About this trial
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 early-stage non-small cell lung cancer (NSCLC) or pulmonary oligometastases.
Eligibility criteria
Qualifiers
Histologically or PET-CT confirmed untreated early-stage non-small cell lung cancer (T1-2N0M0) that is inoperable or where the patient is unwilling to undergo surgery, or PET-CT/chest CT confirmed lung oligometastases (number of metastases ≤3, single lesion diameter ≤5cm).
Age 18 years or older, regardless of gender.
ECOG performance status score of 0-2.
Serum hemoglobin ≥ 80 g/L, platelets ≥ 100,000/μL, absolute neutrophil count ≥ 1,500/μL.
Disqualifiers
Tumors with bronchial invasion are excluded.
Any other disease or condition that contraindicates radiotherapy (e.g., active infections, within 6 months post-myocardial infarction, symptomatic heart disease including unstable angina, congestive heart failure, or uncontrolled arrhythmias).
Pregnant or breastfeeding women, women who have not undergone pregnancy testing, and pregnant individuals.
Individuals with substance abuse issues, chronic alcoholism, or AIDS.
Trial design
Treatments tested in this trial
- Online adaptive SBRT
- Conventional SBRT