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Volumn 165, Issue 2, 2017, Pages 375-382

A Phase I/II study of suberoylanilide hydroxamic acid (SAHA) in combination with trastuzumab (Herceptin) in patients with advanced metastatic and/or local chest wall recurrent HER2-amplified breast cancer: a trial of the ECOG-ACRIN Cancer Research Group (E1104)

(12)  Goldstein, Lori J a   Zhao, Fengmin b   Wang, Molin b   Swaby, Ramona F a,c   Sparano, Joseph A d   Meropol, Neal J a,e   Bhalla, Kapil N f,g   Pellegrino, Christine M d   Katherine Alpaugh, R a   Falkson, Carla I h   Klein, Paula i,j   Sledge, George W k,l  


Author keywords

Anticancer therapy; Histone deacetylase; Resistance; Toxicity; Tumor

Indexed keywords

ALANINE AMINOTRANSFERASE; ALKALINE PHOSPHATASE; ASPARTATE AMINOTRANSFERASE; HEMOGLOBIN; TRASTUZUMAB; VORINOSTAT; ANTINEOPLASTIC AGENT; EPIDERMAL GROWTH FACTOR RECEPTOR 2; HYDROXAMIC ACID; TUMOR MARKER;

EID: 85020517595     PISSN: 01676806     EISSN: 15737217     Source Type: Journal    
DOI: 10.1007/s10549-017-4310-9     Document Type: Article
Times cited : (20)

