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Volumn 17, Issue 5, 2016, Pages 622-631

Safety, tolerability, and preliminary activity of CUDC-907, a first-in-class, oral, dual inhibitor of HDAC and PI3K, in patients with relapsed or refractory lymphoma or multiple myeloma: An open-label, dose-escalation, phase 1 trial

Author keywords

[No Author keywords available]

Indexed keywords

ALKALINE PHOSPHATASE; ANTINEOPLASTIC AGENT; CUDC 907; HISTONE DEACETYLASE INHIBITOR; LOPERAMIDE; PHOSPHATIDYLINOSITOL 3 KINASE INHIBITOR; RITUXIMAB; UNCLASSIFIED DRUG; CUDC-907; HISTONE DEACETYLASE; MORPHOLINE DERIVATIVE; PHOSPHATIDYLINOSITOL 3 KINASE; PYRIMIDINE DERIVATIVE;

EID: 84961933254     PISSN: 14702045     EISSN: 14745488     Source Type: Journal    
DOI: 10.1016/S1470-2045(15)00584-7     Document Type: Article
Times cited : (156)

References (30)
  • 2
    • 84892942381 scopus 로고    scopus 로고
    • New and emerging HDAC inhibitors for cancer treatment
    • West AC, Johnstone RW New and emerging HDAC inhibitors for cancer treatment. J Clin Invest 2014, 124:30-39.
    • (2014) J Clin Invest , vol.124 , pp. 30-39
    • West, A.C.1    Johnstone, R.W.2
  • 3
    • 84887942578 scopus 로고    scopus 로고
    • Phosphatidylinositol 3-kinase (PI3K) inhibitors as cancer therapeutics
    • Akinleye A, Avvaru P, Purqan M, Song Y, Liu D Phosphatidylinositol 3-kinase (PI3K) inhibitors as cancer therapeutics. J Hematol Oncol 2013, 6:88.
    • (2013) J Hematol Oncol , vol.6 , pp. 88
    • Akinleye, A.1    Avvaru, P.2    Purqan, M.3    Song, Y.4    Liu, D.5
  • 4
    • 84864484251 scopus 로고    scopus 로고
    • Cancer network disruption by a single molecule inhibitor targeting both histone deacetylase activity and phosphatidylinositol 3-kinase signaling
    • Qian C, Lai CJ, Bao R, et al. Cancer network disruption by a single molecule inhibitor targeting both histone deacetylase activity and phosphatidylinositol 3-kinase signaling. Clin Cancer Res 2012, 18:4104-4113.
    • (2012) Clin Cancer Res , vol.18 , pp. 4104-4113
    • Qian, C.1    Lai, C.J.2    Bao, R.3
  • 5
    • 84907916640 scopus 로고    scopus 로고
    • PI3K/mTOR inhibition markedly potentiates HDAC inhibitor activity in NHL cells through BIM-and MCL-1-dependent mechanisms in vitro and in vivo
    • Rahmani M, Aust MM, Benson EC, Wallace L, Friedberg J, Grant S PI3K/mTOR inhibition markedly potentiates HDAC inhibitor activity in NHL cells through BIM-and MCL-1-dependent mechanisms in vitro and in vivo. Clin Cancer Res 2014, 20:4849-4860.
    • (2014) Clin Cancer Res , vol.20 , pp. 4849-4860
    • Rahmani, M.1    Aust, M.M.2    Benson, E.C.3    Wallace, L.4    Friedberg, J.5    Grant, S.6
  • 6
    • 84865254848 scopus 로고    scopus 로고
    • Mechanisms of acquired resistance to targeted cancer therapies
    • Lackner MR, Wilson TR, Settleman J Mechanisms of acquired resistance to targeted cancer therapies. Future Oncol 2012, 8:999-1014.
    • (2012) Future Oncol , vol.8 , pp. 999-1014
    • Lackner, M.R.1    Wilson, T.R.2    Settleman, J.3
  • 7
    • 84964685693 scopus 로고    scopus 로고
    • Antitumor activity of CUDC-907, a dual PI3K and HDAC inhibitor, in hematological cancer models
    • Bao R, Wang D, Qu H, et al. Antitumor activity of CUDC-907, a dual PI3K and HDAC inhibitor, in hematological cancer models. Cancer Res 2012, 72(suppl):3744.
    • (2012) Cancer Res , vol.72 , pp. 3744
    • Bao, R.1    Wang, D.2    Qu, H.3
