Actively Recruiting

Age: 18Years +
All Genders
NCT04892849

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

Led by University of Erlangen-Nürnberg Medical School · Updated on 2025-09-17

200

Participants Needed

1

Research Sites

504 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients treatable for head and neck squamous cell carcinoma (palliative), non-small cell lung cancer (palliative or adjuvant), or other solid tumors
  • Indication for systemic therapy with a PD-1/PD-L1 inhibitor according to clinical standards
  • Patients with or without radiation of one or more metastases
  • At least 18 years old
Not Eligible

You will not qualify if you...

  • Diagnosis of melanoma
  • Fertile patients refusing effective contraception during study treatment
  • Persistent drug or alcohol abuse
  • Inability or unwillingness to follow the study protocol
  • Patients in care
  • Inability to speak German
  • Imprisonment by legal or governmental order

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Department of Radiation Oncology, Universitätsklinikum Erlangen

Erlangen, Bavaria, Germany, 91054

Actively Recruiting

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Research Team

M

Markus Hecht, PD Dr.

CONTACT

B

Benjamin Frey, PD Dr. Dr.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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