-
1
-
-
84872967522
-
Cancer statistics, 2013
-
Siegel R, Naishadham D, Jemal A: Cancer statistics, 2013. CA Cancer J Clin 63:11-30, 2013
-
(2013)
CA Cancer J Clin
, vol.63
, pp. 11-30
-
-
Siegel, R.1
Naishadham, D.2
Jemal, A.3
-
2
-
-
79959757619
-
The notorious "drug lag" for oncology drugs in Japan
-
Yonemori K, Hirakawa A, Ando M, et al: The notorious "drug lag" for oncology drugs in Japan. Invest New Drugs 29:706-712, 2011
-
(2011)
Invest New Drugs
, vol.29
, pp. 706-712
-
-
Yonemori, K.1
Hirakawa, A.2
Ando, M.3
-
3
-
-
77952189195
-
Approval of new drugs 1999-2007: Comparison of the US, the EU and Japan situations
-
Tsuji K, Tsutani K: Approval of new drugs 1999-2007: Comparison of the US, the EU and Japan situations. J Clin Pharm Ther 35:289-301, 2010
-
(2010)
J Clin Pharm Ther
, vol.35
, pp. 289-301
-
-
Tsuji, K.1
Tsutani, K.2
-
4
-
-
77957032520
-
PMDA's challenge to accelerate clinical development and review of new drugs in Japan
-
Ichimaru K, Toyoshima S, Uyama Y: PMDA's challenge to accelerate clinical development and review of new drugs in Japan. Clin Pharmacol Ther 88:454-457, 2010
-
(2010)
Clin Pharmacol Ther
, vol.88
, pp. 454-457
-
-
Ichimaru, K.1
Toyoshima, S.2
Uyama, Y.3
-
5
-
-
77952577319
-
Phase I and pharmacokinetic study of ABI-007, albumin-bound paclitaxel, administered every 3 weeks in Japanese patients with solid tumors
-
Yamada K, Yamamoto N, Yamada Y, et al: Phase I and pharmacokinetic study of ABI-007, albumin-bound paclitaxel, administered every 3 weeks in Japanese patients with solid tumors. Jpn J Clin Oncol 40:404-411, 2010
-
(2010)
Jpn J Clin Oncol
, vol.40
, pp. 404-411
-
-
Yamada, K.1
Yamamoto, N.2
Yamada, Y.3
-
6
-
-
32944481043
-
Phase I and pharmacokinetics trial of ABI-007, a novel nanoparticle formulation of paclitaxel in patients with advanced nonhematologic malignancies
-
Nyman DW, Campbell KJ, Hersh E, et al: Phase I and pharmacokinetics trial of ABI-007, a novel nanoparticle formulation of paclitaxel in patients with advanced nonhematologic malignancies. J Clin Oncol 23:7785-7793, 2005
-
(2005)
J Clin Oncol
, vol.23
, pp. 7785-7793
-
-
Nyman, D.W.1
Campbell, K.J.2
Hersh, E.3
-
7
-
-
84863796413
-
An open-label, phase 1 study evaluating safety, tolerability, and pharmacokinetics of linifanib (ABT-869) in Japanese patients with solid tumors
-
Asahina H, Tamura Y, Nokihara H, et al: An open-label, phase 1 study evaluating safety, tolerability, and pharmacokinetics of linifanib (ABT-869) in Japanese patients with solid tumors. Cancer Chemother Pharmacol 69:1477-1486, 2012
-
(2012)
Cancer Chemother Pharmacol
, vol.69
, pp. 1477-1486
-
-
Asahina, H.1
Tamura, Y.2
Nokihara, H.3
-
8
-
-
70350464165
-
Phase I and biomarker study of ABT-869, a multiple receptor tyrosine kinase inhibitor, in patients with refractory solid malignancies
-
Wong CI, Koh TS, Soo R, et al: Phase I and biomarker study of ABT-869, a multiple receptor tyrosine kinase inhibitor, in patients with refractory solid malignancies. J Clin Oncol 27:4718-4726, 2009
-
(2009)
J Clin Oncol
, vol.27
, pp. 4718-4726
-
-
Wong, C.I.1
Koh, T.S.2
Soo, R.3
-
9
-
-
69249187806
-
Safety and pharmacokinetics of panitumumab in Japanese patients with advanced solid tumors
-
Doi T, Ohtsu A, Tahara M, et al: Safety and pharmacokinetics of panitumumab in Japanese patients with advanced solid tumors. Int J Clin Oncol 14:307-314, 2009
-
(2009)
Int J Clin Oncol
, vol.14
, pp. 307-314
-
-
Doi, T.1
Ohtsu, A.2
Tahara, M.3
-
10
-
-
38949178132
-
Dose and schedule study of panitumumab monotherapy in patients with advanced solid malignancies
-
Weiner LM, Belldegrun AS, Crawford J, et al: Dose and schedule study of panitumumab monotherapy in patients with advanced solid malignancies. Clin Cancer Res 14:502-508, 2008
-
(2008)
Clin Cancer Res
, vol.14
, pp. 502-508
-
-
Weiner, L.M.1
Belldegrun, A.S.2
Crawford, J.3
-
11
-
-
77956225558
-
Phase 1 study of the investigational, oral angiogenesis inhibitor motesanib in Japanese patients with advanced solid tumors
-
Fujisaka Y, Yamada Y, Yamamoto N, et al: Phase 1 study of the investigational, oral angiogenesis inhibitor motesanib in Japanese patients with advanced solid tumors. Cancer Chemother Pharmacol 66:935-943, 2010
-
(2010)
Cancer Chemother Pharmacol
, vol.66
, pp. 935-943
-
-
Fujisaka, Y.1
Yamada, Y.2
Yamamoto, N.3
-
12
-
-
34347235531
-
Safety, pharmacokinetics, and efficacy of AMG 706, an oral multikinase inhibitor, in patients with advanced solid tumors
-
Rosen LS, Kurzrock R, Mulay M, et al: Safety, pharmacokinetics, and efficacy of AMG 706, an oral multikinase inhibitor, in patients with advanced solid tumors. J Clin Oncol 25:2369-2376, 2007
-
(2007)
J Clin Oncol
, vol.25
, pp. 2369-2376
-
-
Rosen, L.S.1
Kurzrock, R.2
Mulay, M.3
-
13
-
-
69049085535
-
Phase I, dose escalation and pharmacokinetic study of cediranib (RECENTIN), a highly potent and selective VEGFR signaling inhibitor, in Japanese patients with advanced solid tumors
-
Yamamoto N, Tamura T, Yamamoto N, et al: Phase I, dose escalation and pharmacokinetic study of cediranib (RECENTIN), a highly potent and selective VEGFR signaling inhibitor, in Japanese patients with advanced solid tumors. Cancer Chemother Pharmacol 64:1165-1172, 2009
-
(2009)
Cancer Chemother Pharmacol
, vol.64
, pp. 1165-1172
-
-
Yamamoto, N.1
Tamura, T.2
Yamamoto, N.3
-
14
-
-
34547681379
-
Phase I clinical study of AZD2171, an oral vascular endothelial growth factor signaling inhibitor, in patients with advanced solid tumors
-
