| Erkrankung: | Brustkrebs (Mammakarzinom) |
| Status der Studie: | Studie rekrutiert |
| Studiendesign: | anderes Design |
| Studienart: | Andere Studienart: Register |
| Haupteinschlusskritieren: | - Patients with histological confirmed breast cancer who are pregnant. - Patients < 40 years with histological confirmed breast cancer who are not pregnant (patients who have been pregnant recently can also be collected into this cohort) - Informed consent for data collection (for prospective participants) and biomaterial collection. For retrospective participants an informed consent is not required as long as the data are anonymously captured. |
| Prüfarzt: | Dr. med. Antje Lehnert |
| Weitere Informationen: | Retrospektiv + prospektiv möglich |