-
1
-
-
74049142026
-
The use of novel agents in the treatment of relapsed and refractory multiple myeloma
-
Laubach JP, Mahindra A, Mitsiades CS, et al. The use of novel agents in the treatment of relapsed and refractory multiple myeloma. Leukemia. 2009;23(12):2222-32.
-
(2009)
Leukemia.
, vol.23
, Issue.12
, pp. 2222-2222
-
-
Laubach, J.P.1
Mahindra, A.2
Mitsiades, C.S.3
-
2
-
-
18344394135
-
Proteasome inhibition in the treatment of cancer
-
Richardson PG,Mitsiades C, Hideshima T, Anderson KC. Proteasome inhibition in the treatment of cancer. Cell Cycle. 2005;4(2):290-6. (Pubitemid 41365336)
-
(2005)
Cell Cycle
, vol.4
, Issue.2
, pp. 290-296
-
-
Richardson, P.G.1
Mitsiades, C.2
Hideshima, T.3
Anderson, K.C.4
-
3
-
-
20044396543
-
Phase ii study of proteasome inhibitor bortezomib in relapsed or refractory b-cell non-hodgkin's lymphoma
-
Goy A, Younes A, McLaughlin P, et al. Phase II study of proteasome inhibitor bortezomib in relapsed or refractory B-cell non-Hodgkin's lymphoma. J Clin Oncol. 2005;23(4):667-75.
-
(2005)
J Clin Oncol.
, vol.23
, Issue.4
, pp. 667-665
-
-
Goy, A.1
Younes, A.2
McLaughlin, P.3
-
4
-
-
84862689569
-
Discovery and development of second-generation proteasome inhibitors
-
Kirk CJ. Discovery and development of second-generation proteasome inhibitors. Semin Hematol. 2012;49(3):207-14.
-
(2012)
Semin Hematol.
, vol.49
, Issue.3
, pp. 207-204
-
-
Kirk, C.J.1
-
5
-
-
84864568543
-
Proteasome inhibitors in multiple myeloma: Ten years later
-
May 29. A Comprehensive Review Of PIs Both Old and New
-
Moreau P, Richardson PG, Cavo M, et al. Proteasome inhibitors in multiple myeloma: ten years later. Blood. 2012 May 29. A comprehensive review of PIs, both old and new.
-
(2012)
Blood.
-
-
Moreau, P.1
Richardson, P.G.2
Cavo, M.3
-
6
-
-
84862681257
-
The immunoproteasome as a target in hematologic malignancies
-
Kuhn DJ, Orlowski RZ. The immunoproteasome as a target in hematologic malignancies. Semin Hematol. 2012;49(3):258-62.
-
(2012)
Semin Hematol.
, vol.49
, Issue.3
, pp. 258-252
-
-
Kuhn, D.J.1
Orlowski, R.Z.2
-
7
-
-
84857910414
-
Deubiquitylating enzyme usp-7, a novel therapeutic target in multiple myeloma
-
Chauhan D, Tian Z, Nicholson B, et al. Deubiquitylating enzyme USP-7, a novel therapeutic target in multiple myeloma. ASH Annual Meeting Abstracts. 2009;114(22):610.
-
(2009)
ASH Annual Meeting Abstracts.
, vol.114
, Issue.22
, pp. 610
-
-
Chauhan, D.1
Tian, Z.2
Nicholson, B.3
-
8
-
-
66549099025
-
Targeted inhibition of the immunoproteasome is a potent strategy against models of multiple myeloma that overcomes resistance to conventional drugs and nonspecific proteasome inhibitors
-
An imortant reclinical study of immunoroteasome inhibition in MM
-
Kuhn DJ, Hunsucker SA, Chen Q, et al. Targeted inhibition of the immunoproteasome is a potent strategy against models of multiple myeloma that overcomes resistance to conventional drugs and nonspecific proteasome inhibitors. Blood. 2009;113(19):4667-76. An important preclinical study of immunoproteasome inhibition in MM.
-
(2009)
Blood.
, vol.113
, Issue.19
, pp. 4667-4666
-
-
Kuhn, D.J.1
Hunsucker, S.A.2
Chen, Q.3
-
9
-
-
77953264178
-
Selective inhibition of chymotrypsin-like activity of the immunoproteasome and constitutive proteasome in waldenstrom macroglobulinemia
-
Roccaro AM, Sacco A, Aujay M, et al. Selective inhibition of chymotrypsin-like activity of the immunoproteasome and constitutive proteasome in Waldenstrom macroglobulinemia. Blood. 2010;115(20):4051-60.
-
(2010)
Blood.
