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.
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.
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.
- Conditions
- Cancer, Reproduction, Infertility, Late Effects
- Medical subject headings
- Neoplasms, Infertility
What is being measured
The primary outcome is the main question the study is designed to answer.
Constitution of a harmonized RedCap database
Measured: June 2030
Incidence of azoo/oligozoo/normozoospermia according to the type of cancer treatment.
Measured: 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.
Measured: 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.
Measured: June 2030
Generation of risk categories for sub-fertility and/or hypogonadism
Measured: June 2030
Production of an evidence-based follow-up protocol according to risk categories identified.
Measured: June 2030
Secondary outcomes (12)
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
Frequency of alterations in sperm DNA methylation (target genes)
Subcohort 1
Measured: June 2030
Whole-genome sequencing database including data from subset of patients
Subcohort 2
Measured: June 2030
Database of validated genetic loci and associated with risk of persistent azoo/oligozoospermia and hypogonadism
Subcohort 2
Measured: June 2030
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
Epigenetic clock variations in males following oncological treatments
Subcohort 3
Measured: June 2030
Frequency of Y chromosome loss (mLoY) in males following oncological treatments
Subcohort 3
Measured: 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.
Subcohort 4
Measured: June 2030
Examine decision-making and fertility procedures with anonymous survey to capture lived experiences among AYA cancer survivors.
Subcohort 5
Measured: 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.
Subcohort 4
Measured: June 2030
Examine decision-making and fertility communications with an anonymous survey to capture lived experiences among AYA cancer HCPs.
Subcohort 5
Measured: June 2028
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.
- First posted29 May 2026
- Study start1 Jun 2026 (estimated)
- Primary completion31 May 2030 (estimated)
- Study completion31 May 2031 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for CancerStudies of the same condition, open and under way.
- More trials run by Karolinska InstitutetThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Karolinska Institutet
- Sponsor type
- University, hospital or other
- Collaborators
- Karolinska University Hospital, University of Edinburgh, University of Florence, Linkoeping University, Heidelberg University, Medical University Innsbruck, Ospedale Policlinico San Martino, University of Tartu, University of Leipzig, University of Bern, Université Libre de Bruxelles, Region Stockholm, University of Padova, University of Roma La Sapienza, University Hospital, Rouen, Fundacio Puigvert, Semmelweis University, Lund University, KU Leuven
- Responsible party
- Principal investigator, Kenny Rodriguez-Wallberg, Karolinska Institutet
- Investigators
- Kenny Rodriguez-Wallberg, Prof, MD, Principal investigator, Karolinska Institutet
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.
Study at a glance
From the registry record, last updated by the sponsor on 29 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Frequency and Prediction of Therapy-induced Testicular Dysfunction in AYA Cancer Survivors (ProspectiveMaleAYA)
- ClinicalTrials.gov ID
- NCT07612943
- Acronym / sponsor ID
- FertiTestAYA / v1.0-24/04/2026
- Conditions
- Cancer, Reproduction, Infertility, Late Effects
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 1,000 participants (estimated)
- Lead sponsor
- Karolinska InstitutetUniversity, hospital or other
- Collaborators
- Karolinska University Hospital, University of Edinburgh, University of Florence, Linkoeping University, Heidelberg University, Medical University Innsbruck, Ospedale Policlinico San Martino, University of Tartu, University of Leipzig, University of Bern, Université Libre de Bruxelles, Region Stockholm, University of Padova, University of Roma La Sapienza, University Hospital, Rouen, Fundacio Puigvert, Semmelweis University, Lund University, KU Leuven
- Study start
- 1 Jun 2026 (estimated)
- Primary completion
- 31 May 2030 (estimated)
- Study completion
- 31 May 2031 (estimated)
- First posted
- 29 May 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 15 to 39 years
- Sex
- Male only
- Healthy volunteers
- Not accepted
- Age groups
- 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.
Key inclusion criteria (6 listed)
- 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
Key exclusion criteria (4 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Constitution of a harmonized RedCap database
Time frame: June 2030
Incidence of azoo/oligozoo/normozoospermia according to the type of cancer treatment.
Time frame: 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.
Time frame: 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.
Time frame: June 2030
Generation of risk categories for sub-fertility and/or hypogonadism
Time frame: June 2030
Production of an evidence-based follow-up protocol according to risk categories identified.
Time frame: June 2030
12 secondary outcomes
Frequency of severe sperm DNA fragmentation according to the type of cancer treatment at different time points (pre- and post-therapy)
Time frame: June 2030
Frequency of alterations in sperm DNA methylation (target genes)
Time frame: June 2030
Whole-genome sequencing database including data from subset of patients
Time frame: June 2030
Database of validated genetic loci and associated with risk of persistent azoo/oligozoospermia and hypogonadism
Time frame: June 2030
Validated risk prediction models for chemotherapy induced effects on testicular function pre-post cancer treatment in relation to cancer diagnosis and therapy
Time frame: June 2030
Epigenetic clock variations in males following oncological treatments
Time frame: June 2030
Frequency of Y chromosome loss (mLoY) in males following oncological treatments
Time frame: 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.
Time frame: June 2030
Examine decision-making and fertility procedures with anonymous survey to capture lived experiences among AYA cancer survivors.
Time frame: 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.
Time frame: June 2030
Examine decision-making and fertility communications with an anonymous survey to capture lived experiences among AYA cancer HCPs.
Time frame: June 2028
Examine unmet needs and service gaps with a qualitative interview to capture lived experiences among AYA cancer survivors.
Time frame: June 2028
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 May 2026.
- Individual participant dataSharing planned: Undecided. Upon new ethical approval of additional research, sharing of the study cohort can be allowed.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Kenny Rodriguez-Wallberg, Prof, MD principal investigator
Karolinska Institutet
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.