very latest 24 hours after harvesting.

4.5.2  Cryopreservation of harvested tissue

Slow freezing is currently recommended for the cryopreservation of ovarian tissue because of the higher efficacy of this method in routine clinical practice 12 ,  13 ,  14 .

4.5.3  Transplantation of tissue

Consensus-based Recommendation 4.R37
Expert consensus	Strength of consensus +++
Ovarian tissue must be transplanted orthotopically, i.e. on or into the ovary or close to the ovary in the retroperitoneal space.

Consensus-based Recommendation 4.R38
Expert consensus	Strength of consensus +++
The patientʼs fertility (tubal, uterine and extrauterine factors) must be assessed when transplanting ovarian tissue and, if possible, corrections must carried out where necessary.

4.5.4  Risk of tumor or disease recurrence after retransplantation

( Table 9 )

Table 9  Risk of ovarian metastasis for various tumor types (modified from Dolmans et al. 14 and Bastings et al. 15 ).

High risk	Moderate risk	Low risk
leukemia neuroblastoma Burkittʼs lymphoma ovarian tumors	stage IV breast cancer (lobular subtypes) bowel cancer endometrial carcinoma gastric cancer cervical adenocarcinoma non-Hodgkinʼs lymphoma Ewingʼs sarcoma	stage I – III breast cancer (ductal subtypes) cervical squamous cell carcinoma Hodgkinʼs lymphoma osteosarcoma non-genital rhabdomyosarcoma Wilmsʼ tumor

Consensus-based Statement 4.S24
Expert consensus	Strength of consensus +++
The risk of ovarian metastasis cannot be excluded for any type of tumor. To date, an increased risk has been found for leukemia, neuroblastoma, Burkittʼs lymphoma and malignant ovarian tumors.

Consensus-based Recommendation 4.R39
Expert consensus	Strength of consensus +++
The patient must be informed before harvesting the tissue about the possible risk of transferring malignant cells by transplanting the harvested ovarian tissue.

4.6  Fertility-preserving or fertility-creating/fertility-restoring methods following uterine radiotherapy

Consensus-based Recommendation 4.R40
Expert consensus	Strength of consensus ++
If the patient wishes to have children, the dose administered to the uterus must be kept as low as possible using the latest radiation planning and techniques.

4.7  Combinations of fertility-protecting methods

Consensus-based Recommendation 4.R41
Expert consensus	Strength of consensus +++
The patient must be offered combinations of different fertility-preserving methods (e.g. cryopreservation of oocytes, cryopreservation of ovarian tissue and/or the administration of GnRH agonists) to improve the efficacy of fertility protection methods.

6  Recommendations for Selected Tumor Entities in Women

6.1  Breast cancer

6.1.1  Fertility protection counseling for women with breast cancer

Consensus-based Recommendation 6.R3
Expert consensus	Strength of consensus ++
Every fertile woman with breast cancer who might wish to have children must receive counseling about ovarian toxicity and the available methods to protect fertility before starting any potentially gonadotoxic therapy.

Consensus-based Recommendation 6.R4
Expert consensus	Strength of consensus ++
Patients with metastatic breast cancer must receive individualized information on fertility protection which must also take account of the prognosis of a more limited life expectancy.

6.1.2  Pregnancy after breast cancer

Consensus-based Statement 6.S36
Expert consensus	Strength of consensus ++
According to retrospective observational studies, pregnancy after treatment for breast cancer is not associated with a poorer prognosis with regard to the underlying disease.

6.1.3  Limited fertility due to chemotherapy for breast cancer

The standard chemotherapy protocols to treat breast cancer in young women are anthracycline- and taxane-based chemotherapies. The rule of thumb for persistent amenorrhea following anthracycline-taxane-based regimens is estimated to be 10 – 20% for women aged < 30 years, while the rate of persistent amenorrhea for women aged more than 30 years ranges from 13 – 68%, depending on the patientʼs age 16 ,  17 .

6.1.4  Limited fertility due to radiotherapy

Consensus-based Statement 6.S32
Expert consensus	Strength of consensus +++
Regional radiotherapy to treat breast cancer is not associated with reduced fertility.

6.1.5  Special aspects of fertility protection for women with hormone receptor-positive breast cancer, limited fertility due to endocrine therapy

Consensus-based Recommendation 6.R55
Expert consensus	Strength of consensus ++
If the patient has been carefully informed about the potential risks, pausing anti-tumor endocrine therapy (after a minimum of 2 years of therapy) may be considered to allow the patient to have children, after which the patient would resume therapy.

