An Evaluation of Endobronchial Ultrasound-Transbronchial Needle Aspiration (EBUS-TBNA): Molecular Diagnoses and Patient Satisfaction.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 3/4)
유사 논문P · Population 대상 환자/모집단
306 patients were studied retrospectively, and 39 were studied prospectively, using a questionnaire.
I · Intervention 중재 / 시술
molecular testing
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Clinically, EBUS-TBNA provides genetic diagnoses, which can enable immunotherapy. Patient satisfaction is high, with patients expressing relief after the procedure and finding the staff exceptional.
[BACKGROUND AND AIM] Endobronchial ultrasound-transbronchial needle aspiration (EBUS-TBNA) is a minimally invasive procedure that collects biopsies in patients with mediastinal and/or hilar lymphadeno
- 표본수 (n) 131
- p-value p = 0.004
APA
Wilkinson W, Marshall B, Banerjee A (2026). An Evaluation of Endobronchial Ultrasound-Transbronchial Needle Aspiration (EBUS-TBNA): Molecular Diagnoses and Patient Satisfaction.. Cureus, 18(1), e101092. https://doi.org/10.7759/cureus.101092
MLA
Wilkinson W, et al.. "An Evaluation of Endobronchial Ultrasound-Transbronchial Needle Aspiration (EBUS-TBNA): Molecular Diagnoses and Patient Satisfaction.." Cureus, vol. 18, no. 1, 2026, pp. e101092.
PMID
41658662 ↗
Abstract 한글 요약
[BACKGROUND AND AIM] Endobronchial ultrasound-transbronchial needle aspiration (EBUS-TBNA) is a minimally invasive procedure that collects biopsies in patients with mediastinal and/or hilar lymphadenopathy, often in lung cancer or sarcoidosis. Cancerous biopsies can undergo molecular testing to identify mutations, which may be targeted by immunotherapy. The role of EBUS-TBNA in molecular outcomes has not been studied previously in the United Kingdom. This study also examines patient demographics and satisfaction to comprehensively evaluate EBUS-TBNA. This study aimed to evaluate the EBUS-TBNA service at University Hospital Southampton (UHS), focusing on patient demographics, satisfaction, diagnostic outcomes, procedural statistics, and identifying targetable mutations for immunotherapy.
[METHOD] A total of 306 patients were studied retrospectively, and 39 were studied prospectively, using a questionnaire. Data on their characteristics, reports, diagnoses, and molecular tests were recorded and analyzed using SPSS version 29.
[RESULTS] A total of 47.12% (n = 131) patients were diagnosed with primary lung cancer, 23.38% (n = 65) with sarcoidosis, 9.71% (n = 27) with metastatic cancer, and 1.95% (n = 7) with other diagnoses, such as tuberculosis. Primary lung cancer was categorized as adenocarcinoma (52.31%, n = 68), squamous cell carcinoma (SCC) (25.38%, n = 33), and small cell carcinoma (SCLC) (16.92%, n = 23). Of the primary cancer cases, 60.31% (n = 79) underwent molecular testing. In this cohort, 29.41% (n = 20) of adenocarcinoma cases tested positive for a targetable mutation as follows: 85% (n = 17) were KRAS G12C, and 15% (n = 3) were the EGFR E19del. Overall, 15.27% (n = 20) of EBUS-TBNA procedures for primary lung cancer revealed a clinically actionable variant. Of the 39 patients surveyed, there was a significant difference between the pain experienced (median = 2/10, IQR = 4) and the expected pain (median = 5/10, IQR = 6), as assessed by a Wilcoxon signed-rank test (z = -2.91, p = 0.004). The average staff experience during the EBUS was 9.87/10 (SD = 0.47), and 55.85% (n = 21) waited <1 week for the procedure.
[CONCLUSIONS] EBUS-TBNA's role in diagnosing various conditions, especially primary lung cancer, is clear. Clinically, EBUS-TBNA provides genetic diagnoses, which can enable immunotherapy. Patient satisfaction is high, with patients expressing relief after the procedure and finding the staff exceptional.
[METHOD] A total of 306 patients were studied retrospectively, and 39 were studied prospectively, using a questionnaire. Data on their characteristics, reports, diagnoses, and molecular tests were recorded and analyzed using SPSS version 29.
[RESULTS] A total of 47.12% (n = 131) patients were diagnosed with primary lung cancer, 23.38% (n = 65) with sarcoidosis, 9.71% (n = 27) with metastatic cancer, and 1.95% (n = 7) with other diagnoses, such as tuberculosis. Primary lung cancer was categorized as adenocarcinoma (52.31%, n = 68), squamous cell carcinoma (SCC) (25.38%, n = 33), and small cell carcinoma (SCLC) (16.92%, n = 23). Of the primary cancer cases, 60.31% (n = 79) underwent molecular testing. In this cohort, 29.41% (n = 20) of adenocarcinoma cases tested positive for a targetable mutation as follows: 85% (n = 17) were KRAS G12C, and 15% (n = 3) were the EGFR E19del. Overall, 15.27% (n = 20) of EBUS-TBNA procedures for primary lung cancer revealed a clinically actionable variant. Of the 39 patients surveyed, there was a significant difference between the pain experienced (median = 2/10, IQR = 4) and the expected pain (median = 5/10, IQR = 6), as assessed by a Wilcoxon signed-rank test (z = -2.91, p = 0.004). The average staff experience during the EBUS was 9.87/10 (SD = 0.47), and 55.85% (n = 21) waited <1 week for the procedure.
[CONCLUSIONS] EBUS-TBNA's role in diagnosing various conditions, especially primary lung cancer, is clear. Clinically, EBUS-TBNA provides genetic diagnoses, which can enable immunotherapy. Patient satisfaction is high, with patients expressing relief after the procedure and finding the staff exceptional.
🏷️ 키워드 / MeSH 📖 같은 키워드 OA만
🏷️ 같은 키워드 · 무료전문 — 이 논문 MeSH/keyword 기반
- Chalcone-containing dual-targeting PD-L1/tubulin small molecules: a novel approach for cancer immunotherapy.
- Advances in IL-15-Based Cancer Immunotherapy and Divergent Immunological Effects of IL-2 and IL-15 Signaling via the Shared IL-2Rβγ Receptor.
- Autophagy Modulation in Cancer Immunotherapy, Emerging Molecular Targets and Drug Selection Strategies.
- Aging modulation of the immune system and immunotherapy efficacy in cancer.
- Interplay between natural killer cells and ferroptosis: novel insights in tumor immunity and therapeutic potential.
- Management Dilemma: Myeloperoxidase (MPO)-Positive Vasculitis in a Patient With Metastatic Malignant Melanoma.