About this trial
This study was a single-center, single-arm clinical study to evaluate the safety and efficacy of hypervision proton surgery with single large fractionated doses (34GyE and 39GyE) in the treatment of early peripheral NSCLC.
Eligibility criteria
Qualifiers
The patient must be at least 18 years old
Karnofsky Performance Status > 80
NSCLC confirmed by cytology or histology; for subjects who cannot safely obtain pathological evidence due to factors such as tumor lesion location, patient's underlying diseases, or high puncture risk, after unanimous consent of the multidisciplinary team (MDT) discussion, they meet the clinical diagnostic criteria for NSCLC based on typical imaging features (such as enhanced chest CT and/or PET/CT) combined with clinical manifestations;
Early-stage tumors are defined as T1 (≤3cm) N0M0 based on enhanced computed tomography (CT) and positron emission tomography (PET)
Disqualifiers
Other malignant tumors occurred concurrently within 2 years before enrollment
A history of chest radiotherapy in the past
It is planned to use other anti-tumor treatments within the regimen treatment (within 4 weeks)
Trial design
Treatments tested in this trial
- Hypervision proton surgery
Treatment groups
Sponsors and collaborators
Anhui Provincial Cancer Hospital
Lead sponsor
Anhui Provincial Hospital
Sponsor institution
Anhui Provincial Hospital
Collaborator