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Volumn 59, Issue 14, 2016, Pages 6580-6594

Challenges and perspectives on the development of small-molecule EGFR inhibitors against T790M-mediated resistance in non-small-cell lung cancer: Miniperspective

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE; ANILINE DERIVATIVE; EPIDERMAL GROWTH FACTOR RECEPTOR; EPIDERMAL GROWTH FACTOR RECEPTOR KINASE INHIBITOR; METHIONINE; MUTANT PROTEIN; OSIMERTINIB; PYRIDONE DERIVATIVE; PYRIMIDINE DERIVATIVE; QUINAZOLINE DERIVATIVE; ROCILETINIB; THREONINE; ANTINEOPLASTIC AGENT; EGFR PROTEIN, HUMAN; MOLECULAR LIBRARY; PROTEIN KINASE INHIBITOR;

EID: 84978657458     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/acs.jmedchem.5b00840     Document Type: Review
Times cited : (90)

References (84)
  • 4
    • 14244252225 scopus 로고    scopus 로고
    • The future of adjuvant chemotherapy for resected non-small cell lung cancer
    • Vansteenkiste, J. F.; Schildermans, R. H. The future of adjuvant chemotherapy for resected non-small cell lung cancer Expert Rev. Anticancer Ther. 2005, 5, 165-175 10.1586/14737140.5.1.165
    • (2005) Expert Rev. Anticancer Ther. , vol.5 , pp. 165-175
    • Vansteenkiste, J.F.1    Schildermans, R.H.2
  • 5
    • 0142119289 scopus 로고    scopus 로고
    • Epidermal growth factor receptor in non-small-cell lung carcinomas: Correlation between gene copy number and protein expression and impact on prognosis
    • Hirsch, F. R.; Varella-Garcia, M.; Bunn, P. A., Jr.; Di Maria, M. V.; Veve, R.; Bremmes, R. M.; Barón, A. E.; Zeng, C.; Franklin, W. A. Epidermal growth factor receptor in non-small-cell lung carcinomas: correlation between gene copy number and protein expression and impact on prognosis J. Clin. Oncol. 2003, 21, 3798-3807 10.1200/JCO.2003.11.069
    • (2003) J. Clin. Oncol. , vol.21 , pp. 3798-3807
    • Hirsch, F.R.1    Varella-Garcia, M.2    Bunn, Jr.P.A.3    Di Maria, M.V.4    Veve, R.5    Bremmes, R.M.6    Barón, A.E.7    Zeng, C.8    Franklin, W.A.9
  • 7
    • 33847323129 scopus 로고    scopus 로고
    • Epidermal growth factor receptor mutations in lung cancer
    • Sharma, S. V.; Bell, D. W.; Settleman, J.; Haber, D. A. Epidermal growth factor receptor mutations in lung cancer Nat. Rev. Cancer 2007, 7, 169-181 10.1038/nrc2088
    • (2007) Nat. Rev. Cancer , vol.7 , pp. 169-181
    • Sharma, S.V.1    Bell, D.W.2    Settleman, J.3    Haber, D.A.4
  • 9
    • 0043210670 scopus 로고    scopus 로고
    • FDA drug approval summary gefitinib (ZD1839) (Iressa) tablets
    • Cohen, M. H.; Williams, G. A.; Sridhara, R.; Chen, G.; Pazdur, R. FDA drug approval summary gefitinib (ZD1839) (Iressa) tablets Oncologist 2003, 8, 303-306 10.1634/theoncologist.8-4-303
    • (2003) Oncologist , vol.8 , pp. 303-306