6.1.6  Potential fertility protection methods for patients with breast cancer

( Table 10 )

Table 10  Retrospective studies on methods of cryopreservation in women with breast cancer.

Authors	Study	Number of women	Methods	Country
Lawrenz et al., 2012 18	retrospective, single center	n = 56	ovarian tissue cryopreservation, GnRHa, hormone stimulation and cryopreservation of oocytes, combinations also possible	Germany
Turan et al., 2013 19	retrospective cohort study single center	n = 78	hormone stimulation and cryopreservation of oocytes	USA
Sigismondi et al., 2015 20	retrospective, single center	n = 31	ovarian tissue cryopreservation, hormone stimulation and cryopreservation of oocytes	Italy
Takae et al., 2015 21	retrospective, single center	n = 27	combination of ovarian tissue cryopreservation and hormone stimulation with cryopreservation of oocytes	Japan
Dahhan et al., 2015 22	retrospective, single center	n = 16	hormone stimulation and cryopreservation of oocytes	Netherlands
Oktay et al., 2015 23	retrospective, single center	n = 131	hormone stimulation with/without letrozole and cryopreservation of oocytes	USA

Consensus-based Statement 6.S33
Expert consensus	Strength of consensus +++
Irrespective of the patientʼs hormone status, there are no conclusive data about the potential impact of hormone stimulation for oocyte retrieval before starting planned neoadjuvant systemic therapy for breast cancer on the patientʼs oncologic prognosis.

Consensus-based Recommendation 6.R56
Expert consensus	Strength of consensus ++
Hormone stimulation for oocyte retrieval can be done in patients with hormone receptor-positive breast cancer receiving concomitant anti-hormone treatment (e.g. aromatase inhibitors or tamoxifen).

6.1.7  GnRH agonists (GnRHa) for women with breast cancer

A recent systematic meta-analysis about the use of GnRHa in women with breast cancer 26 evaluated the data from 1962 women, 541 of whom received chemotherapy without GnRHa and 521 of whom were treated with chemotherapy and GnRHa 26 . The rate of spontaneous menstruation recurrence after completing chemotherapy was higher in the group treated with concomitant GnRHa (OR: 2.57; 95% CI: 1.65 – 4.01; p < 0.0001). However, there was no significant difference in pregnancy rates between the two groups. Another recent meta-analysis (n = 1231, 27 ) found a significantly reduced risk of premature ovarian insufficiency (OR: 0.36; 95% CI: 0.41 – 0.73, p < 0.001) for patients who received concomitant GnRHa during chemotherapy, together with a slightly but significantly increased pregnancy rate (OR: 1.83; 95% CI: 1.02 – 3.28; p = 0.041).

6.1.8  Reduced ovarian reserve in women with BRCA1 mutation

Comparative studies have pointed out that women with BRCA1 mutation may have reduced ovarian reserve compared to healthy women 24 ,  25 .

6.2  Ovarian/borderline tumors

6.2.1  Borderline tumors

Consensus-based Recommendation 6.R57
Expert consensus	Strength of consensus +++
After women who have had fertility-preserving surgery to treat an ovarian/borderline tumor and who wish to have children have been informed about the potential risks involved, physicians may consider offering hormone stimulation to them as part of fertility treatment.

Consensus-based Recommendation 6.R58
Expert consensus	Strength of consensus +++
Before undergoing bilateral salpingo-oophorectomy, women should be offered the possibility of cryopreserving unfertilized and fertilized oocytes.

Consensus-based Recommendation 6.R59
Expert consensus	Strength of consensus +++
Cryopreservation of ovarian tissue may be considered.

6.2.2  Ovarian cancer

Consensus-based Statement 6.S34
Expert consensus	Strength of consensus ++
Fertility treatment is possible in patients with early ovarian cancer (FIGO Ia, G1/G2) who were treated using a fertility-preserving approach and were given detailed information about the risks.

6.3  Solid tumors

6.3.1  Sarcomas

Consensus-based Recommendation 6.R60
Expert consensus	Strength of consensus +++
Every fertile woman with sarcoma who may wish to have a child must be informed about the ovarian toxicity of treatment and the methods of preserving fertility before starting a potentially gonadotoxic therapy.

Consensus-based Statement 6.S35
Expert consensus	Strength of consensus ++
There are no indications that pregnancy after treatment for sarcoma will result in a poorer prognosis.

Consensus-based Statement 6.S36
Expert consensus	Strength of consensus ++
Depending on the patientʼs age, chemotherapy to treat osteosarcoma and soft tissue sarcoma will result in primary ovarian insufficiency.

