-
1
-
-
70349687134
-
The role of trastuzumab in the management of HER2-positive metastatic breast cancer: An updated review
-
Tokuda Y, Suzuki Y, Saito Y, Umemura S. The role of trastuzumab in the management of HER2-positive metastatic breast cancer: an updated review. Breast Cancer 2009;16:295-300.
-
(2009)
Breast Cancer
, vol.16
, pp. 295-300
-
-
Tokuda, Y.1
Suzuki, Y.2
Saito, Y.3
Umemura, S.4
-
2
-
-
75449110368
-
The role of EGFR inhibition in the treatment of non-small cell lung cancer
-
Ray M, Salgia R, Vokes EE. The role of EGFR inhibition in the treatment of non-small cell lung cancer. Oncologist 2009;14:1116-1130.
-
(2009)
Oncologist
, vol.14
, pp. 1116-1130
-
-
Ray, M.1
Salgia, R.2
Vokes, E.E.3
-
3
-
-
80052054210
-
Personalizing therapy with targeted agents in non-small cell lung cancer
-
Dienstmann R, Martinez P, Felip E. Personalizing therapy with targeted agents in non-small cell lung cancer. Oncotarget 2011;2:165-177.
-
(2011)
Oncotarget
, vol.2
, pp. 165-177
-
-
Dienstmann, R.1
Martinez, P.2
Felip, E.3
-
5
-
-
33845490014
-
Paclitaxel-carboplatin alone or with bevacizumab for non-small-cell lung cancer
-
Sandler A, Gray R, Perry MC, et al. Paclitaxel-carboplatin alone or with bevacizumab for non-small-cell lung cancer. N Engl J Med 2006;355:2542-2550.
-
(2006)
N Engl J Med
, vol.355
, pp. 2542-2550
-
-
Sandler, A.1
Gray, R.2
Perry, M.C.3
-
6
-
-
33644513730
-
Beyond PTEN mutations: The PI3K pathway as an integrator of multiple inputs during tumorigenesis
-
Cully M, You H, Levine AJ, Mak TW. Beyond PTEN mutations: the PI3K pathway as an integrator of multiple inputs during tumorigenesis. Nat Rev Cancer 2006;6:184-192.
-
(2006)
Nat Rev Cancer
, vol.6
, pp. 184-192
-
-
Cully, M.1
You, H.2
Levine, A.J.3
Mak, T.W.4
-
7
-
-
67749122122
-
Targeting PI3K signalling in cancer: Opportunities, challenges and limitations
-
Engelman JA. Targeting PI3K signalling in cancer: opportunities, challenges and limitations. Nat Rev Cancer 2009;9:550-562.
-
(2009)
Nat Rev Cancer
, vol.9
, pp. 550-562
-
-
Engelman, J.A.1
-
11
-
-
32944457518
-
MTOR inhibition induces upstream receptor tyrosine kinase signaling and activates Akt
-
OReilly KE, Rojo F, She QB, et al. mTOR inhibition induces upstream receptor tyrosine kinase signaling and activates Akt. Cancer Res 2006;66:1500-1508.
-
(2006)
Cancer Res
, vol.66
, pp. 1500-1508
-
-
Oreilly, K.E.1
Rojo, F.2
She, Q.B.3
-
12
-
-
0038335334
-
PI3K/PTEN/AKT pathway. A critical mediator of oncogenic signaling
-
Paez J Sellers WR. PI3K/PTEN/AKT pathway. A critical mediator of oncogenic signaling. Cancer Treat Res 2003;115:145-167.
-
(2003)
Cancer Treat Res
, vol.115
, pp. 145-167
-
-
Paez, J.1
Sellers, W.R.2
-
13
-
-
4344602002
-
The biology and clinical relevance of the PTEN tumor suppressor pathway
-
Sansal I Sellers WR. The biology and clinical relevance of the PTEN tumor suppressor pathway. J Clin Oncol 2004;22:2954-2963.
-
(2004)
J Clin Oncol
, vol.22
, pp. 2954-2963
-
-
Sansal, I.1
Sellers, W.R.2
-
14
-
-
8844222002
-
Frequent activation of AKT in non-small cell lung carcinomas and preneoplastic bronchial lesions
-
Balsara BR, Pei J, Mitsuuchi Y, et al. Frequent activation of AKT in non-small cell lung carcinomas and preneoplastic bronchial lesions. Carcinogenesis 2004;25:2053-2059.
-
(2004)
Carcinogenesis
, vol.25
, pp. 2053-2059
-
-
Balsara, B.R.1
Pei, J.2
Mitsuuchi, Y.3
-
15
-
-
34250161814
-
Prospective study of gefitinib in epidermal growth factor receptor fluorescence in situ hybridization-positive/phospho-Akt-positive or never smoker patients with advanced non-small-cell lung cancer: The ONCOBELL trial
-
Cappuzzo F, Ligorio C, Jnne PA, et al. Prospective study of gefitinib in epidermal growth factor receptor fluorescence in situ hybridization-positive/ phospho-Akt-positive or never smoker patients with advanced non-small-cell lung cancer: the ONCOBELL trial. J Clin Oncol 2007;25:2248-2255.
-
(2007)
J Clin Oncol
, vol.25
, pp. 2248-2255
-
-
Cappuzzo, F.1
Ligorio, C.2
Jnne, P.A.3
-
16
-
-
33644825286
-
Evaluation of two phosphorylation sites improves the prognostic significance of Akt activation in non-small-cell lung cancer tumors
-
Tsurutani J, Fukuoka J, Tsurutani H, et al. Evaluation of two phosphorylation sites improves the prognostic significance of Akt activation in non-small-cell lung cancer tumors. J Clin Oncol 2006;24:306-314.
-
(2006)
J Clin Oncol
, vol.24
, pp. 306-314
-
-
Tsurutani, J.1
Fukuoka, J.2
Tsurutani, H.3
-
17
-
-
31344479312
-
Phosphorylated Akt overexpression and loss of PTEN expression in non-small cell lung cancer confers poor prognosis
-
Tang JM, He QY, Guo RX, Chang XJ. Phosphorylated Akt overexpression and loss of PTEN expression in non-small cell lung cancer confers poor prognosis. Lung Cancer 2006;51:181-191.
-
(2006)
Lung Cancer
, vol.51
, pp. 181-191
-
-
Tang, J.M.1
He, Q.Y.2
Guo, R.X.3
Chang, X.J.4
-
18
-
-
6044230919
-
Phospho-Akt overexpression in non-small cell lung cancer confers significant stage-independent survival disadvantage
-
David O, Jett J, LeBeau H, et al. Phospho-Akt overexpression in non-small cell lung cancer confers significant stage-independent survival disadvantage. Clin Cancer Res 2004;10:6865-6871.
-
(2004)
Clin Cancer Res
, vol.10
, pp. 6865-6871
-
-
David, O.1
Jett, J.2
Lebeau, H.3
-
19
-
-
41849132829
-
Activating E17K mutation in the gene encoding the protein kinase AKT1 in a subset of squamous cell carcinoma of the lung
-
Malanga D, Scrima M, De Marco C, et al. Activating E17K mutation in the gene encoding the protein kinase AKT1 in a subset of squamous cell carcinoma of the lung. Cell Cycle 2008;7:665-669.
-
(2008)
Cell Cycle
, vol.7
, pp. 665-669
-
-
Malanga, D.1
Scrima, M.2
De Marco, C.3
-
20
-
-
51849111556
-
PI3K pathway alterations in cancer: Variations on a theme
-
Yuan TL Cantley LC. PI3K pathway alterations in cancer: variations on a theme. Oncogene 2008;27:5497-5510.
-
(2008)
Oncogene
, vol.27
, pp. 5497-5510
-
-
Yuan, T.L.1
Cantley, L.C.2
-
21
-
-
7844247587
-
Mutation analysis of the PTEN/MMAC1 gene in lung cancer
-
Forgacs E, Biesterveld EJ, Sekido Y, et al. Mutation analysis of the PTEN/MMAC1 gene in lung cancer. Oncogene 1998;17:1557-1565.
