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CancerFertiTestAYANCT07612943

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

An observational study of Cancer and Reproduction, run by Karolinska Institutet.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 15 to 39 years, men only
Conditions the study is for
Cancer, Reproduction, Infertility
How many people
1,000 participants
Where
No sites listed yet
Study dates
1 Jun 2026to 31 May 2031
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 15 to 39 years
  • Men only
  • No healthy volunteers
  • Child, Adult

Study population: 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.

Who may be able to join

  • 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

Who cannot join

  • 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

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Kenny Rodriguez-Wallberg, Prof, MD contact

+46852481213

kenny.rodriguez-wallberg@ki.se

About this study

Official title: 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.

Read the detailed description

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.
Medical subject headings
Neoplasms, Infertility

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Constitution of a harmonized RedCap database

    Measured: June 2030

  2. Incidence of azoo/oligozoo/normozoospermia according to the type of cancer treatment.

    Measured: June 2030

  3. 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.

    Measured: June 2030

  4. 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.

    Measured: June 2030

  5. Generation of risk categories for sub-fertility and/or hypogonadism

    Measured: June 2030

  6. Production of an evidence-based follow-up protocol according to risk categories identified.

    Measured: June 2030

Secondary outcomes (12)
  1. Frequency of severe sperm DNA fragmentation according to the type of cancer treatment at different time points (pre- and post-therapy)

    Subcohort 1

    Measured: June 2030

  2. Frequency of alterations in sperm DNA methylation (target genes)

    Subcohort 1

    Measured: June 2030

  3. Whole-genome sequencing database including data from subset of patients

    Subcohort 2

    Measured: June 2030

  4. Database of validated genetic loci and associated with risk of persistent azoo/oligozoospermia and hypogonadism

    Subcohort 2

    Measured: June 2030

  5. Validated risk prediction models for chemotherapy induced effects on testicular function pre-post cancer treatment in relation to cancer diagnosis and therapy

    Subcohort 2

    Measured: June 2030

  6. Epigenetic clock variations in males following oncological treatments

    Subcohort 3

    Measured: June 2030

  7. Frequency of Y chromosome loss (mLoY) in males following oncological treatments

    Subcohort 3

    Measured: June 2030

  8. Evaluate the general quality of life in male cancer survivors, according to the disease and treatment using the validated questionnaire EORTC-qlq-c30.

    Subcohort 4

    Measured: June 2030

  9. Examine decision-making and fertility procedures with anonymous survey to capture lived experiences among AYA cancer survivors.

    Subcohort 5

    Measured: June 2028

  10. 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.

    Subcohort 4

    Measured: June 2030

  11. Examine decision-making and fertility communications with an anonymous survey to capture lived experiences among AYA cancer HCPs.

    Subcohort 5

    Measured: June 2028

  12. Examine unmet needs and service gaps with a qualitative interview to capture lived experiences among AYA cancer survivors.

    Subcohort 5

    Measured: June 2028

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 May 2026
  2. Study start1 Jun 2026 (estimated)
  3. Primary completion31 May 2030 (estimated)
  4. Study completion31 May 2031 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
1,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07612943
Sponsor's protocol ID
v1.0-24/04/2026
Other IDs
101214879
Acronym
FertiTestAYA
Status last verified
May 2026
First submitted
20 May 2026
Last updated
29 May 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: Upon new ethical approval of additional research, sharing of the study cohort can be allowed.

Questions about this trial

What is this clinical trial studying?

An observational study of Cancer and Reproduction, run by Karolinska Institutet.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 29 May 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Kenny Rodriguez-Wallberg, Prof, MD (+46852481213, kenny.rodriguez-wallberg@ki.se), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Constitution of a harmonized RedCap database (time frame: June 2030). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 May 2026.

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FertiTestAYA Clinical Trial NCT07612943 | AzTrials