    • Cohen, M.H.1    Williams, G.A.2    Sridhara, R.3    Chen, G.4    Pazdur, R.5
  • 11
    • 0041633499 scopus 로고    scopus 로고
    • Erlotinib: A new therapeutic approach for non-small cell lung cancer
    • Bonomi, P. Erlotinib: A new therapeutic approach for non-small cell lung cancer Expert Opin. Invest. Drugs 2003, 12, 1395-1401 10.1517/13543784.12.8.1395
    • (2003) Expert Opin. Invest. Drugs , vol.12 , pp. 1395-1401
    • Bonomi, P.1
  • 12
    • 33847406095 scopus 로고    scopus 로고
    • Structures of lung cancer-derived EGFR mutants and inhibitor complexes: Mechanism of activation and insights into differential inhibitor sensitivity
    • Yun, C. H.; Boggon, T. J.; Li, Y.; Woo, M. S.; Greulich, H.; Meyerson, M.; Eck, M. J. Structures of lung cancer-derived EGFR mutants and inhibitor complexes: Mechanism of activation and insights into differential inhibitor sensitivity Cancer Cell 2007, 11, 217-227 10.1016/j.ccr.2006.12.017
    • (2007) Cancer Cell , vol.11 , pp. 217-227
    • Yun, C.H.1    Boggon, T.J.2    Li, Y.3    Woo, M.S.4    Greulich, H.5    Meyerson, M.6    Eck, M.J.7
  • 13
    • 33748066632 scopus 로고    scopus 로고
    • Kinetic analysis of epidermal growth factor receptor somatic mutant proteins shows increased sensitivity to the epidermal growth factor receptor tyrosine kinase inhibitor, erlotinib
    • Carey, K. D.; Garton, A. J.; Romero, M. S.; Kahler, J.; Thomson, S.; Ross, S.; Park, F.; Haley, J. D.; Gibson, N. M.; Sliwkowski, M. X. Kinetic analysis of epidermal growth factor receptor somatic mutant proteins shows increased sensitivity to the epidermal growth factor receptor tyrosine kinase inhibitor, erlotinib Cancer Res. 2006, 66, 8163-8171 10.1158/0008-5472.CAN-06-0453
    • (2006) Cancer Res. , vol.66 , pp. 8163-8171
    • Carey, K.D.1    Garton, A.J.2    Romero, M.S.3    Kahler, J.4    Thomson, S.5    Ross, S.6    Park, F.7    Haley, J.D.8    Gibson, N.M.9    Sliwkowski, M.X.10
  • 16
    • 49649127657 scopus 로고    scopus 로고
    • Mechanisms of acquired resistance to epidermal growth factor receptor tyrosine kinase inhibitors in non-small-cell lung cancer
    • Engelman, J. A.; Jänne, P. A. Mechanisms of acquired resistance to epidermal growth factor receptor tyrosine kinase inhibitors in non-small-cell lung cancer Clin. Cancer Res. 2008, 14, 2895-2899 10.1158/1078-0432.CCR-07-2248
    • (2008) Clin. Cancer Res. , vol.14 , pp. 2895-2899
    • Engelman, J.A.1    Jänne, P.A.2
  • 17
    • 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.; Miller, V. A.; Politi, K. A.; Riely, G. J.; Somwar, R.; Zakowski, M. F.; Kris, M. G.; Varmus, H. Acquired resistance of lung adenocarcinomas to gefitinib or erlotinib is associated with a second mutation in the EGFR kinase domain PLoS Med. 2005, 10.1371/journal.pmed.0020073
    • (2005) PLoS Med.
    • Pao, W.1    Miller, V.A.2    Politi, K.A.3    Riely, G.J.4    Somwar, R.5    Zakowski, M.F.6    Kris, M.G.7    Varmus, H.8
  • 18
  • 19
    • 0141599428 scopus 로고    scopus 로고
    • Structure of the epidermal growth factor receptor kinase domain alone and in complex with a 4-anilinoquinazoline inhibitor
    • Stamos, J.; Sliwkowski, M. X.; Eigenbrot, C. Structure of the epidermal growth factor receptor kinase domain alone and in complex with a 4-anilinoquinazoline inhibitor J. Biol. Chem. 2002, 277, 46265-46272 10.1074/jbc.M207135200
    • (2002) J. Biol. Chem. , vol.277 , pp. 46265-46272
    • Stamos, J.1    Sliwkowski, M.X.2    Eigenbrot, C.3
  • 20
    • 41649099467 scopus 로고    scopus 로고
    • Structural insights into how irreversible inhibitors can overcome drug resistance in EGFR
    • Michalczyk, A.; Klüter, S.; Rode, H. B.; Simard, J. R.; Grütter, C.; Rabiller, M.; Rauh, D. Structural insights into how irreversible inhibitors can overcome drug resistance in EGFR Bioorg. Med. Chem. 2008, 16, 3482-3488 10.1016/j.bmc.2008.02.053
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 3482-3488
    • Michalczyk, A.1    Klüter, S.2    Rode, H.B.3    Simard, J.R.4    Grütter, C.5    Rabiller, M.6    Rauh, D.7
  • 24
    • 84859418112 scopus 로고    scopus 로고
    • The EGFR T790M mutation in acquired resistance to an irreversible second-generation EGFR inhibitor
    • Kim, Y.; Ko, J.; Cui, Z.; Abolhoda, A.; Ahn, J. S.; Ou, S. H.; Ahn, M. J.; Park, K. The EGFR T790M mutation in acquired resistance to an irreversible second-generation EGFR inhibitor Mol. Cancer Ther. 2012, 11, 784-791 10.1158/1535-7163.MCT-11-0750
    • (2012) Mol. Cancer Ther. , vol.11 , pp. 784-791
    • Kim, Y.1    Ko, J.2    Cui, Z.3    Abolhoda, A.4    Ahn, J.S.5    Ou, S.H.6    Ahn, M.J.7    Park, K.8
  • 34
    • 84959912606 scopus 로고    scopus 로고
    • Clinical activity of the mutant-selective EGFR inhibitor AZD9291 in patients with EGFR inhibitor-resistant non-small cell lung cancer
    • Jiang, T.; Zhou, C. Clinical activity of the mutant-selective EGFR inhibitor AZD9291 in patients with EGFR inhibitor-resistant non-small cell lung cancer Transl. Lung Cancer Res. 2014, 3, 370-372 10.3978/j.issn.2218-6751.2014.08.02
    • (2014) Transl. Lung Cancer Res. , vol.3 , pp. 370-372
    • Jiang, T.1    Zhou, C.2
  • 36
    • 84907049059 scopus 로고    scopus 로고
    • Small-molecule EGFR tyrosine kinase inhibitors for the treatment of cancer
    • Lee, C. C.; Shiao, H. Y.; Wang, W. C.; Hsieh, H. P. Small-molecule EGFR tyrosine kinase inhibitors for the treatment of cancer Expert Opin. Invest. Drugs 2014, 23, 1333-1348 10.1517/13543784.2014.928283
    • (2014) Expert Opin. Invest. Drugs , vol.23 , pp. 1333-1348
    • Lee, C.C.1    Shiao, H.Y.2    Wang, W.C.3    Hsieh, H.P.4
  • 37
    • 84922628379 scopus 로고    scopus 로고
    • Second and third-generation epidermal growth factor receptor tyrosine kinase inhibitors in advanced nonsmall cell lung cancer
    • Liao, B. C.; Lin, C. C.; Yang, C. H. Second and third-generation epidermal growth factor receptor tyrosine kinase inhibitors in advanced nonsmall cell lung cancer Curr. Opin. Oncol. 2015, 27, 94-101 10.1097/CCO.0000000000000164