Consensus-based Recommendation 6.R61
Expert consensus	Strength of consensus +++
Patients with sarcoma should be offered cryopreservation of ovarian tissue to protect fertility. The risk of recurrence caused by transplantation of the tissue cannot be excluded and must be discussed with the patient before harvesting ovarian tissue.

Consensus-based Recommendation 6.R62
Expert consensus	Strength of consensus +++
After the onset of puberty, patients with sarcoma should be informed about the possibility of cryopreserving oocytes, if the start of oncologic therapy can be postponed by at least 2 weeks.

Consensus-based Recommendation 6.R63
Expert consensus	Strength of consensus ++
A GnRH agonist can be administered to patients with sarcoma during gonadotoxic therapy.

6.3.2  Colorectal cancer

Consensus-based Recommendation 6.R64
Expert consensus	Strength of consensus +++
Every fertile woman with colorectal cancer who may wish to have a child must be informed about the ovarian toxicity of treatment and methods of preserving fertility before starting a potentially gonadotoxic therapy.

Consensus-based Statement 6.S37
Expert consensus	Strength of consensus ++
According to case reports, pregnancy after rectal cancer is not associated with a poorer oncologic prognosis.

Consensus-based Statement 6.S38
Expert consensus	Strength of consensus ++
Chemotherapeutic treatment of colorectal cancer with 5-fluorouracil, folinic acid and oxaliplatin is reported to have a low risk of ovarian insufficiency.

Consensus-based Recommendation 6.R65
Expert consensus	Strength of consensus +++
Patients with colorectal cancer should be offered cryopreservation of ovarian tissue to protect fertility. The risk of disease recurrence caused by transplantation cannot be excluded and must be discussed with the patient before harvesting ovarian tissue.

Consensus-based Recommendation 6.R66
Expert consensus	Strength of consensus +++
After the onset of puberty, patients with colorectal cancer should be informed about the possibility of cryopreserving oocytes if the start of oncologic therapy can be postponed by at least 2 weeks.

Consensus-based Recommendation 6.R67
Expert consensus	Strength of consensus ++
A GnRH agonist can be administered to patients with colorectal cancer during gonadotoxic therapy.

6.4  Hematologic disease

6.4.1  Lymphomas (Hodgkinʼs and non-Hodgkinʼs lymphoma)

Consensus-based Statement 6.S39
Expert consensus	Strength of consensus +++
With lymphomas, the risk of primary ovarian insufficiency depends on the chemotherapy protocol used.

Consensus-based Recommendation 6.R68
Expert consensus	Strength of consensus +++
Cryopreservation of ovarian tissue to protect fertility must be offered to patients with lymphoma who are expected to have a high risk of premature ovarian insufficiency from oncologic therapy. The risk of ovarian metastasis is low for Hodgkinʼs lymphoma and high for non-Hodgkinʼs lymphoma and Burkittʼs lymphoma.

Consensus-based Recommendation 6.R69
Expert consensus	Strength of consensus +++
After the onset of puberty, patients with lymphoma should be informed about the possibility of cryopreserving oocytes if the start of oncologic therapy can be postponed by at least 2 weeks.

Consensus-based Recommendation 6.R70
Expert consensus	Strength of consensus +++
A GnRH agonist can be administered to patients with lymphoma during gonadotoxic therapy. This can help prevent thrombocytopenic menorrhagia.

6.4.2  Leukemia

6.4.2.1  Acute lymphatic leukemia (ALL)

Consensus-based Statement 6.S40
Expert consensus	Strength of consensus +++
The risk of infertility after treatment for ALL depends on the protocol used for treatment. Women who were treated with a conditioning protocol to prepare them for stem cell transplantation have a high risk of infertility. Patients treated with a conventional protocol have a low risk of infertility.

Consensus-based Statement 6.S41
Expert consensus	Strength of consensus +++
Depending on the dose, cranial irradiation during treatment for ALL can lead to treatable impairment of the hypothalamic-hypophyseal axis.

Consensus-based Recommendation 6.R71
Expert consensus	Strength of consensus ++
Patients with ALL who have a high risk of POI from therapy and who cannot postpone their gonadotoxic therapy can be offered the option of cryopreserving ovarian tissue to protect their fertility.

Consensus-based Recommendation 6.R72
Expert consensus	Strength of consensus +++
The risk of tumor recurrence after autotransplantation of ovarian tissue is considered to be high in patients with ALL, and autotransplantation is therefore not recommended.

Consensus-based Recommendation 6.R73
Expert consensus	Strength of consensus ++
After the onset of puberty, patients with ALL should be informed about the possibility of cryopreserving oocytes if the start of oncologic therapy can be postponed by at least 2 weeks.

