메뉴 건너뛰기




Volumn 9, Issue 1, 2016, Pages

Acalabrutinib (ACP-196): A selective second-generation BTK inhibitor

Author keywords

[No Author keywords available]

Indexed keywords

ACALABRUTINIB; IBRUTINIB; SPEBRUTINIB; AGAMMAGLOBULINAEMIA TYROSINE KINASE; BENZAMIDE DERIVATIVE; PROTEIN KINASE INHIBITOR; PROTEIN TYROSINE KINASE; PYRAZINE DERIVATIVE;

EID: 84960344942     PISSN: None     EISSN: 17568722     Source Type: Journal    
DOI: 10.1186/s13045-016-0250-9     Document Type: Review
Times cited : (208)

References (37)
  • 1
    • 84894552888 scopus 로고    scopus 로고
    • Obinutuzumab plus chlorambucil in patients with CLL and coexisting conditions
    • 1:CAS:528:DC%2BC2cXlt1ems74%3D 24401022
    • Goede V, Fischer K, Busch R, Engelke A, Eichhorst B, Wendtner CM, et al. Obinutuzumab plus chlorambucil in patients with CLL and coexisting conditions. N Engl J Med. 2014;370(12):1101-10.
    • (2014) N Engl J Med , vol.370 , Issue.12 , pp. 1101-1110
    • Goede, V.1    Fischer, K.2    Busch, R.3    Engelke, A.4    Eichhorst, B.5    Wendtner, C.M.6
  • 2
    • 84950989868 scopus 로고    scopus 로고
    • Bispecific antibodies and their applications
    • Fan G, Wang Z, Hao M, Li J. Bispecific antibodies and their applications. J Hematol Oncol. 2015;8(1):1-14.
    • (2015) J Hematol Oncol , vol.8 , Issue.1 , pp. 1-14
    • Fan, G.1    Wang, Z.2    Hao, M.3    Li, J.4
  • 3
    • 84938506999 scopus 로고    scopus 로고
    • A tetravalent bispecific TandAb (CD19/CD3), AFM11, efficiently recruits T cells for the potent lysis of CD19(+) tumor cells
    • 25875246
    • Reusch U, Duell J, Ellwanger K, Herbrecht C, Knackmuss SH, Fucek I, et al. A tetravalent bispecific TandAb (CD19/CD3), AFM11, efficiently recruits T cells for the potent lysis of CD19(+) tumor cells. MAbs. 2015;7(3):584-604.
    • (2015) MAbs , vol.7 , Issue.3 , pp. 584-604
    • Reusch, U.1    Duell, J.2    Ellwanger, K.3    Herbrecht, C.4    Knackmuss, S.H.5    Fucek, I.6
  • 4
    • 84908213051 scopus 로고    scopus 로고
    • New antibody approaches to lymphoma therapy
    • 25355407 4172963
    • Suresh T, Lee L, Joshi J, Barta S. New antibody approaches to lymphoma therapy. J Hematol Oncol. 2014;7(1):58.
    • (2014) J Hematol Oncol , vol.7 , Issue.1 , pp. 58
    • Suresh, T.1    Lee, L.2    Joshi, J.3    Barta, S.4
  • 5
    • 84925985383 scopus 로고    scopus 로고
    • Blinatumomab: A new era of treatment for adult ALL?
    • 25524799
    • Thomas X. Blinatumomab: a new era of treatment for adult ALL? Lancet Oncol. 2014;16(1):6-7.
    • (2014) Lancet Oncol , vol.16 , Issue.1 , pp. 6-7
    • Thomas, X.1
  • 6
    • 84938574282 scopus 로고    scopus 로고
    • AFM13: A first-in-class tetravalent bispecific anti-CD30/CD16A antibody for NK cell-mediated immunotherapy
    • 26231785 4522136
    • Wu J, Fu J, Zhang M, Liu D. AFM13: a first-in-class tetravalent bispecific anti-CD30/CD16A antibody for NK cell-mediated immunotherapy. J Hematol Oncol. 2015;8:96.