, vol.115
, Issue.20
, pp. 4051-4050
-
-
Roccaro, A.M.1
Sacco, A.2
Aujay, M.3
-
10
-
-
77950238258
-
Evaluation of the proteasome inhibitor mln9708 in preclinical models of human cancer
-
Kupperman E, Lee EC, Cao Y, et al. Evaluation of the proteasome inhibitor MLN9708 in preclinical models of human cancer. Cancer Res. 2010;70(5):1970-80.
-
(2010)
Cancer Res.
, vol.70
, Issue.5
, pp. 80
-
-
Kupperman, E.1
Lee, E.C.2
Cao, Y.3
-
11
-
-
27644562277
-
A novel orally active proteasome inhibitor induces apoptosis in multiple myeloma cells with mechanisms distinct from bortezomib
-
Chauhan D, Catley L, Li G, et al. A novel orally active proteasome inhibitor induces apoptosis in multiple myeloma cells with mechanisms distinct from Bortezomib. Cancer Cell. 2005;8(5):407-19.
-
(2005)
Cancer Cell.
, vol.8
, Issue.5
, pp. 407-409
-
-
Chauhan, D.1
Catley, L.2
Li, G.3
-
12
-
-
77649237033
-
Building on bortezomib: Second-generation proteasome inhibitors as anti-cancer therapy
-
Dick LR, Fleming PE. Building on bortezomib: second-generation proteasome inhibitors as anti-cancer therapy. Drug Discov Today. 2010;15(5-6):243-9.
-
(2010)
Drug Discov Today.
, vol.15
, Issue.5-6
, pp. 243-249
-
-
Dick, L.R.1
Fleming, P.E.2
-
13
-
-
80051691845
-
In vitro and in vivo selective antitumor activity of a novel orally bioavailable proteasome inhibitor mln9708 against multiple myeloma cells
-
An important preclinical study evaluating the activity of MLN9708 in MM
-
Chauhan D, Tian Z, Zhou B, et al. In vitro and in vivo selective antitumor activity of a novel orally bioavailable proteasome inhibitor MLN9708 against multiple myeloma cells. Clin Cancer Res. 2011;17(16):5311-21. An important preclinical study evaluating the activity of MLN9708 in MM.
-
(2011)
Clin Cancer Res.
, vol.17
, Issue.16
, pp. 5311-5311
-
-
Chauhan, D.1
Tian, Z.2
Zhou, B.3
-
14
-
-
41949110089
-
Cep-18770: A novel, orally active proteasome inhibitor with a tumor-selective pharmacologic profile competitive with bortezomib
-
Piva R, Ruggeri B, Williams M, et al. CEP-18770: a novel, orally active proteasome inhibitor with a tumor-selective pharmacologic profile competitive with bortezomib. Blood. 2008;111(5):2765-75.
-
(2008)
Blood.
, vol.111
, Issue.5
, pp. 2765-2765
-
-
Piva, R.1
Ruggeri, B.2
Williams, M.3
-
15
-
-
82555189384
-
Antitumor activity of the investigational proteasome inhibitor mln9708 in mouse models of b-cell and plasma cell malignancies
-
Lee EC, Fitzgerald M, Bannerman B, et al. Antitumor activity of the investigational proteasome inhibitor MLN9708 in mouse models of B-cell and plasma cell malignancies. Clin Cancer Res. 2011;17(23):7313-23.
-
(2011)
Clin Cancer Res.
, vol.17
, Issue.23
, pp. 7313-7313
-
-
Lee, E.C.1
Fitzgerald, M.2
Bannerman, B.3
-
16
-
-
84872197249
-
Tumor drug distribution and target engagement of mln9708, an investigational proteasome inhibitor, in patients with advanced solid tumors
-
abstr 3077
-
Bacco AD, Berger A, Gupta N, et al. Tumor drug distribution and target engagement of MLN9708, an investigational proteasome inhibitor, in patients with advanced solid tumors. J Clin Oncol. 2012;30(suppl):abstr 3077.
-
(2012)
J Clin Oncol.
, vol.30
, Issue.SUPPL.
-
-
Bacco, A.D.1
Berger, A.2
Gupta, N.3
-
17
-
-
75149157969
-
The proteasome inhibitor cep-18770 enhances the anti-myeloma activity of bortezomib and melphalan
-
Sanchez E, Li M, Steinberg JA, et al. The proteasome inhibitor CEP-18770 enhances the anti-myeloma activity of bortezomib and melphalan. Br J Haematol. 2010;148(4):569-81.
-
(2010)
Br J Haematol.
, vol.148
, Issue.4
, pp. 569-561
-
-
Sanchez, E.1
Li, M.2
Steinberg, J.A.3
-
18
-
-
36148944490
-
Potent activity of carfilzomib, a novel, irreversible inhibitor of the ubiquitin-proteasome pathway, against preclinical models of multiple myeloma
-
Kuhn DJ, Chen Q, Voorhees PM, et al. Potent activity of carfilzomib, a novel, irreversible inhibitor of the ubiquitin-proteasome pathway, against preclinical models of multiple myeloma. Blood. 2007;110(9):3281-90.