  • 8
    • 33947496614 scopus 로고    scopus 로고
    • Revised response criteria for malignant lymphoma
    • Cheson BD, Pfistner B, Juweid ME, et al. Revised response criteria for malignant lymphoma. J Clin Oncol 2007, 25:579-586.
    • (2007) J Clin Oncol , vol.25 , pp. 579-586
    • Cheson, B.D.1    Pfistner, B.2    Juweid, M.E.3
  • 9
    • 84988241358 scopus 로고    scopus 로고
    • International uniform response criteria for multiple myeloma
    • Durie BG, Harousseau JL, Miguel JS, et al. International uniform response criteria for multiple myeloma. Leukemia 2006, 20:1467-1473.
    • (2006) Leukemia , vol.20 , pp. 1467-1473
    • Durie, B.G.1    Harousseau, J.L.2    Miguel, J.S.3
  • 10
    • 84964583672 scopus 로고    scopus 로고
    • Spectrum Pharmaceuticals, Inc, Irvine, CA
    • Beleodaq package insert 2014, Spectrum Pharmaceuticals, Spectrum Pharmaceuticals, Inc, Irvine, CA.
    • (2014) Beleodaq package insert
  • 11
    • 84964570567 scopus 로고    scopus 로고
    • Novartis Pharmaceuticals Corporation, East Hanover, NJ
    • Farydak package insert 2015, Novartis Pharmaceuticals Corporation, Novartis Pharmaceuticals Corporation, East Hanover, NJ.
    • (2015) Farydak package insert
  • 12
    • 84964641687 scopus 로고    scopus 로고
    • Celgene Corporation, Summit, NJ
    • Istodax package insert 2014, Celgene Corporation, Celgene Corporation, Summit, NJ.
    • (2014) Istodax package insert
  • 13
    • 72549101701 scopus 로고    scopus 로고
    • Merck & Co, Inc, Whitehouse Station, NJ
    • Zolinza package insert 2006, Merck & Co, Inc, Merck & Co, Inc, Whitehouse Station, NJ.
    • (2006) Zolinza package insert
  • 14
    • 84936159781 scopus 로고    scopus 로고
    • Gilead Sciences, Inc, Foster City, CA
    • Zydelig package insert 2014, Gilead Sciences, Inc, Gilead Sciences, Inc, Foster City, CA.
    • (2014) Zydelig package insert
  • 15
    • 84859413755 scopus 로고    scopus 로고
    • Relapsed/refractory diffuse large B-cell lymphoma
    • Friedberg JW Relapsed/refractory diffuse large B-cell lymphoma. Hematology Am Soc Hematol Educ Program 2011, 2011:498-505.
    • (2011) Hematology Am Soc Hematol Educ Program , vol.2011 , pp. 498-505
    • Friedberg, J.W.1
  • 16
    • 84925622568 scopus 로고    scopus 로고
    • Emerging drugs for diffuse large B-cell lymphoma
    • Mondello P, Younes A Emerging drugs for diffuse large B-cell lymphoma. Expert Rev Anticancer Ther 2015, 15:439-451.
    • (2015) Expert Rev Anticancer Ther , vol.15 , pp. 439-451
    • Mondello, P.1    Younes, A.2
  • 17
    • 84931466697 scopus 로고    scopus 로고
    • Phase 1 first-in-human study of the enhancer of zeste-homolog 2 (EZH2) histome methyl transferase inhibitor E7438 as a single agent in patients with advanced solid tumors or B cell lymphoma
    • Ribrag V, Soria JC, Reyderman L, et al. Phase 1 first-in-human study of the enhancer of zeste-homolog 2 (EZH2) histome methyl transferase inhibitor E7438 as a single agent in patients with advanced solid tumors or B cell lymphoma. Eur J Cancer 2014, 50:197.
    • (2014) Eur J Cancer , vol.50 , pp. 197
    • Ribrag, V.1    Soria, J.C.2    Reyderman, L.3
  • 18
    • 84902334574 scopus 로고    scopus 로고
    • Final results of a phase 1 study of the anti-CD79b antibody-drug conjugate DCDS4501A in relapsed or refractory (R/R) B-cell non-Hodgkin lymphoma (NHL)
