메뉴 건너뛰기




Volumn 7, Issue , 2016, Pages

Circulating tumour DNA profiling reveals heterogeneity of EGFR inhibitor resistance mechanisms in lung cancer patients

(22)  Chabon, Jacob J a,b   Simmons, Andrew D c   Lovejoy, Alexander F a,b   Esfahani, Mohammad S a,b   Newman, Aaron M a,b   Haringsma, Henry J c   Kurtz, David M a,d   Stehr, Henning a,b   Scherer, Florian a,b   Karlovich, Chris A c   Harding, Thomas C c   Durkin, Kathleen A e   Otterson, Gregory A f   Purcell, W Thomas g   Camidge, D Ross g   Goldman, Jonathan W h   Sequist, Lecia V i   Piotrowska, Zofia i   Wakelee, Heather A a   Neal, Joel W a   more..


Author keywords

[No Author keywords available]

Indexed keywords

CIRCULATING TUMOR DNA; DNA; EPIDERMAL GROWTH FACTOR RECEPTOR; EPIDERMAL GROWTH FACTOR RECEPTOR 2; EPIDERMAL GROWTH FACTOR RECEPTOR KINASE INHIBITOR; ERLOTINIB; K RAS PROTEIN; PHOSPHATIDYLINOSITOL 4,5 BISPHOSPHATE 3 KINASE; PHOSPHATIDYLINOSITOL 4,5 BISPHOSPHATE 3 KINASE CATALYTIC SUBUNIT; RETINOBLASTOMA PROTEIN; RETINOBLASTOMA PROTEIN 1; ROCILETINIB; SCATTER FACTOR RECEPTOR; UNCLASSIFIED DRUG; ACRYLAMIDE DERIVATIVE; CRIZOTINIB; PROTEIN KINASE INHIBITOR; PYRAZOLE DERIVATIVE; PYRIDINE DERIVATIVE; PYRIMIDINE DERIVATIVE;

EID: 84974625022     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms11815     Document Type: Article
Times cited : (536)

References (66)
  • 1
    • 2342624080 scopus 로고    scopus 로고
    • EGFR mutations in lung cancer: Correlation with clinical response to gefitinib therapy
    • Paez, J. G. et al. EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy. Science 304, 1497-1500 (2004).
    • (2004) Science , vol.304 , pp. 1497-1500
    • Paez, J.G.1
  • 2
    • 2342471392 scopus 로고    scopus 로고
    • Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib
    • Lynch, T. J. et al. Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib. N. Engl. J. Med. 350, 2129-2139 (2004).
    • (2004) N. Engl. J. Med. , vol.350 , pp. 2129-2139
    • Lynch, T.J.1
  • 3
    • 4444344330 scopus 로고    scopus 로고
    • EGF receptor gene mutations are common in lung cancers from 'never smokers' and are associated with sensitivity of tumors to gefitinib and erlotinib
    • Pao, W. et al. EGF receptor gene mutations are common in lung cancers from 'never smokers' and are associated with sensitivity of tumors to gefitinib and erlotinib. Proc. Natl Acad. Sci. USA 101, 13306-13311 (2004).
    • (2004) Proc. Natl Acad. Sci. USA , vol.101 , pp. 13306-13311
    • Pao, W.1
  • 4
    • 69949162760 scopus 로고    scopus 로고
    • Gefitinib or carboplatin-paclitaxel in pulmonary adenocarcinoma
    • Mok, T. S. et al. Gefitinib or carboplatin-paclitaxel in pulmonary adenocarcinoma. N. Engl. J. Med. 361, 947-957 (2009).
    • (2009) N. Engl. J. Med. , vol.361 , pp. 947-957
    • Mok, T.S.1
  • 5
    • 77953930730 scopus 로고    scopus 로고
    • Gefitinib or chemotherapy for non-small-cell lung cancer with mutated EGFR
    • Maemondo, M. et al. Gefitinib or chemotherapy for non-small-cell lung cancer with mutated EGFR. N. Engl. J. Med. 362, 2380-2388 (2010).
    • (2010) N. Engl. J. Med. , vol.362 , pp. 2380-2388
    • Maemondo, M.1
  • 6
    • 84857502654 scopus 로고    scopus 로고
    • Erlotinib versus standard chemotherapy as first-line treatment for European patients with advanced EGFR mutation-positive non-small-cell lung cancer (EURTAC): A multicentre, open-label, randomised phase 3 trial
    • Rosell, R. et al. Erlotinib versus standard chemotherapy as first-line treatment for European patients with advanced EGFR mutation-positive non-small-cell lung cancer (EURTAC): A multicentre, open-label, randomised phase 3 trial. Lancet Oncol. 13, 239-246 (2012).
    • (2012) Lancet Oncol. , vol.13 , pp. 239-246
    • Rosell, R.1
  • 7
    • 84862785051 scopus 로고    scopus 로고
    • Afatinib versus placebo for patients with advanced, metastatic non-small-cell lung cancer after failure of erlotinib, gefitinib, or both, and one or two lines of chemotherapy (LUX-Lung 1): A phase 2b/3 randomised trial
    • Miller, V. A. et al. Afatinib versus placebo for patients with advanced, metastatic non-small-cell lung cancer after failure of erlotinib, gefitinib, or both, and one or two lines of chemotherapy (LUX-Lung 1): a phase 2b/3 randomised trial. Lancet Oncol. 13, 528-538 (2012).
    • (2012) Lancet Oncol. , vol.13 , pp. 528-538
    • Miller, V.A.1
  • 8
    • 18244371651 scopus 로고    scopus 로고
    • Acquired resistance of lung adenocarcinomas to gefitinib or erlotinib is associated with a second mutation in the EGFR kinase domain
    • Pao, W. et al. Acquired resistance of lung adenocarcinomas to gefitinib or erlotinib is associated with a second mutation in the EGFR kinase domain. PLoS Med. 2, 0225-0235 (2005).
    • (2005) PLoS Med. , vol.2 , pp. 0225-0235
    • Pao, W.1
  • 9
    • 13844317894 scopus 로고    scopus 로고
    • EGFR mutation and resistance of non-small-cell lung cancer to gefitinib
    • Kobayashi, S. et al. EGFR mutation and resistance of non-small-cell lung cancer to gefitinib. N. Engl. J. Med. 352, 786-792 (2005).
    • (2005) N. Engl. J. Med. , vol.352 , pp. 786-792
    • Kobayashi, S.1
  • 10
    • 79953118839 scopus 로고    scopus 로고
    • Genotypic and histological evolution of lung cancers acquiring resistance to EGFR inhibitors
    • 75ra26
    • Sequist, L. V. et al. Genotypic and histological evolution of lung cancers acquiring resistance to EGFR inhibitors. Sci. Transl. Med 3, 75ra26 (2011).
    • (2011) Sci. Transl. Med , vol.3
    • Sequist, L.V.1
  • 11
    • 84877100240 scopus 로고    scopus 로고
    • 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. 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, 2240-2247 (2013).
    • (2013) Clin. Cancer Res. , vol.19 , pp. 2240-2247
    • Yu, H.A.1
  • 12
    • 84887977876 scopus 로고    scopus 로고
    • Discovery of a mutant-selective covalent inhibitor of EGFR that overcomes T790M mediated resistance in NSCLC
    • Walter, A. O. et al. Discovery of a mutant-selective covalent inhibitor of EGFR that overcomes T790M mediated resistance in NSCLC. Cancer Discov. 3, 1404-1415 (2013).
    • (2013) Cancer Discov. , vol.3 , pp. 1404-1415
    • Walter, A.O.1
  • 13
    • 84904898065 scopus 로고    scopus 로고
    • AZD9291, an irreversible EGFR TKI, overcomes T790M-mediated resistance to EGFR inhibitors in lung cancer
    • Cross, D. A. E. et al. AZD9291, an irreversible EGFR TKI, overcomes T790M-mediated resistance to EGFR inhibitors in lung cancer. Cancer Discov. 4, 1046-1061 (2014).
    • (2014) Cancer Discov. , vol.4 , pp. 1046-1061
    • Cross, D.A.E.1
  • 14
    • 84928739294 scopus 로고    scopus 로고
    • AZD9291 in EGFR inhibitor-resistant non-small-cell lung cancer
    • Jänne, P. A. et al. AZD9291 in EGFR inhibitor-resistant non-small-cell lung cancer. N. Engl. J. Med. 372, 1689-1699 (2015).
    • (2015) N. Engl. J. Med. , vol.372 , pp. 1689-1699
    • Jänne, P.A.1
  • 15
    • 84928746232 scopus 로고    scopus 로고
    • Rociletinib in EGFR-mutated non-small-cell lung cancer
    • Sequist, L. V. et al. Rociletinib in EGFR-mutated non-small-cell lung cancer. N. Engl. J. Med. 372, 1700-1709 (2015).
    • (2015) N. Engl. J. Med. , vol.372 , pp. 1700-1709
    • Sequist, L.V.1
  • 16
    • 84930755018 scopus 로고    scopus 로고
    • Acquired EGFR C797S mutation mediates resistance to AZD9291 in non-small cell lung cancer harboring EGFR T790M
    • Thress, K. S. et al. Acquired EGFR C797S mutation mediates resistance to AZD9291 in non-small cell lung cancer harboring EGFR T790M. Nat. Med. 21, 1-5 (2015).
    • (2015) Nat. Med. , vol.21 , pp. 1-5
    • Thress, K.S.1
  • 17
    • 84937414146 scopus 로고    scopus 로고
    • Heterogeneity underlies the emergence of EGFR T790 wild-type clones following treatment of T790M-positive cancers with a third generation EGFR inhibitor
    • Piotrowska, Z. et al. Heterogeneity underlies the emergence of EGFR T790 wild-type clones following treatment of T790M-positive cancers with a third generation EGFR inhibitor. Cancer Discov. 5, 713-722 (2015).
    • (2015) Cancer Discov. , vol.5 , pp. 713-722
    • Piotrowska, Z.1
  • 18
    • 84943744661 scopus 로고    scopus 로고
    • EGFR-independent mechanisms of acquired resistance to AZD9291 in EGFR T790M-positive NSCLC patients
    • Planchard, D. et al. EGFR-independent mechanisms of acquired resistance to AZD9291 in EGFR T790M-positive NSCLC patients. Ann. Oncol. 26, 2073-2078 (2015).
    • (2015) Ann. Oncol. , vol.26 , pp. 2073-2078
    • Planchard, D.1
  • 19
    • 84863393080 scopus 로고    scopus 로고
    • Intratumor heterogeneity and branched evolution revealed by multiregion sequencing
    • Gerlinger, M. et al. Intratumor heterogeneity and branched evolution revealed by multiregion sequencing. N. Engl. J. Med. 366, 883-892 (2012).
    • (2012) N. Engl. J. Med. , vol.366 , pp. 883-892
    • Gerlinger, M.1
  • 20
    • 84880507665 scopus 로고    scopus 로고
    • Mutational heterogeneity in cancer and the search for new cancer-associated genes
    • Lawrence, M. S. et al. Mutational heterogeneity in cancer and the search for new cancer-associated genes. Nature 499, 214-218 (2013).
    • (2013) Nature , vol.499 , pp. 214-218
    • Lawrence, M.S.1
  • 21
    • 84907808265 scopus 로고    scopus 로고
    • Intratumor heterogeneity in localized lung adenocarcinomas delineated by multiregion sequencing
    • Zhang, J. et al. Intratumor heterogeneity in localized lung adenocarcinomas delineated by multiregion sequencing. Science 346, 256-259 (2014).
    • (2014) Science , vol.346 , pp. 256-259
    • Zhang, J.1
  • 22
    • 84907855592 scopus 로고    scopus 로고
    • Spatial and temporal diversity in genomic instability processes defines lung cancer evolution
    • de Bruin, E. C. et al. Spatial and temporal diversity in genomic instability processes defines lung cancer evolution. Science 346, 251-256 (2014).
    • (2014) Science , vol.346 , pp. 251-256
    • De Bruin, E.C.1
  • 23
    • 84864524696 scopus 로고    scopus 로고
    • Lung cancers with acquired resistance to EGFR inhibitors occasionally harbor BRAF gene mutations but lack mutations in KRAS, NRAS, or MEK1
    • Ohashi, K. et al. Lung cancers with acquired resistance to EGFR inhibitors occasionally harbor BRAF gene mutations but lack mutations in KRAS, NRAS, or MEK1. Proc. Natl Acad. Sci. USA 109, E2127-E2133 (2012).
    • (2012) Proc. Natl Acad. Sci. USA , vol.109 , pp. E2127-E2133
    • Ohashi, K.1
  • 24
    • 78349265779 scopus 로고    scopus 로고
    • Reciprocal and complementary role of MET amplification and EGFR T790M mutation in acquired resistance to kinase inhibitors in lung cancer
    • Suda, K. et al. Reciprocal and complementary role of MET amplification and EGFR T790M mutation in acquired resistance to kinase inhibitors in lung cancer. Clin. Cancer Res. 16, 5489-5498 (2010).
    • (2010) Clin. Cancer Res. , vol.16 , pp. 5489-5498
    • Suda, K.1
  • 25
    • 84862999938 scopus 로고    scopus 로고
    • Emergence of KRAS mutations and acquired resistance to anti-EGFR therapy in colorectal cancer
    • Misale, S. et al. Emergence of KRAS mutations and acquired resistance to anti-EGFR therapy in colorectal cancer. Nature 486, 532-536 (2012).
    • (2012) Nature , vol.486 , pp. 532-536
    • Misale, S.1
  • 26
    • 84863000299 scopus 로고    scopus 로고
    • The molecular evolution of acquired resistance to targeted EGFR blockade in colorectal cancers
    • Diaz, L. A. et al. The molecular evolution of acquired resistance to targeted EGFR blockade in colorectal cancers. Nature 486, 537-540 (2012).
    • (2012) Nature , vol.486 , pp. 537-540
    • Diaz, L.A.1
  • 28
    • 84903218109 scopus 로고    scopus 로고
    • An ultrasensitive method for quantitating circulating tumor DNA with broad patient coverage
    • Newman, A. M. et al. An ultrasensitive method for quantitating circulating tumor DNA with broad patient coverage. Nat. Med. 20, 548-554 (2014).
    • (2014) Nat. Med. , vol.20 , pp. 548-554
    • Newman, A.M.1
  • 29
    • 84966365311 scopus 로고    scopus 로고
    • Integrated digital error suppression for improved detection of circulating tumor DNA
    • Newman, A. M. et al. Integrated digital error suppression for improved detection of circulating tumor DNA. Nat. Biotechnol 34, 547-555 (2016).
    • (2016) Nat. Biotechnol , vol.34 , pp. 547-555
    • Newman, A.M.1
  • 30
    • 57849117384 scopus 로고    scopus 로고
    • New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1)
    • Eisenhauer, E. A. et al. New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1). Eur. J. Cancer 45, 228-247 (2009).
    • (2009) Eur. J. Cancer , vol.45 , pp. 228-247
    • Eisenhauer, E.A.1
  • 31
    • 84896371874 scopus 로고    scopus 로고
    • Detection of circulating tumor DNA in early-and late-stage human malignancies
    • Bettegowda, C. et al. Detection of circulating tumor DNA in early-and late-stage human malignancies. Sci. Transl. Med. 6, 224ra24 (2014).
    • (2014) Sci. Transl. Med. , vol.6 , pp. 224-324
    • Bettegowda, C.1
  • 32
    • 84936748494 scopus 로고    scopus 로고
    • Clonal evolution and resistance to EGFR blockade in the blood of colorectal cancer patients
    • Siravegna, G. et al. Clonal evolution and resistance to EGFR blockade in the blood of colorectal cancer patients. Nat. Med. 21, 795-801 (2015).
    • (2015) Nat. Med. , vol.21 , pp. 795-801
    • Siravegna, G.1
  • 33
    • 84942159468 scopus 로고    scopus 로고
    • EGFR mutations and resistance to Irreversible pyrimidine based EGFR inhibitors
    • Ercan, D. et al. EGFR mutations and resistance to Irreversible pyrimidine based EGFR inhibitors. Clin. Cancer Res. 21, 3913-3923 (2015).
    • (2015) Clin. Cancer Res. , vol.21 , pp. 3913-3923
    • Ercan, D.1
  • 34
    • 84938196408 scopus 로고    scopus 로고
    • The allelic context of the C797S mutation acquired upon treatment with third generation EGFR inhibitors impacts sensitivity to subsequent treatment strategies
    • Niederst, M. J. et al. The allelic context of the C797S mutation acquired upon treatment with third generation EGFR inhibitors impacts sensitivity to subsequent treatment strategies. Clin. Cancer Res. 21, 3924-3933 (2015).
    • (2015) Clin. Cancer Res. , vol.21 , pp. 3924-3933
    • Niederst, M.J.1
  • 35
    • 84887497121 scopus 로고    scopus 로고
    • The quest to overcome resistance to EGFR-targeted therapies in cancer
    • Chong, C. R., Jänne, P. A. The quest to overcome resistance to EGFR-targeted therapies in cancer. Nat. Med. 19, 1389-1400 (2013).
    • (2013) Nat. Med. , vol.19 , pp. 1389-1400
    • Chong, C.R.1    Jänne, P.A.2
  • 36
    • 84875950992 scopus 로고    scopus 로고
    • Epidermal growth factor receptor tyrosine kinase inhibitor-resistant disease
    • Ohashi, K., Maruvka, Y. E., Michor, F., Pao, W. Epidermal growth factor receptor tyrosine kinase inhibitor-resistant disease. J. Clin. Oncol. 31, 1070-1080 (2013).
    • (2013) J. Clin. Oncol. , vol.31 , pp. 1070-1080
    • Ohashi, K.1    Maruvka, Y.E.2    Michor, F.3    Pao, W.4
  • 37
    • 84941787370 scopus 로고    scopus 로고
    • Acquired resistance to mutant-selective EGFR inhibitor AZD9291 is associated with increased dependence on RAS signaling in preclinical models
    • Eberlein, C. A. et al. Acquired resistance to mutant-selective EGFR inhibitor AZD9291 is associated with increased dependence on RAS signaling in preclinical models. Cancer Res. 75, 2489-2500 (2015).
    • (2015) Cancer Res. , vol.75 , pp. 2489-2500
    • Eberlein, C.A.1
  • 38
    • 84938274454 scopus 로고    scopus 로고
    • Multi-institutional oncogenic driver mutation analysis in lung adenocarcinoma
    • Sholl, L. M. et al. Multi-institutional oncogenic driver mutation analysis in lung adenocarcinoma. J. Thorac. Oncol. 10, 768-777 (2015).
    • (2015) J. Thorac. Oncol. , vol.10 , pp. 768-777
    • Sholl, L.M.1
  • 39
    • 77954580523 scopus 로고    scopus 로고
    • Multiplicity of EGFR and KRAS mutations in non-small cell lung cancer (NSCLC) patients treated with tyrosine kinase inhibitors
    • Benesova, L., Minarik, M., Jancarikova, D., Belsanova, B., Pesek, M. Multiplicity of EGFR and KRAS mutations in non-small cell lung cancer (NSCLC) patients treated with tyrosine kinase inhibitors. Anticancer Res. 30, 1667-1671 (2010).
    • (2010) Anticancer Res. , vol.30 , pp. 1667-1671
    • Benesova, L.1    Minarik, M.2    Jancarikova, D.3    Belsanova, B.4    Pesek, M.5
  • 40
    • 79952703873 scopus 로고    scopus 로고
    • Comparison of KRAS and EGFR gene status between primary non-small cell lung cancer and local lymph node metastases: Implications for clinical practice
    • Sun, L. et al. Comparison of KRAS and EGFR gene status between primary non-small cell lung cancer and local lymph node metastases: implications for clinical practice. J. Exp. Clin. Cancer Res. 30, 30 (2011).
    • (2011) J. Exp. Clin. Cancer Res. , vol.30 , pp. 30
    • Sun, L.1
  • 41
    • 77649288699 scopus 로고    scopus 로고
    • De novo resistance to epidermal growth factor receptortyrosine inhibitors in EGFR mutation-positive patients with non-small cell lung cancer
    • Takeda, M. et al. De novo resistance to epidermal growth factor receptortyrosine inhibitors in EGFR mutation-positive patients with non-small cell lung cancer. J. Thorac. Oncol. 5, 399-400 (2010).
    • (2010) J. Thorac. Oncol. , vol.5 , pp. 399-400
    • Takeda, M.1
  • 42
    • 15744372810 scopus 로고    scopus 로고
    • KRAS mutations and primary resistance of lung adenocarcinomas to gefitinib or erlotinib
    • Pao, W. et al. KRAS mutations and primary resistance of lung adenocarcinomas to gefitinib or erlotinib. PLoS Med. 2, e17 (2005).
    • (2005) PLoS Med. , vol.2 , pp. e17
    • Pao, W.1
  • 43
    • 77955277111 scopus 로고    scopus 로고
    • Effects of KRAS, BRAF, NRAS, and PIK3CA mutations on the efficacy of cetuximab plus chemotherapy in chemotherapy-refractory metastatic colorectal cancer: A retrospective consortium analysis
    • De Roock, W. et al. Effects of KRAS, BRAF, NRAS, and PIK3CA mutations on the efficacy of cetuximab plus chemotherapy in chemotherapy-refractory metastatic colorectal cancer: a retrospective consortium analysis. Lancet Oncol. 11, 753-762 (2010).
    • (2010) Lancet Oncol. , vol.11 , pp. 753-762
    • De Roock, W.1
  • 44
    • 84986309464 scopus 로고    scopus 로고
    • Osimertinib responses after disease progression in patients who had been receiving rociletinib
    • Sequist, L. V. et al. Osimertinib responses after disease progression in patients who had been receiving rociletinib. JAMA Oncol. 2, 17-19 (2015).
    • (2015) JAMA Oncol. , vol.2 , pp. 17-19
    • Sequist, L.V.1
  • 45
    • 84903482432 scopus 로고    scopus 로고
    • Ceritinib in ALK-rearranged non-small-cell lung cancer
    • Shaw, A. T. et al. Ceritinib in ALK-rearranged non-small-cell lung cancer. N. Engl. J. Med. 370, 1189-1197 (2014).
    • (2014) N. Engl. J. Med. , vol.370 , pp. 1189-1197
    • Shaw, A.T.1
  • 46
    • 84903466222 scopus 로고    scopus 로고
    • The ALK inhibitor ceritinib overcomes crizotinib resistance in non-small cell lung cancer
    • Friboulet, L. et al. The ALK inhibitor ceritinib overcomes crizotinib resistance in non-small cell lung cancer. Cancer Discov. 4, 662-673 (2014).
    • (2014) Cancer Discov. , vol.4 , pp. 662-673
    • Friboulet, L.1
  • 47
    • 38049150665 scopus 로고    scopus 로고
    • MET amplification occurs with or without T790M mutations in EGFR mutant lung tumors with acquired resistance to gefitinib or erlotinib
    • Bean, J. et al. MET amplification occurs with or without T790M mutations in EGFR mutant lung tumors with acquired resistance to gefitinib or erlotinib. Proc. Natl. Acad. Sci. USA 104, 20932-20937 (2007).
    • (2007) Proc. Natl. Acad. Sci. USA , vol.104 , pp. 20932-20937
    • Bean, J.1
  • 48
    • 34249075147 scopus 로고    scopus 로고
    • MET amplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling
    • Engelman, J. A. et al. MET amplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling. Science 316, 1039-1043 (2007).
    • (2007) Science , vol.316 , pp. 1039-1043
    • Engelman, J.A.1
  • 49
    • 84942521073 scopus 로고    scopus 로고
    • Early prediction of response to tyrosine kinase inhibitors by quantification of EGFR mutations in plasma of NSCLC patients
    • Marchetti, A. et al. Early prediction of response to tyrosine kinase inhibitors by quantification of EGFR mutations in plasma of NSCLC patients. J. Thorac. Oncol. 10, 1437-1443 (2015).
    • (2015) J. Thorac. Oncol. , vol.10 , pp. 1437-1443
    • Marchetti, A.1
  • 50
    • 84938399710 scopus 로고    scopus 로고
    • Detection and dynamic changes of EGFR mutations from circulating tumor DNA as a predictor of survival outcomes in NSCLC patients treated with first-line intercalated erlotinib and chemotherapy
    • Mok, T. et al. Detection and dynamic changes of EGFR mutations from circulating tumor DNA as a predictor of survival outcomes in NSCLC patients treated with first-line intercalated erlotinib and chemotherapy. Clin. Cancer Res. 21, 3196-3203 (2015).
    • (2015) Clin. Cancer Res. , vol.21 , pp. 3196-3203
    • Mok, T.1
  • 51
    • 84896539307 scopus 로고    scopus 로고
    • Noninvasive detection of response and resistance in EGFR-mutant lung cancer using quantitative next-generation genotyping of cell-free plasma DNA
    • Oxnard, G. R. et al. Noninvasive detection of response and resistance in EGFR-mutant lung cancer using quantitative next-generation genotyping of cell-free plasma DNA. Clin. Cancer Res. 20, 1698-1705 (2014).
    • (2014) Clin. Cancer Res. , vol.20 , pp. 1698-1705
    • Oxnard, G.R.1
  • 52
    • 84918789657 scopus 로고    scopus 로고
    • Monitoring of epidermal growth factor receptor tyrosine kinase inhibitor-sensitizing and resistance mutations in the plasma DNA of patients with advanced non-small cell lung cancer during treatment with erlotinib
    • Sorensen, B. S. et al. Monitoring of epidermal growth factor receptor tyrosine kinase inhibitor-sensitizing and resistance mutations in the plasma DNA of patients with advanced non-small cell lung cancer during treatment with erlotinib. Cancer 120, 3896-3901 (2014).
    • (2014) Cancer , vol.120 , pp. 3896-3901
    • Sorensen, B.S.1
  • 53
    • 81855208762 scopus 로고    scopus 로고
    • Quantitative detection of EGFR mutations in circulating tumor DNA derived from lung adenocarcinomas
    • Taniguchi, K. et al. Quantitative detection of EGFR mutations in circulating tumor DNA derived from lung adenocarcinomas. Clin. Cancer Res. 17, 7808-7815 (2011).
    • (2011) Clin. Cancer Res. , vol.17 , pp. 7808-7815
    • Taniguchi, K.1
  • 54
    • 84949205332 scopus 로고    scopus 로고
    • EGFR mutation detection in ctDNA from NSCLC patient plasma: A cross-platform comparison of leading technologies to support the clinical development of AZD9291
    • Thress, K. S. et al. EGFR mutation detection in ctDNA from NSCLC patient plasma: a cross-platform comparison of leading technologies to support the clinical development of AZD9291. Lung Cancer 90, 509-515 (2015).
    • (2015) Lung Cancer , vol.90 , pp. 509-515
    • Thress, K.S.1
  • 55
    • 20444498630 scopus 로고    scopus 로고
    • Epidermal growth factor receptor gene and protein and gefitinib sensitivity in non-small-cell lung cancer
    • Cappuzzo, F. et al. Epidermal growth factor receptor gene and protein and gefitinib sensitivity in non-small-cell lung cancer. J. Natl. Cancer Inst. 97, 643-655 (2005).
    • (2005) J. Natl. Cancer Inst. , vol.97 , pp. 643-655
    • Cappuzzo, F.1
  • 56
    • 34249857158 scopus 로고    scopus 로고
    • The prognostic value of chromosome 7 polysomy in non-small cell lung cancer patients treated with gefitinib
    • Buckingham, L. E. et al. The prognostic value of chromosome 7 polysomy in non-small cell lung cancer patients treated with gefitinib. J. Thorac. Oncol. 2, 414-422 (2007).