-
(1998)
Oncogene
, vol.17
, pp. 1557-1565
-
-
Forgacs, E.1
Biesterveld, E.J.2
Sekido, Y.3
-
22
-
-
23444461754
-
PTEN expression in non-small-cell lung cancer: Evaluating its relation to tumor characteristics, allelic loss, and epigenetic alteration
-
Marsit CJ, Zheng S, Aldape K, et al. PTEN expression in non-small-cell lung cancer: evaluating its relation to tumor characteristics, allelic loss, and epigenetic alteration. Hum Pathol 2005;36:768-776.
-
(2005)
Hum Pathol
, vol.36
, pp. 768-776
-
-
Marsit, C.J.1
Zheng, S.2
Aldape, K.3
-
24
-
-
54549094903
-
Somatic mutations affect key pathways in lung adenocarcinoma
-
Ding L, Getz G, Wheeler DA, et al. Somatic mutations affect key pathways in lung adenocarcinoma. Nature 2008;455:1069-1075.
-
(2008)
Nature
, vol.455
, pp. 1069-1075
-
-
Ding, L.1
Getz, G.2
Wheeler, D.A.3
-
25
-
-
24944497744
-
Mutations in the epidermal growth factor receptor and in KRAS are predictive and prognostic indicators in patients with non-small-cell lung cancer treated with chemotherapy alone and in combination with erlotinib
-
Eberhard DA, Johnson BE, Amler LC, et al. Mutations in the epidermal growth factor receptor and in KRAS are predictive and prognostic indicators in patients with non-small-cell lung cancer treated with chemotherapy alone and in combination with erlotinib. J Clin Oncol 2005;23:5900-5909.
-
(2005)
J Clin Oncol
, vol.23
, pp. 5900-5909
-
-
Eberhard, D.A.1
Johnson, B.E.2
Amler, L.C.3
-
26
-
-
79960894047
-
Molecular biomarkers in non-small-cell lung cancer: A retrospective analysis of data from the phase 3 FLEX study
-
OByrne KJ, Gatzemeier U, Bondarenko I, et al. Molecular biomarkers in non-small-cell lung cancer: a retrospective analysis of data from the phase 3 FLEX study. Lancet Oncol 2011;12:795-805.
-
(2011)
Lancet Oncol
, vol.12
, pp. 795-805
-
-
Obyrne, K.J.1
Gatzemeier, U.2
Bondarenko, I.3
-
27
-
-
55449116539
-
Met gene copy number predicts the prognosis for completely resected non-small cell lung cancer
-
Okuda K, Sasaki H, Yukiue H, Yano M, Fujii Y. Met gene copy number predicts the prognosis for completely resected non-small cell lung cancer. Cancer Sci 2008;99:2280-2285.
-
(2008)
Cancer Sci
, vol.99
, pp. 2280-2285
-
-
Okuda, K.1
Sasaki, H.2
Yukiue, H.3
Yano, M.4
Fujii, Y.5
-
28
-
-
60549110433
-
MET increased gene copy number and primary resistance to gefitinib therapy in non-small-cell lung cancer patients
-
Cappuzzo F, Jnne PA, Skokan M, et al. MET increased gene copy number and primary resistance to gefitinib therapy in non-small-cell lung cancer patients. Ann Oncol 2009;20:298-304.
-
(2009)
Ann Oncol
, vol.20
, pp. 298-304
-
-
Cappuzzo, F.1
Jnne, P.A.2
Skokan, M.3
-
29
-
-
34249075147
-
MET amplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling
-
Engelman JA, Zejnullahu K, Mitsudomi T, et al. MET amplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling. Science 2007;316:1039-1043.
-
(2007)
Science
, vol.316
, pp. 1039-1043
-
-
Engelman, J.A.1
Zejnullahu, K.2
Mitsudomi, T.3
-
30
-
-
46749156706
-
Acquired resistance to EGFR tyrosine kinase inhibitors in cancer cells is mediated by loss of IGF-binding proteins
-
Guix M, Faber AC, Wang SE, et al. Acquired resistance to EGFR tyrosine kinase inhibitors in cancer cells is mediated by loss of IGF-binding proteins. J Clin Invest 2008;118:2609-2619.
-
(2008)
J Clin Invest
, vol.118
, pp. 2609-2619
-
-
Guix, M.1
Faber, A.C.2
Wang, S.E.3
-
31
-
-
84872492192
-
PTEN mutation associated with EGFR TKI de novo resistance
-
Kim Y, Ko J, Cui ZY, et al. PTEN mutation associated with EGFR TKI de novo resistance. AACR Meet Abstr 2010;2010:3608.
-
(2010)
AACR Meet Abstr
, vol.2010
, pp. 3608
-
-
Kim, Y.1
Ko, J.2
Cui, Z.Y.3
-
32
-
-
79954620289
-
Transient PI3K inhibition induces apoptosis and overcomes HGF-mediated resistance to EGFR-TKIs in EGFR mutant lung cancer
-
Donev IS, Wang W, Yamada T, et al. Transient PI3K inhibition induces apoptosis and overcomes HGF-mediated resistance to EGFR-TKIs in EGFR mutant lung cancer. Clin Cancer Res 2011;17:2260-2269.
-
(2011)
Clin Cancer Res
, vol.17
, pp. 2260-2269
-
-
Donev, I.S.1
Wang, W.2
Yamada, T.3
-
33
-
-
77954217891
-
Acquired resistance to cetuximab is mediated by increased PTEN instability and leads cross-resistance to gefitinib in HCC827 NSCLC cells
-
Kim SM, Kim JS, Kim JH, et al. Acquired resistance to cetuximab is mediated by increased PTEN instability and leads cross-resistance to gefitinib in HCC827 NSCLC cells. Cancer Lett 2010;296: 150-159.
-
(2010)
Cancer Lett
, vol.296
, pp. 150-159
-
-
Kim, S.M.1
Kim, J.S.2
Kim, J.H.3
-
34
-
-
27944444486
-
Enhanced cytotoxicity induced by gefitinib and specific inhibitors of the Ras or phosphatidyl inositol-3 kinase pathways in non-small cell lung cancer cells
-
Janmaat ML, Rodriguez JA, Gallegos-Ruiz M, Kruyt FA, Giaccone G. Enhanced cytotoxicity induced by gefitinib and specific inhibitors of the Ras or phosphatidyl inositol-3 kinase pathways in non-small cell lung cancer cells. Int J Cancer 2006;118:209-214.
-
(2006)
Int J Cancer
, vol.118
, pp. 209-214
-
-
Janmaat, M.L.1
Rodriguez, J.A.2
Gallegos-Ruiz, M.3
Kruyt, F.A.4
Giaccone, G.5
-
35
-
-
33644685228
-
The phosphatidylinositol-3-kinase inhibitor PX-866 overcomes resistance to the epidermal growth factor receptor inhibitor gefitinib in A-549 human non-small cell lung cancer xenografts
-
Ihle NT, Paine-Murrieta G, Berggren MI, et al. The phosphatidylinositol- 3-kinase inhibitor PX-866 overcomes resistance to the epidermal growth factor receptor inhibitor gefitinib in A-549 human non-small cell lung cancer xenografts. Mol Cancer Ther 2005;4:1349-1357.
-
(2005)
Mol Cancer Ther
, vol.4
, pp. 1349-1357
-
-
Ihle, N.T.1
Paine-Murrieta, G.2
Berggren, M.I.3
-
36
-
-
34547638047
-
Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer
-
Soda M, Choi YL, Enomoto M, et al. Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer. Nature 2007;448:561-566.
-
(2007)
Nature
, vol.448
, pp. 561-566
-
-
Soda, M.1
Choi, Y.L.2
Enomoto, M.3
-
37
-
-
48549098388
-
Identification of novel isoforms of the EML4-ALK transforming gene in non-small cell lung cancer
-
Choi YL, Takeuchi K, Soda M, et al. Identification of novel isoforms of the EML4-ALK transforming gene in non-small cell lung cancer. Cancer Res 2008;68:4971-4976.
-
(2008)
Cancer Res
, vol.68
, pp. 4971-4976
-
-
Choi, Y.L.1
Takeuchi, K.2
Soda, M.3
-
38
-
-
48249114422
-
EML4-ALK fusion gene and efficacy of an ALK kinase inhibitor in lung cancer
-
Koivunen JP, Mermel C, Zejnullahu K, et al. EML4-ALK fusion gene and efficacy of an ALK kinase inhibitor in lung cancer. Clin Cancer Res 2008;14:4275-4283.