-
(2007)
Blood.
, vol.110
, Issue.9
, pp. 3281-3280
-
-
Kuhn, D.J.1
Chen, Q.2
Voorhees, P.M.3
-
19
-
-
34447116376
-
Antitumor activity of pr-171, a novel irreversible inhibitor of the proteasome
-
Demo SD, Kirk CJ, Aujay MA, et al. Antitumor activity of PR-171, a novel irreversible inhibitor of the proteasome. Cancer Res. 2007;67(13):6383-91.
-
(2007)
Cancer Res.
, vol.67
, Issue.13
, pp. 6383-6381
-
-
Demo, S.D.1
Kirk, C.J.2
Aujay, M.A.3
-
20
-
-
78649755360
-
A novel orally active proteasome inhibitor onx 0912 triggers in vitro and in vivo cytotoxicity in multiple myeloma
-
An important preclinical study of ONX 0912 demonstrating activity in MM
-
Chauhan D, Singh AV, Aujay M, et al. A novel orally active proteasome inhibitor ONX 0912 triggers in vitro and in vivo cytotoxicity in multiple myeloma. Blood. 2010;116(23):4906-15. An important preclinical study of ONX 0912 demonstrating activity in MM.
-
(2010)
Blood.
, vol.116
, Issue.23
, pp. 4906-4905
-
-
Chauhan, D.1
Singh, A.V.2
Aujay, M.3
-
21
-
-
84873566163
-
The epoxyketone-based proteasome inhibitors carfilzomib and orally bioavailable oprozomib have anti-resorptive and bone-Anabolic activity in addition to anti-myeloma effects
-
Jul 5
-
Hurchla MA, Garcia-Gomez A, Hornick MC, et al. The epoxyketone-based proteasome inhibitors carfilzomib and orally bioavailable oprozomib have anti-resorptive and bone-Anabolic activity in addition to anti-myeloma effects. Leukemia. 2012;Jul 5.
-
(2012)
Leukemia.
-
-
Hurchla, M.A.1
Garcia-Gomez, A.2
Hornick, M.C.3
-
22
-
-
80053148350
-
Pharmacokinetics, pharmacodynamics, metabolism, distribution, and excretion of carfilzomib in rats
-
Yang J, Wang Z, Fang Y, et al. Pharmacokinetics, pharmacodynamics, metabolism, distribution, and excretion of carfilzomib in rats. Drug Metab Dispos. 2011;39(10):1873-82.
-
(2011)
Drug Metab Dispos.
, vol.39
, Issue.10
, pp. 82
-
-
Yang, J.1
Wang, Z.2
Fang, Y.3
-
23
-
-
79955498420
-
Nonproteasomal targets of the proteasome inhibitors bortezomib and carfilzomib: A link to clinical adverse events
-
Arastu-Kapur S, Anderl JL, Kraus M, et al. Nonproteasomal targets of the proteasome inhibitors bortezomib and carfilzomib: a link to clinical adverse events. Clin Cancer Res. 2011;17(9):2734-43.
-
(2011)
Clin Cancer Res.
, vol.17
, Issue.9
, pp. 2734-2733
-
-
Arastu-Kapur, S.1
Anderl, J.L.2
Kraus, M.3
-
24
-
-
80052784486
-
Carfilzomib interacts synergistically with histone deacetylase inhibitors in mantle cell lymphoma cells in vitro and in vivo
-
Dasmahapatra G, Lembersky D, Son MP, et al. Carfilzomib interacts synergistically with histone deacetylase inhibitors in mantle cell lymphoma cells in vitro and in vivo. Mol Cancer Ther. 2011;10(9):1686-97.
-
(2011)
Mol Cancer Ther.
, vol.10
, Issue.9
, pp. 1686-1687
-
-
Dasmahapatra, G.1
Lembersky, D.2
Son, M.P.3
-
25
-
-
65649139708
-
Design and synthesis of an orally bioavailable and selective peptide epoxyketone proteasome inhibitor (pr-047)
-
Zhou HJ, Aujay MA, Bennett MK, et al. Design and synthesis of an orally bioavailable and selective peptide epoxyketone proteasome inhibitor (PR-047). J Med Chem. 2009;52(9):3028-38.
-
(2009)
J Med Chem.