Consensus-based Recommendation 6.R74
Expert consensus	Strength of consensus +++
A GnRH agonist can be administered to patients with ALL during gonadotoxic therapy. This can help prevent thrombocytopenic menorrhagia.

6.4.2.2  Acute myeloid leukemia (AML)

Consensus-based Statement 6.S42
Expert consensus	Strength of consensus +++
The risk of infertility after treatment for AML depends on the protocol used for treatment. Women treated with a conditioning protocol to prepare them for stem cell transplantation have a high risk of infertility. Patients treated with a conventional protocol have a low risk of infertility.

Consensus-based Recommendation 6.R75
Expert consensus	Strength of consensus +++
Patients with AML who have a high risk of POI from therapy and who cannot postpone their gonadotoxic therapy can be offered the option of cryopreserving ovarian tissue to protect their fertility.

Consensus-based Recommendation 6.R76
Expert consensus	Strength of consensus +++
The risk of tumor recurrence after autotransplantation of ovarian tissue is considered to be high in patients with AML, and autotransplantation is therefore not recommended.

Consensus-based Recommendation 6.R77
Expert consensus	Strength of consensus +++
After the onset of puberty, patients with AML should be informed about the possibility of cryopreserving oocytes if the start of oncologic therapy can be postponed by at least 2 weeks.

Consensus-based Recommendation 6.R78
Expert consensus	Strength of consensus +++
A GnRH agonist can be administered to patients with AML during gonadotoxic therapy. This can help prevent thrombocytopenic menorrhagia.

6.4.2.3  Chronic myelogenous leukemia (CML)

Consensus-based Statement 6.S43
Expert consensus	Strength of consensus +++
The risk of ovarian insufficiency following the administration of tyrosine kinase inhibitors (TKI) is unclear, with TKI reported to have a teratogenic potential.

Consensus-based Recommendation 6.R79
Expert consensus	Strength of consensus +++
The risk of disease recurrence after autotransplantation of ovarian tissue is considered to be high in patients with CML, and autotransplantation is therefore not recommended.

6.4.2.4  Stem cell transplantation

Consensus-based Recommendation 6.R80
Expert consensus	Strength of consensus +++
Women treated with a conditioning protocol to prepare them for stem cell transplantation have a high risk of infertility. These patients must be informed and receive counseling about methods to protect their fertility.

Consensus-based Recommendation 6.R81
Expert consensus	Strength of consensus ++
After the onset of puberty and before starting conditioning for stem cell transplantation, patients should be informed about the possibility of cryopreserving oocytes if the start of oncologic therapy can be postponed by at least 2 weeks.

Consensus-based Recommendation 6.R82
Expert consensus	Strength of consensus +++
Patients can be offered the option of cryopreserving ovarian tissue to protect fertility before undergoing stem cell transplantation.

8  Malignant Disease in Children and Adolescents

In addition to the established methods to protect fertility before and after treatment for malignant disease mainly targeting post-pubertal boys and girls, experimental methods are also available, particularly for prepubertal children. Listed below are instructions concerning the use of fertility protection methods which need to be taken into account before starting therapy.

Consensus-based Recommendation 8.R92
Expert consensus	Strength of consensus +++
The efficacy of administering drugs for fertility protection (e.g. a GnRH agonist) in childhood or early adolescence is still questionable. GnRH agonists must not be administered to prepubertal patients.

Consensus-based Recommendation 8.R93
Expert consensus	Strength of consensus +++
Depending on the expected radiation dose administered to the ovary, the possibility of ovariopexy must be discussed during the tumor conference. The recommendation for ovariopexy must be discussed with the patient and her family.

Consensus-based Recommendation 8.R94
Expert consensus	Strength of consensus +++
After puberty patients can undergo stimulation treatment to cryopreserve oocytes. This must be done before starting treatment for malignant disease if cancer therapy can be postponed by 2 weeks.

Consensus-based Recommendation 8.R95
Expert consensus	Strength of consensus +++
It is currently not clear what the indications for cryopreserving ovarian tissue from prepubertal and peripubertal girls are. The decision for or against cryopreservation requires the type of therapy and the gonadotoxic dose to be weighed up in each individual case.

Consensus-based Recommendation 8.R96
Expert consensus	Strength of consensus +++
After puberty, potential options for fertility preservation include cryopreserving sperm (ejaculation, electrostimulation, testicular biopsy with testicular sperm extraction [TESE]) and cryopreserving testicular tissue as a fertility reserve for assisted reproduction techniques to be used at a later date. The patient and his family must be informed about these options.