    • (2015) J Hematol Oncol , vol.8 , pp. 96
    • Wu, J.1    Fu, J.2    Zhang, M.3    Liu, D.4
  • 7
    • 84938628792 scopus 로고    scopus 로고
    • Blinatumomab: A bispecific T cell engager (BiTE) antibody against CD19/CD3 for refractory acute lymphoid leukemia
    • 26337639 4558758
    • Wu J, Fu J, Zhang M, Liu D. Blinatumomab: a bispecific T cell engager (BiTE) antibody against CD19/CD3 for refractory acute lymphoid leukemia. J Hematol Oncol. 2015;8(1):104.
    • (2015) J Hematol Oncol , vol.8 , Issue.1 , pp. 104
    • Wu, J.1    Fu, J.2    Zhang, M.3    Liu, D.4
  • 8
    • 84959497243 scopus 로고    scopus 로고
    • ABT-199 (venetoclax) and BCL-2 inhibitors in clinical development
    • 26589495 4654800
    • Cang S, Iragavarapu C, Savooji J, Song Y, Liu D. ABT-199 (venetoclax) and BCL-2 inhibitors in clinical development. J Hematol Oncol. 2015;8(1):129.
    • (2015) J Hematol Oncol , vol.8 , Issue.1 , pp. 129
    • Cang, S.1    Iragavarapu, C.2    Savooji, J.3    Song, Y.4    Liu, D.5
  • 10
    • 84938603207 scopus 로고    scopus 로고
    • Therapeutic potential of new B cell-targeted agents in the treatment of elderly and unfit patients with chronic lymphocytic leukemia
    • 26170206 4522086
    • Rai K. Therapeutic potential of new B cell-targeted agents in the treatment of elderly and unfit patients with chronic lymphocytic leukemia. J Hematol Oncol. 2015;8(1):85.
    • (2015) J Hematol Oncol , vol.8 , Issue.1 , pp. 85
    • Rai, K.1
  • 12
    • 84938862553 scopus 로고    scopus 로고
    • MYD88 mutations and response to ibrutinib in Waldenstrom's macroglobulinemia
    • 1:CAS:528:DC%2BC28XkslCqtg%3D%3D 26244327
    • Treon SP, Xu L, Hunter Z. MYD88 mutations and response to ibrutinib in Waldenstrom's macroglobulinemia. N Engl J Med. 2015;373(6):584-6.
    • (2015) N Engl J Med , vol.373 , Issue.6 , pp. 584-586
    • Treon, S.P.1    Xu, L.2    Hunter, Z.3
  • 13
    • 84927155030 scopus 로고    scopus 로고
    • Ibrutinib in previously treated Waldenstrom's macroglobulinemia
    • 1:CAS:528:DC%2BC2MXns1Wrt7w%3D 25853747
    • Treon SP, Tripsas CK, Meid K, Warren D, Varma G, Green R, et al. Ibrutinib in previously treated Waldenstrom's macroglobulinemia. N Engl J Med. 2015;372(15):1430-40.
    • (2015) N Engl J Med , vol.372 , Issue.15 , pp. 1430-1440
    • Treon, S.P.1    Tripsas, C.K.2    Meid, K.3    Warren, D.4    Varma, G.5    Green, R.6
  • 14
    • 84931563809 scopus 로고    scopus 로고
    • The BCL2 antagonist ABT-199 triggers apoptosis, and augments ibrutinib and idelalisib mediated cytotoxicity in CXCR4 Wild-type and CXCR4 WHIM mutated Waldenstrom macroglobulinaemia cells
    • 1:CAS:528:DC%2BC2MXhtVGmsbbF 25582069
    • Cao Y, Yang G, Hunter ZR, Liu X, Xu L, Chen J, et al. The BCL2 antagonist ABT-199 triggers apoptosis, and augments ibrutinib and idelalisib mediated cytotoxicity in CXCR4 Wild-type and CXCR4 WHIM mutated Waldenstrom macroglobulinaemia cells. Br J Haematol. 2015;170(1):134-8.