-
(2008)
Clin Cancer Res
, vol.14
, pp. 4275-4283
-
-
Koivunen, J.P.1
Mermel, C.2
Zejnullahu, K.3
-
39
-
-
82555205478
-
ALK mutations conferring differential resistance to structurally diverse ALK inhibitors
-
Heuckmann JM, Holzel M, Sos ML, et al. ALK mutations conferring differential resistance to structurally diverse ALK inhibitors. Clin Cancer Res 2011;17:7394-7401.
-
(2011)
Clin Cancer Res
, vol.17
, pp. 7394-7401
-
-
Heuckmann, J.M.1
Holzel, M.2
Sos, M.L.3
-
40
-
-
81355124049
-
Crizotinib-resistant mutants of EML4-ALK identified through an accelerated mutagenesis screen
-
Zhang S, Wang F, Keats J, et al. Crizotinib-resistant mutants of EML4-ALK identified through an accelerated mutagenesis screen. Chem Biol Drug Des 2011;78:999-1005.
-
(2011)
Chem Biol Drug des
, vol.78
, pp. 999-1005
-
-
Zhang, S.1
Wang, F.2
Keats, J.3
-
41
-
-
79551559942
-
Multiple mutations and bypass mechanisms can contribute to development of acquired resistance to MET inhibitors
-
Qi J, McTigue MA, Rogers A, et al. Multiple mutations and bypass mechanisms can contribute to development of acquired resistance to MET inhibitors. Cancer Res 2011;71:1081-1091.
-
(2011)
Cancer Res
, vol.71
, pp. 1081-1091
-
-
Qi, J.1
McTigue, M.A.2
Rogers, A.3
-
42
-
-
61549138135
-
Activation of MET by gene amplification or by splice mutations deleting the juxtamembrane domain in primary resected lung cancers
-
Onozato R, Kosaka T, Kuwano H, Sekido Y, Yatabe Y, Mitsudomi T. Activation of MET by gene amplification or by splice mutations deleting the juxtamembrane domain in primary resected lung cancers. J Thorac Oncol 2009;4:5-11.
-
(2009)
J Thorac Oncol
, vol.4
, pp. 5-11
-
-
Onozato, R.1
Kosaka, T.2
Kuwano, H.3
Sekido, Y.4
Yatabe, Y.5
Mitsudomi, T.6
-
43
-
-
41749097250
-
MET gene copy number in non-small cell lung cancer: Molecular analysis in a targeted tyrosine kinase inhibitor nave cohort
-
Beau-Faller M, Ruppert AM, Voegeli AC, et al. MET gene copy number in non-small cell lung cancer: molecular analysis in a targeted tyrosine kinase inhibitor nave cohort. J Thorac Oncol 2008;3:331-339.
-
(2008)
J Thorac Oncol
, vol.3
, pp. 331-339
-
-
Beau-Faller, M.1
Ruppert, A.M.2
Voegeli, A.C.3
-
44
-
-
63849163410
-
Increased MET gene copy number negatively affects survival of surgically resected non-small-cell lung cancer patients
-
Cappuzzo F, Marchetti A, Skokan M, et al. Increased MET gene copy number negatively affects survival of surgically resected non-small-cell lung cancer patients. J Clin Oncol 2009;27:1667-1674.
-
(2009)
J Clin Oncol
, vol.27
, pp. 1667-1674
-
-
Cappuzzo, F.1
Marchetti, A.2
Skokan, M.3
-
45
-
-
0036094196
-
Lack of PTEN expression in non-small cell lung cancer could be related to promoter methylation
-
Soria JC, Lee HY, Lee JI, et al. Lack of PTEN expression in non-small cell lung cancer could be related to promoter methylation. Clin Cancer Res 2002;8:1178-1184.
-
(2002)
Clin Cancer Res
, vol.8
, pp. 1178-1184
-
-
Soria, J.C.1
Lee, H.Y.2
Lee, J.I.3
-
46
-
-
81055149891
-
PF-04691502, a potent and selective oral inhibitor of PI3K and mTOR kinases with antitumor activity
-
Yuan J, Mehta PP, Yin MJ, et al. PF-04691502, a potent and selective oral inhibitor of PI3K and mTOR kinases with antitumor activity. Mol Cancer Ther 2011;10:2189-2199.
-
(2011)
Mol Cancer Ther
, vol.10
, pp. 2189-2199
-
-
Yuan, J.1
Mehta, P.P.2
Yin, M.J.3
-
47
-
-
14144252004
-
Phosphatidylinositol 3-kinase mutations identified in human cancer are oncogenic
-
Kang S, Bader AG, Vogt PK. Phosphatidylinositol 3-kinase mutations identified in human cancer are oncogenic. Proc Natl Acad Sci USA 2005;102:802-807.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 802-807
-
-
Kang, S.1
Bader, A.G.2
Vogt, P.K.3
-
48
-
-
79953024710
-
Phosphoinositide-3-kinase catalytic alpha and KRAS mutations are important predictors of resistance to therapy with epidermal growth factor receptor tyrosine kinase inhibitors in patients with advanced non-small cell lung cancer
-
Ludovini V, Bianconi F, Pistola L, et al. Phosphoinositide-3-kinase catalytic alpha and KRAS mutations are important predictors of resistance to therapy with epidermal growth factor receptor tyrosine kinase inhibitors in patients with advanced non-small cell lung cancer. J Thorac Oncol 2011;6:707-715.
-
(2011)
J Thorac Oncol
, vol.6
, pp. 707-715
-
-
Ludovini, V.1
Bianconi, F.2
Pistola, L.3
-
49
-
-
57349194139
-
Effective use of PI3K and MEK inhibitors to treat mutant Kras G12D and PIK3CA H1047R murine lung cancers
-
Engelman JA, Chen L, Tan X, et al. Effective use of PI3K and MEK inhibitors to treat mutant Kras G12D and PIK3CA H1047R murine lung cancers. Nat Med 2008;14:1351-1356.
-
(2008)
Nat Med
, vol.14
, pp. 1351-1356
-
-
Engelman, J.A.1
Chen, L.2
Tan, X.3
-
50
-
-
63849149937
-
LKB1 and AMP-activated protein kinase control of mTOR signalling and growth
-
Shaw RJ. LKB1 and AMP-activated protein kinase control of mTOR signalling and growth. Acta Physiol (Oxf) 2009;196:65-80.
-
(2009)
Acta Physiol (Oxf)
, vol.196
, pp. 65-80
-
-
Shaw, R.J.1
-
51
-
-
33947100984
-
Dysfunctional AMPK activity, signalling through mTOR and survival in response to energetic stress in LKB1-deficient lung cancer
-
Carretero J, Medina PP, Blanco R, et al. Dysfunctional AMPK activity, signalling through mTOR and survival in response to energetic stress in LKB1-deficient lung cancer. Oncogene 2007;26:1616-1625.
-
(2007)
Oncogene
, vol.26
, pp. 1616-1625
-
-
Carretero, J.1
Medina, P.P.2
Blanco, R.3
-
52
-
-
58749097239
-
LKB1/KRAS mutant lung cancers constitute a genetic subset of NSCLC with increased sensitivity to MAPK and mTOR signalling inhibition
-
Mahoney CL, Choudhury B, Davies H, et al. LKB1/KRAS mutant lung cancers constitute a genetic subset of NSCLC with increased sensitivity to MAPK and mTOR signalling inhibition. Br J Cancer 2009;100:370-375.
-
(2009)
Br J Cancer
, vol.100
, pp. 370-375
-
-
Mahoney, C.L.1
Choudhury, B.2
Davies, H.3
-
53
-
-
34748845413
-
Prevalence and specificity of LKB1 genetic alterations in lung cancers
-
Matsumoto S, Iwakawa R, Takahashi K, et al. Prevalence and specificity of LKB1 genetic alterations in lung cancers. Oncogene 2007;26:5911-5918.
-
(2007)
Oncogene
, vol.26
, pp. 5911-5918
-
-
Matsumoto, S.1
Iwakawa, R.2
Takahashi, K.3
-
54
-
-
70349383772
-
Targeting aberrant PI3K pathway signaling with XL147, a potent, selective and orally bioavailable PI3K inhibitor
-
Shapiro G, Edelman G, Calvo E, et al. Targeting aberrant PI3K pathway signaling with XL147, a potent, selective and orally bioavailable PI3K inhibitor. AACR Meet Abstr 2007;2007: C205.