    • (2015) Curr. Opin. Oncol. , vol.27 , pp. 94-101
    • Liao, B.C.1    Lin, C.C.2    Yang, C.H.3
  • 38
    • 84898026928 scopus 로고    scopus 로고
    • A new challenging and promising era of tyrosine kinase inhibitors
    • Cui, J. J. A new challenging and promising era of tyrosine kinase inhibitors ACS Med. Chem. Lett. 2014, 5, 272-274 10.1021/ml500091p
    • (2014) ACS Med. Chem. Lett. , vol.5 , pp. 272-274
    • Cui, J.J.1
  • 39
    • 84908009315 scopus 로고    scopus 로고
    • Lung cancer research is taking on new challenges: Knowledge of tumors' molecular diversity is opening new pathways to treatment
    • Worley, S. Lung cancer research is taking on new challenges: knowledge of tumors' molecular diversity is opening new pathways to treatment Pharmacol. Ther. 2014, 39, 698-703
    • (2014) Pharmacol. Ther. , vol.39 , pp. 698-703
    • Worley, S.1
  • 41
    • 84863341925 scopus 로고    scopus 로고
    • Design, synthesis, and biological evaluation of novel conformationally constrained inhibitors targeting epidermal growth factor receptor threonine790→methionine790 mutant
    • Chang, S.; Zhang, L.; Xu, S.; Luo, J.; Lu, X.; Zhang, Z.; Xu, T.; Liu, Y.; Tu, Z.; Xu, Y.; Ren, X.; Geng, M.; Ding, J.; Pei, D.; Ding, K. Design, synthesis, and biological evaluation of novel conformationally constrained inhibitors targeting epidermal growth factor receptor threonine790→methionine790 mutant J. Med. Chem. 2012, 55, 2711-2723 10.1021/jm201591k
    • (2012) J. Med. Chem. , vol.55 , pp. 2711-2723
    • Chang, S.1    Zhang, L.2    Xu, S.3    Luo, J.4    Lu, X.5    Zhang, Z.6    Xu, T.7    Liu, Y.8    Tu, Z.9    Xu, Y.10    Ren, X.11    Geng, M.12    Ding, J.13    Pei, D.14    Ding, K.15
  • 42
    • 84927061520 scopus 로고    scopus 로고
    • The next generation of epidermal growth factor receptor tyrosine kinase inhibitors in the treatment of lung cancer
    • Steuer, C. E.; Khuri, F. R.; Ramalingam, S. S. The next generation of epidermal growth factor receptor tyrosine kinase inhibitors in the treatment of lung cancer Cancer 2015, 121, E1-E6 10.1002/cncr.29139
    • (2015) Cancer , vol.121 , pp. E1-E6
    • Steuer, C.E.1    Khuri, F.R.2    Ramalingam, S.S.3
  • 43
    • 84930754135 scopus 로고    scopus 로고
    • Fighting cancer drug resistance: Opportunities and challenges for mutation-specific EGFR inhibitors
    • Juchum, M.; Günther, M.; Laufer, S. A. Fighting cancer drug resistance: opportunities and challenges for mutation-specific EGFR inhibitors Drug Resist. Updates 2015, 20, 12-28 10.1016/j.drup.2015.05.002
    • (2015) Drug Resist. Updates , vol.20 , pp. 12-28
    • Juchum, M.1    Günther, M.2    Laufer, S.A.3
  • 46
    • 33745559710 scopus 로고    scopus 로고
    • The role of nitric oxide in tumour progression
    • Fukumura, D.; Kashiwagi, S.; Jain, R. K. The role of nitric oxide in tumour progression Nat. Rev. Cancer 2006, 6, 521-534 10.1038/nrc1910
    • (2006) Nat. Rev. Cancer , vol.6 , pp. 521-534
    • Fukumura, D.1    Kashiwagi, S.2    Jain, R.K.3
  • 47
    • 47049088507 scopus 로고    scopus 로고
    • Novel therapeutic applications of nitric oxide donors in cancer: Roles in chemo- and immunosensitization to apoptosis and inhibition of metastases
