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ProspectiveMaleAYA - Frequency and Prediction of Therapy-induced Testicular Dysfunction in AYA Cancer Survivors (FertiTestAYA)

28. Mai 2026 aktualisiert von: Kenny Rodriguez-Wallberg, Karolinska Institutet

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.

Studienübersicht

Status

Noch keine Rekrutierung

Detaillierte Beschreibung

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.

Studientyp

Beobachtungs

Einschreibung (Geschätzt)

1000

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Kind
  • Erwachsene

Akzeptiert gesunde Freiwillige

Nein

Probenahmeverfahren

Nicht-Wahrscheinlichkeitsprobe

Studienpopulation

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.

Beschreibung

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

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
Constitution of a harmonized RedCap database
Zeitfenster: June 2030
June 2030
Incidence of azoo/oligozoo/normozoospermia according to the type of cancer treatment.
Zeitfenster: 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.
Zeitfenster: 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.
Zeitfenster: June 2030
June 2030
Generation of risk categories for sub-fertility and/or hypogonadism
Zeitfenster: June 2030
June 2030
Production of an evidence-based follow-up protocol according to risk categories identified.
Zeitfenster: June 2030
June 2030

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Frequency of severe sperm DNA fragmentation according to the type of cancer treatment at different time points (pre- and post-therapy)
Zeitfenster: June 2030
Subcohort 1
June 2030
Frequency of alterations in sperm DNA methylation (target genes)
Zeitfenster: June 2030
Subcohort 1
June 2030
Whole-genome sequencing database including data from subset of patients
Zeitfenster: June 2030
Subcohort 2
June 2030
Database of validated genetic loci and associated with risk of persistent azoo/oligozoospermia and hypogonadism
Zeitfenster: 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
Zeitfenster: June 2030
Subcohort 2
June 2030
Epigenetic clock variations in males following oncological treatments
Zeitfenster: June 2030
Subcohort 3
June 2030
Frequency of Y chromosome loss (mLoY) in males following oncological treatments
Zeitfenster: 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.
Zeitfenster: June 2030
Subcohort 4
June 2030
Examine decision-making and fertility procedures with anonymous survey to capture lived experiences among AYA cancer survivors.
Zeitfenster: 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.
Zeitfenster: June 2030
Subcohort 4
June 2030
Examine decision-making and fertility communications with an anonymous survey to capture lived experiences among AYA cancer HCPs.
Zeitfenster: June 2028
Subcohort 5
June 2028
Examine unmet needs and service gaps with a qualitative interview to capture lived experiences among AYA cancer survivors.
Zeitfenster: June 2028
Subcohort 5
June 2028

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. Juni 2026

Primärer Abschluss (Geschätzt)

31. Mai 2030

Studienabschluss (Geschätzt)

31. Mai 2031

Studienanmeldedaten

Zuerst eingereicht

20. Mai 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

28. Mai 2026

Zuerst gepostet (Tatsächlich)

29. Mai 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

29. Mai 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

28. Mai 2026

Zuletzt verifiziert

1. Mai 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • v1.0-24/04/2026
  • 101214879 (Andere Zuschuss-/Finanzierungsnummer: HORIZON EUROPE)

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

UNENTSCHIEDEN

Beschreibung des IPD-Plans

Upon new ethical approval of additional research, sharing of the study cohort can be allowed.

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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