    • (2015) Br J Haematol , vol.170 , Issue.1 , pp. 134-138
    • Cao, Y.1    Yang, G.2    Hunter, Z.R.3    Liu, X.4    Xu, L.5    Chen, J.6
  • 15
    • 84879748062 scopus 로고    scopus 로고
    • Targeting BTK with ibrutinib in relapsed chronic lymphocytic leukemia
    • 1:CAS:528:DC%2BC3sXhtFygu7zN 23782158 3772525
    • Byrd JC, Furman RR, Coutre SE, Flinn IW, Burger JA, Blum KA, et al. Targeting BTK with ibrutinib in relapsed chronic lymphocytic leukemia. N Engl J Med. 2013;369(1):32-42.
    • (2013) N Engl J Med , vol.369 , Issue.1 , pp. 32-42
    • Byrd, J.C.1    Furman, R.R.2    Coutre, S.E.3    Flinn, I.W.4    Burger, J.A.5    Blum, K.A.6
  • 16
    • 84881225049 scopus 로고    scopus 로고
    • Targeting BTK with ibrutinib in relapsed or refractory mantle-cell lymphoma
    • 1:CAS:528:DC%2BC3sXht1OgtL%2FF 23782157 4513941
    • Wang ML, Rule S, Martin P, Goy A, Auer R, Kahl BS, et al. Targeting BTK with ibrutinib in relapsed or refractory mantle-cell lymphoma. N Engl J Med. 2013;369(6):507-16.
    • (2013) N Engl J Med , vol.369 , Issue.6 , pp. 507-516
    • Wang, M.L.1    Rule, S.2    Martin, P.3    Goy, A.4    Auer, R.5    Kahl, B.S.6
  • 17
    • 84929154536 scopus 로고    scopus 로고
    • The Bruton tyrosine kinase inhibitor ibrutinib with chemoimmunotherapy in patients with chronic lymphocytic leukemia
    • 1:CAS:528:DC%2BC2MXptlGruro%3D 25755291 4424415
    • Brown JR, Barrientos JC, Barr PM, Flinn IW, Burger JA, Tran A, et al. The Bruton tyrosine kinase inhibitor ibrutinib with chemoimmunotherapy in patients with chronic lymphocytic leukemia. Blood. 2015;125(19):2915-22.
    • (2015) Blood , vol.125 , Issue.19 , pp. 2915-2922
    • Brown, J.R.1    Barrientos, J.C.2    Barr, P.M.3    Flinn, I.W.4    Burger, J.A.5    Tran, A.6
  • 18
    • 84950133717 scopus 로고    scopus 로고
    • Ibrutinib as initial therapy for patients with chronic lymphocytic leukemia
    • 1:CAS:528:DC%2BC28Xit10%3D 26639149
    • Burger JA, Tedeschi A, Barr PM, Robak T, Owen C, Ghia P, et al. Ibrutinib as initial therapy for patients with chronic lymphocytic leukemia. N Engl J Med. 2015;373(25):2425-37.
    • (2015) N Engl J Med , vol.373 , Issue.25 , pp. 2425-2437
    • Burger, J.A.1    Tedeschi, A.2    Barr, P.M.3    Robak, T.4    Owen, C.5    Ghia, P.6
  • 19
    • 84977969461 scopus 로고    scopus 로고
    • Abstract 2596: ACP-196: a novel covalent Bruton's tyrosine kinase (Btk) inhibitor with improved selectivity and in vivo target coverage in chronic lymphocytic leukemia (CLL) patients
    • Covey T, Barf T, Gulrajani M, Krantz F, van Lith B, Bibikova E, et al. Abstract 2596: ACP-196: a novel covalent Bruton's tyrosine kinase (Btk) inhibitor with improved selectivity and in vivo target coverage in chronic lymphocytic leukemia (CLL) patients. Cancer Res. 2015;75(15 Supplement):2596.