    • Bonavida, B.; Baritaki, S.; Huerta-Yepez, S.; Vega, M. I.; Chatterjee, D.; Yeung, K. Novel therapeutic applications of nitric oxide donors in cancer: roles in chemo- and immunosensitization to apoptosis and inhibition of metastases Nitric Oxide 2008, 19, 152-157 10.1016/j.niox.2008.04.018
    • (2008) Nitric Oxide , vol.19 , pp. 152-157
    • Bonavida, B.1    Baritaki, S.2    Huerta-Yepez, S.3    Vega, M.I.4    Chatterjee, D.5    Yeung, K.6
  • 49
    • 84879055043 scopus 로고    scopus 로고
    • Novel hybrids of (phenylsulfonyl)furoxan and anilinopyrimidine as potent and selective epidermal growth factor receptor inhibitors for intervention of non-small-cell lung cancer
    • Han, C.; Huang, Z.; Zheng, C.; Wan, L.; Zhang, L.; Peng, S.; Ding, K.; Ji, H.; Tian, J.; Zhang, Y. Novel hybrids of (phenylsulfonyl)furoxan and anilinopyrimidine as potent and selective epidermal growth factor receptor inhibitors for intervention of non-small-cell lung cancer J. Med. Chem. 2013, 56, 4738-4748 10.1021/jm400463q
    • (2013) J. Med. Chem. , vol.56 , pp. 4738-4748
    • Han, C.1    Huang, Z.2    Zheng, C.3    Wan, L.4    Zhang, L.5    Peng, S.6    Ding, K.7    Ji, H.8    Tian, J.9    Zhang, Y.10
  • 50
    • 84879237940 scopus 로고    scopus 로고
    • Nitric oxide donating anilinopyrimidines: Synthesis and biological evaluation as EGFR inhibitors
    • Han, C.; Huang, Z.; Zheng, C.; Wan, L.; Lai, Y.; Peng, S.; Ding, K.; Ji, H.; Zhang, Y. Nitric oxide donating anilinopyrimidines: synthesis and biological evaluation as EGFR inhibitors Eur. J. Med. Chem. 2013, 66, 82-90 10.1016/j.ejmech.2013.05.026
    • (2013) Eur. J. Med. Chem. , vol.66 , pp. 82-90
    • Han, C.1    Huang, Z.2    Zheng, C.3    Wan, L.4    Lai, Y.5    Peng, S.6    Ding, K.7    Ji, H.8    Zhang, Y.9
  • 51
    • 84896796258 scopus 로고    scopus 로고
    • Synthesis and evaluation of 2-anilinopyrimidines bearing 3-aminopropamides as potential epidermal growth factor receptor inhibitors
    • Han, C.; Wan, L.; Ji, H.; Ding, K.; Huang, Z.; Lai, Y.; Peng, S.; Zhang, Y. Synthesis and evaluation of 2-anilinopyrimidines bearing 3-aminopropamides as potential epidermal growth factor receptor inhibitors Eur. J. Med. Chem. 2014, 77, 75-83 10.1016/j.ejmech.2014.02.032
    • (2014) Eur. J. Med. Chem. , vol.77 , pp. 75-83
    • Han, C.1    Wan, L.2    Ji, H.3    Ding, K.4    Huang, Z.5    Lai, Y.6    Peng, S.7    Zhang, Y.8
  • 53
    • 78651260008 scopus 로고    scopus 로고
    • Discovery of selective irreversible inhibitors for EGFR-T790M
    • Zhou, W.; Ercan, D.; Jänne, P. A.; Gray, N. S. Discovery of selective irreversible inhibitors for EGFR-T790M Bioorg. Med. Chem. Lett. 2011, 21, 638-643 10.1016/j.bmcl.2010.12.036
    • (2011) Bioorg. Med. Chem. Lett. , vol.21 , pp. 638-643
    • Zhou, W.1    Ercan, D.2    Jänne, P.A.3    Gray, N.S.4
  • 55
    • 84979908546 scopus 로고    scopus 로고
    • Inhibitors of the epidermal growth factor receptor (EGFR) may provide effective treatment for lung adenocarcinoma
    • Abdel-Magid, A. F. Inhibitors of the epidermal growth factor receptor (EGFR) may provide effective treatment for lung adenocarcinoma ACS Med. Chem. Lett. 2015, 6, 732-733 10.1021/acsmedchemlett.5b00231
