To Explore the Safety and Efficacy of Hypervision Proton Surgery for Early-stage Non-small Cell Lung Cancer

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAnhui Provincial Cancer Hospital

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

12 Participants
are divided into 1 treatment group

Sponsors and collaborators

Anhui Provincial Cancer Hospital

Lead sponsor

Anhui Provincial Hospital

Sponsor institution

Anhui Provincial Hospital

Collaborator