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

2026년 5월 28일 업데이트: 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.

연구 개요

상태

아직 모집하지 않음

상세 설명

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.

연구 유형

관찰

등록 (추정된)

1000

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 어린이
  • 성인

건강한 자원 봉사자를 받아들입니다

아니

샘플링 방법

비확률 샘플

연구 인구

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.

설명

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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

연구는 무엇을 측정합니까?

주요 결과 측정

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

2차 결과 측정

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

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 6월 1일

기본 완료 (추정된)

2030년 5월 31일

연구 완료 (추정된)

2031년 5월 31일

연구 등록 날짜

최초 제출

2026년 5월 20일

QC 기준을 충족하는 최초 제출

2026년 5월 28일

처음 게시됨 (실제)

2026년 5월 29일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 5월 29일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 5월 28일

마지막으로 확인됨

2026년 5월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • v1.0-24/04/2026
  • 101214879 (기타 보조금/기금 번호: HORIZON EUROPE)

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

미정

IPD 계획 설명

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

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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