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Volumn 55, Issue 6, 2010, Pages 1126-1133

Initial testing (stage 1) of the multi-targeted kinase inhibitor sorafenib by the pediatric preclinical testing program

Author keywords

Developmental therapeutics; Preclinical testing; Tyrosine kinases

Indexed keywords

SORAFENIB;

EID: 77958598570     PISSN: 15455009     EISSN: 15455017     Source Type: Journal    
DOI: 10.1002/pbc.22712     Document Type: Article
Times cited : (49)

References (47)
  • 1
    • 12144289677 scopus 로고    scopus 로고
    • Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF
    • Wan PT, Garnett MJ, Roe SM, et al. Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF. Cell 2004; 116: 855-867.
    • (2004) Cell , vol.116 , pp. 855-867
    • Wan, P.T.1    Garnett, M.J.2    Roe, S.M.3
  • 2
    • 33749238553 scopus 로고    scopus 로고
    • Discovery and development of sorafenib: A multikinase inhibitor for treating cancer
    • Wilhelm S, Carter C, Lynch M, et al. Discovery and development of sorafenib: A multikinase inhibitor for treating cancer. Nat Rev Drug Discov 2006; 5: 835-844.
    • (2006) Nat Rev Drug Discov , vol.5 , pp. 835-844
    • Wilhelm, S.1    Carter, C.2    Lynch, M.3
  • 3
    • 33846930383 scopus 로고    scopus 로고
    • The ability of sorafenib to inhibit oncogenic PDGFRbeta and FLT3 mutants and overcome resistance to other small molecule inhibitors
    • Lierman E, Lahortiga I, Van Miegroet H, et al. The ability of sorafenib to inhibit oncogenic PDGFRbeta and FLT3 mutants and overcome resistance to other small molecule inhibitors. Haematologica 2007; 92: 27-34.
    • (2007) Haematologica , vol.92 , pp. 27-34
    • Lierman, E.1    Lahortiga, I.2    Van Miegroet, H.3
  • 4
    • 55749088393 scopus 로고    scopus 로고
    • Preclinical overview of sorafenib, a multikinase inhibitor that targets both Raf and VEGF and PDGF receptor tyrosine kinase signaling
    • Wilhelm SM, Adnane L, Newell P, et al. Preclinical overview of sorafenib, a multikinase inhibitor that targets both Raf and VEGF and PDGF receptor tyrosine kinase signaling. Mol Cancer Ther 2008; 7: 3129-3140.
    • (2008) Mol Cancer Ther , vol.7 , pp. 3129-3140
    • Wilhelm, S.M.1    Adnane, L.2    Newell, P.3
  • 5
    • 38049019119 scopus 로고    scopus 로고
    • Safety and anti-tumor activity of sorafenib (Nexavar) in combination with other anti-cancer agents: A review of clinical trials
    • Takimoto CH, Awada A. Safety and anti-tumor activity of sorafenib (Nexavar) in combination with other anti-cancer agents: A review of clinical trials. Cancer Chemother Pharmacol 2008; 61: 535-548.
    • (2008) Cancer Chemother Pharmacol , vol.61 , pp. 535-548
    • Takimoto, C.H.1    Awada, A.2
  • 6
    • 33846148701 scopus 로고    scopus 로고
    • Sorafenib in advanced clear-cell renal-cell carcinoma
    • Escudier B, Eisen T, Stadler WM, et al. Sorafenib in advanced clear-cell renal-cell carcinoma. N Engl J Med 2007; 356: 125-134.
    • (2007) N Engl J Med , vol.356 , pp. 125-134
    • Escudier, B.1    Eisen, T.2    Stadler, W.M.3
  • 7
    • 47949116252 scopus 로고    scopus 로고
    • Sorafenib in advanced hepatocellular carcinoma
    • Llovet JM, Ricci S, Mazzaferro V, et al. Sorafenib in advanced hepatocellular carcinoma. N Engl J Med 2008; 359: 378-390.