Drevs J, Siegert P, Medinger M, et al: Phase I clinical study of AZD2171, an oral vascular endothelial growth factor signaling inhibitor, in patients with advanced solid tumors. J Clin Oncol 25:3045-3054, 2007
-
(2007)
J Clin Oncol
, vol.25
, pp. 3045-3054
-
-
Drevs, J.1
Siegert, P.2
Medinger, M.3
-
15
-
-
84859712705
-
A Phase I, dose-finding and pharmacokinetic study of olaparib (AZD2281) in Japanese patients with advanced solid tumors
-
Yamamoto N, Nokihara H, Yamada Y, et al: A Phase I, dose-finding and pharmacokinetic study of olaparib (AZD2281) in Japanese patients with advanced solid tumors. Cancer Sci 103:504-509, 2012
-
(2012)
Cancer Sci
, vol.103
, pp. 504-509
-
-
Yamamoto, N.1
Nokihara, H.2
Yamada, Y.3
-
16
-
-
67650471685
-
Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers
-
Fong PC, Boss DS, Yap TA, et al: Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers. N Engl J Med 361:123-134, 2009
-
(2009)
N Engl J Med
, vol.361
, pp. 123-134
-
-
Fong, P.C.1
Boss, D.S.2
Yap, T.A.3
-
17
-
-
84879088068
-
Safety and tolerability of AZD8055 in Japanese patients with advanced solid tumors: A dose-finding phase I study
-
Asahina H, Nokihara H, Yamamoto N, et al: Safety and tolerability of AZD8055 in Japanese patients with advanced solid tumors: A dose-finding phase I study. Invest New Drugs 31:677-684, 2013
-
(2013)
Invest New Drugs
, vol.31
, pp. 677-684
-
-
Asahina, H.1
Nokihara, H.2
Yamamoto, N.3
-
18
-
-
84866928171
-
Safety, tolerability, pharmacokinetics and pharmacodynamics of AZD8055 in advanced solid tumours and lymphoma
-
Naing A, Aghajanian C, Raymond E, et al: Safety, tolerability, pharmacokinetics and pharmacodynamics of AZD8055 in advanced solid tumours and lymphoma. Br J Cancer 107:1093-1099, 2012
-
(2012)
Br J Cancer
, vol.107
, pp. 1093-1099
-
-
Naing, A.1
Aghajanian, C.2
Raymond, E.3
-
19
-
-
84937620913
-
Phase I clinical trial investigating maximum tolerated dose, safety and pharmacokinetics of volasertib in Japanese patients with advanced solid tumours
-
Nokihara H, Yamamoto N, Fujiwara Y, et al: Phase I clinical trial investigating maximum tolerated dose, safety and pharmacokinetics of volasertib in Japanese patients with advanced solid tumours. European Cancer Congress, Amsterdam, the Netherlands, September 27-October 1, 2013
-
European Cancer Congress, Amsterdam, the Netherlands, September 27-October 1, 2013
-
-
Nokihara, H.1
Yamamoto, N.2
Fujiwara, Y.3
-
20
-
-
84655164874
-
A phase I, dose-escalation study of the novel Polo-like kinase inhibitor volasertib (BI 6727) in patients with advanced solid tumours
-
Schöffski P, Awada A, Dumez H, et al: A phase I, dose-escalation study of the novel Polo-like kinase inhibitor volasertib (BI 6727) in patients with advanced solid tumours. Eur J Cancer 48:179-186, 2012
-
(2012)
Eur J Cancer
, vol.48
, pp. 179-186
-
-
Schöffski, P.1
Awada, A.2
Dumez, H.3
-
21
-
-
39749126801
-
Phase I clinical and pharmacokinetic study of 3-weekly, 3-h infusion of ixabepilone (BMS-247550), an epothilone B analog, in Japanese patients with refractory solid tumors
-
Shimizu T, Yamamoto N, Yamada Y, et al: Phase I clinical and pharmacokinetic study of 3-weekly, 3-h infusion of ixabepilone (BMS-247550), an epothilone B analog, in Japanese patients with refractory solid tumors. Cancer Chemother Pharmacol 61:751-758, 2008
-
(2008)
Cancer Chemother Pharmacol
, vol.61
, pp. 751-758
-
-
Shimizu, T.1
Yamamoto, N.2
Yamada, Y.3
-
22
-
-
34047212584
-
Phase I study of the novel epothilone analog ixabepilone (BMS-247550) in patients with advanced solid tumors and lymphomas
-
Aghajanian C, Burris HA 3rd, Jones S, et al: Phase I study of the novel epothilone analog ixabepilone (BMS-247550) in patients with advanced solid tumors and lymphomas. J Clin Oncol 25:1082-1088, 2007
-
(2007)
J Clin Oncol
, vol.25
, pp. 1082-1088
-
-
Aghajanian, C.1
Burris, H.A.2
Jones, S.3
-
23
-
-
84867577176
-
A phase I study of BMS-690514 in Japanese patients with advanced or metastatic solid tumors
-
Nokihara H, Yamamoto N, Yamada Y, et al: A phase I study of BMS-690514 in Japanese patients with advanced or metastatic solid tumors. Cancer Chemother Pharmacol 70:559-565, 2012
-
(2012)
Cancer Chemother Pharmacol
, vol.70
, pp. 559-565
-
-
Nokihara, H.1
Yamamoto, N.2
Yamada, Y.3
-
24
-
-
84876671596
-
Phase I-IIa study of BMS-690514, an EGFR, HER-2 and -4 and VEGFR-1 to -3 oral tyrosine kinase inhibitor, in patients with advanced or metastatic solid tumours
-
Soria JC, Baselga J, Hanna N, et al: Phase I-IIa study of BMS-690514, an EGFR, HER-2 and -4 and VEGFR-1 to -3 oral tyrosine kinase inhibitor, in patients with advanced or metastatic solid tumours. Eur J Cancer 49:1815-1824, 2013
-
(2013)
Eur J Cancer
, vol.49
, pp. 1815-1824
-
-
Soria, J.C.1
Baselga, J.2
Hanna, N.3
-
25
-
-
84937620914
-
Phase 1 dose escalating study of BMS-754807 in Japanese patients with advanced solid tumors
-
Tamura Y, Nokihara H, Yamamoto N, et al: Phase 1 dose escalating study of BMS-754807 in Japanese patients with advanced solid tumors. The 10th Annual Meeting of the Japanese Society of Medical Oncology, Osaka, Japan, July 26-28, 2012
-
The 10th Annual Meeting of the Japanese Society of Medical Oncology, Osaka, Japan, July 26-28, 2012
-
-
Tamura, Y.1
Nokihara, H.2
Yamamoto, N.3
-
26
-
-
77955265956
-
A Phase 1 clinical study of temsirolimus (CCI-779) in Japanese patients with advanced solid tumors
-
Fujisaka Y, Yamada Y, Yamamoto N, et al: A Phase 1 clinical study of temsirolimus (CCI-779) in Japanese patients with advanced solid tumors. Jpn J Clin Oncol 40:732-738, 2010
