Chemosensitivity During Phases of the Menstrual Cycle in Breast Cancer Patients

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study is a prospective, multicenter study in which a serum sample will be collected at the day of starting neo adjuvant treatment in breast cancer patients

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 59
Healthy Volunteers: f
View:

• Women with a new diagnosis of triple negative breast cancer who have not yet started systemic treatment.

• Patients with stage I-III disease, patient with locoregional recurrence who have not been treated with chemotherapy before. ,

• Aged \< 60 years

• Women having a (regular) physiological menstrual cycle

• Patients who are assigned to receive neoadjuvant chemotherapy with or without immunotherapy, targeted therapy and endocrine therapy

• Patients must be systemic treatment naïve for current malignancy (e.g. no chemotherapy, hormonal therapy or targeted therapy)

• Signed written informed consent

Locations
Other Locations
Netherlands
Antoni van Leeuwenhoek
RECRUITING
Amsterdam
Contact Information
Primary
Sabine Linn, MD
s.linn@nki.nl
+31205129111
Backup
Ingrid Mandjes
i.mandjes@nki.nl
Time Frame
Start Date: 2025-10-14
Estimated Completion Date: 2036-07-15
Participants
Target number of participants: 100
Treatments
Other: Blood sample
Collection of serum blood sample at day of start neo adjuvant treatment
Related Therapeutic Areas
Sponsors
Leads: The Netherlands Cancer Institute

This content was sourced from clinicaltrials.gov