References (31)
  • 2
    • 0036274359 scopus 로고    scopus 로고
    • The fundamental role of epigenetic events in cancer
    • COI: 1:CAS:528:DC%2BD38XksFOmsrw%3D, PID: 12042769
    • Jones PA, Baylin SB (2002) The fundamental role of epigenetic events in cancer. Nat Rev Genet 3:415–428. doi:10.1038/nrg816
    • (2002) Nat Rev Genet , vol.3 , pp. 415-428
    • Jones, P.A.1    Baylin, S.B.2
  • 3
    • 0141953936 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: from chromatin remodeling to experimental cancer therapeutics
    • COI: 1:CAS:528:DC%2BD3sXotFKlsLY%3D, PID: 14529477
    • Arts J, de Schepper S, Van Emelen K (2003) Histone deacetylase inhibitors: from chromatin remodeling to experimental cancer therapeutics. Curr Med Chem 10:2343–2350. doi:10.2174/0929867033456657
    • (2003) Curr Med Chem , vol.10 , pp. 2343-2350
    • Arts, J.1    de Schepper, S.2    Van Emelen, K.3
  • 4
    • 0034885248 scopus 로고    scopus 로고
    • A phase I dose escalation and bioavailability study of oral sodium phenylbutyrate in patients with refractory solid tumor malignancies
    • COI: 1:CAS:528:DC%2BD3MXmsVOmtrY%3D, PID: 11489804
    • Gilbert J, Baker SD, Bowling MK, Grochow L, Figg WD, Zabelina Y, Donehower RC, Carducci MA (2001) A phase I dose escalation and bioavailability study of oral sodium phenylbutyrate in patients with refractory solid tumor malignancies. Clin Cancer Res 7:2292–2300
    • (2001) Clin Cancer Res , vol.7 , pp. 2292-2300
    • Gilbert, J.1    Baker, S.D.2    Bowling, M.K.3    Grochow, L.4    Figg, W.D.5    Zabelina, Y.6    Donehower, R.C.7    Carducci, M.A.8
  • 6
    • 84925506096 scopus 로고    scopus 로고
    • Cyclic depsipeptides as potential cancer therapeutics
    • COI: 1:CAS:528:DC%2BC2MXhsV2gtbc%3D, PID: 25419631
    • Kitagaki J, Shi G, Miyauchi S, Murakami S, Yang Y (2015) Cyclic depsipeptides as potential cancer therapeutics. Anticancer Drugs 26:259–271. doi:10.1097/CAD.0000000000000183
    • (2015) Anticancer Drugs , vol.26 , pp. 259-271
    • Kitagaki, J.1    Shi, G.2    Miyauchi, S.3    Murakami, S.4    Yang, Y.5
  • 7
    • 0035525781 scopus 로고    scopus 로고
    • Inhibitor of histone deacetylation, depsipeptide (FR901228), in the treatment of peripheral and cutaneous T-cell lymphoma: a case report
    • COI: 1:CAS:528:DC%2BD3MXotVegt74%3D, PID: 11675364
    • Piekarz RL, Robey R, Sandor V, Bakke S, Wilson WH, Dahmoush L, Kingma DM, Turner ML, Altemus R, Bates SE (2001) Inhibitor of histone deacetylation, depsipeptide (FR901228), in the treatment of peripheral and cutaneous T-cell lymphoma: a case report. Blood 98:2865–2868. doi:10.1182/blood.V98.9.2865
    • (2001) Blood , vol.98 , pp. 2865-2868
    • Piekarz, R.L.1    Robey, R.2    Sandor, V.3    Bakke, S.4    Wilson, W.H.5    Dahmoush, L.6    Kingma, D.M.7    Turner, M.L.8    Altemus, R.9    Bates, S.E.10
  • 9
    • 0036906832 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: from target to clinical trials
    • COI: 1:CAS:528:DC%2BD38XptFCjs7s%3D
    • Kelly WK, O’Connor OA, Marks PA (2002) Histone deacetylase inhibitors: from target to clinical trials. Expert Opin Inv Drug 11:1695–1713. doi:10.1517/13543784.11.12.1695
    • (2002) Expert Opin Inv Drug , vol.11 , pp. 1695-1713
    • Kelly, W.K.1    O’Connor, O.A.2    Marks, P.A.3
  • 10
    • 33845996135 scopus 로고    scopus 로고
    • Phase 2 trial of oral vorinostat (suberoylanilide hydroxamic acid, SAHA) for refractory cutaneous T-cell lymphoma (CTCL)
    • COI: 1:CAS:528:DC%2BD2sXivVyrt7g%3D, PID: 16960145
    • Duvic M, Talpur R, Ni X, Zhang C, Hazarika P, Kelly C, Chiao JH, Reilly JF, Ricker JL, Richon VM, Frankel SR (2007) Phase 2 trial of oral vorinostat (suberoylanilide hydroxamic acid, SAHA) for refractory cutaneous T-cell lymphoma (CTCL). Blood 109:31–39. doi:10.1182/blood-2006-06-025999
    • (2007) Blood , vol.109 , pp. 31-39
    • Duvic, M.1    Talpur, R.2    Ni, X.3    Zhang, C.4    Hazarika, P.5    Kelly, C.6    Chiao, J.H.7    Reilly, J.F.8    Ricker, J.L.9    Richon, V.M.10    Frankel, S.R.11
  • 12
    • 0002478350 scopus 로고    scopus 로고
    • Malignant tumors of the breast
    • Devita JVT, Hellman S, Rosenberg SA, (eds), Lippincott-Raven Publishers, Philadelphia