, vol.52
, Issue.9
, pp. 3028-3028
-
-
Zhou, H.J.1
Aujay, M.A.2
Bennett, M.K.3
-
26
-
-
77951682116
-
Pharmacodynamic and efficacy studies of the novel proteasome inhibitor npi-0052 (marizomib) in a human plasmacytoma xenograft murine model
-
Singh AV, Palladino MA, Lloyd GK, et al. Pharmacodynamic and efficacy studies of the novel proteasome inhibitor NPI-0052 (marizomib) in a human plasmacytoma xenograft murine model. Br J Haematol. 2010;149(4):550-9.
-
(2010)
Br J Haematol.
, vol.149
, Issue.4
, pp. 550-559
-
-
Singh, A.V.1
Palladino, M.A.2
Lloyd, G.K.3
-
27
-
-
79951684725
-
Marizomib, a proteasome inhibitor for all seasons: Preclinical profile and a framework for clinical trials
-
Potts BC, Albitar MX, Anderson KC, et al. Marizomib, a proteasome inhibitor for all seasons: preclinical profile and a framework for clinical trials. Curr Cancer Drug Targets. 2011;11(3):254-84.
-
(2011)
Curr Cancer Drug Targets.
, vol.11
, Issue.3
, pp. 254-254
-
-
Potts, B.C.1
Albitar, M.X.2
Anderson, K.C.3
-
28
-
-
84872192025
-
Selective inhibition of the proteasome's {beta}2 catalytic subunit alone does not induce cytotoxicity, but resensitizes bortezomib-refractory myeloma cells for bortezomib treatment
-
Kraus M, Florea B, Bader J, et al. Selective inhibition of the proteasome's {beta}2 catalytic subunit alone does not induce cytotoxicity, but resensitizes bortezomib-refractory myeloma cells for bortezomib treatment. ASH Annual Meeting Abstracts. 2011;118(21):2915.
-
(2011)
ASH Annual Meeting Abstracts.
, vol.118
, Issue.21
, pp. 2915
-
-
Kraus, M.1
Florea, B.2
Bader, J.3
-
29
-
-
38949125853
-
Combination of proteasome inhibitors bortezomib and npi-0052 trigger in vivo synergistic cytotoxicity in multiple myeloma
-
Chauhan D, Singh A, Brahmandam M, et al. Combination of proteasome inhibitors bortezomib and NPI-0052 trigger in vivo synergistic cytotoxicity in multiple myeloma. Blood. 2008;111 (3):1654-64.
-
(2008)
Blood.
, vol.111
, Issue.3
, pp. 1654-1654
-
-
Chauhan, D.1
Singh, A.2
Brahmandam, M.3
-
30
-
-
77949315484
-
Combination of novel proteasome inhibitor npi-0052 and lenalidomide trigger in vitro and in vivo synergistic cytotoxicity in multiple myeloma
-
A study describing the potent combinational effect of lenalidomide and NPI-834-A study describing the po0052 and showing synergy preclinically against MM
-
Chauhan D, Singh AV, Ciccarelli B, et al. Combination of novel proteasome inhibitor NPI-0052 and lenalidomide trigger in vitro and in vivo synergistic cytotoxicity in multiple myeloma. Blood. 2010;115(4):834-45. A study describing the potent combinational effect of lenalidomide and NPI-0052 and showing synergy preclinically against MM.
-
(2010)
Blood.
, vol.115
, Issue.4
, pp. 834-835
-
-
Chauhan, D.1
Singh, A.V.2
Ciccarelli, B.3
-
31
-
-
64749088834
-
Emerging treatments for multiple myeloma: Beyond immunomodulatory drugs and bortezomib
-
Mitsiades CS, Hideshima T, Chauhan D, et al. Emerging treatments for multiple myeloma: beyond immunomodulatory drugs and bortezomib. Semin Hematol. 2009;46(2):166-75.
-
(2009)
Semin Hematol.
, vol.46
, Issue.2
, pp. 166-165
-
-
Mitsiades, C.S.1
Hideshima, T.2
Chauhan, D.3
-
32
-
-
34948881265
-
Salinosporamide a (npi-0052) potentiates apoptosis, suppresses osteoclastogenesis, and inhibits invasion through down-modulation of nf-kappab regulated gene products
-
Ahn KS, Sethi G, Chao TH, et al. Salinosporamide A (NPI-0052) potentiates apoptosis, suppresses osteoclastogenesis, and inhibits invasion through down-modulation of NF-kappaB regulated gene products. Blood. 2007;110(7):2286-95.
-
(2007)
Blood.
, vol.110
, Issue.7
, pp. 2286-2285
-
-
Ahn, K.S.1
Sethi, G.2
Chao, T.H.3
-
33
-
-
37249013214
-
-
US National Institute of Health. [cited 2012 July 31]; Available from
-
US National Institute of Health. ClinicalTrial.gov. 2012 [cited 2012 July 31]; Available from: http://clinicaltrials.gov/.
