- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07612943
ProspectiveMaleAYA - Frequency and Prediction of Therapy-induced Testicular Dysfunction in AYA Cancer Survivors (FertiTestAYA)
Frequency and Prediction of Therapy-induced Testicular Dysfunction in AYA Cancer Survivors (ProspectiveMaleAYA)
This study describes the ProspectiveMaleAYA cohort, a multicentre, prospective, longitudinal European study designed to investigate the long-term impact of cancer and cancer treatments on reproductive and endocrine health in adolescent and young adult (AYA) male cancer patients. Addressing major gaps in standardized prospective data, particularly for long-term fertility, hypogonadism, and the effects of newer systemic therapies, the study will harmonize data collection across centres and follow patients from diagnosis through post-treatment survivorship.
Comprehensive clinical, oncologic, reproductive, hormonal, biological, and patient-reported outcomes will be collected at predefined intervals to evaluate testicular dysfunction, fertility impairment, oligo/azoospermia, sexual health, and quality of life. Sub-cohorts will enable focused analyses of genetic and epigenetic sperm changes, whole-genome sequencing to identify susceptibility to reproductive and organ toxicity, accelerated aging markers following specific treatments, access to and satisfaction with fertility counselling, and sexual health dysfunctions. The overarching aim is to identify risk factors and predictive markers, develop individualized risk stratification and prediction models, and support precision, patient-centred survivorship care for male AYA cancer survivors.
Aperçu de l'étude
Statut
Les conditions
Description détaillée
In the past two decades, knowledge regarding the gonadotoxicity of cancer treatments and their impact on fertility and pregnancy outcomes has expanded. However, prospective, standardized, longitudinal data remain largely unavailable, particularly for:
- long-term endocrine and reproductive outcomes,
- effects of novel systemic therapies (e.g., immunotherapy, targeted therapies)
To address this gap, we will conduct a prospective, multicentre, longitudinal cohort study (ProspectiveMaleAYA cohort) in adolescent and young adult (AYA) male cancer patients.
Participants will be enrolled for this study after having received a diagnosis of primary cancer (no relapse or secondary cancers) and if they will receive or are already receiving oncological treatment. Clinical, oncologic, reproductive, endocrine, biological and patient-reported data will be collected at predefined follow-up intervals. Substudies including analyses of biological materials will be conducted in sub-cohorts.
The study aims to harmonize data collection across participating European centres and to set up a large-scale network structure of emerging data collection programmes to evaluate the gonadotoxic risk, including the prevalence and course of testicular dysfunction and/or fertility impairment and oligo/azoospermia following specific treatments, identification of further risk factors and predictive markers to enhance precision survivorship research in this field. In addition to clinical information, whole genome sequencing data will be generated for selected individuals with evidence of varying impact of gonadotoxic therapies on reproductive function. The aim is to find genetic variants associated with risk of reproductive and organ toxicity, and to build and enhance individual predictive risk models for gonadotoxic therapies. Additionally, data on sexual health, quality of life and subjective health status shall be analysed to support patient-centric care.
The objectives of this prospective analysis of European adolescent and young adult (AYA) cancer patient cohorts are:
- Establish harmonized prospective databases with relevant clinical characteristics at time of diagnosis, cancer therapy received and post-cancer clinical and reproductive outcomes by following AYA cancer patients longitudinally.
- Evaluate the impact of cancer treatment on long-term fertility according to cancer type, patient characteristics (pre- and post-treatment) and treatment modalities in a male AYA population
- Establish predictive parameters for the recovery of spermatogenesis and for the later development of hypogonadism
- Classification of patients into low-, medium- and high-risk groups for the development of hypogonadism and infertility.
For specific sub-cohorts, the following objectives are planned:
- Sub-cohort 1: Determine the duration of genetic/epigenetic alterations in spermatozoa to define the minimum time-period after AYA cancer treatment to attempt safe conception.
- Sub-cohort 2: i) To set up a genetic database based on whole genome sequencing of AYAs of the cohort; ii) To evaluate the role of genetic background on determining persistent damage to testicular function (reproductive and endocrine); iii) To develop prediction models for organ toxicities in cancer patients.
- Sub-cohort 3: i) To test and evaluate the magnitude of accelerated aging following oncological treatments BEP (testicular cancer) or ABVD (Hodgkin lymphoma) through epigenetic clock and mosaic Y chromosome loss (mLoY); ii) To assess the role of clinical and the genetic factors in accelerated aging following oncological treatments.
- Sub-cohort 4: Evaluate the frequency and entity of sexual health dysfunctions in male cancer survivors, according to the disease and treatment.
- Sub-cohort 5: Mapping access and barriers to reproductive counseling and FP, and evaluating the satisfaction with these programs.
