About this trial
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
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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
Disqualifiers
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
Trial population
Young women diagnosed at age 40 years or younger with stage I-III invasive breast cancer between January 2000 and December 2025 and harboring a germline pathogenic variant in a breast cancer susceptibility gene other than BRCA1/2, including TP53, PALB2, PTEN, CDH1, STK11, CHEK2, ATM, BARD1, RAD51C, and RAD51D.
Trial design
Cohort
Retrospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Cumulative Incidence of Pregnancy After Breast Cancer Diagnosis
Invasive Disease-Free Survival (iDFS)
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: