-
1
-
-
79953118839
-
Genotypic and histological evolution of lung cancers acquiring resistance to EGFR inhibitors
-
75ra26
-
Sequist, L.V., Waltman, B.A., Dias-Santagata, D., et al. Genotypic and histological evolution of lung cancers acquiring resistance to EGFR inhibitors. Sci. Transl. Med., 3(March (75)), 2011 75ra26.
-
(2011)
Sci. Transl. Med.
, vol.3
, Issue.March (75)
-
-
Sequist, L.V.1
Waltman, B.A.2
Dias-Santagata, D.3
-
2
-
-
84877100240
-
Analysis of tumor specimens at the time of acquired resistance to EGFR-TKI therapy in 155 patients with EGFR-mutant lung cancers
-
Yu, H.A., Arcila, M.E., Rekhtman, N., et al. Analysis of tumor specimens at the time of acquired resistance to EGFR-TKI therapy in 155 patients with EGFR-mutant lung cancers. Clin. Cancer Res. 19 (2013), 2240–2247.
-
(2013)
Clin. Cancer Res.
, vol.19
, pp. 2240-2247
-
-
Yu, H.A.1
Arcila, M.E.2
Rekhtman, N.3
-
3
-
-
84930755018
-
Acquired EGFR C797S mutation mediates resistance to AZD9291 in non-small cell lung cancer harboring EGFR T790M
-
Thress, K.S., Paweletz, C.P., Felip, E., et al. Acquired EGFR C797S mutation mediates resistance to AZD9291 in non-small cell lung cancer harboring EGFR T790M. Nat. Med. 21 (2015), 560–562.
-
(2015)
Nat. Med.
, vol.21
, pp. 560-562
-
-
Thress, K.S.1
Paweletz, C.P.2
Felip, E.3
-
4
-
-
84987849616
-
Acquired resistance of EGFR-mutant lung cancer to a T790M-specific EGFR inhibitor: emergence of a third mutation (C797S) in the EGFR tyrosine kinase domain
-
Yu, H.A., Tian, S.K., Drilon, A.E., et al. Acquired resistance of EGFR-mutant lung cancer to a T790M-specific EGFR inhibitor: emergence of a third mutation (C797S) in the EGFR tyrosine kinase domain. JAMA Oncol. 1 (2015), 982–984.
-
(2015)
JAMA Oncol.
, vol.1
, pp. 982-984
-
-
Yu, H.A.1
Tian, S.K.2
Drilon, A.E.3
-
5
-
-
84973438966
-
High MET amplification level as a resistance mechanism to osimertinib (AZD9291) in a patient that symptomatically responded to crizotinib treatment post-osimertinib progression
-
Ou, S.H., Agarwal, N., Ali, S.M., High MET amplification level as a resistance mechanism to osimertinib (AZD9291) in a patient that symptomatically responded to crizotinib treatment post-osimertinib progression. Lung Cancer 98 (2016), 59–61.
-
(2016)
Lung Cancer
, vol.98
, pp. 59-61
-
-
Ou, S.H.1
Agarwal, N.2
Ali, S.M.3
-
6
-
-
84974625022
-
Circulating tumour DNA profiling reveals heterogeneity of EGFR inhibitor resistance mechanisms in lung cancer patients
-
Chabon, J.J., Simmons, A.D., Lovejoy, A.F., et al. Circulating tumour DNA profiling reveals heterogeneity of EGFR inhibitor resistance mechanisms in lung cancer patients. Nat. Commun., 7(June), 2016, 11815.
-
(2016)
Nat. Commun.
, vol.7
, Issue.June
, pp. 11815
-
-
Chabon, J.J.1
Simmons, A.D.2
Lovejoy, A.F.3
-
7
-
-
84938597193
-
Emergence of RET rearrangement co- existing with activated EGFR mutation in EGFR-mutated NSCLC patients who had progressed on first- or second-generation EGFR TKI
-
Klempner, S.J., Bazhenova, L.A., Braiteh, F.S., et al. Emergence of RET rearrangement co- existing with activated EGFR mutation in EGFR-mutated NSCLC patients who had progressed on first- or second-generation EGFR TKI. Lung Cancer 89 (2015), 357–359.
