Padeliporfin VTP Using Robotic Assisted Bronchoscopy in Peripheral Lung Cancer

Inclusion Criteria: Age ≥18 Patients with primary lung lesions who are at high risk for primary lung cancer. 2.1.Biopsy with intraoperative confirmation of malignancy using on-site cytology will be used as final inclusion prior to study treatment. All patients will be approved by a multi-disciplinary team (thoracic surgery, interventional pulmonology, medical oncology and radiation oncology) as appropriate for bronchoscopic VTP prior to surgical resection. Tumor size targeted for VTP treatment ≤ 2 cm (Part A) and <3cm (Part B), based on CT scan, including solid or semi-solid tumors. EBUS mediastinal staging performed intraoperative prior to VTP treatment with rapid on-site evaluation negative for nodal involvement of malignancy. Tumor is ≥ 2cm from the central bronchial tree (distal 2 cm of the trachea, carina, and named major lobar bronchi up to their first bifurcation) (Timmerman, 2018). Lung lesion is not contiguous with and ≥ 1 cm from the pleura/fissures. Patient is eligible to undergo bronchoscopy under general anesthesia. Tumor is accessible for Padeliporfin VTP treatment via robotic bronchoscopy ECOG performance score 0-2 Estimated life expectancy of ≥3 months Adequate organ system function Negative serum pregnancy test Exclusion Criteria: Patient has a centrally located lung lesion, as defined by RTOG within 2 cm of the proximal bronchial tree, or within 2 cm of other major mediastinal structure (aorta, heart, trachea, pericardium, superior vena cava, pulmonary artery, esophagus, vertebra's body or spinal canal). Patient has a lung lesion located less than 1 cm from the pleura or fissure Patient has a lung cancer lesion >2cm in diameter, for the expansion cohort lesion >2-3 cm Patient has cytologic or histologic evidence of nodal disease Tumor invades major vessels Prior exposure to VTP or PDT treatments Pregnant or breastfeeding women Receiving any other investigational treatment Co-morbidities: Baseline hypoxia with O2 saturation <92% on 2L NC or more of oxygen New York Heart Association (NYHA) stage III/IV heart failure Unstable coronary artery disease or MI within the last 6 months Uncontrollable clinically serious arrhythmia Decompensated/clinically worsening interstitial lung disease or obstructive lung disease. Unstable cerebrovascular or peripheral vascular disease Inability to stop anticoagulation or anti-platelet therapy peri-procedure Evidence of clinically active infection requiring systemic (any route) antibiotic therapy. All prior infections must have resolved following optimal therapy. Patient has any acute or chronic condition assessed as clinically significant by Investigator which may preclude bronchoscopy procedure History of medical or psychiatric disease which, in the view of the investigator, would preclude safe treatment or acceptable study compliance Known severe pulmonary hypertension (mean pulmonary arterial pressure ≥ 50 mmHg) Patient has a cancer diagnosis with active disease requiring further cancer therapy. Patient has had major surgery within the last 4 weeks. Patient has porphyria or hypersensitivity to padeliporfin or porphyrin-like compounds or to any of its excipients.