    • (2008) N Engl J Med , vol.359 , pp. 378-390
    • Llovet, J.M.1    Ricci, S.2    Mazzaferro, V.3
  • 8
    • 77953271584 scopus 로고    scopus 로고
    • Patterns of molecular response to and relapse after combination of sorafenib, idarubicin, and cytarabine in patients with newly diagnosed FLT3-mutant acute myeloid leukemia (AML)
    • Abstr #2079.
    • Al-Kali A, Jones D, Cortes J, et al. Patterns of molecular response to and relapse after combination of sorafenib, idarubicin, and cytarabine in patients with newly diagnosed FLT3-mutant acute myeloid leukemia (AML). Blood 2009; 114: Abstr #2079.
    • (2009) Blood , vol.114
    • Al-Kali, A.1    Jones, D.2    Cortes, J.3
  • 9
    • 34147135644 scopus 로고    scopus 로고
    • A fluorescence microplate cytotoxicity assay with a 4-log dynamic range that identifies synergistic drug combinations
    • Frgala T, Kalous O, Proffitt RT, et al. A fluorescence microplate cytotoxicity assay with a 4-log dynamic range that identifies synergistic drug combinations. Mol Cancer Ther 2007; 6: 886-897.
    • (2007) Mol Cancer Ther , vol.6 , pp. 886-897
    • Frgala, T.1    Kalous, O.2    Proffitt, R.T.3
  • 10
    • 36849020943 scopus 로고    scopus 로고
    • Initial testing (stage 1) of the proteasome inhibitor bortezomib by the pediatric preclinical testing program
    • Houghton PJ, Morton CL, Kolb EA, et al. Initial testing (stage 1) of the proteasome inhibitor bortezomib by the pediatric preclinical testing program. Pediatr Blood Cancer 2007; 50: 37-45.
    • (2007) Pediatr Blood Cancer , vol.50 , pp. 37-45
    • Houghton, P.J.1    Morton, C.L.2    Kolb, E.A.3
  • 11
    • 0023731771 scopus 로고
    • Experimental chemotherapy of human medulloblastoma cell lines and transplantable xenografts with bifunctional alkylating agents
    • Friedman HS, Colvin OM, Skapek SX, et al. Experimental chemotherapy of human medulloblastoma cell lines and transplantable xenografts with bifunctional alkylating agents. Cancer Res 1988; 48: 4189-4195.
    • (1988) Cancer Res , vol.48 , pp. 4189-4195
    • Friedman, H.S.1    Colvin, O.M.2    Skapek, S.X.3
  • 12
    • 2342531648 scopus 로고    scopus 로고
    • Characterization of childhood acute lymphoblastic leukemia xenograft models for the preclinical evaluation of new therapies
    • Liem NL, Papa RA, Milross CG, et al. Characterization of childhood acute lymphoblastic leukemia xenograft models for the preclinical evaluation of new therapies. Blood 2004; 103: 3905-3914.
    • (2004) Blood , vol.103 , pp. 3905-3914
    • Liem, N.L.1    Papa, R.A.2    Milross, C.G.3
  • 13
    • 34447249881 scopus 로고    scopus 로고
    • The pediatric preclinical testing program: Description of models and early testing results
    • Houghton PJ, Morton CL, Tucker C, et al. The pediatric preclinical testing program: Description of models and early testing results. Pediatr Blood Cancer 2006; 49: 928-940.
    • (2006) Pediatr Blood Cancer , vol.49 , pp. 928-940
    • Houghton, P.J.1    Morton, C.L.2    Tucker, C.3
  • 14
    • 0036045473 scopus 로고    scopus 로고
    • Amplification of a novel c-Kit activating mutation Asn(822)-Lys in the Kasumi-1 cell line: A t(8;21)-Kit mutant model for acute myeloid leukemia
    • Beghini A, Magnani I, Ripamonti CB, et al. Amplification of a novel c-Kit activating mutation Asn(822)-Lys in the Kasumi-1 cell line: A t(8;21)-Kit mutant model for acute myeloid leukemia. Hematol J 2002; 3: 157-163.