-
(2012)
ClinicalTrial.gov.
-
-
-
34
-
-
72549116835
-
A phase 1 dose escalation study of the safety and pharmacokinetics of the novel proteasome inhibitor carfilzomib (pr-171) in patients with hematologic malignancies
-
O'Connor OA, Stewart AK, Vallone M, et al. A phase 1 dose escalation study of the safety and pharmacokinetics of the novel proteasome inhibitor carfilzomib (PR-171) in patients with hematologic malignancies. Clin Cancer Res. 2009;15(22):7085-91.
-
(2009)
Clin Cancer Res.
, vol.15
, Issue.22
, pp. 7085-7081
-
-
O'Connor, O.A.1
Stewart, A.K.2
Vallone, M.3
-
35
-
-
50249150555
-
Phase 1 single agent antitumor activity of twice weekly consecutive day dosing of the proteasome inhibitor carfilzomib (pr-171) in hematologic malignancies
-
Alsina M, Trudel S, Vallone M, et al. Phase 1 single agent antitumor activity of twice weekly consecutive day dosing of the proteasome inhibitor carfilzomib (PR-171) in hematologic malignancies. ASH Annual Meeting Abstracts. 2007;110(11):411.
-
(2007)
ASH Annual Meeting Abstracts.
, vol.110
, Issue.11
, pp. 411
-
-
Alsina, M.1
Trudel, S.2
Vallone, M.3
-
36
-
-
84865712581
-
A phase 1 single-Agent study of twice-weekly consecutive-day dosing of the proteasome inhibitor carfilzomib in patients with relapsed or refractory multiple myeloma or lymphoma
-
Jul 3. This important phase I study of carfilzomib in relapsed/refractory MM established the dose and schedule of carfilzomib in this setting
-
Alsina M, Trudel S, Furman RR, et al. A phase 1 single-Agent study of twice-weekly consecutive-day dosing of the proteasome inhibitor carfilzomib in patients with relapsed or refractory multiple myeloma or lymphoma. Clin Cancer Res. 2012;Jul 3. This important phase I study of carfilzomib in relapsed/refractory MM established the dose and schedule of carfilzomib in this setting.
-
(2012)
Clin Cancer Res.
-
-
Alsina, M.1
Trudel, S.2
Furman, R.R.3
-
37
-
-
84862495709
-
Multivariate modelling reveals evidence of a dose-response relationship in phase 2 studies of single-Agent carfilzomib
-
Squifflet P, Michiels S, Siegel DS, et al. Multivariate modelling reveals evidence of a dose-response relationship in phase 2 studies of single-Agent carfilzomib. ASH Annual Meeting Abstracts. 2011;118(21):1877.
-
(2011)
ASH Annual Meeting Abstracts.
, vol.118
, Issue.21
, pp. 1877
-
-
Squifflet, P.1
Michiels, S.2
Siegel, D.S.3
-
38
-
-
84862486640
-
A phase 1b/2 study of prolonged infusion carfilzomib in patients with relapsed and/or refractory (r/r) multiple myeloma: Updated efficacy and tolerability from the completed 20/56 mg/m2 expansion cohort of px-171-007
-
Papadopoulos KP, Lee P, Singhal S, et al. A phase 1b/2 study of prolonged infusion carfilzomib in patients with relapsed and/or refractory (R/R) multiple myeloma: updated efficacy and tolerability from the completed 20/56 mg/m2 expansion cohort of PX-171-007. ASH Annual Meeting Abstracts. 2011;118(21):2930.
-
(2011)
ASH Annual Meeting Abstracts.
, vol.118
, Issue.21
, pp. 2930
-
-
Papadopoulos, K.P.1
Lee, P.2
Singhal, S.3
-
39
-
-
84859760906
-
Integrated safety from phase 2 studies of monotherapy carfilzomib in patients with relapsed and refractory multiple myeloma (mm): An updated analysis
-
Singhal S, Siegel DS, Martin T, et al. Integrated safety from phase 2 studies of monotherapy carfilzomib in patients with relapsed and refractory Multiple Myeloma (MM): an updated analysis. ASH Annual Meeting Abstracts. 2011;118(21):1876.
-
(2011)
ASH Annual Meeting Abstracts.
, vol.118
, Issue.21
, pp. 1876
-
-
Singhal, S.1
Siegel, D.S.2
Martin, T.3
-
40
-
-
84867295563
-
A phase 2 study of singleagent carfilzomib (px-171-003-A1) in patients with relapsed and refractory multiple myeloma
-
Jul 25. This Pivotal Phase II Study Of Carfilzomib In Relapsedrefractory MM Demonstrated Response Benefit In This Heavily Pretreated Advanced Patient Population
-
Siegel DS, Martin T, Wang M, et al. A phase 2 study of singleagent carfilzomib (PX-171-003-A1) in patients with relapsed and refractory multiple myeloma. Blood. 2012;Jul 25. This pivotal phase II study of carfilzomib in relapsed/refractory MM demonstrated response benefit in this heavily pretreated, advanced patient population.