-
(2007)
AACR Meet Abstr
, vol.2007
-
-
Shapiro, G.1
Edelman, G.2
Calvo, E.3
-
55
-
-
34547172596
-
A transforming mutation in the pleckstrin homology domain of AKT1 in cancer
-
Carpten JD, Faber AL, Horn C, et al. A transforming mutation in the pleckstrin homology domain of AKT1 in cancer. Nature 2007;448:439-444.
-
(2007)
Nature
, vol.448
, pp. 439-444
-
-
Carpten, J.D.1
Faber, A.L.2
Horn, C.3
-
56
-
-
0024376173
-
Ras oncogenes in human cancer: A review
-
Bos JL. ras oncogenes in human cancer: a review. Cancer Res 1989;49:4682-4689.
-
(1989)
Cancer Res
, vol.49
, pp. 4682-4689
-
-
Bos, J.L.1
-
58
-
-
84872493314
-
The mTOR inhibitor deforolimus is efficacious in models of mutant KRAS lung cancer
-
Abstract 1887
-
Haines B, Bittinger M, Chenard M, et al. The mTOR inhibitor deforolimus is efficacious in models of mutant KRAS lung cancer. AACR Meet Abstr 2009;2009: Abstract 1887.
-
(2009)
AACR Meet Abstr
, vol.2009
-
-
Haines, B.1
Bittinger, M.2
Chenard, M.3
-
59
-
-
77952238072
-
Potentiating the antitumor effects of chemotherapy with the selective PI3K inhibitor XL147
-
Foster P. Potentiating the antitumor effects of chemotherapy with the selective PI3K inhibitor XL147. AACR Meet Abstr 2007;2007: C199.
-
(2007)
AACR Meet Abstr
, vol.2007
-
-
Foster, P.1
-
60
-
-
58249120506
-
Mutations in the phosphatidylinositol-3-kinase pathway predict for antitumor activity of the inhibitor PX-866 whereas oncogenic Ras is a dominant predictor for resistance
-
Ihle NT, Lemos R Jr, Wipf P, et al. Mutations in the phosphatidylinositol-3-kinase pathway predict for antitumor activity of the inhibitor PX-866 whereas oncogenic Ras is a dominant predictor for resistance. Cancer Res 2009;69:143-150.
-
(2009)
Cancer Res
, vol.69
, pp. 143-150
-
-
Ihle, N.T.1
Lemos Jr., R.2
Wipf, P.3
-
61
-
-
33746257209
-
The evolution of phosphatidylinositol 3-kinases as regulators of growth and metabolism
-
Engelman JA, Luo J, Cantley LC. The evolution of phosphatidylinositol 3-kinases as regulators of growth and metabolism. Nat Rev Genet 2006;7:606-619.
-
(2006)
Nat Rev Genet
, vol.7
, pp. 606-619
-
-
Engelman, J.A.1
Luo, J.2
Cantley, L.C.3
-
62
-
-
84856988295
-
A dose-escalation study with the novel formulation of the oral pan-class i PI3K inhibitor BEZ235, solid dispersion system (SDS) sachet, in patients with advanced solid tumors
-
Peyton JD, Rodon Ahnert J, Burris H, et al. A dose-escalation study with the novel formulation of the oral pan-class I PI3K inhibitor BEZ235, solid dispersion system (SDS) sachet, in patients with advanced solid tumors. ASCO Meet Abstr 2011;29:3066.
-
(2011)
ASCO Meet Abstr
, vol.29
, pp. 3066
-
-
Peyton, J.D.1
Rodon Ahnert, J.2
Burris, H.3
-
63
-
-
84856071447
-
Phase I, dose-escalation study of BKM120, an oral pan-Class i PI3K inhibitor, in patients with advanced solid tumors
-
Bendell JC, Rodon J, Burris HA, et al. Phase I, dose-escalation study of BKM120, an oral pan-Class I PI3K inhibitor, in patients with advanced solid tumors. J Clin Oncol 2012;30:282-290.
-
(2012)
J Clin Oncol
, vol.30
, pp. 282-290
-
-
Bendell, J.C.1
Rodon, J.2
Burris, H.A.3
-
64
-
-
84901982336
-
Biological characterization of NVP-BKM120, a novel inhibitor of phosphoinositide 3-kinase in phase I/II clinical trials
-
Voliva CF, Pecchi S, Burger M, et al. Biological characterization of NVP-BKM120, a novel inhibitor of phosphoinositide 3-kinase in phase I/II clinical trials. AACR Meet Abstr 2010;2010:4498.
-
(2010)
AACR Meet Abstr
, vol.2010
, pp. 4498
-
-
Voliva, C.F.1
Pecchi, S.2
Burger, M.3
-
65
-
-
77956566979
-
A phase i dose-escalation study of XL147 (SAR245408), a PI3K inhibitor administered orally to patients (pts) with advanced malignancies
-
Edelman G, Bedell C, Shapiro G, et al. A phase I dose-escalation study of XL147 (SAR245408), a PI3K inhibitor administered orally to patients (pts) with advanced malignancies. ASCO Meet Abstr 2010;28:3004.
-
(2010)
ASCO Meet Abstr
, vol.28
, pp. 3004
-
-
Edelman, G.1
Bedell, C.2
Shapiro, G.3
-
66
-
-
79952665848
-
A phase i safety and pharmacokinetic (PK) study of the PI3K inhibitor XL147 (SAR245408) in combination with paclitaxel (P) and carboplatin (C) in patients (pts) with advanced solid tumors
-
Traynor AM, Kurzrock R, Bailey HH, et al. A phase I safety and pharmacokinetic (PK) study of the PI3K inhibitor XL147 (SAR245408) in combination with paclitaxel (P) and carboplatin (C) in patients (pts) with advanced solid tumors. ASCO Meet Abstr 2010;28:3078.
-
(2010)
ASCO Meet Abstr
, vol.28
, pp. 3078
-
-
Traynor, A.M.1
Kurzrock, R.2
Bailey, H.H.3
-
67
-
-
79959343185
-
A phase i safety and pharmacokinetic (PK) study of the PI3K inhibitor XL147 (SAR245408) in combination with erlotinib in patients (pts) with advanced solid tumors
-
Moldovan C, Soria J, LoRusso P, et al. A phase I safety and pharmacokinetic (PK) study of the PI3K inhibitor XL147 (SAR245408) in combination with erlotinib in patients (pts) with advanced solid tumors. ASCO Meet Abstr 2010;28:3070.
-
(2010)
ASCO Meet Abstr
, vol.28
, pp. 3070
-
-
Moldovan, C.1
Soria, J.2
Lorusso, P.3
-
68
-
-
4444223702
-
Molecular pharmacology and antitumor activity of PX-866, a novel inhibitor of phosphoinositide-3-kinase signaling
-
Ihle NT, Williams R, Chow S, et al. Molecular pharmacology and antitumor activity of PX-866, a novel inhibitor of phosphoinositide-3-kinase signaling. Mol Cancer Ther 2004;3:763-772.
-
(2004)
Mol Cancer Ther
, vol.3
, pp. 763-772
-
-
Ihle, N.T.1
Williams, R.2
Chow, S.3
-
69
-
-
79952686437
-
Final results from a phase I, dose-escalation study of PX-866, an irreversible, pan-isoform inhibitor of PI3 kinase
-
Jimeno A, Herbst RS, Falchook GS, et al. Final results from a phase I, dose-escalation study of PX-866, an irreversible, pan-isoform inhibitor of PI3 kinase. ASCO Meet Abstr 2010;28:3089.
-
(2010)
ASCO Meet Abstr
, vol.28
, pp. 3089
-
-
Jimeno, A.1
Herbst, R.S.2
Falchook, G.S.3
-
70
-
-
84863847137
-
GDC-0941, a potent, selective, orally bioavailable inhibitor of class i PI3K
-
Friedman L. GDC-0941, a potent, selective, orally bioavailable inhibitor of class I PI3K. AACR Meet Abstr 2008;2008:LB-110.
