Abstract
Radiofrequency ablation (RFA) can be a therapeutic
option in medically inoperable lung cancer patients. In
this study, we evaluated a prototype bipolar RFA device
applicator that can be deployed from a standard
endobronchial ultrasound (EBUS) bronchoscope to
determine feasibility and histopathological analysis in
animal models. Rabbit lung cancers were created by
transbronchial injection of VX2 rabbit cancer cells.
Once the tumors were developed, they were ablated
transpleurally, under EBUS guidance using the prototype
RFA device. The animals were then sacrificed for
specimen resection. Pig inflammatory lung pseudo-tumors
and lymphadenopathy were created by transbronchial
injection of a talc paste and ablated transbronchially
under EBUS guidance. Pigs were evaluated at five days,
two weeks, and four weeks following ablation by
bronchoscopy and cone-beam computed tomography before
necropsy. Nicotinamide adenine dinucleotide hydrogen
diaphorase staining was employed to measure the
ablation area. Twenty-four VX2 rabbit tumors were
ablated. The total ablated area ranged from 0.6 to 3.0
cm2 (mean: 1.8 cm2), corresponding to a total energy
range of 1 to 6 kJ. Six pig lung pseudo-tumors and five
mediastinal lymph nodes (LNs) were ablated. Adjacent
airway ulceration was observed in three ablations of
LNs. These airway complications resolved within four
weeks of RFA without any treatment. There was no
hemoptysis, air embolism, respiratory distress, or
other serious complication noted. In these two animal
models, we provide evidence that EBUS-guided bipolar
RFA is feasible and histopathology shows that can
ablate lung tumors and mediastinal lymph nodes under
real-time ultrasound guidance.
PMID: 32057971 [PubMed - as supplied by publisher]
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pubmed: caandvteortroorpul
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