-
(2012)
Blood.
-
-
Siegel, D.S.1
Martin, T.2
Wang, M.3
-
41
-
-
84862507585
-
An open-label, single-Arm, phase 2 (px-171-004) study of single-Agent carfilzomib in bortezomib-naive patients with relapsed and/or refractory multiple myeloma
-
Vij R, Wang M, Kaufman JL, et al. An open-label, single-Arm, phase 2 (PX-171-004) study of single-Agent carfilzomib in bortezomib-naive patients with relapsed and/or refractory multiple myeloma. Blood. 2012;119(24):5661-70.
-
(2012)
Blood.
, vol.119
, Issue.24
, pp. 5661-5660
-
-
Vij, R.1
Wang, M.2
Kaufman, J.L.3
-
42
-
-
84859785906
-
The speed of response to single-Agent carfilzomib in patients with relapsed and/or refractory multiple myeloma: An exploratory analysis of results from 2 multicenter phase 2 clinical trials
-
Wang L, Siegel DS, Jakubowiak AJ, et al. The speed of response to single-Agent carfilzomib in patients with relapsed and/or refractory multiple myeloma: an exploratory analysis of results from 2 multicenter phase 2 clinical trials. ASH Annual Meeting Abstracts. 2011;118(21):3969.
-
(2011)
ASH Annual Meeting Abstracts.
, vol.118
, Issue.21
, pp. 3969
-
-
Wang, L.1
Siegel, D.S.2
Jakubowiak, A.J.3
-
43
-
-
84866311322
-
A phase i/ii study of carfilzomib (cfz) as a replacement for bortezomib (btz) for multiple myeloma (mm) patients (pts) progressing while receiving a btz-containing combination regimen
-
abstr 8098
-
Berenson JR, Yellin O, Dichmann R, et al. A phase I/II study of carfilzomib (CFZ) as a replacement for bortezomib (BTZ) for multiple myeloma (MM) patients (Pts) progressing while receiving a BTZ-containing combination regimen. J Clin Oncol. 2012;30 (suppl):abstr 8098.
-
(2012)
J Clin Oncol.
, vol.30
, Issue.SUPPL.
-
-
Berenson, J.R.1
Yellin, O.2
Dichmann, R.3
-
44
-
-
84865333050
-
A phase 1/2 study of carfilzomib in combination with lenalidomide and low-dose dexamethasone as a frontline treatment for multiple myeloma
-
This seminal study of carfilzomib, lenalidomide, and dexamethasone in newly diagnosed MM showed remarkable activity (ORR of 94%) and favorable tolerability, with a low overall rate of treatment -emergent peripheral neuropathy (23%)
-
Jakubowiak AJ, Dytfeld D, Griffith KA, et al. A phase 1/2 study of carfilzomib in combination with lenalidomide and low-dose dexamethasone as a frontline treatment for multiple myeloma. Blood. 2012. This seminal study of carfilzomib, lenalidomide, and dexamethasone in newly diagnosed MM showed remarkable activity (ORR of 94%) and favorable tolerability, with a low overall rate of treatment -emergent peripheral neuropathy (23%).
-
(2012)
Blood.
-
-
Jakubowiak, A.J.1
Dytfeld, D.2
Griffith, K.A.3
-
45
-
-
84864568291
-
Carfilzomib combined with thalidomide and dexamethasone (carthadex) as induction treatment prior to high-dose melphalan (hdm) in newly diagnosed patients with multiple myeloma (mm)
-
Sonneveld P, Hacker E, Zweegman S, et al. Carfilzomib Combined with Thalidomide and Dexamethasone (CARTHADEX) as induction treatment prior to High-Dose Melphalan (HDM) in newly diagnosed patients with Multiple Myeloma (MM). A Trial of the European Myeloma Network EMN. ASH Annual Meeting Abstracts. 2011;118(21):633.
-
(2011)
A Trial of the European Myeloma Network EMN. ASH Annual Meeting Abstracts.
, vol.118
, Issue.21
, pp. 633
-
-
Sonneveld, P.1
Hacker, E.2
Zweegman, S.3
-
46
-
-
84867313110
-
A phase i/ii trial of cyclophosphamide, carfilzomib, thalidomide, and dexamethasone (cyclone) in patients with newly diagnosed multiple myeloma
-
abstr 8010
-
Mikhael J, Reeder CB, Libby EN, et al. A phase I/II trial of cyclophosphamide, carfilzomib, thalidomide, and dexamethasone (CYCLONE) in patients with newly diagnosed multiple myeloma. J Clin Oncol. 2012;30(suppl):abstr 8010.
