Skip to content

Genomic and Epigenomic alterations after Cancer treatment In Pregnancy.

Genomic and Epigenomic alterations after Cancer treatment In Pregnancy. - GE-CIP

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON51958
Enrollment
60
Registered
2021-09-24
Start date
2022-06-13
Completion date
Unknown
Last updated
2024-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chemo therapy Pregnancy

Interventions

None listed

Sponsors

UZ Leuven
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: ancer in pregnancy - CT-treated arm (n=150) • Histological proven cancer during pregnancy (any type and stage) • (Former) participation in part I.IA of the CIP-study S25470 (and I.IB for the placental sub study) • Treatment during pregnancy with one or a combination of the following chemotherapeutic agents: - Cyclophosphamide - Anthracyclines - Taxanes - Platinum derivates • Gestational age (GA) at birth >=24 weeks Cancer in pregnancy - CT-untreated arm (n=150) • No treatment during pregnancy or surgery only (subgroup 1) • Radiotherapy and/or systemic treatment (other than CT) during pregnancy (subgroup 2) • GA at birth >=24 weeks

Exclusion criteria

Exclusion criteria: Exclusion criteria for the three study groups • GA at birth

Design outcomes

Primary

MeasureTime frame
determination of potential (sub)chromosomal alterations and/or changes in DNA methylation in cord blood and buccal cells of the newborn, and the association with chemotherapy concentrations measured in respectively placental or newborn tissue.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)