-
1
-
-
84894552888
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
9
-
-
84955491187
-
Targeting BCL2 with venetoclax in relapsed chronic lymphocytic leukemia
-
26639348
-
Roberts AW, Davids MS, Pagel JM, Kahl BS, Puvvada SD, Gerecitano JF, et al. Targeting BCL2 with venetoclax in relapsed chronic lymphocytic leukemia. N Engl J Med. 2016;374(4):311-22.
-
(2016)
N Engl J Med
, vol.374
, Issue.4
, pp. 311-322
-
-
Roberts, A.W.1
Davids, M.S.2
Pagel, J.M.3
Kahl, B.S.4
Puvvada, S.D.5
Gerecitano, J.F.6
-
10
-
-
84938603207
-
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
-
11
-
-
84978025178
-
Ibrutinib for B cell malignancies
-
Novero A, Ravella PM, Chen Y, Dous G, Liu D. Ibrutinib for B cell malignancies. Experimental Hematology & Oncology. 2014;3(1):1-7.
-
(2014)
Experimental Hematology & Oncology
, vol.3
, Issue.1
, pp. 1-7
-
-
Novero, A.1
Ravella, P.M.2
Chen, Y.3
Dous, G.4
Liu, D.5
-
12
-
-
84938862553
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
24
-
-
84955481177
-
Acalabrutinib (ACP-196) in relapsed chronic lymphocytic leukemia
-
26641137
-
Byrd JC, Harrington B, O'Brien S, Jones JA, Schuh A, Devereux S, et al. Acalabrutinib (ACP-196) in relapsed chronic lymphocytic leukemia. N Engl J Med. 2016;374(4):323-32.
-
(2016)
N Engl J Med
, vol.374
, Issue.4
, pp. 323-332
-
-
Byrd, J.C.1
Harrington, B.2
O'Brien, S.3
Jones, J.A.4
Schuh, A.5
Devereux, S.6
-
25
-
-
84977930710
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
33
-
-
85016649923
-
Novel ALK inhibitors in clinical use and development
-
25888090 4349797
-
Iragavarapu C, Mustafa M, Akinleye A, Furqan M, Mittal V, Cang S, et al. Novel ALK inhibitors in clinical use and development. J Hematol Oncol. 2015;8(1):17.
-
(2015)
J Hematol Oncol
, vol.8
, Issue.1
, pp. 17
-
-
Iragavarapu, C.1
Mustafa, M.2
Akinleye, A.3
Furqan, M.4
Mittal, V.5
Cang, S.6
-
34
-
-
84924149342
-
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
-
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
-
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
-
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
|