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BREVITY-02
RNA Disruption Assay (RDA)-Breast Cancer Response Evaluation for Individualized Therapy (BREVITY / BREVITY-02 in Germany)
Brief Summary: The current study aims to provide validation results of RNA Disruption Assay (RDA) as a tumour response assessment tool that uses tumour core biopsies taken starting from 35 +/- 4 days after the initiation of neoadjuvant chemotherapy
Minimum Age: 18 Years
Sex: Female
Inclusion Criteria:
- Women aged at least 18 years;
- Patients must be able to provide informed consent and sign the informed consent form to participate in the RDA study before any study procedures starts;
- Newly diagnosed clinical stage I, II or III breast cancer with complete surgical excision of the breast cancer after neoadjuvant therapy as the treatment goal;
- Tumour size at least 1 cm in one dimension by clinical or radiographic exam (WHO criteria);
- Must have histological confirmation of invasive breast cancer of any subtype or grade;
- Patient is scheduled for neoadjuvant chemotherapy +/- antibodies and +/- other drugs according to Standard of Care;
- Patient willing to have 2 research core needle biopsies (for RDA) taken at 2 collection timepoints during neoadjuvant chemotherapy treatment.
Exclusion Criteria:
- Patient who has had prior local (i.e. surgery or radiotherapy) or systemic (i.e. endocrine or cytotoxic) therapy for the current breast cancer;
- Participation in another interventional clinical trial with concurrent treatment with experimental drugs;
- Stage IV breast cancer;
- Bilateral, multifocal or multicentric breast tumour;
- Prior malignant disease except curatively treated basalioma of the skin or pTis of the cervix uteri;
- Concurrent pregnancy;
- Breast feeding woman;
- Concurrent medical, psychiatric or addictive disorders that may limit the ability to give informed consent or complete the trial;
- Reasons indicating risk of poor compliance with study procedures;
- Patient not able to consent
C-Patrol
Einarmige, prospektive Nicht-interventionelle Studie zur Erfassung von klinischen Therapiedaten und Lebensqualitätsdaten von Patientinnen mit platinsensitivem, BRCA-mutierten Ovarialkarzinomrezidiv unter Olaparibtherapie
Beobachtungsstudie gemäß Arzneimittelgesetz (AMG, §67(6))
OPAL
Registerplattform Mammakarzinom-OPAL:
Treatment and Outcome of Patients with Advanced breast cancer: cLinical research platform for real world data (OPAL)
P4-Studie
Prospektive Studie zur Vorhersage der Rezidivwahrscheinlichkeit nach neo-adjuvanter, Anthrazyklin-basierter Chemotherapie durch PITX2 bei Patientinnen mit Östrogenrezeptor-positivem Brustkrebs (P4-Studie)
PERFORM
PERFORM: An EPidEmiological, PRospective Cohort Study to Generate Real-world Evidence in Patients With HR+/HER2- Advanced Breast Cancer Treated in the First-line Setting as per Current Standard Of Care With an EndocRine-based Palbociclib CoMbination Therapy
Praegnant
Prospektives AkadEmisches translationales Forschungsnetzwerk zur Optimierung der onkoloGischen Versorgungsqualität iN der Adjuvanten und fortgeschritteneN/ meTastasierten Situation: Versorgungsforschung, Pharmakogenetik, Biomarker, Pharmakoökonomie
REGSA
Deutsche prospektive Registerstudie zur Erfassung der Behandlungspraxis von gynäkologischen Sarkomen in der klinischen Routine.
Nicht-interventionelle prospektive Registerstudie (REGSA)
RIBANNA
Eine nicht-interventionelle Studie für postmenopausale Frauen mit einem HR+/HER2- lokal fortgeschrittenen/metastasierten Brustkrebs zur Bewertung der Effektivität des Behandlungsalgorithmus, beginnend mit Kisqali® (RIBociclib) in Kombination mit einem Aromatasehemmer oder mit einer ENdokriNen Therapie oder mit einer ChemotherApie als Erstlinientherapie in der klinischen Routine
SCORE
Nicht-interventionelle Beobachtungsstudie (NIS):
Identifikation von Faktoren zur Ermittlung eines Scores für die Vorhersage der Non-Compliance in der Routinetherapie des rezidivierenden Ovarialkarzinoms mit Ovastat®
Smaragd
SMARAGD – Registerplattform Ovarial-/Endometriumkarzinom
Clinical Research Platform on Ovarian, Fallopian Tube, Primary
Peritoneal, and Endometrial Cancer Treatment and Outcomes