    • (2015) Cancer Res , vol.75 , Issue.15 , pp. 2596
    • Covey, T.1    Barf, T.2    Gulrajani, M.3    Krantz, F.4    Van Lith, B.5    Bibikova, E.6
  • 20
    • 84977961466 scopus 로고    scopus 로고
    • Abstract 1757: The novel BTK inhibitor CC-292 exerts in vitro and in vivo antitumor activity, interferes with adhesion, cell migration, and synergizes with lenalidomide in MCL models
    • Vidal-Crespo A, Rodríguez V, Matas-Céspedes A, Campos E, López-Guillermo A, Roué G, et al. Abstract 1757: the novel BTK inhibitor CC-292 exerts in vitro and in vivo antitumor activity, interferes with adhesion, cell migration, and synergizes with lenalidomide in MCL models. Cancer Res. 2014;74(19 Supplement):1757.
    • (2014) Cancer Res , vol.74 , Issue.19 , pp. 1757
    • Vidal-Crespo, A.1    Rodríguez, V.2    Matas-Céspedes, A.3    Campos, E.4    López-Guillermo, A.5    Roué, G.6
  • 21
    • 84977966160 scopus 로고    scopus 로고
    • Abstract 2597: BGB-3111 is a novel and highly selective Bruton's tyrosine kinase (BTK) inhibitor
    • Na L, Zhijian S, Ye L, Mingming G, Yilu Z, Dongping Z, et al. Abstract 2597: BGB-3111 is a novel and highly selective Bruton's tyrosine kinase (BTK) inhibitor. Cancer Res. 2015;75:2597.
    • (2015) Cancer Res , vol.75 , pp. 2597
    • Na, L.1    Zhijian, S.2    Ye, L.3    Mingming, G.4    Yilu, Z.5    Dongping, Z.6
  • 22
    • 84960359160 scopus 로고    scopus 로고
    • The BTK inhibitor, Bgb-3111, is safe, tolerable, and highly active in patients with relapsed/refractory B-cell malignancies: Initial report of a phase 1 first-in-human trial
    • Tam C, Grigg AP, Opat S, Ku M, Gilbertson M, Anderson MA, et al. The BTK inhibitor, Bgb-3111, is safe, tolerable, and highly active in patients with relapsed/refractory B-cell malignancies: initial report of a phase 1 first-in-human trial. Blood. 2015;126(23):832.
    • (2015) Blood , vol.126 , Issue.23 , pp. 832
    • Tam, C.1    Grigg, A.P.2    Opat, S.3    Ku, M.4    Gilbertson, M.5    Anderson, M.A.6
  • 23
    • 84958230944 scopus 로고    scopus 로고
    • A phase 1 clinical trial of the selective BTK inhibitor ONO/GS-4059 in relapsed and refractory mature B-cell malignancies
    • 26542378 4731845
    • Walter HS, Rule SA, Dyer MJS, Karlin L, Jones C, Cazin B, et al. A phase 1 clinical trial of the selective BTK inhibitor ONO/GS-4059 in relapsed and refractory mature B-cell malignancies. Blood. 2016;127(4):411-9.
    • (2016) Blood , vol.127 , Issue.4 , pp. 411-419
    • Walter, H.S.1    Rule, S.A.2    Dyer, M.J.S.3    Karlin, L.4    Jones, C.5    Cazin, B.6
  • 25
    • 84977930710 scopus 로고    scopus 로고
    • Abstract 1744: ACP-196: a second generation Btk inhibitor demonstrates biologic activity in a canine model of B-cell non-Hodgkin lymphoma
    • Gardner∗ HL, Harrington∗ BK, Izumi R, Hamdy A, Kaptein A, Lith BV, et al. Abstract 1744: ACP-196: a second generation Btk inhibitor demonstrates biologic activity in a canine model of B-cell non-Hodgkin lymphoma. Cancer Res. 2014;74(19 Supplement):1744.
    • (2014) Cancer Res , vol.74 , Issue.19 , pp. 1744
    • Gardner, H.L.1    Harrington, B.K.2    Izumi, R.3    Hamdy, A.4    Kaptein, A.5    Lith, B.V.6
  • 26
    • 84977942416 scopus 로고    scopus 로고
    • ACP-196 is a second generation inhibitor of Bruton tyrosine kinase (BTK) with enhanced target specificity
    • Harrington BK, Gulrajani M, Covey T, Kaptein A, Van Lith B, Izumi R, et al. ACP-196 is a second generation inhibitor of Bruton tyrosine kinase (BTK) with enhanced target specificity. Blood. 2015;126(23):2908.
    • (2015) Blood , vol.126 , Issue.23 , pp. 2908
    • Harrington, B.K.1    Gulrajani, M.2    Covey, T.3    Kaptein, A.4    Van Lith, B.5    Izumi, R.6
  • 27
    • 84977936070 scopus 로고    scopus 로고
    • Abstract 408: ACP-196, an orally bioavailable covalent selective inhibitor of Btk, modulates the innate tumor microenvironment, exhibits antitumor efficacy and enhances gemcitabine activity in pancreatic cancer
    • Lannutti BJ, Gulrajani M, Krantz F, Bibikova E, Covey T, Jessen K, et al. Abstract 408: ACP-196, an orally bioavailable covalent selective inhibitor of Btk, modulates the innate tumor microenvironment, exhibits antitumor efficacy and enhances gemcitabine activity in pancreatic cancer. Cancer Res. 2015;75(15 Supplement):408.
    • (2015) Cancer Res , vol.75 , Issue.15 , pp. 408
    • Lannutti, B.J.1    Gulrajani, M.2    Krantz, F.3    Bibikova, E.4    Covey, T.5    Jessen, K.6
  • 28
    • 84960463221 scopus 로고    scopus 로고
    • Abstract 2624: The novel Bruton's tyrosine kinase inhibitor ACP-196 shows in vivo efficacy against human chronic lymphocytic leukemia cells xenografted to the NSG mouse model
    • Niemann CU, Montraveta A, Herman SEM, Ingallinera T, Barf T, Colomer D, et al. Abstract 2624: the novel Bruton's tyrosine kinase inhibitor ACP-196 shows in vivo efficacy against human chronic lymphocytic leukemia cells xenografted to the NSG mouse model. Cancer Res. 2014;74(19 Supplement):2624.
    • (2014) Cancer Res , vol.74 , Issue.19 , pp. 2624
    • Niemann, C.U.1    Montraveta, A.2    Herman, S.E.M.3    Ingallinera, T.4    Barf, T.5    Colomer, D.6
  • 29
    • 84977951072 scopus 로고    scopus 로고
    • The Bruton tyrosine kinase (BTK) inhibitor ACP-196 demonstrates clinical activity in two mouse models of chronic lymphocytic leukemia
    • Herman SEM, Montraveta A, Niemann CU, Mora-Jensen H, Gulrajani M, Krantz F, et al. The Bruton tyrosine kinase (BTK) inhibitor ACP-196 demonstrates clinical activity in two mouse models of chronic lymphocytic leukemia. Blood. 2015;126(23):2920.
    • (2015) Blood , vol.126 , Issue.23 , pp. 2920
    • Herman, S.E.M.1    Montraveta, A.2    Niemann, C.U.3    Mora-Jensen, H.4    Gulrajani, M.5    Krantz, F.6
  • 30
    • 84890438137 scopus 로고    scopus 로고
    • Modeling tumor-host interactions of chronic lymphocytic leukemia in xenografted mice to study tumor biology and evaluate targeted therapy
    • 1:CAS:528:DC%2BC3sXhvFCqtbbN 23619564 4126654
    • Herman SE, Sun X, McAuley EM, Hsieh MM, Pittaluga S, Raffeld M, et al. Modeling tumor-host interactions of chronic lymphocytic leukemia in xenografted mice to study tumor biology and evaluate targeted therapy. Leukemia. 2013;27(12):2311-21.
