13 Acquired resistance to EGFR inhibition: evolution from adenocarcinoma to small cell lung cancer (SCLC)

Lung Cancer ◽  
2013 ◽  
Vol 79 ◽  
pp. S5
Author(s):  
C. Moss ◽  
P. Cane ◽  
E. Mclean ◽  
G. Santis ◽  
K. Tobal ◽  
...  
2020 ◽  
Vol 16 (21) ◽  
pp. 1537-1547
Author(s):  
Fumio Imamura ◽  
Madoka Kimura ◽  
Yukihiro Yano ◽  
Masahide Mori ◽  
Hidekazu Suzuki ◽  
...  

Aim: Osimertinib is a key drug for EGFR mutation-positive non-small-cell lung cancer (NSCLC). As the hazards ratio of overall survival in comparison with first-generation EGFR-tyrosine kinase inhibitors was almost similar between FLAURA and ARCHER 1050, salvage use of osimertinib is still a treatment option. Patients & methods: We retrospectively analyzed the clinical courses of EGFR mutation-positive NSCLC patients who were potential candidates for salvage osimertinib. Results: Among 524 patients enrolled from five hospitals, 302 patients underwent biopsy, with 52.6% detection rate of T790M. Osimertinib was administered in 93.6% of the T790M-positive patients. The overall response rate and median progression-free survival time of osimertinib were calculated with 147 patients, to be 55.6% and 17.2 months, respectively. Conclusion: Osimertinib is active for T790M-driven acquired resistance in EGFR-mutant NSCLC, but the detection of T790M was unsatisfactory. Clinical Trial Registration: UMIN000028989 (UMIN Clinical Trials Registry)


2021 ◽  
Author(s):  
Hideko Isozaki ◽  
Ammal Abbasi ◽  
Naveed Nikpour ◽  
Adam Langenbucher ◽  
Wenjia Su ◽  
...  

2019 ◽  
Vol 13 (10) ◽  
pp. 1019-1028 ◽  
Author(s):  
Niki Karachaliou ◽  
Jordi Codony-Servat ◽  
Jillian Wilhelmina Paulina Bracht ◽  
Masaoki Ito ◽  
Martyna Filipska ◽  
...  

PLoS ONE ◽  
2016 ◽  
Vol 11 (9) ◽  
pp. e0162925 ◽  
Author(s):  
Fei Yan ◽  
Jiuxia Pang ◽  
Yong Peng ◽  
Julian R. Molina ◽  
Ping Yang ◽  
...  

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