    • Winer E, Morrow M, Osborne CK (2000) Malignant tumors of the breast. In: Devita JVT, Hellman S, Rosenberg SA (eds) Cancer: principles and practice of oncology, 6th edn. Lippincott-Raven Publishers, Philadelphia, pp 1651–1716
    • (2000) Cancer: principles and practice of oncology , pp. 1651-1716
    • Winer, E.1    Morrow, M.2    Osborne, C.K.3
  • 14
    • 0034600849 scopus 로고    scopus 로고
    • The ErbB signaling network: receptor heterodimerization in development and cancer
    • COI: 1:CAS:528:DC%2BD3cXlt1ajtLY%3D, PID: 10880430
    • Olayioye MA, Neve RM, Lane HA, Hynes NE (2000) The ErbB signaling network: receptor heterodimerization in development and cancer. EMBO J 19:3159–3167. doi:10.1093/emboj/19.13.3159
    • (2000) EMBO J , vol.19 , pp. 3159-3167
    • Olayioye, M.A.1    Neve, R.M.2    Lane, H.A.3    Hynes, N.E.4
  • 17
    • 0036633164 scopus 로고    scopus 로고
    • Constitutive and inducible Akt activity promotes resistance to chemotherapy, trastuzumab, or tamoxifen in breast cancer cells
    • COI: 1:CAS:528:DC%2BD38XlsFSmtLk%3D, PID: 12479367
    • Clark AS, West K, Streicher S, Dennis PA (2002) Constitutive and inducible Akt activity promotes resistance to chemotherapy, trastuzumab, or tamoxifen in breast cancer cells. Mol Cancer Ther 1:707–717
    • (2002) Mol Cancer Ther , vol.1 , pp. 707-717
    • Clark, A.S.1    West, K.2    Streicher, S.3    Dennis, P.A.4
  • 18
    • 0035915421 scopus 로고    scopus 로고
    • Insulin-like growth factor-I receptor signaling and resistance to trastuzumab (Herceptin)
    • COI: 1:CAS:528:DC%2BD38XltVWluw%3D%3D
    • Lu YH, Zi XL, Zhao YH, Mascarenhas D, Pollak M (2001) Insulin-like growth factor-I receptor signaling and resistance to trastuzumab (Herceptin). J Natl Cancer I 93:1852–1857. doi:10.1093/jnci/93.24.1852
    • (2001) J Natl Cancer I , vol.93 , pp. 1852-1857
    • Lu, Y.H.1    Zi, X.L.2    Zhao, Y.H.3    Mascarenhas, D.4    Pollak, M.5
  • 19
    • 0037240275 scopus 로고    scopus 로고
    • ErbB (HER) receptors can abrogate antiestrogen action in human breast cancer by multiple signaling mechanisms
    • COI: 1:CAS:528:DC%2BD3sXnt1yisw%3D%3D, PID: 12538508
    • Kurokawa H, Arteaga CL (2003) ErbB (HER) receptors can abrogate antiestrogen action in human breast cancer by multiple signaling mechanisms. Clin Cancer Res 9:511S–515S
    • (2003) Clin Cancer Res , vol.9 , pp. 511S-515S
    • Kurokawa, H.1    Arteaga, C.L.2
  • 20
    • 0034596309 scopus 로고    scopus 로고
    • Histone deacetylase inhibitors: inducers of differentiation or apoptosis of transformed cells
    • COI: 1:CAS:528:DC%2BD3cXlvFyhsb8%3D
    • Marks PA, Richon VM, Rifkind RA (2000) Histone deacetylase inhibitors: inducers of differentiation or apoptosis of transformed cells. J Natl Cancer I 92:1210–1216. doi:10.1093/jnci/92.15.1210
    • (2000) J Natl Cancer I , vol.92 , pp. 1210-1216
    • Marks, P.A.1    Richon, V.M.2    Rifkind, R.A.3
  • 21
    • 0034730127 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor selectively induces p21(WAF1) expression and gene-associated histone acetylation
    • COI: 1:CAS:528:DC%2BD3cXmtlehsL4%3D, PID: 10954755
    • Richon VM, Sandhoff TW, Rifkind RA, Marks PA (2000) Histone deacetylase inhibitor selectively induces p21(WAF1) expression and gene-associated histone acetylation. Proc Natl Acad Sci USA 97:10014–10019. doi:10.1073/pnas.180316197
    • (2000) Proc Natl Acad Sci USA , vol.97 , pp. 10014-10019
    • Richon, V.M.1    Sandhoff, T.W.2    Rifkind, R.A.3    Marks, P.A.4
  • 22
    • 1642490813 scopus 로고    scopus 로고
    • Histone deacetylase inhibitor LAQ824 down-regulates HER2 and sensitizes human breast cancer cells to trastuzumab, taxotere, gemcitabine, and epothilone B
    • COI: 1:CAS:528:DC%2BD3sXosVCqt7g%3D, PID: 14578462
    • Fuino L, Bali P, Wittmann S, Donapaty S, Guo F, Yamaguchi H, Wang HG, Atadja P, Bhalla K (2003) Histone deacetylase inhibitor LAQ824 down-regulates HER2 and sensitizes human breast cancer cells to trastuzumab, taxotere, gemcitabine, and epothilone B. Mol Cancer Ther 2:971–984
    • (2003) Mol Cancer Ther , vol.2 , pp. 971-984
    • Fuino, L.1    Bali, P.2    Wittmann, S.3    Donapaty, S.4    Guo, F.5    Yamaguchi, H.6    Wang, H.G.7    Atadja, P.8    Bhalla, K.9
  • 23
