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ENB and Photodynamic Therapy in the Treatment for Early Lung Cancer

The Application of Electro-magnetic Navigation Bronchoscopy (ENB) and Photodynamic Therapy in the Treatment for Early Lung Cancer

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03211078
Enrollment
10
Registered
2017-07-07
Start date
2016-10-14
Completion date
2017-09-15
Last updated
2017-07-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer

Keywords

Early lung cancer, Photodynamic therapy, ENB

Brief summary

With the increased incidence of lung cancer and prevalence of low dose CT screening, treating of early lung cancer has becoming an important issue in the clinical practice of thoracic oncology. In this clinical study, the investigators will evaluate whether superDimension (superD) ENB (Electromagnetic navigation bronchoscopy) in combination with interstitial photodynamic therapy can provide the chance of tumor eradication.

Detailed description

Lung cancer is the one the major cause of cancer death all over the world especially in Asia. The prevalence of low dose CT screening has made more patients of lung cancer treated in the early stage. The treatment of choice for of early lung cancer is surgical resection. However, several difficulties exist in surgery for treating early lung cancer. eg. Some presenting as multi-focal lesions, which cannot be completely eradicated by surgical resection. Electromagnetic navigation bronchoscopy (ENB)(superDimension™ Navigation System, super-D ENB) is a novel technique, which uses an image guided localization system to direct steerable bronchoscopic tools to predetermined points within the bronchial tree. This technology allows improved access to peripheral lesions in particular. Photodynamic therapy (PDT) has been adopted an effective treatment option for the central located lung cancer by using photosensitizer which is focally retained in the tumor leading to tumor-specific abrasion by irradiating with a certain wave-length of light. The most frequently used and commercially available photosensitizer for lung cancer is PDT with Photofrin under 623 nm red light irradiation. For the peripheral lung cancer which cannot be approached by bronchoscopy, interstitial PDT with the aids of CT guided catheter implantation has been adopted. However, there are potential disadvantages of such approach including 1) bleeding or hemothorax during CT-guided catheter implantation; 2) dislodging of the catheter after lung collapse in the procedure; 3) unable to treat other lesion after pneumothorax. In the current proposal, the investigators use ENB in combination with PDT to handle to test the feasibility of super-D ENB guided-PDT to treat small lung cancer which cannot be eradicated through surgical resection.

Interventions

PROCEDUREsuper-D ENB guided-PDT

PDT with super-D EBN localization will be given for treating the target lung lesion. Intrvenous photofrin (2mg/kg) will be given 48 hours before intervention. After localization of the tumor by ENB, a 630nm of light will be give for the lesion with the dosage of 2oo J/cm. Intravenous general anesthesia and endobronchial intubation will be performed under the whole procedure.

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Multiple small lung cancer which cannot be completely removed by surgical resection. 2. Patient with small early lung cancer with diameter less than 1 cm and with high surgical risk precluding surgery. 3. Patient with small early lung cancer with diameter less than 1 cm but unwilling to receive surgical intervention. 4. Age above 20 years old and who can do the bronchoscopy test

Exclusion criteria

1\. Bleeding tendency. 2 .Poor cardiopulmonary function with intolerance to bronchoscopy examination.

Design outcomes

Primary

MeasureTime frameDescription
Disease-free survival5 yearsThe time interval between enrollment and the earliest onset of any of the following events,: tumor local recurrence , distant metastasis, and mortality

Secondary

MeasureTime frameDescription
post-operative complication3 monthdefined as any deviation from the normal postoperative course
post-operative pulmonary function6, 12, and 24 monthsthe pulmonary function at 6, 12, and 24 months post-operation
overall survival5 yearsThe time interval between enrollment and death

Countries

Taiwan

Contacts

Primary ContactJang-Ming Lee, MD. PhD.
jmlee@ntu.edu.tw
Backup ContactPeiwen Yang, PhD.
pwy1210@gmail.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026