-
(2015)
Lung Cancer
, vol.89
, pp. 357-359
-
-
Klempner, S.J.1
Bazhenova, L.A.2
Braiteh, F.S.3
-
8
-
-
85024488073
-
Genomic profiling of circulating tumor DNA in relapsed EGFR-mutated lung adenocarcinoma reveals an acquired FGFR3-TACC3 fusion
-
pii: S1525-7304
-
Allen, J.M., Schrock, A.B., Erlich, R.L., et al. Genomic profiling of circulating tumor DNA in relapsed EGFR-mutated lung adenocarcinoma reveals an acquired FGFR3-TACC3 fusion. Clin. Lung Cancer 22:December (16) (2016), 30382–30385 pii: S1525-7304.
-
(2016)
Clin. Lung Cancer
, vol.22
, Issue.December (16)
, pp. 30382-30385
-
-
Allen, J.M.1
Schrock, A.B.2
Erlich, R.L.3
-
9
-
-
84957052714
-
Metastatic EML4-ALK fusion detected by circulating DNA genotyping in an EGFR-mutated NSCLC patient and successful management by adding ALK inhibitors: a case report
-
Liang, W., He, Q., Chen, Y., et al. Metastatic EML4-ALK fusion detected by circulating DNA genotyping in an EGFR-mutated NSCLC patient and successful management by adding ALK inhibitors: a case report. BMC Cancer, 16(February (62)), 2016, 12.
-
(2016)
BMC Cancer
, vol.16
, Issue.February (62)
, pp. 12
-
-
Liang, W.1
He, Q.2
Chen, Y.3
-
10
-
-
84887491073
-
Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing
-
Frampton, G.M., Fichtenholtz, A., Otto, G.A., et al. Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing. Nat. Biotechnol. 31 (2013), 1023–1031.
-
(2013)
Nat. Biotechnol.
, vol.31
, pp. 1023-1031
-
-
Frampton, G.M.1
Fichtenholtz, A.2
Otto, G.A.3
-
11
-
-
85015316213
-
Emergence of preexisting MET Y1230C mutation as a resistance mechanism to crizotinib in NSCLC with MET exon 14 skipping
-
Ou, S.I., Young, L., Schrock, A.B., et al. Emergence of preexisting MET Y1230C mutation as a resistance mechanism to crizotinib in NSCLC with MET exon 14 skipping. J. Thorac. Oncol. 12 (2017), 137–140.
-
(2017)
J. Thorac. Oncol.
, vol.12
, pp. 137-140
-
-
Ou, S.I.1
Young, L.2
Schrock, A.B.3
-
12
-
-
84897018525
-
Integrative and comparative genomic analysis of lung squamous cell carcinomas in East Asian patients
-
Kim, Y., Hammerman, P.S., Kim, J., et al. Integrative and comparative genomic analysis of lung squamous cell carcinomas in East Asian patients. J. Clin. Oncol. 32 (2014), 121–128.
-
(2014)
J. Clin. Oncol.
, vol.32
, pp. 121-128
-
-
Kim, Y.1
Hammerman, P.S.2
Kim, J.3
-
13
-
-
84905508021
-
FGFR1/3 tyrosine kinase fusions define a unique molecular subtype of non-small cell lung cancer
-
Wang, R., Wang, L., Li, Y., et al. FGFR1/3 tyrosine kinase fusions define a unique molecular subtype of non-small cell lung cancer. Clin. Cancer Res. 20 (2014), 4107–4114.
-
(2014)
Clin. Cancer Res.
, vol.20
, pp. 4107-4114
-
-
Wang, R.1
Wang, L.2
Li, Y.3
-
14
-
-
84919724844
-
Identification of recurrent FGFR3-TACC3 fusion oncogenes from lung adenocarcinoma
-
Capelletti, M., Dodge, M.E., Ercan, D., et al. Identification of recurrent FGFR3-TACC3 fusion oncogenes from lung adenocarcinoma. Clin. Cancer Res. 20 (2014), 6551–6558.
-
(2014)
Clin. Cancer Res.
, vol.20
, pp. 6551-6558
-
-
Capelletti, M.1
Dodge, M.E.2
Ercan, D.3
-
15
-
-
84976314171
-
FGFR3-TACC3 fusion proteins act as naturally occurring drivers of tumor resistance by functionally substituting for EGFR/ERK signaling
-
Daly, C., Castanaro, C., Zhang, W., et al. FGFR3-TACC3 fusion proteins act as naturally occurring drivers of tumor resistance by functionally substituting for EGFR/ERK signaling. Oncogene 36 (2017), 471–481.
-
(2017)
Oncogene
, vol.36
, pp. 471-481
-
-
Daly, C.1
Castanaro, C.2
Zhang, W.3
|