RecruitingNCT04892849

Clinical Benefit and Biomarker Analysis of Combination of PD-1/PD-L1 Immune Checkpoint Inhibitors and Radiotherapy

Clinical Benefit and Biomarker Analysis of Combination of PD-1/PD-L1 Immune Checkpoint Inhibitors and Radiotherapy in NSCLC, HNSCC and Other Solid Tumors


Sponsor

University of Erlangen-Nürnberg Medical School

Enrollment

200 participants

Start Date

Apr 30, 2021

Study Type

OBSERVATIONAL

Conditions

Summary

Inhibitors of the programmed cell death protein 1 (PD-1)/PD-L1 immune checkpoint signaling pathway are already approved in the treatment of various tumor entities in relapsed or metastatic stages. Different exploratory trials suggest that the combination of radiotherapy and PD-1/PD-L1 inhibitors is highly effective, especially in oligometastatic stages and if all lesions are treated with ablative radiotherapy. In addition, the role of predictive biomarkers is becoming increasingly important for future therapy algorithms. First data, also from our group, indicate clearly that dynamic changes of immune cells and their activation markers in the peripheral blood (immune matrix) can be used as predictive biomarkers. During the planned STICI-02 trial predictive immune matrix derived from the STICI01 trial (NCT03453892) will be validated in the groups of patient suffering from HNSCC (palliative), NSCLC (separately palliative and adjuvant) and "other solid tumors" (including in particular esophageal carcinomas, urothelial and renal carcinomas, small cell bronchial carcinomas and squamous cell carcinomas of the skin \[depending on the current drug approval\]). Within the framework of scientific accompanying projects, the predictive value of markers in tumor tissue and of pattern radiomics analyses will be analyzed accompanying the immunophenotyping in peripheral blood. The side effects


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This observational study is tracking how well PD-1/PD-L1 immunotherapy drugs (checkpoint inhibitors) work for patients with head and neck cancer, lung cancer, or other solid tumors, both alone and combined with radiation therapy. Researchers are also studying biomarkers to understand why some patients respond better than others. **You may be eligible if...** - You are 18 or older with head and neck squamous cell cancer, non-small cell lung cancer, or another solid tumor - Your doctor has recommended a PD-1/PD-L1 immunotherapy drug as part of your standard care - You may or may not be receiving radiation to cancer deposits - You can read and understand German **You may NOT be eligible if...** - You have melanoma - You are not willing to use effective contraception if you are of childbearing potential - You have ongoing serious drug or alcohol abuse - You are under legal custody or imprisoned - You are unwilling or unable to follow the study protocol Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

OTHERConventional Therapy acc. to prevailing clincal approved schemes

The study is observational. The treatment-plan of the underlying disease remains unchanged. The treatment of the patient is according to the prevailing clinical approved schemes at the respective entities. Blood will be drawn from patients at several time points during and after RT and ICI for detailed immunomonitoring of the patients.


Locations(1)

Department of Radiation Oncology, Universitätsklinikum Erlangen

Erlangen, Bavaria, Germany

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT04892849


Related Trials