    • (2007) J. Thorac. Oncol. , vol.2 , pp. 414-422
    • Buckingham, L.E.1
  • 57
    • 27244451321 scopus 로고    scopus 로고
    • Epidermal growth factor receptor gene mutations and increased copy numbers predict gefitinib sensitivity in patients with recurrent non-small-cell lung cancer
    • Takano, T. et al. Epidermal growth factor receptor gene mutations and increased copy numbers predict gefitinib sensitivity in patients with recurrent non-small-cell lung cancer. J. Clin. Oncol. 23, 6829-6837 (2005).
    • (2005) J. Clin. Oncol. , vol.23 , pp. 6829-6837
    • Takano, T.1
  • 58
    • 33750962024 scopus 로고    scopus 로고
    • Molecular predictors of outcome with gefitinib in a phase III placebo-controlled study in advanced non-small-cell lung cancer
    • Hirsch, F. R. et al. Molecular predictors of outcome with gefitinib in a phase III placebo-controlled study in advanced non-small-cell lung cancer. J. Clin. Oncol. 24, 5034-5042 (2006).
    • (2006) J. Clin. Oncol. , vol.24 , pp. 5034-5042
    • Hirsch, F.R.1
  • 60
    • 84859169877 scopus 로고    scopus 로고
    • The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity
    • 603-307
    • Barretina, J. et al. The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity. Nature 483, 603-307 (2012).
    • (2012) Nature , vol.483
    • Barretina, J.1
  • 61
    • 84995454099 scopus 로고    scopus 로고
    • Prime, version 4.0 (Schrödinger, LLC, New York, NY
    • Schrödinger Release 2015-2: Prime, version 4.0 (Schrödinger, LLC, New York, NY, 2015).
    • (2015) Schrödinger Release , pp. 2015-2022
  • 62
    • 1842532008 scopus 로고    scopus 로고
    • A hierarchical approach to all-atom protein loop prediction
    • Jacobson, M. P. et al. A hierarchical approach to all-atom protein loop prediction. Proteins 55, 351-367 (2004).
    • (2004) Proteins , vol.55 , pp. 351-367
    • Jacobson, M.P.1
  • 63
    • 84946228623 scopus 로고    scopus 로고
    • Schrödinger Release New York, NY, 2015. Maestro-Desmond Interoperability Tools, version 4.2 (Schrödinger, New York, NY
    • Schrödinger Release 2015-2: Desmond Molecular Dynamics System, version 4.2 (D. E. Shaw Research, New York, NY, 2015. Maestro-Desmond Interoperability Tools, version 4.2 (Schrödinger, New York, NY, 2015).
    • (2015) Desmond Molecular Dynamics System, Version 4.2 (D. E. Shaw Research , pp. 2015-2022
  • 65
    • 84883178389 scopus 로고    scopus 로고
    • Functional DNA quantification guides accurate next-generation sequencing mutation detection in formalin-fixed, paraffin-embedded tumor biopsies
    • Sah, S. et al. Functional DNA quantification guides accurate next-generation sequencing mutation detection in formalin-fixed, paraffin-embedded tumor biopsies. Genome Med. 5, 77 (2013).
    • (2013) Genome Med. , vol.5 , pp. 77
    • Sah, S.1
  • 66
    • 84874519595 scopus 로고    scopus 로고
    • Targeted, high-depth, next-generation sequencing of cancer genes in formalin-fixed, paraffin-embedded and fine-needle aspiration tumor specimens
    • Hadd, A. G. et al. Targeted, high-depth, next-generation sequencing of cancer genes in formalin-fixed, paraffin-embedded and fine-needle aspiration tumor specimens. J. Mol. Diagn. 15, 234-247 (2013).
    • (2013) J. Mol. Diagn. , vol.15 , pp. 234-247
    • Hadd, A.G.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.