-
(2010)
Jpn J Clin Oncol
, vol.40
, pp. 732-738
-
-
Fujisaka, Y.1
Yamada, Y.2
Yamamoto, N.3
-
27
-
-
2942735384
-
Safety and pharmacokinetics of escalated doses of weekly intravenous infusion of CCI-779, a novel mTOR inhibitor, in patients with cancer
-
Raymond E, Alexandre J, Faivre S, et al: Safety and pharmacokinetics of escalated doses of weekly intravenous infusion of CCI-779, a novel mTOR inhibitor, in patients with cancer. J Clin Oncol 22:2336-2347, 2004
-
(2004)
J Clin Oncol
, vol.22
, pp. 2336-2347
-
-
Raymond, E.1
Alexandre, J.2
Faivre, S.3
-
28
-
-
84937620915
-
A Phase 1 study evaluating the safety profile and pharmacokinetics of CS1008 (Tigatuzumab), humanized monoclonal antibody targeting death receptor 5 (DR5), in Japanese patients with advanced solid tumours
-
Nokihara H, Yamamoto N, Yamada Y, et al: A Phase 1 study evaluating the safety profile and pharmacokinetics of CS1008 (Tigatuzumab), humanized monoclonal antibody targeting death receptor 5 (DR5), in Japanese patients with advanced solid tumours. 22nd EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics, Berlin, Germany, November 16-19, 2010
-
22nd EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics, Berlin, Germany, November 16-19, 2010
-
-
Nokihara, H.1
Yamamoto, N.2
Yamada, Y.3
-
29
-
-
77649301860
-
Phase I trial of weekly tigatuzumab, an agonistic humanized monoclonal antibody targeting death receptor 5 (DR5)
-
Forero-Torres A, Shah J, Wood T, et al: Phase I trial of weekly tigatuzumab, an agonistic humanized monoclonal antibody targeting death receptor 5 (DR5). Cancer Biother Radiopharm 25:13-19, 2010
-
(2010)
Cancer Biother Radiopharm
, vol.25
, pp. 13-19
-
-
Forero-Torres, A.1
Shah, J.2
Wood, T.3
-
30
-
-
0033865075
-
DX-8951f, a hexacyclic camptothecin analog, on a daily-times-five schedule: A phase I and pharmacokinetic study in patients with advanced solid malignancies
-
Rowinsky EK, Johnson TR, Geyer CE Jr, et al: DX-8951f, a hexacyclic camptothecin analog, on a daily-times-five schedule: A phase I and pharmacokinetic study in patients with advanced solid malignancies. J Clin Oncol 18:3151-3163, 2000
-
(2000)
J Clin Oncol
, vol.18
, pp. 3151-3163
-
-
Rowinsky, E.K.1
Johnson, T.R.2
Geyer, C.E.3
-
31
-
-
0034548798
-
Phase I and pharmacokinetic study of the camptothecin analog DX-8951f administered as a 30-minute infusion every 3 weeks in patients with advanced cancer
-
Boige V, Raymond E, Faivre S, et al: Phase I and pharmacokinetic study of the camptothecin analog DX-8951f administered as a 30-minute infusion every 3 weeks in patients with advanced cancer. J Clin Oncol 18:3986-3992, 2000
-
(2000)
J Clin Oncol
, vol.18
, pp. 3986-3992
-
-
Boige, V.1
Raymond, E.2
Faivre, S.3
-
32
-
-
28444465958
-
Phase I pharmacokinetic and pharmacogenomic study of E7070 administered once every 21 days
-
Yamada Y, Yamamoto N, Shimoyama T, et al: Phase I pharmacokinetic and pharmacogenomic study of E7070 administered once every 21 days. Cancer Sci 96:721-728, 2005
-
(2005)
Cancer Sci
, vol.96
, pp. 721-728
-
-
Yamada, Y.1
Yamamoto, N.2
Shimoyama, T.3
-
33
-
-
0037102283
-
Phase I and pharmacokinetic study of E7070, a novel chloroindolyl sulfonamide cell-cycle inhibitor, administered as a one-hour infusion every three weeks in patients with advanced cancer
-
Raymond E, ten Bokkel Huinink WW, Taïeb J, et al: Phase I and pharmacokinetic study of E7070, a novel chloroindolyl sulfonamide cell-cycle inhibitor, administered as a one-hour infusion every three weeks in patients with advanced cancer. J Clin Oncol 20:3508-3521, 2002
-
(2002)
J Clin Oncol
, vol.20
, pp. 3508-3521
-
-
Raymond, E.1
Ten Bokkel Huinink, W.W.2
Taïeb, J.3
-
34
-
-
79954609271
-
Phase I dose-escalation study and biomarker analysis of E7080 in patients with advanced solid tumors
-
Yamada K, Yamamoto N, Yamada Y, et al: Phase I dose-escalation study and biomarker analysis of E7080 in patients with advanced solid tumors. Clin Cancer Res 17:2528-2537, 2011
-
(2011)
Clin Cancer Res
, vol.17
, pp. 2528-2537
-
-
Yamada, K.1
Yamamoto, N.2
Yamada, Y.3
-
35
-
-
84860780755
-
A phase I study of E7080, a multitargeted tyrosine kinase inhibitor, in patients with advanced solid tumours
-
Boss DS, Glen H, Beijnen JH, et al: A phase I study of E7080, a multitargeted tyrosine kinase inhibitor, in patients with advanced solid tumours. Br J Cancer 106:1598-1604, 2012
-
(2012)
Br J Cancer
, vol.106
, pp. 1598-1604
-
-
Boss, D.S.1
Glen, H.2
Beijnen, J.H.3
-
36
-
-
84937620916
-
A Phase 1 Study of necitumumab (anti-EGFR monoclonal antibody) in Japanese patients with advanced solid tumors
-
Nokihara H, Yamamoto N, Tamura Y, et al: A Phase 1 Study of necitumumab (anti-EGFR monoclonal antibody) in Japanese patients with advanced solid tumors. The 12th Annual Meeting of the Japanese Society of Medical Oncology, Fukuoka, Japan, July 17-19, 2014
-
The 12th Annual Meeting of the Japanese Society of Medical Oncology, Fukuoka, Japan, July 17-19, 2014
-
-
Nokihara, H.1
Yamamoto, N.2
Tamura, Y.3
-
37
-
-
77949726425
-
A phase I pharmacologic study of necitumumab (IMC-11F8), a fully human IgG1 monoclonal antibody directed against EGFR in patients with advanced solid malignancies
-
Kuenen B, Witteveen PO, Ruijter R, et al: A phase I pharmacologic study of necitumumab (IMC-11F8), a fully human IgG1 monoclonal antibody directed against EGFR in patients with advanced solid malignancies. Clin Cancer Res 16:1915-1923, 2010
