Transbroncheal Novel PDT Peripheral Lung Tumor Ablation With 5-ALA

The primary objective of this study is to develop an innovative photodynamic therapy (PDT) approach for the treatment of peripheral lung tumors. Current treatments for lung tumors (either primary lung cancer or metastases from other malignant tumors) include surgery, chemotherapy (including targeted and immunotherapy), and radiation therapy. The choice of treatment depends on tumor size, stage, genetic profile, and the patient's physical condition to ensure the most appropriate approach. For early-stage peripheral lung tumors, the ongoing goal in medical technology is to develop minimally invasive treatment methods that could potentially replace existing surgical techniques, even those that are minimally invasive. Emerging treatments such as computed tomography (CT)-guided percutaneous ablation, bronchoscopic-guided radiofrequency ablation (RFA), microwave ablation, and photodynamic therapy (PDT) are under active research for minimally invasive management of malignant lung tumors without the need for incisions. PDT uses a specialized photosensitizing drug that selectively accumulates in cancer cells. When exposed to a specific wavelength of light, the drug is activated, generating free radicals that destroy the tumor cells. Currently, PDT is applied to early-stage lung cancers of the central airways or for advanced tumors causing airway obstruction. With advancements in medical technology, electromagnetic navigation bronchoscopy (EMB) in a hybrid operating room (Hybrid OR) can guide photodynamic therapy fibers directly to the tumor site for precise treatment. There are currently three clinical trials (by Concordia in the U.S., Tokyo Medical University in Japan, and National Taiwan University Hospital) investigating PDT for lung cancer. Initial findings from these trials suggest that PDT is safe and effective but has limitations. Though the treatment fibers can be accurately guided to the tumor, the penetration depth of light is limited, reaching only 1.5 to 2 cm in diameter. As a result, multiple guided light exposures are necessary to cover the entire tumor area to achieve complete curative resection, which increases the complexity of the procedure. Light travels in straight lines and, when encountering tissue, undergoes three effects: penetration, absorption, and reflection, which limit its tissue penetration. In 2003, Dr. Friedberg in the U.S. proposed a novel light-exposure method. He infused high-refractive-index substances such as mineral oil into the airways, allowing the light to reflect and propagate along the bronchial walls, enabling greater tissue coverage beyond straight-line transmission. However, mineral oil can cause severe lung inflammation (lipoid pneumonia) if aspirated into the airways, limiting its clinical application. Our research team discovered that Lipiodol, a poppy seed oil mixed with iodine ions (RI: 1.47), widely used in lymphatic imaging and hepatic tumor embolization, could be a suitable substitute for mineral oil. Lipiodol has been used for many years in airway infusion for lung tumor visualization, and while there have been reports of pneumonia as a complication, patients generally recover fully with short-term conventional treatment. Studies have shown that even when infused up to 20 ml via bronchoscopy, Lipiodol does not cause severe complications, making it a promising candidate for novel PDT methods to overcome light penetration limitations. Based on this principle, our research team proposed using electromagnetic navigation bronchoscopy to infuse Lipiodol into the bronchial segment near peripheral lung tumors. By completely enveloping the tumor in Lipiodol, light exposure therapy applied to the proximal airway would allow the light to reach the Lipiodol-infused lung tissue, including the tumor and its supplying microvasculature and lymphatic structures. This would selectively kill the tumor and potential early micro-metastases. We conducted a series of preclinical trials using pigs as models, demonstrating that Lipiodol can be infused into the peripheral lung tumor region via bronchoscopy. Furthermore, PDT with 200 J/cm (400 mW/cm for 500 seconds) was safe in Lipiodol-containing lung tissues. A multicenter U.S. clinical trial (ClinicalTrials.gov Identifier: NCT02916745) is investigating PDT for peripheral lung tumors. In this trial, patients receive an intravenous injection of Photofrin (2 mg/kg) 48 hours before treatment. Using EMB and endobronchial ultrasound (EBUS), the treatment fiber is inserted into the tumor for light exposure (200 J/cm, 400 mW/cm for 500 seconds). By January 2019, five patients had been enrolled with no severe complications reported, confirming the safety and feasibility of this approach. Building on this study, our team proposed a pilot clinical trial to evaluate the safety and effectiveness of our novel PDT method for peripheral lung tumors. From October 2021 to February 2022, three clinical cases were completed, with at least one month of follow-up indicating that the treatment was safe and feasible. All patients successfully completed the treatment without acute severe complications. One patient died six weeks post-treatment due to disease progression, unrelated to treatment complications. The limited treatment effect may be due to the low light dosage used for safety reasons, as tumor reduction was not significant in the follow-up. However, pathology from one patient showed partial tumor necrosis, and the surrounding normal lung tissue exhibited only mild inflammation, indicating that the light exposure method did not cause significant damage to normal tissue and had some therapeutic effect. Further clinical trials are needed to determine the optimal light dosage. In the NCT02916745 trial, two cases received multiple light exposures from different angles (one case with three sessions and another with four), with no significant complications. Dr. Allison reported a case where a patient unable to undergo standard treatment received two light exposures 48 hours apart, with no complications and a positive outcome. Based on our single-session trial from 2022, which showed no complications, we are currently conducting a clinical trial with the same light dosage (confirmed not to cause thermal injury or lung damage) but employing multiple light exposures from different angles. We are also testing additional light exposure 48 hours later to determine the feasibility of this approach. Aside from Sodium Porfimer, other photosensitizers have been approved for PDT, such as 5-Aminolevulinic Acid (5-ALA), which is approved for brain cancer surgery. Like Sodium Porfimer, 5-ALA is a precursor to heme, working through the same photodynamic mechanism. When administered, 5-ALA or Sodium Porfimer accumulates Protoporphyrin IX (PpIX) in certain cells (e.g., cancer cells), and light exposure (630 nm) activates PpIX to generate oxygen free radicals, destroying the tumor tissue. 5-ALA has been approved by the U.S. FDA and Taiwan's FDA for brain cancer surgery, with clinical trials demonstrating its safety in other cancers such as bladder and esophageal cancer. Compared to Sodium Porfimer, 5-ALA has the same therapeutic mechanism but a shorter half-life. It can be taken orally 2-4 hours before treatment, requires only one day of post-treatment light avoidance, and is more cost-effective. This has led us to propose this clinical trial to replace Sodium Porfimer with 5-ALA for our novel PDT approach to treating peripheral lung tumors.