AI Article Synopsis

  • Ultrathin bronchoscopy shows a higher diagnostic yield for small peripheral lung lesions compared to thin bronchoscopy, but the difference in the number of tumor cells in non-small cell lung cancer (NSCLC) remains unclear.
  • A study analyzed data from 175 patients, comparing tumor cell counts from NSCLC lesions using both types of bronchoscopes; the ultrathin group had smaller lesions but similar diagnostic yields.
  • Results indicated no significant differences in maximum tumor cell counts or success rates of genetic analysis between the two techniques, suggesting similar effectiveness for NSCLC sample collection.

Article Abstract

Ultrathin bronchoscopy has been reported to have a higher diagnostic yield than thin bronchoscopy for small peripheral lung lesions in transbronchial biopsy under radial endobronchial ultrasonography (EBUS). However, data comparing the number of tumor cells in non-small cell lung cancer (NSCLC) are limited. We retrospectively compared the number of NSCLC tumor cells in peripheral lung lesions obtained using an ultrathin bronchoscope and a thin bronchoscope with radial EBUS between April 2020 and October 2021. In all patients, we used virtual bronchoscopic navigation (VBN) software, and guide sheaths were used in thin bronchoscopy cases. A total of 175 patients were enrolled in this study. Ultrathin bronchoscopy cases (n = 69) had lesions with a smaller diameter that are more peripherally located compared to thin bronchoscopy cases (n = 106) (median, 25.0 vs. 26.5 mm, mean bronchial generations accessed by bronchoscopy; 4.4±1.2 vs. 3.8±1.0, respectively; p<0.010). There were no significant differences in the overall diagnostic yield (ultrathin vs. thin bronchoscopy cases, 68.1% vs. 72.6%, p = 0.610) or diagnostic yield in only lung cancer cases (78.6% vs. 78.5%, p = 1.000). In histologically NSCLC cases (n = 102), the maximum number of tumor cells per slide as the primary endpoint was similar (average, 307.6±246.7 vs. 328.7±314.9, p = 0.710). The success rate of the Oncomine™ analysis did not differ significantly (80.0% vs. 55.6%, p = 0.247). The yield of NSCLC tumor cells was not different between the samples obtained by the ultrathin bronchoscope and those obtained by the thin bronchoscope.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449145PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0290609PLOS

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