    • 0034297220 scopus 로고    scopus 로고
    • Suberoylanilide hydroxamic acid as a potential therapeutic agent for human breast cancer treatment
    • COI: 1:CAS:528:DC%2BD3cXot1WgtL4%3D, PID: 11126200
    • Huang LL, Pardee AB (2000) Suberoylanilide hydroxamic acid as a potential therapeutic agent for human breast cancer treatment. Mol Med 6:849–866
    • (2000) Mol Med , vol.6 , pp. 849-866
    • Huang, L.L.1    Pardee, A.B.2
  • 24
    • 0043288724 scopus 로고    scopus 로고
    • Heat shock protein 90 as a molecular target for cancer therapeutics
    • COI: 1:CAS:528:DC%2BD3sXislOrtb8%3D, PID: 12676580
    • Isaacs JS, Xu W, Neckers L (2003) Heat shock protein 90 as a molecular target for cancer therapeutics. Cancer Cell 3:213–217
    • (2003) Cancer Cell , vol.3 , pp. 213-217
    • Isaacs, J.S.1    Xu, W.2    Neckers, L.3
  • 26
    • 0037149539 scopus 로고    scopus 로고
    • Tumor biology—Herceptin acts as an anti-angiogenic cocktail
    • COI: 1:CAS:528:DC%2BD38XisFSmsL4%3D, PID: 11907566
    • Izumi Y, Xu L, di Tomaso E, Fukumura D, Jain RK (2002) Tumor biology—Herceptin acts as an anti-angiogenic cocktail. Nature 416:279–280. doi:10.1038/416279b
    • (2002) Nature , vol.416 , pp. 279-280
    • Izumi, Y.1    Xu, L.2    di Tomaso, E.3    Fukumura, D.4    Jain, R.K.5
  • 27
    • 0024536437 scopus 로고
    • Optimal two-stage designs for phase II clinical trials
    • COI: 1:STN:280:DyaL1M7ps1SjsQ%3D%3D, PID: 2702835
    • Simon R (1989) Optimal two-stage designs for phase II clinical trials. Control Clin Trials 10:1–10
    • (1989) Control Clin Trials , vol.10 , pp. 1-10
    • Simon, R.1
  • 29
    • 79958084461 scopus 로고    scopus 로고
    • A phase II study of the histone deacetylase inhibitor vorinostat combined with tamoxifen for the treatment of patients with hormone therapy-resistant breast cancer
    • COI: 1:CAS:528:DC%2BC3MXntV2hsbg%3D, PID: 21559012
    • Munster PN, Thurn KT, Thomas S, Raha P, Lacevic M, Miller A, Melisko M, Ismail-Khan R, Rugo H, Moasser M, Minton SE (2011) A phase II study of the histone deacetylase inhibitor vorinostat combined with tamoxifen for the treatment of patients with hormone therapy-resistant breast cancer. Br J Cancer 104:1828–1835. doi:10.1038/bjc.2011.156
    • (2011) Br J Cancer , vol.104 , pp. 1828-1835
    • Munster, P.N.1    Thurn, K.T.2    Thomas, S.3    Raha, P.4    Lacevic, M.5    Miller, A.6    Melisko, M.7    Ismail-Khan, R.8    Rugo, H.9    Moasser, M.10    Minton, S.E.11
  • 30
    • 79957514394 scopus 로고    scopus 로고
    • HDAC inhibitor SNDX-275 enhances efficacy of trastuzumab in erbB2-overexpressing breast cancer cells and exhibits potential to overcome trastuzumab resistance
    • COI: 1:CAS:528:DC%2BC3MXmslyhsbg%3D, PID: 21497990
    • Huang X, Wang S, Lee CK, Yang X, Liu B (2011) HDAC inhibitor SNDX-275 enhances efficacy of trastuzumab in erbB2-overexpressing breast cancer cells and exhibits potential to overcome trastuzumab resistance. Cancer Lett 307:72–79. doi:10.1016/j.canlet.2011.03.019
    • (2011) Cancer Lett , vol.307 , pp. 72-79
    • Huang, X.1    Wang, S.2    Lee, C.K.3    Yang, X.4    Liu, B.5
  • 31
    • 84879834815 scopus 로고    scopus 로고
    • Randomized phase II, double-blind, placebo-controlled study of exemestane with or without entinostat in postmenopausal women with locally recurrent or metastatic estrogen receptor-positive breast cancer progressing on treatment with a nonsteroidal aromatase inhibitor
    • COI: 1:CAS:528:DC%2BC3sXhtVSntbrF, PID: 23650416
    • Yardley DA, Ismail-Khan RR, Melichar B, Lichinitser M, Munster PN, Klein PM, Cruickshank S, Miller KD, Lee MJ, Trepel JB (2013) Randomized phase II, double-blind, placebo-controlled study of exemestane with or without entinostat in postmenopausal women with locally recurrent or metastatic estrogen receptor-positive breast cancer progressing on treatment with a nonsteroidal aromatase inhibitor. J Clin Oncol 31:2128–2135. doi:10.1200/JCO.2012.43.7251
    • (2013) J Clin Oncol , vol.31 , pp. 2128-2135
    • Yardley, D.A.1    Ismail-Khan, R.R.2    Melichar, B.3    Lichinitser, M.4    Munster, P.N.5    Klein, P.M.6    Cruickshank, S.7    Miller, K.D.8    Lee, M.J.9    Trepel, J.B.10


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