ICK-Breast: Immunotherapy-related CRP Kinetics in Early and Metastatic Triple-negative Breast Cancer

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

ICK-breast is a prospective, multicentric, non-interventional investigator-initiated trial (IIT) that aims to investigate the prognostic value of CRP kinetics in early and advanced or metastatic triple negative breast cancer (TNBC) under immune checkpoint inhibitor (ICI) therapy on pathological complete response (pCR) and event-free survival in early TNBC patients, and objective response rate (ORR), progression-free survival (PFS) and overall survival (OS) in advanced or metastatic TNBC.

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

• women ≥ 18 years of age

• histologically proven early or advanced or metastatic invasive breast cancer irrespective of therapy line

• ER-negative and progesterone receptor (PR)-negative and human epidermal growth factor receptor 2 (HER2)-negative (IHC 0-2+, Fluorescence In Situ Hybridization (FISH) neg.)

• patients with advanced or metastatic disease must be programmed cell death ligand 1 (PD-L1)-positive (IC ≥ 1 or combined positive score (CPS) ≥ 10) in the experimental group

• planned ICI therapy in combination with chemotherapy in the experimental group

• written informed consent into ICK-breast

Locations
Other Locations
Germany
Department of Women's Health
RECRUITING
Tübingen
Contact Information
Primary
Tobias Engler, Dr.
Tobias.Engler@med.uni-tuebingen.de
07071 29 82211
Time Frame
Start Date: 2024-06-01
Estimated Completion Date: 2035-04
Participants
Target number of participants: 225
Treatments
Control Group
Chemotherapy without immunotherapy
Experimental Group
Chemotherapy in combination with immunotherapy
Related Therapeutic Areas
Sponsors
Leads: University Hospital Tuebingen
Collaborators: University Hospital Ulm, University Hospital Freiburg

This content was sourced from clinicaltrials.gov

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