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

2026年5月28日 更新者: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.

調査の概要

状態

まだ募集していません

詳細な説明

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.

研究の種類

観察的

入学 (推定)

1000

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 子
  • 大人

健康ボランティアの受け入れ

いいえ

サンプリング方法

非確率サンプル

調査対象母集団

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.

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

この研究は何を測定していますか?

主要な結果の測定

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

二次結果の測定

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

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年6月1日

一次修了 (推定)

2030年5月31日

研究の完了 (推定)

2031年5月31日

試験登録日

最初に提出

2026年5月20日

QC基準を満たした最初の提出物

2026年5月28日

最初の投稿 (実際)

2026年5月29日

学習記録の更新

投稿された最後の更新 (実際)

2026年5月29日

QC基準を満たした最後の更新が送信されました

2026年5月28日

最終確認日

2026年5月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • v1.0-24/04/2026
  • 101214879 (その他の助成金/資金番号:HORIZON EUROPE)

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

未定

IPD プランの説明

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

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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