    • (2002) Hematol J , vol.3 , pp. 157-163
    • Beghini, A.1    Magnani, I.2    Ripamonti, C.B.3
  • 15
    • 33847195060 scopus 로고    scopus 로고
    • Antitumor activity of sorafenib in FLT3-driven leukemic cells
    • Auclair D, Miller D, Yatsula V, et al. Antitumor activity of sorafenib in FLT3-driven leukemic cells. Leukemia 2007; 21: 439-445.
    • (2007) Leukemia , vol.21 , pp. 439-445
    • Auclair, D.1    Miller, D.2    Yatsula, V.3
  • 16
    • 39149129114 scopus 로고    scopus 로고
    • Mutant FLT3: A direct target of sorafenib in acute myelogenous leukemia
    • Zhang W, Konopleva M, Shi YX, et al. Mutant FLT3: A direct target of sorafenib in acute myelogenous leukemia. J Natl Cancer Inst 2008; 100: 184-198.
    • (2008) J Natl Cancer Inst , vol.100 , pp. 184-198
    • Zhang, W.1    Konopleva, M.2    Shi, Y.X.3
  • 17
    • 77949887020 scopus 로고    scopus 로고
    • FLT3 mutant allelic burden and clinical status are predictive of response to FLT3 inhibitors in AML
    • Pratz KW, Sato T, Murphy KM, et al. FLT3 mutant allelic burden and clinical status are predictive of response to FLT3 inhibitors in AML. Blood 2009; 115: 1425-1432.
    • (2009) Blood , vol.115 , pp. 1425-1432
    • Pratz, K.W.1    Sato, T.2    Murphy, K.M.3
  • 18
    • 34548061196 scopus 로고    scopus 로고
    • Sorafenib inhibits the imatinib-resistant KITT670I gatekeeper mutation in gastrointestinal stromal tumor
    • Guo T, Agaram NP, Wong GC, et al. Sorafenib inhibits the imatinib-resistant KITT670I gatekeeper mutation in gastrointestinal stromal tumor. Clin Cancer Res 2007; 13: 4874-4881.
    • (2007) Clin Cancer Res , vol.13 , pp. 4874-4881
    • Guo, T.1    Agaram, N.P.2    Wong, G.C.3
  • 19
    • 51049092292 scopus 로고    scopus 로고
    • Sorafenib potently inhibits papillary thyroid carcinomas harboring RET/PTC1 rearrangement
    • Henderson YC, Ahn SH, Kang Y, et al. Sorafenib potently inhibits papillary thyroid carcinomas harboring RET/PTC1 rearrangement. Clin Cancer Res 2008; 14: 4908-4914.
    • (2008) Clin Cancer Res , vol.14 , pp. 4908-4914
    • Henderson, Y.C.1    Ahn, S.H.2    Kang, Y.3
  • 20
    • 33644747449 scopus 로고    scopus 로고
    • BAY 43-9006 inhibition of oncogenic RET mutants
    • Carlomagno F, Anaganti S, Guida T, et al. BAY 43-9006 inhibition of oncogenic RET mutants. J Natl Cancer Inst 2006; 98: 326-334.
    • (2006) J Natl Cancer Inst , vol.98 , pp. 326-334
    • Carlomagno, F.1    Anaganti, S.2    Guida, T.3
  • 21
    • 34250675667 scopus 로고    scopus 로고
    • Sorafenib inhibits imatinib-resistant KIT and platelet-derived growth factor receptor beta gatekeeper mutants
    • Guida T, Anaganti S, Provitera L, et al. Sorafenib inhibits imatinib-resistant KIT and platelet-derived growth factor receptor beta gatekeeper mutants. Clin Cancer Res 2007; 13: 3363-3369.