Type d'étude
Inscription (Estimé)
Contacts et emplacements
Coordonnées de l'étude
- Nom: Kenny Rodriguez-Wallberg, Prof, MD
- Numéro de téléphone: +46852481213
- E-mail: kenny.rodriguez-wallberg@ki.se
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
- Adulte
Accepte les volontaires sains
Méthode d'échantillonnage
Population étudiée
Multi-center study on European AYA patient cohorts.
Prospective observational multicohort study including male AYA cancer patients enrolled after a diagnosis of primary cancer and followed at 1, 2 and 3 years post diagnosis.
The cohort database will be maintained to allow additional follow-up >3 years after reconsent to allow for further longitudinal research.
The subjects will be recruited at ~16 European Centres with expertise in oncofertility.
La description
Inclusion Criteria:
- Subjects with male internal and external genitalia
- Age at cancer diagnosis 15-39 years old
- Subjects planned to or having received oncologic treatment
- Subjects able to provide semen sample
- Information available on cancer treatment and medical history
- Patients (or parents in case of minors) who signed informed consent
Exclusion Criteria:
- individuals presenting with relapse or secondary cancers at time of inclusion
- subjects who were not treated with oncological treatment
- subjects who underwent bilateral orchiectomy
- patients with a diagnosis of azoospermia or testicular failure previously to cancer diagnosis
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
Constitution of a harmonized RedCap database
Délai: June 2030
|
June 2030
|
|
Incidence of azoo/oligozoo/normozoospermia according to the type of cancer treatment.
Délai: June 2030
|
June 2030
|
|
Incidence of overt and compensated hypogonadism according to the type of cancer treatment through the measurement of Testosterone, LH, FSH (Inhibin B) pre/post treatment.
Délai: June 2030
|
June 2030
|
|
Correlation between hormonal values /routine sperm parameters and clinical characteristics (testis volume, andrological history) at baseline with the development of azoo/oligozoospermia and/or hypogonadism post-therapy according to the type of treatment.
Délai: June 2030
|
June 2030
|
|
Generation of risk categories for sub-fertility and/or hypogonadism
Délai: June 2030
|
June 2030
|
|
Production of an evidence-based follow-up protocol according to risk categories identified.
Délai: June 2030
|
June 2030
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Frequency of severe sperm DNA fragmentation according to the type of cancer treatment at different time points (pre- and post-therapy)
Délai: June 2030
|
Subcohort 1
|
June 2030
|
|
Frequency of alterations in sperm DNA methylation (target genes)
Délai: June 2030
|
Subcohort 1
|
June 2030
|
|
Whole-genome sequencing database including data from subset of patients
Délai: June 2030
|
Subcohort 2
|
June 2030
|
|
Database of validated genetic loci and associated with risk of persistent azoo/oligozoospermia and hypogonadism
Délai: June 2030
|
Subcohort 2
|
June 2030
|
|
Validated risk prediction models for chemotherapy induced effects on testicular function pre-post cancer treatment in relation to cancer diagnosis and therapy
Délai: June 2030
|
Subcohort 2
|
June 2030
|
|
Epigenetic clock variations in males following oncological treatments
Délai: June 2030
|
Subcohort 3
|
June 2030
|
|
Frequency of Y chromosome loss (mLoY) in males following oncological treatments
Délai: June 2030
|
Subcohort 3
|
June 2030
|
|
Evaluate the general quality of life in male cancer survivors, according to the disease and treatment using the validated questionnaire EORTC-qlq-c30.
Délai: June 2030
|
Subcohort 4
|
June 2030
|
|
Examine decision-making and fertility procedures with anonymous survey to capture lived experiences among AYA cancer survivors.
Délai: June 2028
|
Subcohort 5
|
June 2028
|
|
Evaluate the frequency and entity of sexual health dysfunctions in male cancer survivors, according to the disease and treatment using the validated questionnaire EORTC-SH22.
Délai: June 2030
|
Subcohort 4
|
June 2030
|
|
Examine decision-making and fertility communications with an anonymous survey to capture lived experiences among AYA cancer HCPs.
Délai: June 2028
|
Subcohort 5
|
June 2028
|
|
Examine unmet needs and service gaps with a qualitative interview to capture lived experiences among AYA cancer survivors.
Délai: June 2028
|
Subcohort 5
|
June 2028
|
Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Les enquêteurs
- Chercheur principal: Kenny Rodriguez-Wallberg, Prof, MD, Karolinska Institutet
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- v1.0-24/04/2026
- 101214879 (Autre subvention/numéro de financement: HORIZON EUROPE)
Plan pour les données individuelles des participants (IPD)
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Description du régime IPD
Informations sur les médicaments et les dispositifs, documents d'étude
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