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Clinical Trials/NCT07591532
NCT07591532Not yet recruitingNot Applicable

Retrospective Observational Study on the Prognostic Impact of Pregnancy in Young Women With Breast Cancer Harboring a Germline Pathogenic Variant in Breast Cancer-related Genes Other Than BRCA1/2: the "Beyond BRCA BCY Collaboration"

Jules Bordet Institute0 sites2,200 target enrollmentStarted: June 1, 2026Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
2,200
Primary Endpoint
Cumulative Incidence of Pregnancy After Breast Cancer Diagnosis

Study Overview

Brief Summary

The present study aims to refine the understanding of the prognostic impact of pregnancy after breast cancer in young women harboring germline pathogenic variants in breast cancer susceptibility genes other than BRCA

Detailed Description

This retrospective, multicenter, observational study aims to evaluate the prognostic impact of pregnancy after breast cancer diagnosis in young women harboring germline pathogenic variants in breast cancer susceptibility genes other than BRCA1/2, including TP53, PALB2, PTEN, CDH1, STK11, CHEK2, ATM, BARD1, RAD51C, and RAD51D.

Although pregnancy after breast cancer has been shown to be safe in the overall population of young breast cancer survivors and in carriers of BRCA1/2 pathogenic variants, evidence remains limited for patients with pathogenic variants in other breast cancer susceptibility genes. This knowledge gap represents a relevant unmet need in oncofertility counseling and survivorship care.

The study will include patients diagnosed with stage I-III invasive breast cancer at age 40 years or younger between January 2000 and December 2025. The primary objectives are to assess the prognostic impact of pregnancy after breast cancer diagnosis and to evaluate the cumulative incidence of pregnancy in this population. Secondary objectives include the assessment of pregnancy, fetal, and obstetrical outcomes, the safety of assisted reproductive technology procedures, patterns of care including risk-reducing surgeries, survival outcomes according to clinicopathologic and genetic subgroups, and the occurrence of second primary malignancies.

Data will be collected retrospectively from participating centers within the Beyond BRCA BCY Collaboration.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to 40 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Diagnosis of stage I-III invasive breast cancer between January 2000 and December 2025
  • Age at breast cancer diagnosis ≤40 years
  • Germline pathogenic variant in at least one of the following breast cancer susceptibility genes other than BRCA: TP53, PALB2, PTEN, CDH1, STK11, CHEK2, ATM, BARD1, RAD51C, or RAD51D

Exclusion Criteria

  • Known germline pathogenic variant in breast cancer susceptibility genes without a diagnosis of invasive breast cancer
  • Diagnosis of ovarian cancer or other malignancies without a prior history of invasive breast cancer
  • Diagnosis of invasive breast cancer with germline variants of uncertain significance in breast cancer susceptibility genes
  • De novo stage IV breast cancer

Arms & Interventions

Pregnant cohort

Women with one or more pregnancies any time after breast cancer diagnosis

Non-pregnant cohort

Women with no subsequent pregnancies after breast cancer diagnosis

Outcomes

Primary Outcomes

Cumulative Incidence of Pregnancy After Breast Cancer Diagnosis

Time Frame: Up to 20 years from breast cancer diagnosis

Invasive Disease-Free Survival (iDFS)

Time Frame: Up to 20 years from breast cancer diagnosis

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

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