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Clinical Trials in Taiwan / NCT07396259
Recruiting Observational

Predicting Clinical Efficacy of Immunotherapy Using Pre-treatment andContinuousMonitoring of PD-L1 TPS/CPS on CTCs, and Immunity Exhaustion Scores

NCT07396259 · tracked via the Priya Life Science Taiwan tracker
Phase
Observational
Started
2025-02-25
Last updated
2026-02-09

Condition(s) studied

Circulating Tumor Cells (CTCs)ImmunotherapyPD-L1 ExpressionLiquidbiopsies

Study summary

Head and neck cancer is ranked among the fifth to eighth most prevalent cancers worldwide and is associated with a high mortality rate. Immunotherapy has been established as the first-line standard of care for recurrent and metastatic head and neck cancer. However, patient selection is currently guided by the histological Combined Positive Score (CPS) (KN-048) or Tumor Proportion Score (TPS) (KN-040).

A significant limitation is the inability to re-test tumor tissue when disease status changes necessitate therapeutic adjustment, as new tissue is often unavailable. Consequently, liquid biopsy, which allows for repeatable testing and thus constitutes a dynamic biomarker, becomes crucial. Nevertheless, its definitive role in predicting the efficacy of IT has yet to be thoroughly investigated.

In this study, our team endeavors to define the CPS score of peripheral circulating tumor cells (CTCs) and evaluate the predictive ability of CTC TPS/CPS for clinical response, using objective clinical outcomes as the ultimate measure.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
-Inclusion Criteria: Cancer Subjects- Age: 18 years of age or older. Diagnosis: Confirmed diagnosis of Head and Neck Cancer with plans to undergo immunotherapy. Life Expectancy: Evaluated by a physician to have a life expectancy of at least 3 months. Pathology/Biomarkers: Must have an available tissue biopsy or existing tissue staining results for PD-L1 TPS and/or PD-L1 CPS at this hospital. Healthy Subjects- Health Status: No prior diagnosis of any cancer. Age: 18 years of age or older. -Exclusion Criteria: Mental Health: Presence of psychiatric disorders. Comorbidities: Presence of uncontrolled complications. Logistics: Difficulty with blood collection or unwillingness to comply with follow-up blood draw schedules. Clinical Judgment: Individuals assessed by the physician as unsuitable for enrollment in the study.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Linkou Chang Gung Memorial Hospital Taoyuan City Recruiting

More Chang Gung Memorial Hospital trials in Taiwan

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07396259 on ClinicalTrials.gov ↗ ← All trials in Taiwan