About this trial

In the past two decades, the evidence-based knowledge on the prevalence and risk factors for gonads impairment, including infertility, following cancer and numerous cancer treatment regimen has significantly increased. However, data remains mostly insufficient for individualized prediction of (future) fertility and pregnancy potential, including the use and success of artificial reproductive technologies (ART). Furthermore, therapies have become increasingly complex as more recent treatment regimen have continuously also implemented novel treatment approaches (e.g. immune therapies such as checkpoint inhibitors) for which no comprehensive data regarding its impact on fertility and pregnancy outcomes is available, yet.

It is crucial to carefully balance risk-benefit between fertility preservation (FP) procedures and potential of gonadal function/fertility impairment, to examine the efficiency and safety, as well as to assess patients' satisfaction regarding the FP procedures. Answering these questionsis highly relevant as it has been shown that fertility capacity and post-treatment gonadal function may represent a significant part of quality of life in young cancer survivors.

The study therefore aim to set up a large-scale registry of emerging data collection programmes to evaluate the gonadotoxic risks, including the prevalence and course of ovarian dysfunction and/or fertility impairment and premature ovarian insufficiency following specific treatments, identification of further risk factors and predictive markers to enhance precision survivorship research in this field. Additionally, data on the use of fertility preservation/hormonal treatment and patients' satisfaction related to these procedures in Europe will be analysed to support patient-centric care.

Reproductive health counselling should not be limited to evaluating the risk of gonadotoxicity and offering fertility preservation to those at risk. It should also include evaluating the impact on post-treatment sexuality, menopausal symptoms management, and the counselling on contraception.

In addition to clinical information, whole genome sequence data will be generated for selected study participants with evidence of varying impact of gonadotoxic therapies on reproductive function to find genetic variants associated with risk of reproductive and organ toxicity.

The data collection will focus on all different cancer diseases, including diseases which are less common such as different types of sarcomas. This will be a significant development to the current state of information in existing registries.

The primary objectives of this prospective analysis of European ongoing adolescent and young adult (AYA) cancer patient cohorts are:

1. To establish a database with relevant clinical characteristics at time of diagnosis, cancer therapy received and post-cancer clinical and reproductive outcomes by following AYA cancer patients longitudinally. 2. To evaluate the effect of cancer therapies on ovarian function and reproductive potential. 3. To evaluate fertility preservation measures performed, their risks and efficacy. 4. To evaluate the impact of fertility preservation measures on the risk of cancer relapse. 5. To evaluate occurrence of pregnancies/live births naturally conceived (including unplanned) or through medical assistance post-cancer and the obstetrical complications and neonatal health following the use of cryopreserved oocytes or gonadal tissue. 6. To set up a genetic database based on whole genome sequencing of AYAs of the cohort. For this objective a Substudy 1 : " Development of risk prediction models based on clinical and genetic data " will be conducted. 7. To develop prediction models for organ toxicities in cancer patients (objective included in Substudy 1). 8. To evaluate the effect of cancer therapies on sexuality and quality of life. For this objective a Substudy 2 : "Sexual Health" will be conducted. 9. To evaluate the use and counselling on contraception. For this objective, a Substudy 3 : "Contraception" will be conducted. 10. To describe management of treatment-induced premature ovarian insufficiency (POI) and menopausal symptoms. For this objective a Substudy 4 "Management of POI and Menopause Symptoms" will be conducted. 11. To explore patient's satisfaction receiving counseling and/or undergoing fertility preservation. For this objective a Substudy 5 on "Satisfaction with Fertility Preservation" will be conducted.

Eligibility criteria

Qualifiers

Female cancer patients aged between 15 and 39 years at diagnosis.

Receiving a diagnosis of primary cancer 01/01/2025 or later

Treated with chemotherapy and/or targeted therapy/immunotherapy and/or radiotherapy/ radioactive iodine therapy and/or gynaecological surgery.

Detailed information on treatment received available.

Disqualifiers

Pre-existing known POI at cancer diagnosis.

Treated by surgery alone (except gynaecological surgery).

Patients with relapse or secondary malignant neoplasms at time of inclusion or having received already treatments for cancer

Adult individuals subject of a measure of legal protection and/or patients with severe mental disorders.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed

Locations

This trial has no locations

Sponsors and collaborators

Karolinska Institutet

Lead sponsor

Region Stockholm

Collaborator

University of Bern

Collaborator

Institut National de la Santé Et de la Recherche Médicale, France

Collaborator

University of Leipzig

Collaborator

Université Libre de Bruxelles

Collaborator

Ospedale Policlinico San Martino

Collaborator

Linkoeping University

Collaborator

University of Tartu

Collaborator

University Hospital Heidelberg

Collaborator

Medical University Innsbruck

Collaborator

University of Edinburgh

Collaborator

Hospital Clínico Universitario de Valencia

Collaborator

Careggi Hospital

Collaborator

University of Genova

Collaborator

Vrije Universiteit Brussel

Collaborator

Aix Marseille Université

Collaborator

Centre Leon Berard

Collaborator

Istituto Europeo di Oncologia

Collaborator

European Union

Collaborator

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Collaborator

Institute of Oncology Ljubljana

Collaborator

University Hospital, Angers

Collaborator

Hopital Antoine Beclere

Collaborator

Universitair Ziekenhuis Brussel

Collaborator