-
(2008)
AACR Meet Abstr
, vol.2008
-
-
Friedman, L.1
-
71
-
-
84861963385
-
A phase i dose-escalation study to evaluate GDC-0941, a pan-PI3K inhibitor, administered QD or BID in patients with advanced or metastatic solid tumors
-
Von Hoff DD, LoRusso P, Demetri GD, et al. A phase I dose-escalation study to evaluate GDC-0941, a pan-PI3K inhibitor, administered QD or BID in patients with advanced or metastatic solid tumors. ASCO Meet Abstr 2011;29:3052.
-
(2011)
ASCO Meet Abstr
, vol.29
, pp. 3052
-
-
Von Hoff, D.D.1
Lorusso, P.2
Demetri, G.D.3
-
72
-
-
84861992072
-
A phase i study evaluating GDC-0941, an oral phosphoinositide-3 kinase (PI3K) inhibitor, in patients with advanced solid tumors or multiple myeloma
-
Moreno Garcia V, Baird RD, Shah KJ, et al. A phase I study evaluating GDC-0941, an oral phosphoinositide-3 kinase (PI3K) inhibitor, in patients with advanced solid tumors or multiple myeloma. ASCO Meet Abstr 2011;29:3021.
-
(2011)
ASCO Meet Abstr
, vol.29
, pp. 3021
-
-
Moreno Garcia, V.1
Baird, R.D.2
Shah, K.J.3
-
73
-
-
80054717796
-
Clinical combination of the MEK inhibitor GDC-0973 and the PI3K inhibitor GDC-0941: A first-in-human phase Ib study testing daily and intermittent dosing schedules in patients with advanced solid tumors
-
Shapiro G, LoRusso P, Kwak EL, et al. Clinical combination of the MEK inhibitor GDC-0973 and the PI3K inhibitor GDC-0941: a first-in-human phase Ib study testing daily and intermittent dosing schedules in patients with advanced solid tumors. ASCO Meet Abstr 2011;29:3005.
-
(2011)
ASCO Meet Abstr
, vol.29
, pp. 3005
-
-
Shapiro, G.1
Lorusso, P.2
Kwak, E.L.3
-
74
-
-
84863828298
-
A phase Ib study to evaluate the PI3-kinase inhibitor GDC-0941 with paclitaxel (P) and carboplatin (C), with and without bevacizumab (BEV), in patients with advanced non-small cell lung cancer (NSCLC)
-
Besse B, Soria J, Gomez-Roca C, et al. A phase Ib study to evaluate the PI3-kinase inhibitor GDC-0941 with paclitaxel (P) and carboplatin (C), with and without bevacizumab (BEV), in patients with advanced non-small cell lung cancer (NSCLC). ASCO Meet Abstr 2011;29:3044.
-
(2011)
ASCO Meet Abstr
, vol.29
, pp. 3044
-
-
Besse, B.1
Soria, J.2
Gomez-Roca, C.3
-
75
-
-
79960253536
-
A first-in-human phase i study of intravenous PI3K inhibitor BAY 80-6946 in patients with advanced solid tumors: Results of dose-escalation phase
-
Patnaik A, Appleman LJ, Mountz JM, et al. A first-in-human phase I study of intravenous PI3K inhibitor BAY 80-6946 in patients with advanced solid tumors: results of dose-escalation phase. ASCO Meet Abstr 2011;29:3035.
-
(2011)
ASCO Meet Abstr
, vol.29
, pp. 3035
-
-
Patnaik, A.1
Appleman, L.J.2
Mountz, J.M.3
-
76
-
-
77954567174
-
Biologic effects of NVP-BEZ235, an orally available dual PI3K/mTOR inhibitor, in human breast, lung, colon, pancreas, and liver cancer cell lines in vitro
-
Abstract 2816
-
Finn R, Dering J, Portillo D, et al. Biologic effects of NVP-BEZ235, an orally available dual PI3K/mTOR inhibitor, in human breast, lung, colon, pancreas, and liver cancer cell lines in vitro. AACR Meet Abstr 2009;2009: Abstract 2816.
-
(2009)
AACR Meet Abstr
, vol.2009
-
-
Finn, R.1
Dering, J.2
Portillo, D.3
-
77
-
-
79956078123
-
The dual PI3K/mTOR inhibitor BEZ235 is effective in lung cancer cell lines
-
Herrera VA, Zeindl-Eberhart E, Jung A, Huber RM, Bergner A. The dual PI3K/mTOR inhibitor BEZ235 is effective in lung cancer cell lines. Anticancer Res 2011;31:849-854.
-
(2011)
Anticancer Res
, vol.31
, pp. 849-854
-
-
Herrera, V.A.1
Zeindl-Eberhart, E.2
Jung, A.3
Huber, R.M.4
Bergner, A.5
-
78
-
-
79958816470
-
The combination of RAD001 and NVP-BEZ235 exerts synergistic anticancer activity against non-small cell lung cancer in vitro and in vivo
-
Xu CX, Li Y, Yue P, et al. The combination of RAD001 and NVP-BEZ235 exerts synergistic anticancer activity against non-small cell lung cancer in vitro and in vivo. PLoS ONE 2011;6:e20899.
-
(2011)
PLoS ONE
, vol.6
-
-
Xu, C.X.1
Li, Y.2
Yue, P.3
-
79
-
-
77956602070
-
First-in-human phase i study of the oral PI3K inhibitor BEZ235 in patients (pts) with advanced solid tumors
-
Burris H, Rodon J, Sharma S, et al. First-in-human phase I study of the oral PI3K inhibitor BEZ235 in patients (pts) with advanced solid tumors. ASCO Meet Abstr 2010;28:3005.
-
(2010)
ASCO Meet Abstr
, vol.28
, pp. 3005
-
-
Burris, H.1
Rodon, J.2
Sharma, S.3
-
80
-
-
79958164013
-
XL765 targets tumor growth, survival, and angiogenesis in preclinical models by dual inhibition of PI3K and mTOR
-
Laird AD. XL765 targets tumor growth, survival, and angiogenesis in preclinical models by dual inhibition of PI3K and mTOR. AACR Meet Abstr 2007;2007: B250.
-
(2007)
AACR Meet Abstr
, vol.2007
-
-
Laird, A.D.1
-
81
-
-
77957104533
-
A phase i dose-escalation study of the safety, pharmacokinetics (PK), and pharmacodynamics of XL765 (SAR245409), a PI3K/TORC1/TORC2 inhibitor administered orally to patients (pts) with advanced malignancies
-
Brana I, LoRusso P, Baselga J, et al. A phase I dose-escalation study of the safety, pharmacokinetics (PK), and pharmacodynamics of XL765 (SAR245409), a PI3K/TORC1/TORC2 inhibitor administered orally to patients (pts) with advanced malignancies. ASCO Meet Abstr 2010;28:3030.
-
(2010)
ASCO Meet Abstr
, vol.28
, pp. 3030
-
-
Brana, I.1
Lorusso, P.2
Baselga, J.3
-
82
-
-
79951612370
-
A phase i safety and pharmacokinetic (PK) study of PI3K/TORC1/TORC2 inhibitor XL765 (SAR245409) in combination with erlotinib (E) in patients (pts) with advanced solid tumors
-
Cohen RB, Janne PA, Engelman JA, et al. A phase I safety and pharmacokinetic (PK) study of PI3K/TORC1/TORC2 inhibitor XL765 (SAR245409) in combination with erlotinib (E) in patients (pts) with advanced solid tumors. ASCO Meet Abstr 2010;28:3015.
-
(2010)
ASCO Meet Abstr
, vol.28
, pp. 3015
-
-
Cohen, R.B.1
Janne, P.A.2
Engelman, J.A.3
-
83
-
-
79952646251
-
A first-in-human, phase l study to evaluate the dual PI3K/mTOR inhibitor GDC-0980 administered QD in patients with advanced solid tumors or non-Hodgkins lymphoma
-
Dolly S, Wagner AJ, Bendell JC, et al. A first-in-human, phase l study to evaluate the dual PI3K/mTOR inhibitor GDC-0980 administered QD in patients with advanced solid tumors or non-Hodgkins lymphoma. ASCO Meet Abstr 2010;28:3079.
-
(2010)
ASCO Meet Abstr
, vol.28
, pp. 3079
-
-
Dolly, S.1
Wagner, A.J.2
Bendell, J.C.3
-
84
-
-
80054740282
-
A first-in-human phase i study to evaluate GDC-0980, an oral PI3K/mTOR inhibitor, administered QD in patients with advanced solid tumors
-
Wagner AJ, Bendell JC, Dolly S, et al. A first-in-human phase I study to evaluate GDC-0980, an oral PI3K/mTOR inhibitor, administered QD in patients with advanced solid tumors. ASCO Meet Abstr 2011;29:3020.
