Immune-Marker Platform for Patients With Advanced Lung Cancer

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorTechnische Universität Dresden

About this trial

The goal of this observational study is to better understand how the immune system and certain tumor markers are linked to treatment response in patients with advanced non-small cell lung cancer (NSCLC) who receive immunochemotherapy.

The investigators aim to answer the following questions:

* Can the investigators successfully analyze immune markers and gene activity from small tumor samples (biopsies)? * Are these markers connected to how well patients respond to immunochemotherapy and how their disease progresses?

What will participants do?

* Provide tumor tissue samples (biopsies) at key points: before treatment, about 6 weeks after starting immunochemotherapy, and if the cancer grows or treatment changes. * Allow their tumor samples to be analyzed in the lab using advanced techniques to measure immune and genetic markers. * Share clinical information (such as treatment response and disease progression) so investigators can study how it relates to these markers.

This study does not test a new drug or treatment.

Eligibility criteria

Qualifiers

Written informed consent of the patient

Consent of participation in the national Network for Genomic Medicine in Lung Cancer (nNGM)

Advanced lung cancer with non-curative treatment option (NSCLC)

No targetable driver mutation detected, defined as no targetable drive mutation in ALK, EGFR, BRAF, HER2, MET, NTRK, RET, ROS1

Disqualifiers

Any condition representing an unjustified risk for obtaining an additional biopsy sample (if needed) in the view of the investigator

Incapability of understanding the purpose and possible consequences of the trial

Substance abuse, medical, psychological or social conditions that may interfere with the subject's cooperation with the requirements of the trial or evaluation of the study results

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

500 Participants
are grouped into 2 trial groups

Sponsors and collaborators

Technische Universität Dresden

Lead sponsor

Deutsche Krebshilfe e.V., Bonn (Germany)

Collaborator

Universitätsklinikum Köln

Collaborator