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Radiofrequency ablation (RFA) can be a therapeutic option in medically inoperable lung cancer patients. In

 


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

Management of cancer-related thrombosis in the era of 


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the 2019 ITAC-CME clinical practice guidelines. On 


behalf of the Groupe Francophone Thrombose et Cancer 


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Authors: Rafii H, Frère C, Benzidia I, Crichi B, Andre 


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Marjanovic Z, Ait Abdallah N, Yannoutsos A, Farge D


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