    • (2007) Clin Cancer Res , vol.13 , pp. 3363-3369
    • Guida, T.1    Anaganti, S.2    Provitera, L.3
  • 22
    • 67650351086 scopus 로고    scopus 로고
    • Structural and functional alterations of FLT3 in acute myeloid leukemia
    • Meshinchi S, Appelbaum FR. Structural and functional alterations of FLT3 in acute myeloid leukemia. Clin Cancer Res 2009; 15: 4263-4269.
    • (2009) Clin Cancer Res , vol.15 , pp. 4263-4269
    • Meshinchi, S.1    Appelbaum, F.R.2
  • 23
    • 77950612017 scopus 로고    scopus 로고
    • Prevalence and prognostic significance of KIT mutations in pediatric patients with core binding factor AML enrolled on serial pediatric cooperative trials for de novo AML
    • Pollard JA, Alonzo TA, Gerbing RB, et al. Prevalence and prognostic significance of KIT mutations in pediatric patients with core binding factor AML enrolled on serial pediatric cooperative trials for de novo AML. Blood 2010; 115: 2372-2379.
    • (2010) Blood , vol.115 , pp. 2372-2379
    • Pollard, J.A.1    Alonzo, T.A.2    Gerbing, R.B.3
  • 24
    • 4944249117 scopus 로고    scopus 로고
    • BAY 43-9006 exhibits broad spectrum oral antitumor activity and targets the RAF/MEK/ERK pathway and receptor tyrosine kinases involved in tumor progression and angiogenesis
    • Wilhelm SM, Carter C, Tang L, et al. BAY 43-9006 exhibits broad spectrum oral antitumor activity and targets the RAF/MEK/ERK pathway and receptor tyrosine kinases involved in tumor progression and angiogenesis. Cancer Res 2004; 64: 7099-7109.
    • (2004) Cancer Res , vol.64 , pp. 7099-7109
    • Wilhelm, S.M.1    Carter, C.2    Tang, L.3
  • 25
    • 33846212284 scopus 로고    scopus 로고
    • Sorafenib blocks the RAF/MEK/ERK pathway, inhibits tumor angiogenesis, and induces tumor cell apoptosis in hepatocellular carcinoma model PLC/PRF/5
    • Liu L, Cao Y, Chen C, et al. Sorafenib blocks the RAF/MEK/ERK pathway, inhibits tumor angiogenesis, and induces tumor cell apoptosis in hepatocellular carcinoma model PLC/PRF/5. Cancer Res 2006; 66: 11851-11858.
    • (2006) Cancer Res , vol.66 , pp. 11851-11858
    • Liu, L.1    Cao, Y.2    Chen, C.3
  • 26
    • 27144502652 scopus 로고    scopus 로고
    • The role of Mcl-1 downregulation in the proapoptotic activity of the multikinase inhibitor BAY 43-9006
    • Yu C, Bruzek LM, Meng XW, et al. The role of Mcl-1 downregulation in the proapoptotic activity of the multikinase inhibitor BAY 43-9006. Oncogene 2005; 24: 6861-6869.
    • (2005) Oncogene , vol.24 , pp. 6861-6869
    • Yu, C.1    Bruzek, L.M.2    Meng, X.W.3
  • 27
    • 56249096211 scopus 로고    scopus 로고
    • Sorafenib inhibits signal transducer and activator of transcription 3 signaling associated with growth arrest and apoptosis of medulloblastomas
    • Yang F, Van Meter TE, Buettner R, et al. Sorafenib inhibits signal transducer and activator of transcription 3 signaling associated with growth arrest and apoptosis of medulloblastomas. Mol Cancer Ther 2008; 7: 3519-3526.