-
(2010)
Clin Cancer Res
, vol.16
, pp. 1915-1923
-
-
Kuenen, B.1
Witteveen, P.O.2
Ruijter, R.3
-
38
-
-
77649213706
-
Phase I pharmacologic and biologic study of ramucirumab (IMC-1121B), a fully human immunoglobulin G1 monoclonal antibody targeting the vascular endothelial growth factor receptor-2
-
Spratlin JL, Cohen RB, Eadens M, et al: Phase I pharmacologic and biologic study of ramucirumab (IMC-1121B), a fully human immunoglobulin G1 monoclonal antibody targeting the vascular endothelial growth factor receptor-2. J Clin Oncol 28:780-787, 2010
-
(2010)
J Clin Oncol
, vol.28
, pp. 780-787
-
-
Spratlin, J.L.1
Cohen, R.B.2
Eadens, M.3
-
39
-
-
33646477959
-
Phase I and pharmacokinetic study of edotecarin, a novel topoisomerase I inhibitor, administered once every 3 weeks in patients with solid tumors
-
Yamada Y, Tamura T, Yamamoto N, et al: Phase I and pharmacokinetic study of edotecarin, a novel topoisomerase I inhibitor, administered once every 3 weeks in patients with solid tumors. Cancer Chemother Pharmacol 58:173-182, 2006
-
(2006)
Cancer Chemother Pharmacol
, vol.58
, pp. 173-182
-
-
Yamada, Y.1
Tamura, T.2
Yamamoto, N.3
-
40
-
-
33751292216
-
A phase I study of the safety and pharmacokinetics of edotecarin (J-107088), a novel topoisomerase I inhibitor, in patients with advanced solid tumors
-
Hurwitz HI, Cohen RB, McGovren JP, et al: A phase I study of the safety and pharmacokinetics of edotecarin (J-107088), a novel topoisomerase I inhibitor, in patients with advanced solid tumors. Cancer Chemother Pharmacol 59:139-147, 2007
-
(2007)
Cancer Chemother Pharmacol
, vol.59
, pp. 139-147
-
-
Hurwitz, H.I.1
Cohen, R.B.2
McGovren, J.P.3
-
41
-
-
0033658605
-
Pharmacokinetic and pharmacodynamic analysis of bisacetato-ammine-dichloro-cyclohexylamine-platinum(IV) (JM216) administered once a day for five consecutive days: A phase I study
-
Kurata T, Tamura T, Sasaki Y, et al: Pharmacokinetic and pharmacodynamic analysis of bisacetato-ammine-dichloro-cyclohexylamine-platinum(IV) (JM216) administered once a day for five consecutive days: A phase I study. Jpn J Clin Oncol 30:377-384, 2000
-
(2000)
Jpn J Clin Oncol
, vol.30
, pp. 377-384
-
-
Kurata, T.1
Tamura, T.2
Sasaki, Y.3
-
42
-
-
0030742993
-
Phase I and pharmacokinetic study of an oral platinum complex given daily for 5 days in patients with cancer
-
McKeage MJ, Raynaud F, Ward J, et al: Phase I and pharmacokinetic study of an oral platinum complex given daily for 5 days in patients with cancer. J Clin Oncol 15:2691-2700, 1997
-
(1997)
J Clin Oncol
, vol.15
, pp. 2691-2700
-
-
McKeage, M.J.1
Raynaud, F.2
Ward, J.3
-
43
-
-
33847256149
-
Phase 1 clinical study of pegylated liposomal doxorubicin (JNS002) in Japanese patients with solid tumors
-
Fujisaka Y, Horiike A, Shimizu T, et al: Phase 1 clinical study of pegylated liposomal doxorubicin (JNS002) in Japanese patients with solid tumors. Jpn J Clin Oncol 36:768-774, 2006
-
(2006)
Jpn J Clin Oncol
, vol.36
, pp. 768-774
-
-
Fujisaka, Y.1
Horiike, A.2
Shimizu, T.3
-
44
-
-
0029038996
-
Liposomal doxorubicin: Antitumor activity and unique toxicities during two complementary phase I studies
-
Uziely B, Jeffers S, Isacson R, et al: Liposomal doxorubicin: Antitumor activity and unique toxicities during two complementary phase I studies. J Clin Oncol 13:1777-1785, 1995
-
(1995)
J Clin Oncol
, vol.13
, pp. 1777-1785
-
-
Uziely, B.1
Jeffers, S.2
Isacson, R.3
-
45
-
-
0042284740
-
Phase I and pharmacokinetic study of KRN5500, a spicamycin derivative, for patients with advanced solid tumors
-
Yamamoto N, Tamura T, Kamiya Y, et al: Phase I and pharmacokinetic study of KRN5500, a spicamycin derivative, for patients with advanced solid tumors. Jpn J Clin Oncol 33:302-308, 2003
-
(2003)
Jpn J Clin Oncol
, vol.33
, pp. 302-308
-
-
Yamamoto, N.1
Tamura, T.2
Kamiya, Y.3
-
46
-
-
70149124715
-
Phase I and pharmacokinetic study of vorinostat (suberoylanilide hydroxamic acid) in Japanese patients with solid tumors
-
Fujiwara Y, Yamamoto N, Yamada Y, et al: Phase I and pharmacokinetic study of vorinostat (suberoylanilide hydroxamic acid) in Japanese patients with solid tumors. Cancer Sci 100:1728-1734, 2009
-
(2009)
Cancer Sci
, vol.100
, pp. 1728-1734
-
-
Fujiwara, Y.1
Yamamoto, N.2
Yamada, Y.3
-
47
-
-
21244464349
-
Phase I study of an oral histone deacetylase inhibitor, suberoylanilide hydroxamic acid, in patients with advanced cancer
-
Kelly WK, O'Connor OA, Krug LM, et al: Phase I study of an oral histone deacetylase inhibitor, suberoylanilide hydroxamic acid, in patients with advanced cancer. J Clin Oncol 23:3923-3931, 2005
-
(2005)
J Clin Oncol
, vol.23
, pp. 3923-3931
-
-
Kelly, W.K.1
O'Connor, O.A.2
Krug, L.M.3
-
48
-
-
79960918427
-
Phase I study of LY2181308, an antisense oligonucleotide against survivin, in patients with advanced solid tumors
-
Tanioka M, Nokihara H, Yamamoto N, et al: Phase I study of LY2181308, an antisense oligonucleotide against survivin, in patients with advanced solid tumors. Cancer Chemother Pharmacol 68:505-511, 2011
-
(2011)
Cancer Chemother Pharmacol
, vol.68
, pp. 505-511
-
-
Tanioka, M.1
Nokihara, H.2
Yamamoto, N.3
-
49
-
-
62549160588
-
First-in-class, first-in-human phase I results of targeted agents: Highlights of the 2008 American Society of Clinical Oncology meeting
-
Molckovsky A, Siu LL: First-in-class, first-in-human phase I results of targeted agents: Highlights of the 2008 American Society of Clinical Oncology meeting. J Hematol Oncol 1:20, 2008
-
(2008)
