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Earlier Detection and Optimization of Treatment and Prognosis for Patients With Early-onset Colorectal Cancer (BIO-EOCRC)

Netherlands Cancer Institute (NKI) logo

Netherlands Cancer Institute (NKI)

Status

Enrolling

Conditions

Early-onset Colorectal Cancer

Treatments

Other: No intervention; observational

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The study aims to collect high quality clinical data on lifestyle and patient biomaterials prior to start or during / after treatment of early-onset colorectal cancer (EOCRC) and to inform on treatment and survival outcomes of EOCRC patients.

Full description

The current study will be complementary to COMPRAYA, a prospective cohort study focused on risk factors of impaired medical and psychosocial outcomes of adolescents and young adults with cancer (AYA) and to GENAYA, focused on genetic testing of AYA. The collected data and materials will be essential for an in-depth analysis of the epidemiology, exposomes and pathophysiology of EOCRC and compare this with average-onset CRC (AOCRC) and healthy controls. These data will facilitate multiomics studies and the identification of high-risk profiles and blood- and/or stool-based biomarkers, which in turn will enable the development of prevention and early detection strategies to ultimately improve prognosis and the prevalence, risk factors and mechanisms of impaired health outcomes (short- and long-term medical and psychosocial effects and late effects) over time among EOCRC patients wil be examined.

Enrollment

300 estimated patients

Sex

All

Ages

18 to 49 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with locoregional or metastatic colorectal cancer (CRC)
  • Histologically proven CRC
  • Age 18 - 49 years at time of first CRC diagnosis
  • Able to understand the informed consent form
  • Provide written informed consent.

Exclusion criteria

  • Mentally incompetent patients based on the opinion of treating physician
  • Inability to understand the Dutch language

Trial contacts and locations

1

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Central trial contact

Ruud Weijer, PhD

Data sourced from clinicaltrials.gov

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