    • (2008) Mol Cancer Ther , vol.7 , pp. 3519-3526
    • Yang, F.1    Van Meter, T.E.2    Buettner, R.3
  • 28
    • 27444436166 scopus 로고    scopus 로고
    • Apoptosis induced by the kinase inhibitor BAY 43-9006 in human leukemia cells involves down-regulation of Mcl-1 through inhibition of translation
    • Rahmani M, Davis EM, Bauer C, et al. Apoptosis induced by the kinase inhibitor BAY 43-9006 in human leukemia cells involves down-regulation of Mcl-1 through inhibition of translation. J Biol Chem 2005; 280: 35217-35227.
    • (2005) J Biol Chem , vol.280 , pp. 35217-35227
    • Rahmani, M.1    Davis, E.M.2    Bauer, C.3
  • 29
    • 34548412863 scopus 로고    scopus 로고
    • The multikinase inhibitor sorafenib induces apoptosis in highly imatinib mesylate-resistant bcr/abl+ human leukemia cells in association with signal transducer and activator of transcription 5 inhibition and myeloid cell leukemia-1 down-regulation
    • Rahmani M, Nguyen TK, Dent P, et al. The multikinase inhibitor sorafenib induces apoptosis in highly imatinib mesylate-resistant bcr/abl+ human leukemia cells in association with signal transducer and activator of transcription 5 inhibition and myeloid cell leukemia-1 down-regulation. Mol Pharmacol 2007; 72: 788-795.
    • (2007) Mol Pharmacol , vol.72 , pp. 788-795
    • Rahmani, M.1    Nguyen, T.K.2    Dent, P.3
  • 30
    • 51049101063 scopus 로고    scopus 로고
    • Down-regulation of myeloid cell leukemia-1 through inhibiting Erk/Pin 1 pathway by sorafenib facilitates chemosensitization in breast cancer
    • Ding Q, Huo L, Yang JY, et al. Down-regulation of myeloid cell leukemia-1 through inhibiting Erk/Pin 1 pathway by sorafenib facilitates chemosensitization in breast cancer. Cancer Res 2008; 68: 6109-6117.
    • (2008) Cancer Res , vol.68 , pp. 6109-6117
    • Ding, Q.1    Huo, L.2    Yang, J.Y.3
  • 31
    • 77949887020 scopus 로고    scopus 로고
    • FLT3-mutant allelic burden and clinical status are predictive of response to FLT3 inhibitors in AML
    • Pratz KW, Sato T, Murphy KM, et al. FLT3-mutant allelic burden and clinical status are predictive of response to FLT3 inhibitors in AML. Blood 2010; 115: 1425-1432.
    • (2010) Blood , vol.115 , pp. 1425-1432
    • Pratz, K.W.1    Sato, T.2    Murphy, K.M.3
  • 32
    • 33847118123 scopus 로고    scopus 로고
    • Sorafenib (BAY 43-9006) inhibits tumor growth and vascularization and induces tumor apoptosis and hypoxia in RCC xenograft models
    • Chang YS, Adnane J, Trail PA, et al. Sorafenib (BAY 43-9006) inhibits tumor growth and vascularization and induces tumor apoptosis and hypoxia in RCC xenograft models. Cancer Chemother Pharmacol 2007; 59: 561-574.
    • (2007) Cancer Chemother Pharmacol , vol.59 , pp. 561-574
    • Chang, Y.S.1    Adnane, J.2    Trail, P.A.3
  • 33
    • 34147161209 scopus 로고    scopus 로고
    • Inhibition of tumor endothelial ERK activation, angiogenesis, and tumor growth by sorafenib (BAY43-9006)
    • Murphy DA, Makonnen S, Lassoued W, et al. Inhibition of tumor endothelial ERK activation, angiogenesis, and tumor growth by sorafenib (BAY43-9006). Am J Pathol 2006; 169: 1875-1885.