-
(2011)
ASCO Meet Abstr
, vol.29
, pp. 3020
-
-
Wagner, A.J.1
Bendell, J.C.2
Dolly, S.3
-
85
-
-
2542547908
-
Perifosine, a novel alkylphospholipid, inhibits protein kinase B activation
-
Kondapaka SB, Singh SS, Dasmahapatra GP, Sausville EA, Roy KK. Perifosine, a novel alkylphospholipid, inhibits protein kinase B activation. Mol Cancer Ther 2003;2:1093-1103.
-
(2003)
Mol Cancer Ther
, vol.2
, pp. 1093-1103
-
-
Kondapaka, S.B.1
Singh, S.S.2
Dasmahapatra, G.P.3
Sausville, E.A.4
Roy, K.K.5
-
86
-
-
77958485501
-
In vitro and in vivo antitumor activities of MK-2206, a new allosteric Akt inhibitor
-
Abstract 3714
-
Lu W, Defeo-Jones D, Davis L, et al. In vitro and in vivo antitumor activities of MK-2206, a new allosteric Akt inhibitor. AACR Meeting Abstracts 2009;2009:Abstract 3714.
-
(2009)
AACR Meeting Abstracts
, vol.2009
-
-
Lu, W.1
Defeo-Jones, D.2
Davis, L.3
-
87
-
-
0021215741
-
Phase i study of tricyclic nucleoside phosphate using a five-day continuous infusion schedule
-
Feun LG, Savaraj N, Bodey GP, et al. Phase I study of tricyclic nucleoside phosphate using a five-day continuous infusion schedule. Cancer Res 1984;44:3608-3612.
-
(1984)
Cancer Res
, vol.44
, pp. 3608-3612
-
-
Feun, L.G.1
Savaraj, N.2
Bodey, G.P.3
-
88
-
-
84863854918
-
Triciribine phosphate (TCN-P) in advanced non-small cell lung cancer (NSCLC): Phase II trial
-
Lyss AP, Morrell LE, Perry MC. Triciribine phosphate (TCN-P) in advanced non-small cell lung cancer (NSCLC): phase II trial. ASCO Mee Abstr 1996:1151.
-
(1996)
ASCO Mee Abstr
, pp. 1151
-
-
Lyss, A.P.1
Morrell, L.E.2
Perry, M.C.3
-
89
-
-
77954615408
-
MK-2206, an allosteric Akt inhibitor, enhances antitumor efficacy by standard chemotherapeutic agents or molecular targeted drugs in vitro and in vivo
-
Hirai H, Sootome H, Nakatsuru Y, et al. MK-2206, an allosteric Akt inhibitor, enhances antitumor efficacy by standard chemotherapeutic agents or molecular targeted drugs in vitro and in vivo. Mol Cancer Ther 2010;9:1956-1967.
-
(2010)
Mol Cancer Ther
, vol.9
, pp. 1956-1967
-
-
Hirai, H.1
Sootome, H.2
Nakatsuru, Y.3
-
90
-
-
84856008240
-
Impact of AKT inhibitor MK-2206 on erlotinib resistance in non-small cell lung cancer (NSCLC)
-
Mack PC, Farneth N, Mahaffey C, et al. Impact of AKT inhibitor MK-2206 on erlotinib resistance in non-small cell lung cancer (NSCLC). ASCO Meet Abstr 2011;29:7573.
-
(2011)
ASCO Meet Abstr
, vol.29
, pp. 7573
-
-
MacK, P.C.1
Farneth, N.2
Mahaffey, C.3
-
91
-
-
77956587792
-
First-in-class phase i trial of a selective Akt inhibitor, MK2206 (MK), evaluating alternate day (QOD) and once weekly (QW) doses in advanced cancer patients (pts) with evidence of target modulation and antitumor activity
-
Yap TA, Patnaik A, Fearen I, et al. First-in-class phase I trial of a selective Akt inhibitor, MK2206 (MK), evaluating alternate day (QOD) and once weekly (QW) doses in advanced cancer patients (pts) with evidence of target modulation and antitumor activity. ASCO Meet Abstr 2010;28:3009.
-
(2010)
ASCO Meet Abstr
, vol.28
, pp. 3009
-
-
Yap, T.A.1
Patnaik, A.2
Fearen, I.3
-
92
-
-
80054760775
-
A phase i dose-escalation study of oral MK-2206 (allosteric AKT inhibitor) with oral selumetinib (AZD6244; MEK inhibitor) in patients with advanced or metastatic solid tumors
-
Tolcher AW, Baird RD, Patnaik A, et al. A phase I dose-escalation study of oral MK-2206 (allosteric AKT inhibitor) with oral selumetinib (AZD6244; MEK inhibitor) in patients with advanced or metastatic solid tumors. ASCO Meet Abstr 2011;29:3004.
-
(2011)
ASCO Meet Abstr
, vol.29
, pp. 3004
-
-
Tolcher, A.W.1
Baird, R.D.2
Patnaik, A.3
-
93
-
-
80054747639
-
Safety, pharmacokinetics (PK), pharmacodynamics (PD), and clinical activity of the oral AKT inhibitor GSK2141795 (GSK795) in a phase i first-in-human study
-
Burris HA, Siu LL, Infante JR, et al. Safety, pharmacokinetics (PK), pharmacodynamics (PD), and clinical activity of the oral AKT inhibitor GSK2141795 (GSK795) in a phase I first-in-human study. ASCO Meet Abstr 2011;29:3003.
-
(2011)
ASCO Meet Abstr
, vol.29
, pp. 3003
-
-
Burris, H.A.1
Siu, L.L.2
Infante, J.R.3
-
94
-
-
70349637311
-
Efficacy of everolimus (RAD001) in patients with advanced NSCLC previously treated with chemotherapy alone or with chemotherapy and EGFR inhibitors
-
Soria JC, Shepherd FA, Douillard JY, et al. Efficacy of everolimus (RAD001) in patients with advanced NSCLC previously treated with chemotherapy alone or with chemotherapy and EGFR inhibitors. Ann Oncol 2009;20:1674-1681.
-
(2009)
Ann Oncol
, vol.20
, pp. 1674-1681
-
-
Soria, J.C.1
Shepherd, F.A.2
Douillard, J.Y.3
-
95
-
-
77958161544
-
Phase II trial of gefitinib and everolimus in advanced non-small cell lung cancer
-
Price KA, Azzoli CG, Krug LM, et al. Phase II trial of gefitinib and everolimus in advanced non-small cell lung cancer. J Thorac Oncol 2010;5:1623-1629.
-
(2010)
J Thorac Oncol
, vol.5
, pp. 1623-1629
-
-
Price, K.A.1
Azzoli, C.G.2
Krug, L.M.3
-
96
-
-
84863852095
-
Everolimus, an mTOR inhibitor, in combination with docetaxel for second- or third-line therapy of advanced-stage non-small cell lung cancer: A phase II study
-
Khuri FR, Owonikoko TK, Subramanian J, et al. Everolimus, an mTOR inhibitor, in combination with docetaxel for second- or third-line therapy of advanced-stage non-small cell lung cancer: a phase II study. ASCO Meet Abstr 2011;29:e13601.
-
(2011)
ASCO Meet Abstr
, vol.29
-
-
Khuri, F.R.1
Owonikoko, T.K.2
Subramanian, J.3
-
97
-
-
76749109738
-
A phase 1/2 study investigating the combination of RAD001 (R) (everolimus) and erlotinib (E) as 2nd and 3rd line therapy in patients (pts) with advanced non-small cell lung cancer (NSCLC) previously treated with chemotherapy (C): Phase 1 results
-
Papadimitrakopoulou V, Blumenschein GR, Leighl NB, et al. A phase 1/2 study investigating the combination of RAD001 (R) (everolimus) and erlotinib (E) as 2nd and 3rd line therapy in patients (pts) with advanced non-small cell lung cancer (NSCLC) previously treated with chemotherapy (C): phase 1 results. ASCO Meet Abstr 2008;26:8051.