    • Palanca-Wessels MC, Salles GA, Czuczman MS, et al. Final results of a phase 1 study of the anti-CD79b antibody-drug conjugate DCDS4501A in relapsed or refractory (R/R) B-cell non-Hodgkin lymphoma (NHL). Blood 2013, 122:4400.
    • (2013) Blood , vol.122 , pp. 4400
    • Palanca-Wessels, M.C.1    Salles, G.A.2    Czuczman, M.S.3
  • 19
    • 84938553527 scopus 로고    scopus 로고
    • The oral selective inhibitor of nuclear export (SINE) selinexor (KPT-330) demonstrates broad and durable clinical activity in relapsed/refractory non Hodgkin's lymphoma
    • Kuruvilla J, Byrd JC, Flynn J, et al. The oral selective inhibitor of nuclear export (SINE) selinexor (KPT-330) demonstrates broad and durable clinical activity in relapsed/refractory non Hodgkin's lymphoma. Blood 2014, 124:396.
    • (2014) Blood , vol.124 , pp. 396
    • Kuruvilla, J.1    Byrd, J.C.2    Flynn, J.3
  • 20
    • 84959270269 scopus 로고    scopus 로고
    • BET-Bromodomain (BRD) inhibitor OTX015: final results of the dose-finding part of a phase I study in hematologic malignancies
    • Herait P, Domret H, Thieblemont C, et al. BET-Bromodomain (BRD) inhibitor OTX015: final results of the dose-finding part of a phase I study in hematologic malignancies. Ann Oncol 2015, 26(suppl 2):ii10-ii11.
    • (2015) Ann Oncol , vol.26 , pp. ii10-ii11
    • Herait, P.1    Domret, H.2    Thieblemont, C.3
  • 21
    • 84858118200 scopus 로고    scopus 로고
    • Phase 2 trial of alisertib (MLN8237), an investigational, potent inhibitor of aurora A kinase (AAK), in patients (pts) with aggressive B-and T-cell non-Hodgkin lymphoma (NHL)
    • Friedberg JW, Mahadevan D, Jung J, et al. Phase 2 trial of alisertib (MLN8237), an investigational, potent inhibitor of aurora A kinase (AAK), in patients (pts) with aggressive B-and T-cell non-Hodgkin lymphoma (NHL). Blood 2011, 118:95.
    • (2011) Blood , vol.118 , pp. 95
    • Friedberg, J.W.1    Mahadevan, D.2    Jung, J.3
  • 22
    • 84964583680 scopus 로고    scopus 로고
    • Panobinostat as salvage treatment for patients with relapsed/refractory diffuse large B-cell lymphoma not eligible to high dose therapy: a phase II study of the Fondazione Italiana Linfomi (FIL)
    • Zaja F, Volpetti S, Chiappella A, et al. Panobinostat as salvage treatment for patients with relapsed/refractory diffuse large B-cell lymphoma not eligible to high dose therapy: a phase II study of the Fondazione Italiana Linfomi (FIL). Blood 2014, 124:1755.
    • (2014) Blood , vol.124 , pp. 1755
    • Zaja, F.1    Volpetti, S.2    Chiappella, A.3
  • 23
    • 84961658075 scopus 로고    scopus 로고
    • A phase II study of single agent mocetinostat, an oral isotype-selective histone deacetylase (HDAC) inhibitor, in patients with diffuse large cell B-cell (DLBCL) and follicular (FL) lymphomas
    • Crump M, Andreadis C, Assouline SE, et al. A phase II study of single agent mocetinostat, an oral isotype-selective histone deacetylase (HDAC) inhibitor, in patients with diffuse large cell B-cell (DLBCL) and follicular (FL) lymphomas. J Clin Oncol 2013, 31:8535.
    • (2013) J Clin Oncol , vol.31 , pp. 8535
    • Crump, M.1    Andreadis, C.2    Assouline, S.E.3
  • 24
    • 84964627790 scopus 로고    scopus 로고
    • An open-label phase II study of buparlisib (BKM120) in patients with relapsed and refractory diffuse large B-cell lymphoma, mantle cell lymphoma or follicular lymphoma