J Hematol Oncol
, vol.1
, pp. 20
-
-
Molckovsky, A.1
Siu, L.L.2
-
50
-
-
84878662338
-
Phase I study of oral gemcitabine prodrug (LY2334737) in Japanese patients with advanced solid tumors
-
Yamamoto N, Nokihara H, Yamada Y, et al: Phase I study of oral gemcitabine prodrug (LY2334737) in Japanese patients with advanced solid tumors. Cancer Chemother Pharmacol 71:1645-1655, 2013
-
(2013)
Cancer Chemother Pharmacol
, vol.71
, pp. 1645-1655
-
-
Yamamoto, N.1
Nokihara, H.2
Yamada, Y.3
-
51
-
-
47949130807
-
Oral administration of gemcitabine in patients with refractory tumors: A clinical and pharmacologic study
-
Veltkamp SA, Jansen RS, Callies S, et al: Oral administration of gemcitabine in patients with refractory tumors: A clinical and pharmacologic study. Clin Cancer Res 14:3477-3486, 2008
-
(2008)
Clin Cancer Res
, vol.14
, pp. 3477-3486
-
-
Veltkamp, S.A.1
Jansen, R.S.2
Callies, S.3
-
52
-
-
84903820094
-
A phase 1 and dose-finding study of LY2523355 (litronesib), an Eg5 inhibitor, in Japanese patients with advanced solid tumors
-
Wakui H, Yamamoto N, Kitazono S, et al: A phase 1 and dose-finding study of LY2523355 (litronesib), an Eg5 inhibitor, in Japanese patients with advanced solid tumors. Cancer Chemother Pharmacol 74:15-23, 2014
-
(2014)
Cancer Chemother Pharmacol
, vol.74
, pp. 15-23
-
-
Wakui, H.1
Yamamoto, N.2
Kitazono, S.3
-
53
-
-
84859806868
-
Phase I study for ridaforolimus, an oral mTOR inhibitor, in Japanese patients with advanced solid tumors
-
Seki Y, Yamamoto N, Tamura Y, et al: Phase I study for ridaforolimus, an oral mTOR inhibitor, in Japanese patients with advanced solid tumors. Cancer Chemother Pharmacol 69:1099-1105, 2012
-
(2012)
Cancer Chemother Pharmacol
, vol.69
, pp. 1099-1105
-
-
Seki, Y.1
Yamamoto, N.2
Tamura, Y.3
-
54
-
-
38649140450
-
Phase I trial of the novel mammalian target of rapamycin inhibitor deforolimus (AP23573; MK-8669) administered intravenously daily for 5 days every 2 weeks to patients with advanced malignancies
-
Mita MM, Mita AC, Chu QS, et al: Phase I trial of the novel mammalian target of rapamycin inhibitor deforolimus (AP23573; MK-8669) administered intravenously daily for 5 days every 2 weeks to patients with advanced malignancies. J Clin Oncol 26:361-367, 2008
-
(2008)
J Clin Oncol
, vol.26
, pp. 361-367
-
-
Mita, M.M.1
Mita, A.C.2
Chu, Q.S.3
-
55
-
-
63149129641
-
A phase I trial to determine the safety, tolerability, and maximum tolerated dose of deforolimus in patients with advanced malignancies
-
Hartford CM, Desai AA, Janisch L, et al: A phase I trial to determine the safety, tolerability, and maximum tolerated dose of deforolimus in patients with advanced malignancies. Clin Cancer Res 15:1428-1434, 2009
-
(2009)
Clin Cancer Res
, vol.15
, pp. 1428-1434
-
-
Hartford, C.M.1
Desai, A.A.2
Janisch, L.3
-
56
-
-
84937620917
-
Phase I study of anti-PD-1 antibody ONO-4538 in Japanese patients with advanced solid tumors
-
Yamamoto N, Nokihara H, Yasuhide Y, et al: Phase I study of anti-PD-1 antibody ONO-4538 in Japanese patients with advanced solid tumors. The 10th Annual Meeting of the Japanese Society of Medical Oncology, Osaka, Japan, July 26-28, 2012
-
The 10th Annual Meeting of the Japanese Society of Medical Oncology, Osaka, Japan, July 26-28, 2012
-
-
Yamamoto, N.1
Nokihara, H.2
Yasuhide, Y.3
-
57
-
-
84862859820
-
Safety, activity, and immune correlates of anti-PD-1 antibody in cancer
-
Topalian SL, Hodi FS, Brahmer JR, et al: Safety, activity, and immune correlates of anti-PD-1 antibody in cancer. N Engl J Med 366:2443-2454, 2012
-
(2012)
N Engl J Med
, vol.366
, pp. 2443-2454
-
-
Topalian, S.L.1
Hodi, F.S.2
Brahmer, J.R.3
-
58
-
-
84937620918
-
Phase IA/IB study of the anti-MET antibody onartuzumab (MetMAb) in patients with solid tumors or MET-positive lung cancer
-
Horinouchi H, Nakamichi S, Wakui H, et al: Phase IA/IB study of the anti-MET antibody onartuzumab (MetMAb) in patients with solid tumors or MET-positive lung cancer. 15th World Conference on Lung Cancer, Sydney, Australia, October 27-30, 2013
-
15th World Conference on Lung Cancer, Sydney, Australia, October 27-30, 2013
-
-
Horinouchi, H.1
Nakamichi, S.2
Wakui, H.3
-
59
-
-
84890108571
-
Randomized phase II trial of onartuzumab in combination with erlotinib in patients with advanced non-small-cell lung cancer
-
Spigel DR, Ervin TJ, Ramlau RA, et al: Randomized phase II trial of onartuzumab in combination with erlotinib in patients with advanced non-small-cell lung cancer. J Clin Oncol 31:4105-4114, 2013
-
(2013)
J Clin Oncol
, vol.31
, pp. 4105-4114
-
-
Spigel, D.R.1
Ervin, T.J.2
Ramlau, R.A.3
-
60
-
-
63849224412
-
Phase I and pharmacokinetic study of HER2-targeted rhuMAb 2C4 (Pertuzumab, RO4368451) in Japanese patients with solid tumors
-
Yamamoto N, Yamada Y, Fujiwara Y, et al: Phase I and pharmacokinetic study of HER2-targeted rhuMAb 2C4 (Pertuzumab, RO4368451) in Japanese patients with solid tumors. Jpn J Clin Oncol 39:260-266, 2009
-
(2009)
Jpn J Clin Oncol
, vol.39
, pp. 260-266
-
-
Yamamoto, N.1
Yamada, Y.2
Fujiwara, Y.3
-
61
-
-
20244378677
-
Phase I clinical study of pertuzumab, a novel HER dimerization inhibitor, in patients with advanced cancer
-
Agus DB, Gordon MS, Taylor C, et al: Phase I clinical study of pertuzumab, a novel HER dimerization inhibitor, in patients with advanced cancer. J Clin Oncol 23:2534-2543, 2005
-
(2005)
J Clin Oncol
, vol.23
, pp. 2534-2543
-
-
Agus, D.B.1
Gordon, M.S.2
Taylor, C.3
-
62
-
-
84937620919
-
