Ireland
--:--IST
Recruiting Not applicable

Phase I Study of Carbon-Ion Lattice Radiotherapy for Large Thoracic Tumors

NCT07744074 · tracked via the Priya Life Science China tracker
Phase
Not applicable
Started
2026-05-26
Last updated
2026-08-04

Condition(s) studied

Carbon Ion Radiotheray

Investigational drug(s) / intervention(s)

Carbon ion - Lattice radioIon Lattice Radiation Therapy for Thoracic bulky solid tumors

Carbon ion - Lattice radioIon Lattice Radiation Therapy for Thoracic bulky solid tumors: Carbon ion - Lattice radioIon Lattice Radiation Therapy for Thoracic bulky solid tumors

Study summary

This is the first prospective clinical study to evaluate the efficacy and safety of induction chemoimmunotherapy followed by carbon ion radiotherapy and consolidation immunotherapy in patients with unresectable locally advanced non-small cell lung cancer (NSCLC). Based on this prospective study, tumor tissue, blood, urine, and stool samples from participants will be collected and analyzed to identify predictive markers of treatment response.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Age ≥ 18 years old; 2. Pathologically confirmed thoracic solid malignant tumors; 3. Local recurrence or failure of prior standard therapies (including surgery, radiotherapy, systemic therapy, etc.), deemed unsuitable for or lacking standard treatment options following Multidisciplinary Team (MDT) evaluation, and planned to receive heavy-ion radiotherapy; 4. Maximum diameter of the target lesion ≥ 4.5 cm; 5. Eastern Cooperative Oncology Group (ECOG) performance status of 0-2; 6. Life expectancy ≥ 6 months; 7. Signed informed consent. Exclusion Criteria: 1. Tumors adjacent to critical organs at risk (OARs) where dose constraints cannot be met through plan optimization; 2. Prior radiotherapy to the intended treatment area, where re-irradiation would fail to meet normal tissue dose constraints; 3. Presence of recognized standard treatment options for which the patient is eligible (e.g., radical surgery, concurrent chemoradiotherapy, or standard systemic therapy); 4. Primary hematologic malignancies; 5. Uncontrolled severe comorbidities, including active infections, unstable cardiovascular or cerebrovascular diseases, and severe hepatic or renal insufficiency; 6. Other diseases deemed by the investigator to compromise patient safety; 7. Psychiatric disorders or cognitive impairment that would prevent cooperation with treatment; 8. Pregnancy or lactation.

Primary outcome measure(s)

  • Dose-Limiting Toxicities — 90 days
    To determine the dose-limiting toxicities (DLTs) of carbon ion - lattice radiotherapy (CI-LRT) in this population.

Trial sites (1)

FacilityCityRegionStatus
Zhejiang Cancer Hospital Hangzhou Zhejiang Recruiting
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 NCT07744074 on ClinicalTrials.gov ↗ ← All trials in China