    • Younes A, Salles G, Bociek RG, et al. An open-label phase II study of buparlisib (BKM120) in patients with relapsed and refractory diffuse large B-cell lymphoma, mantle cell lymphoma or follicular lymphoma. Blood 2014, 124:1718.
    • (2014) Blood , vol.124 , pp. 1718
    • Younes, A.1    Salles, G.2    Bociek, R.G.3
  • 25
    • 84887321322 scopus 로고    scopus 로고
    • A phase II study of PXD101 (belinostat) in relapsed and refractory aggressive B-cell lymphomas (rel/ref ABCL): SWOG S0520
    • Persky DO, Bernstein SH, Goldman BH, et al. A phase II study of PXD101 (belinostat) in relapsed and refractory aggressive B-cell lymphomas (rel/ref ABCL): SWOG S0520. J Clin Oncol 2012, 30:e18536.
    • (2012) J Clin Oncol , vol.30 , pp. e18536
    • Persky, D.O.1    Bernstein, S.H.2    Goldman, B.H.3
  • 26
    • 43049092663 scopus 로고    scopus 로고
    • Phase II trial of oral vorinostat (suberoylanilide hydroxamic acid) in relapsed diffuse large-B-cell lymphoma
    • Crump M, Coiffier B, Jacobsen ED, et al. Phase II trial of oral vorinostat (suberoylanilide hydroxamic acid) in relapsed diffuse large-B-cell lymphoma. Ann Oncol 2008, 19:964-969.
    • (2008) Ann Oncol , vol.19 , pp. 964-969
    • Crump, M.1    Coiffier, B.2    Jacobsen, E.D.3
  • 27
    • 77955643796 scopus 로고    scopus 로고
    • The clinical development of histone deacetylase inhibitors as targeted anticancer drugs
    • Marks PA The clinical development of histone deacetylase inhibitors as targeted anticancer drugs. Expert Opin Investig Drugs 2010, 19:1049-1066.
    • (2010) Expert Opin Investig Drugs , vol.19 , pp. 1049-1066
    • Marks, P.A.1
  • 28
    • 77957965500 scopus 로고    scopus 로고
    • Salvage regimens with autologous transplantation for relapsed large B-cell lymphoma in the rituximab era
    • Gisselbrecht C, Glass B, Mounier N, et al. Salvage regimens with autologous transplantation for relapsed large B-cell lymphoma in the rituximab era. J Clin Oncol 2010, 28:4184-4190.
    • (2010) J Clin Oncol , vol.28 , pp. 4184-4190
    • Gisselbrecht, C.1    Glass, B.2    Mounier, N.3
  • 29
    • 77955872819 scopus 로고    scopus 로고
    • Response to second-line therapy defines the potential for cure in patients with recurrent diffuse large B-cell lymphoma: implications for the development of novel therapeutic strategies
    • Elstrom RL, Martin P, Ostrow K, et al. Response to second-line therapy defines the potential for cure in patients with recurrent diffuse large B-cell lymphoma: implications for the development of novel therapeutic strategies. Clin Lymphoma Myeloma Leuk 2010, 10:192-196.
    • (2010) Clin Lymphoma Myeloma Leuk , vol.10 , pp. 192-196
    • Elstrom, R.L.1    Martin, P.2    Ostrow, K.3
  • 30
    • 84879385620 scopus 로고    scopus 로고
    • MYC/BCL2 protein coexpression contributes to the inferior survival of activated B-cell subtype of diffuse large B-cell lymphoma and demonstrates high-risk gene expression signatures: a report from The International DLBCL Rituximab-CHOP Consortium Program
    • Hu S, Xu-Monette ZY, Tzankov A, et al. MYC/BCL2 protein coexpression contributes to the inferior survival of activated B-cell subtype of diffuse large B-cell lymphoma and demonstrates high-risk gene expression signatures: a report from The International DLBCL Rituximab-CHOP Consortium Program. Blood 2013, 121:4021-4031.
    • (2013) Blood , vol.121 , pp. 4021-4031
    • Hu, S.1    Xu-Monette, Z.Y.2    Tzankov, A.3


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