    • (2013) Leukemia , vol.27 , Issue.12 , pp. 2311-2321
    • Herman, S.E.1    Sun, X.2    McAuley, E.M.3    Hsieh, M.M.4    Pittaluga, S.5    Raffeld, M.6
  • 31
    • 84896453785 scopus 로고    scopus 로고
    • Movement toward optimization of CLL therapy
    • 1:CAS:528:DC%2BC2cXlt1ems7k%3D 24645950
    • Rai KR, Barrientos JC. Movement toward optimization of CLL therapy. N Engl J Med. 2014;370(12):1160-2.
    • (2014) N Engl J Med , vol.370 , Issue.12 , pp. 1160-1162
    • Rai, K.R.1    Barrientos, J.C.2
  • 32
    • 84927638285 scopus 로고    scopus 로고
    • Idelalisib: First-in-class PI3K delta inhibitor for the treatment of chronic lymphocytic leukemia, small lymphocytic leukemia, and follicular lymphoma
    • 1:CAS:528:DC%2BC2MXmtVahsrk%3D 25670221
    • Yang Q, Modi P, Newcomb T, Queva C, Gandhi V. Idelalisib: first-in-class PI3K delta inhibitor for the treatment of chronic lymphocytic leukemia, small lymphocytic leukemia, and follicular lymphoma. Clin Cancer Res. 2015;21(7):1537-42.
    • (2015) Clin Cancer Res , vol.21 , Issue.7 , pp. 1537-1542
    • Yang, Q.1    Modi, P.2    Newcomb, T.3    Queva, C.4    Gandhi, V.5
  • 34
    • 84924149342 scopus 로고    scopus 로고
    • Selective inhibitors of nuclear export (SINE) - A novel class of anti-cancer agents
    • 25316614 4200201
    • Parikh K, Cang S, Sekhri A, Liu D. Selective inhibitors of nuclear export (SINE) - a novel class of anti-cancer agents. J Hematol Oncol. 2014;7(1):78.
    • (2014) J Hematol Oncol , vol.7 , Issue.1 , pp. 78
    • Parikh, K.1    Cang, S.2    Sekhri, A.3    Liu, D.4
  • 35
    • 84978024579 scopus 로고    scopus 로고
    • Selective inhibitors of nuclear export (SINE) in hematological malignancies
    • 25745591 4350974
    • Das A, Wei G, Parikh K, Liu D. Selective inhibitors of nuclear export (SINE) in hematological malignancies. Exp Hematol Oncol. 2015;4:7.
    • (2015) Exp Hematol Oncol , vol.4 , pp. 7
    • Das, A.1    Wei, G.2    Parikh, K.3    Liu, D.4
  • 36
    • 84873540049 scopus 로고    scopus 로고
    • ABT-199, a potent and selective BCL-2 inhibitor, achieves antitumor activity while sparing platelets
    • 1:CAS:528:DC%2BC3sXjslagtQ%3D%3D 23291630
    • Souers AJ, Leverson JD, Boghaert ER, Ackler SL, Catron ND, Chen J, et al. ABT-199, a potent and selective BCL-2 inhibitor, achieves antitumor activity while sparing platelets. Nat Med. 2013;19(2):202-8.
    • (2013) Nat Med , vol.19 , Issue.2 , pp. 202-208
    • Souers, A.J.1    Leverson, J.D.2    Boghaert, E.R.3    Ackler, S.L.4    Catron, N.D.5    Chen, J.6
  • 37
    • 84977961468 scopus 로고    scopus 로고
    • In vitro and in vivo characterization of CD19/CD3 Tandab AFM11 and CD19/CD16A Tandab AFM12 targeting NHL
    • Zhao X, Rajasekaran N, Reusch U, Weichel M, Ellwanger K, Marschner J-P, et al. In vitro and in vivo characterization of CD19/CD3 Tandab AFM11 and CD19/CD16A Tandab AFM12 targeting NHL. Blood. 2015;126(23):2763.
    • (2015) Blood , vol.126 , Issue.23 , pp. 2763
    • Zhao, X.1    Rajasekaran, N.2    Reusch, U.3    Weichel, M.4    Ellwanger, K.5    Marschner, J.-P.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.