-
(2012)
J Clin Oncol.
, vol.30
, Issue.SUPPL.
-
-
Mikhael, J.1
Reeder, C.B.2
Libby, E.N.3
-
47
-
-
84867825131
-
Phase i/ii study of carfilzomib plus melphalan-prednisone (cmp) in elderly patients with de novo multiple myeloma
-
abstr 8009
-
Kolb B, Hulin C, Caillot D, et al. Phase I/II study of carfilzomib plus melphalan-prednisone (CMP) in elderly patients with de novo multiple myeloma. J Clin Oncol. 2012;30(suppl):abstr 8009.
-
(2012)
J Clin Oncol.
, vol.30
, Issue.SUPPL.
-
-
Kolb, B.1
Hulin, C.2
Caillot, D.3
-
48
-
-
84872200272
-
-
European Medicines Agency [cited 2012 July 31]; Available from
-
European Medicines Agency. EU Clinical Trials Register. 2012 [cited 2012 July 31]; Available from: https://www.clinicaltrialsregister.eu.
-
(2012)
EU Clinical Trials Register.
-
-
-
49
-
-
84863713771
-
Flat-dosing versus bsa-based dosing for mln9708, an investigational proteasome inhibitor: Population pharmacokinetic (pk) analysis of pooled data from 4 phase-1 studies
-
Gupta N, Saleh M, Venkatakrishnan K. Flat-dosing versus BSA-based dosing for MLN9708, an investigational proteasome inhibitor: Population Pharmacokinetic (PK) analysis of pooled data from 4 phase-1 studies. ASH Annual Meeting Abstracts. 2011;118(21):1433.
-
(2011)
ASH Annual Meeting Abstracts.
, vol.118
, Issue.21
, pp. 1433
-
-
Gupta, N.1
Saleh, M.2
Venkatakrishnan, K.3
-
50
-
-
84872183328
-
Weekly dosing of the investigational oral proteasome inhibitor mln9708 in patients (pts) with relapsed/refractory multiple myeloma (mm): A phase i study
-
abstr 8034
-
Kumar S, Bensinger W, Reeder CB, et al. Weekly dosing of the investigational oral proteasome inhibitor MLN9708 in patients (pts) with relapsed/refractory multiple myeloma (MM): A phase I study. J Clin Oncol. 2012;30(suppl):abstr 8034.
-
(2012)
J Clin Oncol.
, vol.30
, Issue.SUPPL.
-
-
Kumar, S.1
Bensinger, W.2
Reeder, C.B.3
-
51
-
-
84872886249
-
Phase i study of twice-weekly dosing of the investigational oral proteasome inhibitor mln9708 in patients (pts) with relapsed and/or refractory multiple myeloma (mm)
-
abstr 8017
-
Lonial S, Baz RC, Wang M, et al. Phase I study of twice-weekly dosing of the investigational oral proteasome inhibitor MLN9708 in patients (pts) with relapsed and/or refractory multiple myeloma (MM). J Clin Oncol. 2012;30(suppl):abstr 8017.
-
(2012)
J Clin Oncol.
, vol.30
, Issue.SUPPL.
-
-
Lonial, S.1
Baz, R.C.2
Wang, M.3
-
52
-
-
85051761722
-
Mln9708, an investigational proteasome inhibitor, in patients (pts) with relapsed/refractory lymphoma: Emerging data from a phase i dose-escalation study
-
abstr 8064
-
Martin P, Chang JE, Rifkin RM, et al. MLN9708, an investigational proteasome inhibitor, in patients (pts) with relapsed/refractory lymphoma: Emerging data from a phase I dose-escalation study. J Clin Oncol. 2012 30(suppl):abstr 8064.
-
(2012)
J Clin Oncol.
, Issue.SUPPL.
, pp. 30
-
-
Martin, P.1
Chang, J.E.2
Rifkin, R.M.3
-
53
-
-
84872196659
-
MLN9708, an investigational proteasome inhibitor, in patients (pts) with solid tumors: Updated phase I results
-
abstr e13603
-
Smith DC, Sullivan D, Infante JR, et al.MLN9708, an investigational proteasome inhibitor, in patients (pts) with solid tumors: Updated phase I results. J Clin Oncol. 2012;30:suppl; abstr e13603.
-
(2012)
J Clin Oncol.
, vol.30
, Issue.SUPPL.