    • (2015) ACS Med. Chem. Lett. , vol.6 , pp. 732-733
    • Abdel-Magid, A.F.1
  • 57
    • 84887920359 scopus 로고    scopus 로고
    • Design, synthesis, and biological evaluation of 2-oxo-3,4-dihydropyrimido[4,5-d]pyrimidinyl derivatives as new irreversible epidermal growth factor receptor inhibitors with improved pharmacokinetic properties
    • Xu, S.; Xu, T.; Zhang, L.; Zhang, Z.; Luo, J.; Liu, Y.; Lu, X.; Tu, Z.; Ren, X.; Ding, K. Design, synthesis, and biological evaluation of 2-oxo-3,4-dihydropyrimido[4,5-d]pyrimidinyl derivatives as new irreversible epidermal growth factor receptor inhibitors with improved pharmacokinetic properties J. Med. Chem. 2013, 56, 8803-8813 10.1021/jm4012388
    • (2013) J. Med. Chem. , vol.56 , pp. 8803-8813
    • Xu, S.1    Xu, T.2    Zhang, L.3    Zhang, Z.4    Luo, J.5    Liu, Y.6    Lu, X.7    Tu, Z.8    Ren, X.9    Ding, K.10
  • 58
    • 84886494418 scopus 로고    scopus 로고
    • Discovery of pteridin-7(8H)-one-based irreversible inhibitors targeting the epidermal growth factor receptor (EGFR) kinase T790M/L858R mutant
    • Zhou, W.; Liu, X.; Tu, Z.; Zhang, L.; Ku, X.; Bai, F.; Zhao, Z.; Xu, Y.; Ding, K.; Li, H. Discovery of pteridin-7(8H)-one-based irreversible inhibitors targeting the epidermal growth factor receptor (EGFR) kinase T790M/L858R mutant J. Med. Chem. 2013, 56, 7821-7837 10.1021/jm401045n
    • (2013) J. Med. Chem. , vol.56 , pp. 7821-7837
    • Zhou, W.1    Liu, X.2    Tu, Z.3    Zhang, L.4    Ku, X.5    Bai, F.6    Zhao, Z.7    Xu, Y.8    Ding, K.9    Li, H.10
  • 65
    • 79960110757 scopus 로고    scopus 로고
    • Afatinib (BIBW 2992) development in non-small-cell lung cancer
    • Hirsh, V. Afatinib (BIBW 2992) development in non-small-cell lung cancer Future Oncol. 2011, 7, 817-825 10.2217/fon.11.62
    • (2011) Future Oncol. , vol.7 , pp. 817-825
    • Hirsh, V.1
  • 66
    • 84933565203 scopus 로고    scopus 로고
    • Next-generation covalent irreversible kinase inhibitors in NSCLC: Focus on afatinib
    • Hirsh, V. Next-generation covalent irreversible kinase inhibitors in NSCLC: focus on afatinib BioDrugs 2015, 29, 167-183 10.1007/s40259-015-0130-9
    • (2015) BioDrugs , vol.29 , pp. 167-183
    • Hirsh, V.1
  • 68
    • 84928405077 scopus 로고    scopus 로고
    • Afatinib is especially effective against non-small cell lung cancer carrying an EGFR exon 19 deletion
    • Banno, E.; Togashi, Y.; Kobayashi, Y.; Hayashi, H.; Mitsudomi, T.; Nishio, K. Afatinib is especially effective against non-small cell lung cancer carrying an EGFR exon 19 deletion Anticancer Res. 2015, 35, 2005-2008
    • (2015) Anticancer Res. , vol.35 , pp. 2005-2008
    • Banno, E.1    Togashi, Y.2    Kobayashi, Y.3    Hayashi, H.4    Mitsudomi, T.5    Nishio, K.6
  • 71
    • 84979908556 scopus 로고    scopus 로고
    • TAS-2913 is a mutant selective EGFR inhibitor for NSCLC: Characterization against EGFR T790M in cell and xenograft models
    • Miyadera, K.; Kato, M.; Takahashi, I.; Ito, K.; Aoyagi, Y.; Fukasawa, K.; Sagara, T.; Yonekura, K.; Iwasawa, Y.; Utsugi, T. TAS-2913 is a mutant selective EGFR inhibitor for NSCLC: characterization against EGFR T790M in cell and xenograft models Eur. J. Cancer 2012, 48 (Suppl. 6) 44 10.1016/S0959-8049(12)71940-8
