Chemosensitivity During Phases of the Menstrual Cycle in Breast Cancer Patients

ConditionBreast Cancer
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-59
SponsorThe Netherlands Cancer Institute

About this trial

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 criteria

Qualifiers

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

Disqualifiers

Oral contraception (OAC)

Hormonal intra-uterine device (IUD, Mirena)

No ovarian function suppression to preserve fertility

Other forms of hormonal contraception, including but not limited to: nuva-ring, Implanon, prikpil

Trial design

Treatments tested in this trial

  • Blood sample

Treatment groups

100 Participants
are divided into 1 treatment group