-
(2008)
ASCO Meet Abstr
, vol.26
, pp. 8051
-
-
Papadimitrakopoulou, V.1
Blumenschein, G.R.2
Leighl, N.B.3
-
98
-
-
79959208568
-
Inhibition of mTOR by temsirolimus contributes to prolonged survival of mice with pleural dissemination of non-small-cell lung cancer cells
-
Ohara T, Takaoka M, Toyooka S, et al. Inhibition of mTOR by temsirolimus contributes to prolonged survival of mice with pleural dissemination of non-small-cell lung cancer cells. Cancer Sci 2011;102:1344-1349.
-
(2011)
Cancer Sci
, vol.102
, pp. 1344-1349
-
-
Ohara, T.1
Takaoka, M.2
Toyooka, S.3
-
99
-
-
85059107658
-
In vitro treatment of non-small cell lung cancer cells with temsirolimus and/or docetaxel: Does alternating the sequence affect the outcome?
-
Huang C, Misra J, Van Veldhuizen PJ, et al. In vitro treatment of non-small cell lung cancer cells with temsirolimus and/or docetaxel: does alternating the sequence affect the outcome? ASCO Meet Abstr 2011;29: e13515.
-
(2011)
ASCO Meet Abstr
, vol.29
-
-
Huang, C.1
Misra, J.2
Van Veldhuizen, P.J.3
-
100
-
-
33750321673
-
A phase i and pharmacokinetic study of temsirolimus (CCI-779) administered intravenously daily for 5 days every 2 weeks to patients with advanced cancer
-
Hidalgo M, Buckner JC, Erlichman C, et al. A phase I and pharmacokinetic study of temsirolimus (CCI-779) administered intravenously daily for 5 days every 2 weeks to patients with advanced cancer. Clin Cancer Res 2006;12:5755-5763.
-
(2006)
Clin Cancer Res
, vol.12
, pp. 5755-5763
-
-
Hidalgo, M.1
Buckner, J.C.2
Erlichman, C.3
-
101
-
-
35848959875
-
A randomized, phase II trial of two dose levels of temsirolimus (CCI-779) in patients with extensive-stage small-cell lung cancer who have responding or stable disease after induction chemotherapy: A trial of the Eastern Cooperative Oncology Group (E1500)
-
Pandya KJ, Dahlberg S, Hidalgo M, et al.; Eastern Cooperative Oncology Group (E1500). A randomized, phase II trial of two dose levels of temsirolimus (CCI-779) in patients with extensive-stage small-cell lung cancer who have responding or stable disease after induction chemotherapy: a trial of the Eastern Cooperative Oncology Group (E1500). J Thorac Oncol 2007;2:1036-1041.
-
(2007)
J Thorac Oncol
, vol.2
, pp. 1036-1041
-
-
Pandya, K.J.1
Dahlberg, S.2
Hidalgo, M.3
-
102
-
-
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 2008;26:361-367.
-
(2008)
J Clin Oncol
, vol.26
, pp. 361-367
-
-
Mita, M.M.1
Mita, A.C.2
Chu, Q.S.3
-
103
-
-
51349164790
-
Inhibition of mTORC1 leads to MAPK pathway activation through a PI3K-dependent feedback loop in human cancer
-
Carracedo A, Ma L, Teruya-Feldstein J, et al. Inhibition of mTORC1 leads to MAPK pathway activation through a PI3K-dependent feedback loop in human cancer. J Clin Invest 2008;118:3065-3074.
-
(2008)
J Clin Invest
, vol.118
, pp. 3065-3074
-
-
Carracedo, A.1
Ma, L.2
Teruya-Feldstein, J.3
-
105
-
-
75149112670
-
AZD8055 is a potent, selective, and orally bioavailable ATP-competitive mammalian target of rapamycin kinase inhibitor with in vitro and in vivo antitumor activity
-
Chresta CM, Davies BR, Hickson I, et al. AZD8055 is a potent, selective, and orally bioavailable ATP-competitive mammalian target of rapamycin kinase inhibitor with in vitro and in vivo antitumor activity. Cancer Res 2010;70:288-298.
-
(2010)
Cancer Res
, vol.70
, pp. 288-298
-
-
Chresta, C.M.1
Davies, B.R.2
Hickson, I.3
-
106
-
-
79951651465
-
First-in-human phase i study exploring three schedules of OSI-027, a novel small molecule TORC1/TORC2 inhibitor, in patients with advanced solid tumors and lymphoma
-
Tan DS, Dumez H, Olmos D, et al. First-in-human phase I study exploring three schedules of OSI-027, a novel small molecule TORC1/TORC2 inhibitor, in patients with advanced solid tumors and lymphoma. ASCO Meet Abstr 2010;28:3006.
-
(2010)
ASCO Meet Abstr
, vol.28
, pp. 3006
-
-
Tan, D.S.1
Dumez, H.2
Olmos, D.3
-
107
-
-
79952257687
-
Sorafenib treatment efficacy and KRAS biomarker status in the Biomarker-Integrated Approaches of Targeted Therapy for Lung Cancer Elimination (BATTLE) trial
-
Herbst RS, Blumenschein GR, Kim ES, et al. Sorafenib treatment efficacy and KRAS biomarker status in the Biomarker-Integrated Approaches of Targeted Therapy for Lung Cancer Elimination (BATTLE) trial. ASCO Meet Abstr 2010;28:7609.
-
(2010)
ASCO Meet Abstr
, vol.28
, pp. 7609
-
-
Herbst, R.S.1
Blumenschein, G.R.2
Kim, E.S.3
-
108
-
-
78049425319
-
Anaplastic lymphoma kinase inhibition in non-small-cell lung cancer
-
Kwak EL, Bang YJ, Camidge DR, et al. Anaplastic lymphoma kinase inhibition in non-small-cell lung cancer. N Engl J Med 2010;363:1693-1703.
-
(2010)
N Engl J Med
, vol.363
, pp. 1693-1703
-
-
Kwak, E.L.1
Bang, Y.J.2
Camidge, D.R.3
-
109
-
-
79960889662
-
Erlotinib versus chemotherapy as first-line treatment for patients with advanced EGFR mutation-positive non-small-cell lung cancer (OPTIMAL, CTONG-0802): A multicentre, open-label, randomised, phase 3 study
-
Zhou C, Wu YL, Chen G, et al. Erlotinib versus chemotherapy as first-line treatment for patients with advanced EGFR mutation-positive non-small-cell lung cancer (OPTIMAL, CTONG-0802): a multicentre, open-label, randomised, phase 3 study. Lancet Oncol 2011;12:735-742.
-
(2011)
Lancet Oncol
, vol.12
, pp. 735-742
-
-
Zhou, C.1
Wu, Y.L.2
Chen, G.3
-
110
-
-
73349129405
-
Differential induction of apoptosis in HER2 and EGFR addicted cancers following PI3K inhibition
-
Faber AC, Li D, Song Y, et al. Differential induction of apoptosis in HER2 and EGFR addicted cancers following PI3K inhibition. Proc Natl Acad Sci USA 2009;106:19503-19508.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 19503-19508
-
-
Faber, A.C.1
Li, D.2
Song, Y.3
-
111
-
-
20044364940
-
Clinical and biological features associated with epidermal growth factor receptor gene mutations in lung cancers
-
Shigematsu H, Lin L, Takahashi T, et al. Clinical and biological features associated with epidermal growth factor receptor gene mutations in lung cancers. J Natl Cancer Inst 2005;97:339-346.
-
(2005)
J Natl Cancer Inst
, vol.97
, pp. 339-346
-
-
Shigematsu, H.1
Lin, L.2
Takahashi, T.3
-
112
-
-
52049090365
-
Role of KRAS and EGFR as biomarkers of response to erlotinib in National Cancer Institute of Canada Clinical Trials Group Study BR.21
-
Zhu CQ, da Cunha Santos G, Ding K, et al.; National Cancer Institute of Canada Clinical Trials Group Study BR.21. Role of KRAS and EGFR as biomarkers of response to erlotinib in National Cancer Institute of Canada Clinical Trials Group Study BR.21. J Clin Oncol 2008;26:4268-4275.
-
(2008)
J Clin Oncol
, vol.26
, pp. 4268-4275
-
-
Zhu, C.Q.1
Da Cunha Santos, G.2
Ding, K.3
-
113
-
-
69949186250
-
Screening for epidermal growth factor receptor mutations in lung cancer
-
Rosell R, Moran T, Queralt C, et al.; Spanish Lung Cancer Group. Screening for epidermal growth factor receptor mutations in lung cancer. N Engl J Med 2009;361:958-967.
