RecruitingPhase 2NCT06730295

Elimination of PTV Margins Based on Online Adaptive Stereotactic Radiotherapy for Centrally Located Early-stage Non-small Cell Lung Cancer

Elimination of PTV Margins Based on Online Adaptive Stereotactic Radiotherapy for Centrally Located Early-stage Non-small Cell Lung Cancer: a Prospective, Single-arm, Phase II Study


Sponsor

Sun Yat-sen University

Enrollment

52 participants

Start Date

Dec 10, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This study aims to explore the safety and efficacy of eliminating the PTV (planning target volume) margins based on online adaptive stereotactic radiotherapy for patients with centrally located early-stage non-small cell lung cancer (NSCLC).


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing an adaptive radiation therapy technique for people with early-stage lung cancer located near the center of the chest (centrally located). By using real-time imaging to adapt the radiation field each session, doctors may be able to safely eliminate safety margins around the tumor, potentially reducing side effects to nearby healthy tissue. **You may be eligible if...** - You have confirmed early-stage non-small cell lung cancer (T1-2N0M0) or locally recurrent early-stage NSCLC that cannot be surgically removed (or you choose not to have surgery) - Your tumor is centrally located in the lung - You are 18 or older in good to moderate health (ECOG 0-2) - Your blood counts, kidney, and liver function are within required ranges - Your lung function (FEV1) is at least 0.5 liters **You may NOT be eligible if...** - You have an active infection, had a heart attack within 6 months, or have uncontrolled heart disease - You are pregnant or breastfeeding - You have a substance abuse disorder, chronic alcoholism, or AIDS - You have uncontrolled seizures or severe psychiatric conditions - You have a history of severe allergies Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

RADIATIONOnline adaptive SBRT

Online adaptive SBRT (without PTV expansion margin). The total dose will be 39-42Gy/3 fractions, administered once daily. FBCT and 4DCT will be acquired.


Locations(1)

Sun Yat-sen University Cancer Center

Guangzhou, Guangdong, China

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NCT06730295


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