    • (2006) Am J Pathol , vol.169 , pp. 1875-1885
    • Murphy, D.A.1    Makonnen, S.2    Lassoued, W.3
  • 34
    • 44149115014 scopus 로고    scopus 로고
    • Initial testing (stage 1) of sunitinib by the Pediatric Preclinical Testing Program
    • Maris JM, Courtright J, Houghton PJ, et al. Initial testing (stage 1) of sunitinib by the Pediatric Preclinical Testing Program. Pediatr Blood Cancer 2008; 51: 42-48.
    • (2008) Pediatr Blood Cancer , vol.51 , pp. 42-48
    • Maris, J.M.1    Courtright, J.2    Houghton, P.J.3
  • 35
    • 38549164180 scopus 로고    scopus 로고
    • Initial testing of the VEGFR inhibitor AZD2171 by the pediatric preclinical testing program
    • Maris JM, Courtright J, Houghton PJ, et al. Initial testing of the VEGFR inhibitor AZD2171 by the pediatric preclinical testing program. Pediatr Blood Cancer 2008; 50: 581-587.
    • (2008) Pediatr Blood Cancer , vol.50 , pp. 581-587
    • Maris, J.M.1    Courtright, J.2    Houghton, P.J.3
  • 36
    • 16644379604 scopus 로고    scopus 로고
    • Hotspot mutations of BRAF gene are not associated with pediatric solid neoplasms
    • Miao J, Kusafuka T, Fukuzawa M. Hotspot mutations of BRAF gene are not associated with pediatric solid neoplasms. Oncol Rep 2004; 12: 1269-1272.
    • (2004) Oncol Rep , vol.12 , pp. 1269-1272
    • Miao, J.1    Kusafuka, T.2    Fukuzawa, M.3
  • 37
    • 8844252330 scopus 로고    scopus 로고
    • Mutation analysis of the Ras pathway genes NRAS, HRAS, KRAS and BRAF in glioblastomas
    • Knobbe CB, Reifenberger J, Reifenberger G. Mutation analysis of the Ras pathway genes NRAS, HRAS, KRAS and BRAF in glioblastomas. Acta Neuropathol 2004; 108: 467-470.
    • (2004) Acta Neuropathol , vol.108 , pp. 467-470
    • Knobbe, C.B.1    Reifenberger, J.2    Reifenberger, G.3
  • 38
    • 13544251719 scopus 로고    scopus 로고
    • Mutations in the BRAF and N-ras genes in childhood acute lymphoblastic leukaemia
    • Gustafsson B, Angelini S, Sander B, et al. Mutations in the BRAF and N-ras genes in childhood acute lymphoblastic leukaemia. Leukemia 2005; 19: 310-312.
    • (2005) Leukemia , vol.19 , pp. 310-312
    • Gustafsson, B.1    Angelini, S.2    Sander, B.3
  • 39
    • 43049124130 scopus 로고    scopus 로고
    • BRAF gene duplication constitutes a mechanism of MAPK pathway activation in low-grade astrocytomas
    • Pfister S, Janzarik WG, Remke M, et al. BRAF gene duplication constitutes a mechanism of MAPK pathway activation in low-grade astrocytomas. J Clin Invest 2008; 118: 1739-1749.
    • (2008) J Clin Invest , vol.118 , pp. 1739-1749
    • Pfister, S.1    Janzarik, W.G.2    Remke, M.3
  • 40
    • 55349107544 scopus 로고    scopus 로고
    • Tandem duplication producing a novel oncogenic BRAF fusion gene defines the majority of pilocytic astrocytomas
    • Jones DT, Kocialkowski S, Liu L, et al. Tandem duplication producing a novel oncogenic BRAF fusion gene defines the majority of pilocytic astrocytomas. Cancer Res 2008; 68: 8673-8677.