Phase I and pharmacokinetics/pharmacodynamics study of a MEK inhibitor RO4987655 in patients with advanced solid tumors
-
Yamada Y, Nokihara H, Yamamoto N, et al: Phase I and pharmacokinetics/pharmacodynamics study of a MEK inhibitor RO4987655 in patients with advanced solid tumors. The 12th Annual Meeting of the Japanese Society of Medical Oncology, Fukuoka, Japan, July 17-19, 2014
-
The 12th Annual Meeting of the Japanese Society of Medical Oncology, Fukuoka, Japan, July 17-19, 2014
-
-
Yamada, Y.1
Nokihara, H.2
Yamamoto, N.3
-
63
-
-
84865702746
-
Phase I dose-escalation study of the safety, pharmacokinetics, and pharmacodynamics of the MEK inhibitor RO4987655 (CH4987655) in patients with advanced solid tumors
-
Leijen S, Middleton MR, Tresca P, et al: Phase I dose-escalation study of the safety, pharmacokinetics, and pharmacodynamics of the MEK inhibitor RO4987655 (CH4987655) in patients with advanced solid tumors. Clin Cancer Res 18:4794-4805, 2012
-
(2012)
Clin Cancer Res
, vol.18
, pp. 4794-4805
-
-
Leijen, S.1
Middleton, M.R.2
Tresca, P.3
-
64
-
-
37249041552
-
Phase I dose-finding and pharmacokinetic study of the oral epidermal growth factor receptor tyrosine kinase inhibitor Ro50-8231 (erlotinib) in Japanese patients with solid tumors
-
Yamamoto N, Horiike A, Fujisaka Y, et al: Phase I dose-finding and pharmacokinetic study of the oral epidermal growth factor receptor tyrosine kinase inhibitor Ro50-8231 (erlotinib) in Japanese patients with solid tumors. Cancer Chemother Pharmacol 61:489-496, 2008
-
(2008)
Cancer Chemother Pharmacol
, vol.61
, pp. 489-496
-
-
Yamamoto, N.1
Horiike, A.2
Fujisaka, Y.3
-
65
-
-
0035398631
-
Phase I and pharmacologic study of OSI-774, an epidermal growth factor receptor tyrosine kinase inhibitor, in patients with advanced solid malignancies
-
Hidalgo M, Siu LL, Nemunaitis J, et al: Phase I and pharmacologic study of OSI-774, an epidermal growth factor receptor tyrosine kinase inhibitor, in patients with advanced solid malignancies. J Clin Oncol 19:3267-3279, 2001
-
(2001)
J Clin Oncol
, vol.19
, pp. 3267-3279
-
-
Hidalgo, M.1
Siu, L.L.2
Nemunaitis, J.3
-
66
-
-
84883490437
-
Phase I and pharmacokinetic/pharmacodynamic study of RO5126766, a first-in-class dual Raf/MEK inhibitor, in Japanese patients with advanced solid tumors
-
Honda K, Yamamoto N, Nokihara H, et al: Phase I and pharmacokinetic/pharmacodynamic study of RO5126766, a first-in-class dual Raf/MEK inhibitor, in Japanese patients with advanced solid tumors. Cancer Chemother Pharmacol 72:577-584, 2013
-
(2013)
Cancer Chemother Pharmacol
, vol.72
, pp. 577-584
-
-
Honda, K.1
Yamamoto, N.2
Nokihara, H.3
-
67
-
-
84865749357
-
First-in-human, phase I dose-escalation study of the safety, pharmacokinetics, and pharmacodynamics of RO5126766, a first-in-class dual MEK/RAF inhibitor in patients with solid tumors
-
Martinez-Garcia M, Banerji U, Albanell J, et al: First-in-human, phase I dose-escalation study of the safety, pharmacokinetics, and pharmacodynamics of RO5126766, a first-in-class dual MEK/RAF inhibitor in patients with solid tumors. Clin Cancer Res 18:4806-4819, 2012
-
(2012)
Clin Cancer Res
, vol.18
, pp. 4806-4819
-
-
Martinez-Garcia, M.1
Banerji, U.2
Albanell, J.3
-
68
-
-
0033863452
-
Phase I and pharmacokinetic study of a new taxoid, RPR 109881A, given as a 1-hour intravenous infusion in patients with advanced solid tumors
-
Kurata T, Shimada Y, Tamura T, et al: Phase I and pharmacokinetic study of a new taxoid, RPR 109881A, given as a 1-hour intravenous infusion in patients with advanced solid tumors. J Clin Oncol 18:3164-3171, 2000
-
(2000)
J Clin Oncol
, vol.18
, pp. 3164-3171
-
-
Kurata, T.1
Shimada, Y.2
Tamura, T.3
-
69
-
-
0035990845
-
Phase I clinical and pharmacokinetic studies of the taxoid derivative RPR 109881A administered as a 1-hour or a 3-hour infusion in patients with advanced solid tumors
-
Sessa C, Cuvier C, Caldiera S, et al: Phase I clinical and pharmacokinetic studies of the taxoid derivative RPR 109881A administered as a 1-hour or a 3-hour infusion in patients with advanced solid tumors. Ann Oncol 13:1140-1150, 2002
-
(2002)
Ann Oncol
, vol.13
, pp. 1140-1150
-
-
Sessa, C.1
Cuvier, C.2
Caldiera, S.3
-
70
-
-
84885457420
-
A first-in-human, phase 1, dose-escalation study of dinaciclib, a novel cyclin-dependent kinase inhibitor, administered weekly in subjects with advanced malignancies
-
Nemunaitis JJ, Small KA, Kirschmeier P, et al: A first-in-human, phase 1, dose-escalation study of dinaciclib, a novel cyclin-dependent kinase inhibitor, administered weekly in subjects with advanced malignancies. J Transl Med 11:259-263, 2013
-
(2013)
J Transl Med
, vol.11
, pp. 259-263
-
-
Nemunaitis, J.J.1
Small, K.A.2
Kirschmeier, P.3
-
71
-
-
84937620920
-
Phase I dose escalation study of oral bosutinib (SKI-606) in patients with advanced malignant solid tumors
-
Yamamoto N, Yasuhide Y, Nokihara H, et al: Phase I dose escalation study of oral bosutinib (SKI-606) in patients with advanced malignant solid tumors. The 7th Annual Meeting of the Japanese Society of Medical Oncology, Nagoya, Japan, March 20-21, 2009
-
The 7th Annual Meeting of the Japanese Society of Medical Oncology, Nagoya, Japan, March 20-21, 2009
-
-
Yamamoto, N.1
Yasuhide, Y.2
Nokihara, H.3
-
72
-
-
84857090723
-
Phase I study of bosutinib, a src/abl tyrosine kinase inhibitor, administered to patients with advanced solid tumors
-
Daud AI, Krishnamurthi SS, Saleh MN, et al: Phase I study of bosutinib, a src/abl tyrosine kinase inhibitor, administered to patients with advanced solid tumors. Clin Cancer Res 18:1092-1100, 2012
