MA15.07 Survival Benefit From Immunocheckpoint Inhibitors in Stage IV Non-small Cell Lung Cancer Patients ≥75 Years Old of Age

2021 ◽  
Vol 16 (10) ◽  
pp. S936
Author(s):  
S. Takamori ◽  
T. Komiya ◽  
E. Powell
2010 ◽  
Vol 28 (15_suppl) ◽  
pp. e18058-e18058
Author(s):  
R. F. Tartari ◽  
C. Abreu Nunes ◽  
J. Moreira ◽  
F. Bortolon ◽  
D. L. Da Silva ◽  
...  

2013 ◽  
Vol 5 (3) ◽  
pp. 1063-1067 ◽  
Author(s):  
RAFAELA FESTUGATTO TARTARI ◽  
JANE MARIA ULBRICH-KULCZYNSKI ◽  
ANTÔNIO FABIANO FERREIRA FILHO

2021 ◽  
pp. e20200584
Author(s):  
Juliana Guarize1 ◽  
Elena Guerini Rocco2 ◽  
Filippo de Marinis3 ◽  
Giulia Sedda4 ◽  
Luca Bertolaccini4 ◽  
...  

Objective: EBUS-TBNA cytological sampling is routinely performed for pathological diagnosis, mediastinal staging, and molecular testing in lung cancer patients. EBUS-TBNA samples are not formally accepted for testing programmed death-ligand 1 (PD-L1) expression. The objective of the study was to compare the feasibility, reproducibility, and accuracy of PD-L1 expression assessment in cytological specimens and histological samples. Methods: We prospectively collected histological (transbronchial forceps biopsy) and cytological (EBUS-TBNA) samples from peribronchial neoplastic lesions during an endoscopic procedure at the same target lesion for the pathological diagnosis and molecular assessment of stage IV non-small cell lung cancer (NSCLC). Results: Fifteen patients underwent the procedure. Adequate cytological samples (at least 100 neoplastic cells) were obtained in 12 cases (92.3%). Assessment of PD-L1 expression was similar between histological and cytological samples (agreement rate = 92%). Sensitivity and diagnostic accuracy of EBUS-TBNA cytological specimens were 88.9% and 100%, respectively. Conclusions: The evaluation of PD-L1 expression in EBUS-TBNA cytological specimens is feasible and presents good reproducibility when compared with routine histological samples. EBUS-TBNA cytological samples could be used for the assessment of PD-L1 expression in patients with NSCLC as a minimally invasive approach in stage IV NSCLC cancer patients.


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