-
-
Smith, D.C.1
Sullivan, D.2
Infante, J.R.3
-
54
-
-
84872188377
-
Oral weekly mln9708, an investigational proteasome inhibitor, in combination with lenalidomide and dexamethasone in patients (pts) with previously untreated multiple myeloma (mm): A phase i/ii study
-
abstr 8033. This encouraging clinical study of MLN9708 in combination with lenalidomide and dexamethasone as an all oral regimen in newly diagnosed MM, demonstrated 100% ORR and favorable tolerability
-
Richardson PG, Berdeja JG, Niesvizky R, et al. Oral weekly MLN9708, an investigational proteasome inhibitor, in combination with lenalidomide and dexamethasone in patients (pts) with previously untreated multiple myeloma (MM): A phase I/II study. J Clin Oncol. 2012;30(suppl):abstr 8033. This encouraging clinical study of MLN9708 in combination with lenalidomide and dexamethasone as an all oral regimen in newly diagnosed MM, demonstrated 100% ORR and favorable tolerability.
-
(2012)
J Clin Oncol.
, vol.30
, Issue.SUPPL.
-
-
Richardson, P.G.1
Berdeja, J.G.2
Niesvizky, R.3
-
55
-
-
77949432502
-
Clinical trial of the novel structure proteasome inhibitor npi-0052 in patients with relapsed and relapsed/refractory multiple myeloma (r/r mm)
-
suppl; abstr 8505
-
Hofmeister CC, Richardson P, Zimmerman T, et al. Clinical trial of the novel structure proteasome inhibitor NPI-0052 in patients with relapsed and relapsed/refractory multiple myeloma (r/r MM). J Clin Oncol. 2009;27(15s):suppl; abstr 8505.
-
(2009)
J Clin Oncol.
, vol.27
, Issue.15 S
-
-
Hofmeister, C.C.1
Richardson, P.2
Zimmerman, T.3
-
56
-
-
79953092305
-
Phase 1 clinical trial of the novel structure proteasome inhibitor npi-0052
-
Spencer A, Millward M, Mainwaring P, et al. Phase 1 clinical trial of the novel structure proteasome inhibitor NPI-0052. ASH Annual Meeting Abstracts. 2009;114(22):2693.
-
(2009)
ASH Annual Meeting Abstracts.
, vol.114
, Issue.22
, pp. 2693
-
-
Spencer, A.1
Millward, M.2
Mainwaring, P.3
-
57
-
-
84857919694
-
Phase 1 clinical evaluation of twice-weekly marizomib (npi-0052), a novel proteasome inhibitor, in patients with relapsed/refractory multiple myeloma (mm)
-
Richardson PG, Spencer A, Cannell P, et al. Phase 1 clinical evaluation of twice-weekly marizomib (NPI-0052), a novel proteasome inhibitor, in patients with relapsed/refractory Multiple Myeloma (MM). ASH Annual Meeting Abstracts. 2011;118 (21):302.
-
(2011)
ASH Annual Meeting Abstracts.
, vol.118
, Issue.21
, pp. 302
-
-
Richardson, P.G.1
Spencer, A.2
Cannell, P.3
-
58
-
-
84875495677
-
Phase 1 clinical trial of the novel proteasome inhibitor marizomib with the histone deacetylase inhibitor vorinostat in patients with melanoma pancreatic and lung cancer based on in vitro assessments of the combination
-
Nov 12
-
Millward M, Price T, Townsend A, et al. Phase 1 clinical trial of the novel proteasome inhibitor marizomib with the histone deacetylase inhibitor vorinostat in patients with melanoma, pancreatic and lung cancer based on in vitro assessments of the combination. Invest New Drugs. 2011 Nov 12.
-
(2011)
Invest New Drugs.
-
-
Millward, M.1
Price, T.2
Townsend, A.3
-
59
-
-
78649681350
-
Efficacy and safety of onceweekly bortezomib in multiple myeloma patients
-
Bringhen S, Larocca A, Rossi D, et al. Efficacy and safety of onceweekly bortezomib in multiple myeloma patients. Blood. 2010;116 (23):4745-53.
-
(2010)
Blood.
, vol.116
, Issue.23
, pp. 4745-4743
-
-
Bringhen, S.1
Larocca, A.2
Rossi, D.3
-
60
-
-
81155138545
-
A phase i, open-label, dose-escalation study of the novel oral proteasome inhibitor (pi) onx 0912 in patients with advanced refractory or recurrent solid tumors
-
abstr 3075
-
Papadopoulos KP, Mendelson DS, Tolcher AW, et al. A phase I, open-label, dose-escalation study of the novel oral proteasome inhibitor (PI) ONX 0912 in patients with advanced refractory or recurrent solid tumors. J Clin Oncol. 2011;29:suppl; abstr 3075.
-
(2011)
J Clin Oncol.
, vol.29
, Issue.SUPPL.
-
-
Papadopoulos, K.P.1
Mendelson, D.S.2
Tolcher, A.W.3
|