    • (2008) Cancer Res , vol.68 , pp. 8673-8677
    • Jones, D.T.1    Kocialkowski, S.2    Liu, L.3
  • 41
    • 52649172327 scopus 로고    scopus 로고
    • Frequent gains at chromosome 7q34 involving BRAF in pilocytic astrocytoma
    • Bar EE, Lin A, Tihan T, et al. Frequent gains at chromosome 7q34 involving BRAF in pilocytic astrocytoma. J Neuropathol Exp Neurol 2008; 67: 878-887.
    • (2008) J Neuropathol Exp Neurol , vol.67 , pp. 878-887
    • Bar, E.E.1    Lin, A.2    Tihan, T.3
  • 42
    • 38049097938 scopus 로고    scopus 로고
    • Identification of genotype-correlated sensitivity to selective kinase inhibitors by using high-throughput tumor cell line profiling
    • McDermott U, Sharma SV, Dowell L, et al. Identification of genotype-correlated sensitivity to selective kinase inhibitors by using high-throughput tumor cell line profiling. Proc Natl Acad Sci USA 2007; 104: 19936-19941.
    • (2007) Proc Natl Acad Sci USA , vol.104 , pp. 19936-19941
    • McDermott, U.1    Sharma, S.V.2    Dowell, L.3
  • 43
    • 33748325763 scopus 로고    scopus 로고
    • Sorafenib in advanced melanoma: A Phase II randomised discontinuation trial analysis
    • Eisen T, Ahmad T, Flaherty KT, et al. Sorafenib in advanced melanoma: A Phase II randomised discontinuation trial analysis. Br J Cancer 2006; 95: 581-586.
    • (2006) Br J Cancer , vol.95 , pp. 581-586
    • Eisen, T.1    Ahmad, T.2    Flaherty, K.T.3
  • 44
    • 76249091731 scopus 로고    scopus 로고
    • Phase I study of sorafenib in children with refractory solid tumors: A Children's Oncology Group Phase I Consortium trial
    • Abstr #10012.
    • Widemann BC, Fox E, Adamson PC, et al. Phase I study of sorafenib in children with refractory solid tumors: A Children's Oncology Group Phase I Consortium trial. J Clin Oncol 2009; 27: Abstr #10012.
    • (2009) J Clin Oncol , vol.27
    • Widemann, B.C.1    Fox, E.2    Adamson, P.C.3
  • 45
    • 69249221392 scopus 로고    scopus 로고
    • Compassionate use of sorafenib in FLT3-ITD-positive acute myeloid leukemia: Sustained regression before and after allogeneic stem cell transplantation
    • Metzelder S, Wang Y, Wollmer E, et al. Compassionate use of sorafenib in FLT3-ITD-positive acute myeloid leukemia: Sustained regression before and after allogeneic stem cell transplantation. Blood 2009; 113: 6567-6571.
    • (2009) Blood , vol.113 , pp. 6567-6571
    • Metzelder, S.1    Wang, Y.2    Wollmer, E.3
  • 46
    • 56949083913 scopus 로고    scopus 로고
    • Sorafenib (Nexavar) induces molecular remission and regression of extramedullary disease in a patient with FLT3-ITD+ acute myeloid leukemia
    • Safaian NN, Czibere A, Bruns I, et al. Sorafenib (Nexavar) induces molecular remission and regression of extramedullary disease in a patient with FLT3-ITD+ acute myeloid leukemia. Leuk Res 2009; 33: 348-350.
    • (2009) Leuk Res , vol.33 , pp. 348-350
    • Safaian, N.N.1    Czibere, A.2    Bruns, I.3
  • 47
    • 51649092873 scopus 로고    scopus 로고
    • Molecular characterization of the pediatric preclinical testing panel
    • Neale G, Su X, Morton CL, et al. Molecular characterization of the pediatric preclinical testing panel. Clin Cancer Res 2008; 14: 4572-4583.
    • (2008) Clin Cancer Res , vol.14 , pp. 4572-4583
    • Neale, G.1    Su, X.2    Morton, C.L.3


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