-
(2012)
Clin Cancer Res
, vol.18
, pp. 1092-1100
-
-
Daud, A.I.1
Krishnamurthi, S.S.2
Saleh, M.N.3
-
73
-
-
27144531036
-
A Phase I study of the angiogenesis inhibitor SU5416 (semaxanib) in solid tumours, incorporating dynamic contrast MR pharmacodynamic end points
-
O'Donnell A, Padhani A, Hayes C, et al: A Phase I study of the angiogenesis inhibitor SU5416 (semaxanib) in solid tumours, incorporating dynamic contrast MR pharmacodynamic end points. Br J Cancer 93:876-883, 2005
-
(2005)
Br J Cancer
, vol.93
, pp. 876-883
-
-
O'Donnell, A.1
Padhani, A.2
Hayes, C.3
-
74
-
-
79955552390
-
Phase I, pharmacokinetic, and biological studies of TSU-68, a novel multiple receptor tyrosine kinase inhibitor, administered after meals with solid tumors
-
Murakami H, Ueda Y, Shimoyama T, et al: Phase I, pharmacokinetic, and biological studies of TSU-68, a novel multiple receptor tyrosine kinase inhibitor, administered after meals with solid tumors. Cancer Chemother Pharmacol 67:1119-1128, 2011
-
(2011)
Cancer Chemother Pharmacol
, vol.67
, pp. 1119-1128
-
-
Murakami, H.1
Ueda, Y.2
Shimoyama, T.3
-
75
-
-
79955566755
-
Phase I and pharmacokinetic study of TSU-68, a novel multiple receptor tyrosine kinase inhibitor, by twice daily oral administration between meals in patients with advanced solid tumors
-
Ueda Y, Shimoyama T, Murakami H, et al: Phase I and pharmacokinetic study of TSU-68, a novel multiple receptor tyrosine kinase inhibitor, by twice daily oral administration between meals in patients with advanced solid tumors. Cancer Chemother Pharmacol 67:1101-1109, 2011
-
(2011)
Cancer Chemother Pharmacol
, vol.67
, pp. 1101-1109
-
-
Ueda, Y.1
Shimoyama, T.2
Murakami, H.3
-
76
-
-
84896035233
-
Phase 1 and dose-finding study of patritumab (U3-1287), a human monoclonal antibody targeting HER3, in Japanese patients with advanced solid tumors
-
Wakui H, Yamamoto N, Nakamichi S, et al: Phase 1 and dose-finding study of patritumab (U3-1287), a human monoclonal antibody targeting HER3, in Japanese patients with advanced solid tumors. Cancer Chemother Pharmacol 73:511-516, 2014
-
(2014)
Cancer Chemother Pharmacol
, vol.73
, pp. 511-516
-
-
Wakui, H.1
Yamamoto, N.2
Nakamichi, S.3
-
77
-
-
84878958728
-
Phase I study of U3-1287, a fully human anti-HER3 monoclonal antibody, in patients with advanced solid tumors
-
LoRusso P, Jänne PA, Oliveira M, et al: Phase I study of U3-1287, a fully human anti-HER3 monoclonal antibody, in patients with advanced solid tumors. Clin Cancer Res 19:3078-3087, 2013
-
(2013)
Clin Cancer Res
, vol.19
, pp. 3078-3087
-
-
LoRusso, P.1
Jänne, P.A.2
Oliveira, M.3
-
78
-
-
0035871444
-
Phase I trial of 72-hour continuous infusion UCN-01 in patients with refractory neoplasms
-
Sausville EA, Arbuck SG, Messmann R, et al: Phase I trial of 72-hour continuous infusion UCN-01 in patients with refractory neoplasms. J Clin Oncol 19:2319-2333, 2001
-
(2001)
J Clin Oncol
, vol.19
, pp. 2319-2333
-
-
Sausville, E.A.1
Arbuck, S.G.2
Messmann, R.3
-
79
-
-
84937620921
-
A phase 1 study of cabozantinib in Japanese patients with advanced solid tumors: Anti-tumor activity in NSCLC and GIST
-
Nokihara H, Yamamoto N, Nakamichi S, et al: A phase 1 study of cabozantinib in Japanese patients with advanced solid tumors: Anti-tumor activity in NSCLC and GIST. The 11th Annual Meeting of the Japanese Society of Medical Oncology, Sendai, Japan, August 29-31, 2013
-
The 11th Annual Meeting of the Japanese Society of Medical Oncology, Sendai, Japan, August 29-31, 2013
-
-
Nokihara, H.1
Yamamoto, N.2
Nakamichi, S.3
-
80
-
-
79959936054
-
Activity of XL184 (cabozantinib), an oral tyrosine kinase inhibitor, in patients with medullary thyroid cancer
-
Kurzrock R, Sherman SI, Ball DW, et al: Activity of XL184 (cabozantinib), an oral tyrosine kinase inhibitor, in patients with medullary thyroid cancer. J Clin Oncol 29:2660-2666, 2011
-
(2011)
J Clin Oncol
, vol.29
, pp. 2660-2666
-
-
Kurzrock, R.1
Sherman, S.I.2
Ball, D.W.3
-
81
-
-
0036980346
-
ZD0473 pharmacokinetics in Japanese patients: A Phase I dose-escalation study
-
Murakami H, Tamura T, Yamada Y, et al: ZD0473 pharmacokinetics in Japanese patients: A Phase I dose-escalation study. Eur J Cancer 38:S1-S5, 2002
-
(2002)
Eur J Cancer
, vol.38
, pp. S1-S5
-
-
Murakami, H.1
Tamura, T.2
Yamada, Y.3
-
82
-
-
0037673681
-
Phase I pharmacokinetic trial of the selective oral epidermal growth factor receptor tyrosine kinase inhibitor gefitinib ('Iressa', ZD1839) in Japanese patients with solid malignant tumors
-
Nakagawa K, Tamura T, Negoro S, et al: Phase I pharmacokinetic trial of the selective oral epidermal growth factor receptor tyrosine kinase inhibitor gefitinib ('Iressa', ZD1839) in Japanese patients with solid malignant tumors. Ann Oncol 14:922-930, 2003
-
(2003)
Ann Oncol
, vol.14
, pp. 922-930
-
-
Nakagawa, K.1
Tamura, T.2
Negoro, S.3
-
83
-
-
0036569870
-
ZD1839, a selective oral epidermal growth factor receptor-tyrosine kinase inhibitor, is well tolerated and active in patients with solid, malignant tumors: Results of a phase I trial
-
Ranson M, Hammond LA, Ferry D, et al: ZD1839, a selective oral epidermal growth factor receptor-tyrosine kinase inhibitor, is well tolerated and active in patients with solid, malignant tumors: Results of a phase I trial. J Clin Oncol 20:2240-2250, 2002
-
(2002)
J Clin Oncol
, vol.20
, pp. 2240-2250
-
-
Ranson, M.1
Hammond, L.A.2
Ferry, D.3
-
84
-
-
