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Not yet recruiting NCT07523464

Centrally Confined 8Gy/1f to Tumor Core Followed by Concurrent Chemoradiotherapy for Unresectable Stage III NSCLC

Phase I Interventional Locally-Advanced Non-Small Cell Lung Cancer Radiotherapy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Centrally Confined 8 Gy/1 Fraction Immune-Priming Radiotherapy to the Tumor Core Followed by Definitive Concurrent Chemoradiotherapy.
Who it may be relevant to
Registry conditions: Locally-Advanced Non-Small Cell Lung Cancer, Radiotherapy. Basic parameters: 18 years — 75 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

A Single-Arm Phase I Clinical Study of Centrally Confined 8 Gy/1 Fraction Immune-Priming Radiotherapy to the Tumor Core Followed by Definitive Concurrent Chemoradiotherapy in Unresectable Stage III Non-Small Cell Lung Cancer

Overview

This is a single-center, prospective, open-label, single-arm phase I exploratory study designed to evaluate the safety and feasibility of a novel central immune-priming radiotherapy strategy in patients with unresectable stage III non-small cell lung cancer (NSCLC). The investigational approach consists of a single 8 Gy/1 fraction radiotherapy dose delivered to the central subregion of the primary tumor, with rapid dose fall-off to keep the peripheral tumor margin dose below 4 Gy, followed by one cycle of PD-(L)1 inhibitor, and then standard concurrent chemoradiotherapy (cCRT) approximately one week later. Patients without disease progression after cCRT will subsequently receive consolidation immune checkpoint inhibitor therapy. The primary objective is to assess the safety and feasibility of this lead-in immune-priming strategy, particularly whether it can be integrated into standard cCRT and subsequent immunotherapy without unacceptable toxicity or treatment delay. The primary endpoint is the dose-limiting toxicity (DLT) rate, with the DLT observation window defined from initiation of the priming radiotherapy to 6-8 weeks after completion of cCRT. Secondary objectives include the on-time initiation rate of cCRT, cCRT completion rate, initiation rate of consolidation immunotherapy, acute and subacute toxicity profile, preliminary efficacy signals, and dynamic changes in peripheral lymphocyte counts. Exploratory analyses will investigate peripheral immune cell subsets, circulating tumor DNA (ctDNA), T-cell receptor (TCR) clonality, cytokine changes, and their associations with toxicity and clinical outcomes. The study will adopt a safety run-in plus expansion design, with an initial cohort of 6 patients and expansion to 24 patients if safety is acceptable.

Interventions

  • Radiation Centrally Confined 8 Gy/1 Fraction Immune-Priming Radiotherapy to the Tumor Core Followed by Definitive Concurrent Chemoradiotherapy
    Centrally Confined 8 Gy/1 Fraction Immune-Priming Radiotherapy to the Tumor Core Followed by Definitive Concurrent Chemoradiotherapy

Primary outcome measures

  • Dose-limiting toxicity (DLT) rate [Time frame: From the start of priming radiotherapy to 6-8 weeks after completion of cCRT]

Eligibility criteria

Inclusion criteria

  • Age 18 to 75 years;
  • Histologically or cytologically confirmed NSCLC;
  • Unresectable stage III disease according to the AJCC 8th edition;
  • Negative for driver gene alterations;
  • Considered suitable for definitive cCRT by MDT discussion or investigator judgment;
  • ECOG performance status 0-1;
  • Presence of a clearly delineable pulmonary primary lesion allowing centrally confined priming treatment planning;
  • Adequate major organ function as required by the study;
  • Willingness to participate and provision of written informed consent.

Exclusion criteria

  • Presence of distant metastasis;
  • Positive driver gene alterations;
  • Prior definitive thoracic radiotherapy or prior systemic antitumor treatment for the current disease;
  • Active autoimmune disease or need for long-term systemic immunosuppressive therapy;
  • Active interstitial lung disease, prior severe radiation pneumonitis, or immune-related pneumonitis;
  • Special primary tumor location such that safety constraints for centrally confined priming radiotherapy cannot be met;
  • Primary lesion immediately adjacent to the main bronchus, carina, major vessels, or esophagus, such that the investigator judges the lead-in intervention to be excessively risky;
  • Pregnancy or lactation;
  • Any other condition that, in the opinion of the investigator, makes the patient unsuitable for this study.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07523464 · 2026ky476

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