Consensus-based Statement 8.S48
Expert consensus	Strength of consensus +++
The cryopreservation of immature testicular tissue extracted by biopsy before the onset of puberty is still in its experimental stages. The subsequent maturation of sperm from spermatogonial stem cells, which would be necessary for this approach, is currently not yet possible in humans. Transplanting cryopreserved tissue always carries the risk of transplanting malignant cells.

9  Psychological and Ethical Aspects of Fertility Preservation

Consensus-based Statement 9.S49
Expert consensus	Strength of consensus +++
All patients of reproductive age with malignant disease and children with malignant disease and their parents should be offered counseling and advice on fertility protection using a biopsychosocial framework. Information about the options for and the limits of fertility protection should be made available to affected patients both orally and in writing (e.g., in the form of publications like “Die Blauen Ratgeber” – a German series of publications issued by the German Cancer Society) through low-threshold publications which enable patients to make their decisions based on informed consent.

Consensus-based Statement 9.S50
Expert consensus	Strength of consensus +++
During open-ended counseling, the different options and perspectives available must be presented and discussed without bias or preference: oncologic therapy without fertility protection, oncologic therapy after fertility protection measures, and pregnancy, childbirth and starting a family must be discussed in ways that take account of different healing processes and courses of disease.

Appendix to the Guideline

A standard operating procedure (SOP) on managing the contact with a patient before the patient starts oncologic treatment which will reduce their fertility while the patient may still want to have children is included in the appendix of the long (German) version of the guideline, together with leaflets on preserving fertility which were compiled together with the German Cancer Society (DKG).

Guideline Program. Editors.

Leading Professional Medical Associations

German Society of Gynecology and Obstetrics (Deutsche Gesellschaft für Gynäkologie und Geburtshilfe e. V. [DGGG]) Head Office of DGGG and Professional Societies Hausvogteiplatz 12, DE-10117 Berlin info@dggg.de http://www.dggg.de/

President of DGGG Prof. Dr. Birgit Seelbach-Göbel Universität Regensburg Klinik für Geburtshilfe und Frauenheilkunde St. Hedwig-Krankenhaus Barmherzige Brüder Steinmetzstraße 1–3, DE-93049 Regensburg

DGGG Guidelines Representative Prof. Dr. med. Matthias W. Beckmann Universitätsklinikum Erlangen, Frauenklinik Universitätsstraße 21–23, DE-91054 Erlangen

Prof. Dr. med. Erich-Franz Solomayer Universitätsklinikum des Saarlandes Geburtshilfe und Reproduktionsmedizin Kirrberger Straße, Gebäude 9, DE-66421 Homburg

Guidelines Coordination Dr. med. Paul Gaß, Christina Fuchs, Marion Gebhardt Universitätsklinikum Erlangen Frauenklinik Universitätsstraße 21–23 DE-91054 Erlangen fk-dggg-leitlinien@uk-erlangen.de http://www.dggg.de/leitlinienstellungnahmen

Austrian Society of Gynecology and Obstetrics (Österreichische Gesellschaft für Gynäkologie und Geburtshilfe [OEGGG]) Innrain 66A, AT-6020 Innsbruck stephanie.leutgeb@oeggg.at http://www.oeggg.at

President of OEGGG Prof. Dr. med. Petra Kohlberger Universitätsklinik für Frauenheilkunde Wien Währinger Gürtel 18–20, AT-1180 Wien

OEGGG Guidelines Representative Prof. Dr. med. Karl Tamussino Universitätsklinik für Frauenheilkunde und Geburtshilfe Graz Auenbruggerplatz 14 AT-8036 Graz

Prof. Dr. med. Hanns Helmer Universitätsklinik für Frauenheilkunde Wien Währinger Gürtel 18–20, AT-1090 Wien

Swiss Society of Gynecology and Obstetrics (Schweizerische Gesellschaft für Gynäkologie und Geburtshilfe [SGGG]) Gynécologie Suisse SGGG Altenbergstraße 29, Postfach 6, CH-3000 Bern 8 sekretariat@sggg.ch http://www.sggg.ch/

President of SGGG Dr. med. David Ehm FMH für Geburtshilfe und Gynäkologie Nägeligasse 13 CH-3011 Bern

SGGG Guidelines Representative Prof. Dr. med. Daniel Surbek Universitätsklinik für Frauenheilkunde Geburtshilfe und feto-maternale Medizin Inselspital Bern Effingerstraße 102 CH-3010 Bern

Prof. Dr. med. René Hornung Kantonsspital St. Gallen, Frauenklinik Rorschacher Straße 95, CH-9007 St. Gallen