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

Last updated: September 10, 2025
Sponsor: University of Erlangen-Nürnberg Medical School
Overall Status: Active - Recruiting

Phase

N/A

Condition

Carcinoma

Head And Neck Cancer

Urothelial Carcinoma

Treatment

Conventional Therapy acc. to prevailing clincal approved schemes

Clinical Study ID

NCT04892849
ST-ICI02
  • Ages > 18
  • All Genders

Study 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 Criteria

Inclusion

Inclusion Criteria:

  • Patients treatable for HNSCC (palliative), NSCLC (separately palliative andadjuvant) or "other solid tumour"

  • Indication for system therapy with a PD-1/PD-L1 inhibitor according to clinicalstandards

  • Patients without or with radiation of one or more metastases

  • Age at least 18 years

Exclusion

Exclusion Criteria:

  • Melanoma patients

  • Fertile patients who refuse effective contraception during study treatment

  • Persistent drug and/or alcohol abuse

  • Patients not able or willing to behave according to study protocol

  • Patients in care

  • Patients that are not able to speak German

  • Patients which are imprisoned according to legal or governmental order

Both gender are included into the study, a maximum age was not defined.

Study Design

Total Participants: 200
Treatment Group(s): 1
Primary Treatment: Conventional Therapy acc. to prevailing clincal approved schemes
Phase:
Study Start date:
April 30, 2021
Estimated Completion Date:
December 31, 2030

Connect with a study center

  • Department of Radiation Oncology, Universitätsklinikum Erlangen

    Erlangen, Bavaria 91054
    Germany

    Site Not Available

  • Department of Radiation Oncology, Universitätsklinikum Erlangen

    Erlangen 2929567, Bavaria 2951839 91054
    Germany

    Active - Recruiting

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