    • (2012) Eur. J. Cancer , vol.48 , pp. 44
    • Miyadera, K.1    Kato, M.2    Takahashi, I.3    Ito, K.4    Aoyagi, Y.5    Fukasawa, K.6    Sagara, T.7    Yonekura, K.8    Iwasawa, Y.9    Utsugi, T.10
  • 72
    • 84979919957 scopus 로고    scopus 로고
    • TAS-121, a highly potent and mutant-specific EGFR inhibitor, overcomes T790M-acquired resistance with promising antitumor activity through specific inhibition of mutant EGFR signaling
    • Kato, M.; Miyadera, K.; Ito, K.; Aoyagi, Y.; Hashimoto, A.; Yonekura, K.; Iwasawa, Y.; Utsugi, T. TAS-121, a highly potent and mutant-specific EGFR inhibitor, overcomes T790M-acquired resistance with promising antitumor activity through specific inhibition of mutant EGFR signaling Eur. J. Cancer 2014, 50, 128 10.1016/S0959-8049(14)70527-1
    • (2014) Eur. J. Cancer , vol.50 , pp. 128
    • Kato, M.1    Miyadera, K.2    Ito, K.3    Aoyagi, Y.4    Hashimoto, A.5    Yonekura, K.6    Iwasawa, Y.7    Utsugi, T.8
  • 73
    • 85020269696 scopus 로고    scopus 로고
    • Abstract C112: Characterization of TAS-121, a novel mutant-specific EGFR-TKI, on pharmacokinetics, pharmacodynamics, and antitumor activity
    • Kato, M.; Miyadera, K.; Shibata, Y.; Ito, K.; Aoyagi, Y.; Chiba, M. Abstract C112: Characterization of TAS-121, a novel mutant-specific EGFR-TKI, on pharmacokinetics, pharmacodynamics, and antitumor activity Mol. Cancer Ther. 2013, 12, C112 10.1158/1535-7163.TARG-13-C112
    • (2013) Mol. Cancer Ther. , vol.12 , pp. C112
    • Kato, M.1    Miyadera, K.2    Shibata, Y.3    Ito, K.4    Aoyagi, Y.5    Chiba, M.6
  • 74
    • 85020281446 scopus 로고    scopus 로고
    • Abstract C111: In vitro characterization of TAS-121, a novel, highly potent, and mutant-specific EGFR-TKI
    • Ito, K.; Miyadera, K.; Aoyagi, Y.; Kato, M.; Kato, M.; Yonekura, K.; Iwasawa, Y.; Utsugi, T. Abstract C111: In vitro characterization of TAS-121, a novel, highly potent, and mutant-specific EGFR-TKI Mol. Cancer Ther. 2013, 12, C111 10.1158/1535-7163.TARG-13-C111
    • (2013) Mol. Cancer Ther. , vol.12 , pp. C111
    • Ito, K.1    Miyadera, K.2    Aoyagi, Y.3    Kato, M.4    Kato, M.5    Yonekura, K.6    Iwasawa, Y.7    Utsugi, T.8
  • 76
    • 84975874463 scopus 로고    scopus 로고
    • HM61713, an EGFR-mutant selective inhibitor
    • Kim, D. W. HM61713, an EGFR-mutant selective inhibitor Ann. Oncol. 2015, 26, ii14 10.1093/annonc/mdv088.2
    • (2015) Ann. Oncol. , vol.26 , pp. ii14
    • Kim, D.W.1
  • 80
    • 84938263349 scopus 로고    scopus 로고
    • Parallel phase 1 clinical trials in the US and in China: Accelerating the test of avitinib in lung cancer as a novel inhibitor selectively targeting mutated EGFR and overcoming T790M-induced resistance
    • Xu, X. Parallel phase 1 clinical trials in the US and in China: accelerating the test of avitinib in lung cancer as a novel inhibitor selectively targeting mutated EGFR and overcoming T790M-induced resistance Chin. J. Cancer 2015, 34, 1-3 10.1186/s40880-015-0029-3
    • (2015) Chin. J. Cancer , vol.34 , pp. 1-3
    • Xu, X.1


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