33645732100
-
Phase I clinical evaluation of weekly administration of the novel vascular-targeting agent, ZD6126, in patients with solid tumors
-
Beerepoot LV, Radema SA, Witteveen EO, et al: Phase I clinical evaluation of weekly administration of the novel vascular-targeting agent, ZD6126, in patients with solid tumors. J Clin Oncol 24:1491-1498, 2006
-
(2006)
J Clin Oncol
, vol.24
, pp. 1491-1498
-
-
Beerepoot, L.V.1
Radema, S.A.2
Witteveen, E.O.3
-
85
-
-
33846844387
-
A phase I dose-escalation study of ZD6474 in Japanese patients with solid, malignant tumors
-
Tamura T, Minami H, Yamada Y, et al: A phase I dose-escalation study of ZD6474 in Japanese patients with solid, malignant tumors. J Thorac Oncol 1:1002-1009, 2006
-
(2006)
J Thorac Oncol
, vol.1
, pp. 1002-1009
-
-
Tamura, T.1
Minami, H.2
Yamada, Y.3
-
86
-
-
23844544081
-
Clinical evaluation of ZD6474, an orally active inhibitor of VEGF and EGF receptor signaling, in patients with solid, malignant tumors
-
Holden SN, Eckhardt SG, Basser R, et al: Clinical evaluation of ZD6474, an orally active inhibitor of VEGF and EGF receptor signaling, in patients with solid, malignant tumors. Ann Oncol 16:1391-1397, 2005
-
(2005)
Ann Oncol
, vol.16
, pp. 1391-1397
-
-
Holden, S.N.1
Eckhardt, S.G.2
Basser, R.3
-
87
-
-
84857055503
-
Patient selection for oncology phase I trials: A multi-institutional study of prognostic factors
-
Olmos D, A'Hern RP, Marsoni S, et al: Patient selection for oncology phase I trials: A multi-institutional study of prognostic factors. J Clin Oncol 30:996-1004, 2012
-
(2012)
J Clin Oncol
, vol.30
, pp. 996-1004
-
-
Olmos, D.1
A'Hern, R.P.2
Marsoni, S.3
-
88
-
-
76749161498
-
Phase I oncology studies: Evidence that in the era of targeted therapies patients on lower doses do not fare worse
-
Jain RK, Lee JJ, Hong D, et al: Phase I oncology studies: Evidence that in the era of targeted therapies patients on lower doses do not fare worse. Clin Cancer Res 16:1289-1297, 2010
-
(2010)
Clin Cancer Res
, vol.16
, pp. 1289-1297
-
-
Jain, R.K.1
Lee, J.J.2
Hong, D.3
-
89
-
-
66849118694
-
Dose escalation methods in phase I cancer clinical trials
-
Le Tourneau C, Lee JJ, Siu LL: Dose escalation methods in phase I cancer clinical trials. J Natl Cancer Inst 101:708-720, 2009
-
(2009)
J Natl Cancer Inst
, vol.101
, pp. 708-720
-
-
Le Tourneau, C.1
Lee, J.J.2
Siu, L.L.3
-
90
-
-
77950505295
-
Choice of starting dose for molecularly targeted agents evaluated in first-in-human phase I cancer clinical trials
-
Le Tourneau C, Stathis A, Vidal L, et al: Choice of starting dose for molecularly targeted agents evaluated in first-in-human phase I cancer clinical trials. J Clin Oncol 28:1401-1407, 2010
-
(2010)
J Clin Oncol
, vol.28
, pp. 1401-1407
-
-
Le Tourneau, C.1
Stathis, A.2
Vidal, L.3
-
91
-
-
41549095568
-
Treatment outcome and survival in participants of phase I oncology trials carried out from 2003 to 2006 at Institut Gustave Roussy
-
Italiano A, Massard C, Bahleda R, et al: Treatment outcome and survival in participants of phase I oncology trials carried out from 2003 to 2006 at Institut Gustave Roussy. Ann Oncol 19:787-792, 2008
-
(2008)
Ann Oncol
, vol.19
, pp. 787-792
-
-
Italiano, A.1
Massard, C.2
Bahleda, R.3
-
92
-
-
84864047388
-
Change in tumor size by RECIST correlates linearly with overall survival in phase I oncology studies
-
Jain RK, Lee JJ, Ng C, et al: Change in tumor size by RECIST correlates linearly with overall survival in phase I oncology studies. J Clin Oncol 30:2684-2690, 2012
-
(2012)
J Clin Oncol
, vol.30
, pp. 2684-2690
-
-
Jain, R.K.1
Lee, J.J.2
Ng, C.3
-
93
-
-
14544284502
-
Risks and benefits of phase 1 oncology trials, 1991 through 2002
-
Horstmann E, McCabe MS, Grochow L, et al: Risks and benefits of phase 1 oncology trials, 1991 through 2002. N Engl J Med 352:895-904, 2005
-
(2005)
N Engl J Med
, vol.352
, pp. 895-904
-
-
Horstmann, E.1
McCabe, M.S.2
Grochow, L.3
-
94
-
-
0036727187
-
Prospective exploratory analysis of the association between tumor response, quality of life, and expenditures among patients receiving paclitaxel monotherapy for refractory metastatic breast cancer
-
Modi S, Panageas KS, Duck ET, et al: Prospective exploratory analysis of the association between tumor response, quality of life, and expenditures among patients receiving paclitaxel monotherapy for refractory metastatic breast cancer. J Clin Oncol 20:3665-3673, 2002
-
(2002)
J Clin Oncol
, vol.20
, pp. 3665-3673
-
-
Modi, S.1
Panageas, K.S.2
Duck, E.T.3
-
95
-
-
0034605462
-
Response rates, survival, and chemotherapy trials
-
Pazdur R: Response rates, survival, and chemotherapy trials. J Natl Cancer Inst 92:1552-1553, 2000
-
(2000)
J Natl Cancer Inst
, vol.92
, pp. 1552-1553
-
-
Pazdur, R.1
-
96
-
-
5644246195
-
Tumor response and survival end points in clinical trials: A clinician's perspective
-
Lokich J: Tumor response and survival end points in clinical trials: A clinician's perspective. Am J Clin Oncol 27:494-496, 2004
-
(2004)
Am J Clin Oncol
, vol.27
, pp. 494-496
-
-
Lokich, J.1
-
97
-
-
66749124176
-
Prospective validation of a prognostic score to improve patient selection for oncology phase I trials
-
Arkenau HT, Barriuso J, Olmos D, et al: Prospective validation of a prognostic score to improve patient selection for oncology phase I trials. J Clin Oncol 27:2692-2696, 2009
-
(2009)
J Clin Oncol
, vol.27
, pp. 2692-2696
-
-
Arkenau, H.T.1
Barriuso, J.2
Olmos, D.3
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