-
(2009)
N Engl J Med
, vol.361
, pp. 958-967
-
-
Rosell, R.1
Moran, T.2
Queralt, C.3
-
114
-
-
69949162760
-
Gefitinib or carboplatin-paclitaxel in pulmonary adenocarcinoma
-
Mok TS, Wu YL, Thongprasert S, et al. Gefitinib or carboplatin-paclitaxel in pulmonary adenocarcinoma. N Engl J Med 2009;361:947-957.
-
(2009)
N Engl J Med
, vol.361
, pp. 947-957
-
-
Mok, T.S.1
Wu, Y.L.2
Thongprasert, S.3
-
115
-
-
84872499747
-
-
Wellcome TrustSanger Institute Cancer Genome Project. Accessed April 26
-
Wellcome TrustSanger Institute Cancer Genome Project. Available at http://www.sanger.ac.uk/cosmic. Accessed April 26, 2012.
-
(2012)
-
-
-
116
-
-
20444498630
-
Epidermal growth factor receptor gene and protein and gefitinib sensitivity in non-small-cell lung cancer
-
Cappuzzo F, Hirsch FR, Rossi E, et al. Epidermal growth factor receptor gene and protein and gefitinib sensitivity in non-small-cell lung cancer. J Natl Cancer Inst 2005;97:643-655.
-
(2005)
J Natl Cancer Inst
, vol.97
, pp. 643-655
-
-
Cappuzzo, F.1
Hirsch, F.R.2
Rossi, E.3
-
117
-
-
33750962024
-
Molecular predictors of outcome with gefitinib in a phase III placebo-controlled study in advanced non-small-cell lung cancer
-
Hirsch FR, Varella-Garcia M, Bunn PA Jr, et al. Molecular predictors of outcome with gefitinib in a phase III placebo-controlled study in advanced non-small-cell lung cancer. J Clin Oncol 2006;24:5034-5042.
-
(2006)
J Clin Oncol
, vol.24
, pp. 5034-5042
-
-
Hirsch, F.R.1
Varella-Garcia, M.2
Bunn Jr., P.A.3
-
118
-
-
37549060017
-
EML4-ALK fusion is linked to histological characteristics in a subset of lung cancers
-
Inamura K, Takeuchi K, Togashi Y, et al. EML4-ALK fusion is linked to histological characteristics in a subset of lung cancers. J Thorac Oncol 2008;3:13-17.
-
(2008)
J Thorac Oncol
, vol.3
, pp. 13-17
-
-
Inamura, K.1
Takeuchi, K.2
Togashi, Y.3
-
119
-
-
40149109522
-
EML4-ALK fusion lung cancer: A rare acquired event
-
Perner S, Wagner PL, Demichelis F, et al. EML4-ALK fusion lung cancer: a rare acquired event. Neoplasia 2008;10:298-302.
-
(2008)
Neoplasia
, vol.10
, pp. 298-302
-
-
Perner, S.1
Wagner, P.L.2
Demichelis, F.3
-
120
-
-
65249095599
-
The EML4-ALK fusion gene is involved in various histologic types of lung cancers from nonsmokers with wild-type EGFR and KRAS
-
Wong DW, Leung EL, So KK, et al.; University of Hong Kong Lung Cancer Study Group. The EML4-ALK fusion gene is involved in various histologic types of lung cancers from nonsmokers with wild-type EGFR and KRAS. Cancer 2009;115:1723-1733.
-
(2009)
Cancer
, vol.115
, pp. 1723-1733
-
-
Wong, D.W.1
Leung, E.L.2
So, K.K.3
-
121
-
-
31544462584
-
Somatic mutations lead to an oncogenic deletion of met in lung cancer
-
Kong-Beltran M, Seshagiri S, Zha J, et al. Somatic mutations lead to an oncogenic deletion of met in lung cancer. Cancer Res 2006;66:283-289.
-
(2006)
Cancer Res
, vol.66
, pp. 283-289
-
-
Kong-Beltran, M.1
Seshagiri, S.2
Zha, J.3
-
123
-
-
38049150665
-
MET amplification occurs with or without T790M mutations in EGFR mutant lung tumors with acquired resistance to gefitinib or erlotinib
-
Bean J, Brennan C, Shih JY, et al. MET amplification occurs with or without T790M mutations in EGFR mutant lung tumors with acquired resistance to gefitinib or erlotinib. Proc Natl Acad Sci USA 2007;104:20932-20937.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 20932-20937
-
-
Bean, J.1
Brennan, C.2
Shih, J.Y.3
-
124
-
-
62449250134
-
MET gene amplification or EGFR mutation activate MET in lung cancers untreated with EGFR tyrosine kinase inhibitors
-
Kubo T, Yamamoto H, Lockwood WW, et al. MET gene amplification or EGFR mutation activate MET in lung cancers untreated with EGFR tyrosine kinase inhibitors. Int J Cancer 2009;124:1778-1784.
-
(2009)
Int J Cancer
, vol.124
, pp. 1778-1784
-
-
Kubo, T.1
Yamamoto, H.2
Lockwood, W.W.3
-
125
-
-
15744372810
-
KRAS mutations and primary resistance of lung adenocarcinomas to gefitinib or erlotinib
-
Pao W, Wang TY, Riely GJ, et al. KRAS mutations and primary resistance of lung adenocarcinomas to gefitinib or erlotinib. PLoS Med 2005;2:e17.
-
(2005)
PLoS Med
, vol.2
-
-
Pao, W.1
Wang, T.Y.2
Riely, G.J.3
-
126
-
-
34548446446
-
PIK3CA mutation and amplification in human lung cancer
-
Okudela K, Suzuki M, Kageyama S, et al. PIK3CA mutation and amplification in human lung cancer. Pathol Int 2007;57:664-671.
-
(2007)
Pathol Int
, vol.57
, pp. 664-671
-
-
Okudela, K.1
Suzuki, M.2
Kageyama, S.3
-
127
-
-
11144358645
-
High frequency of mutations of the PIK3CA gene in human cancers
-
Samuels Y, Wang Z, Bardelli A, et al. High frequency of mutations of the PIK3CA gene in human cancers. Science 2004;304:554.
-
(2004)
Science
, vol.304
, pp. 554
-
-
Samuels, Y.1
Wang, Z.2
Bardelli, A.3
-
128
-
-
33846252977
-
PTEN and PIK3CA expression is associated with prolonged survival after gefitinib treatment in EGFR-mutated lung cancer patients
-
Endoh H, Yatabe Y, Kosaka T, Kuwano H, Mitsudomi T. PTEN and PIK3CA expression is associated with prolonged survival after gefitinib treatment in EGFR-mutated lung cancer patients. J Thorac Oncol 2006;1:629-634.
-
(2006)
J Thorac Oncol
, vol.1
, pp. 629-634
-
-
Endoh, H.1
Yatabe, Y.2
Kosaka, T.3
Kuwano, H.4
Mitsudomi, T.5
-
129
-
-
33751084640
-
PIK3CA mutation status in Japanese lung cancer patients
-
Kawano O, Sasaki H, Endo K, et al. PIK3CA mutation status in Japanese lung cancer patients. Lung Cancer 2006;54:209-215.
-
(2006)
Lung Cancer
, vol.54
, pp. 209-215
-
-
Kawano, O.1
Sasaki, H.2
Endo, K.3
-
130
-
-
52049099853
-
PIK3CA mutations and copy number gains in human lung cancers
-
Yamamoto H, Shigematsu H, Nomura M, et al. PIK3CA mutations and copy number gains in human lung cancers. Cancer Res 2008;68:6913-6921.
-
(2008)
Cancer Res
, vol.68
, pp. 6913-6921
-
-
Yamamoto, H.1
Shigematsu, H.2
Nomura, M.3
-
131
-
-
34548485621
-
PIK3CA gene amplification in Japanese non-small cell lung cancer
-
Kawano O, Sasaki H, Okuda K, et al. PIK3CA gene amplification in Japanese non-small cell lung cancer. Lung Cancer 2007;58:159-160.
-
(2007)
Lung Cancer
, vol.58
, pp. 159-160
-
-
Kawano, O.1
Sasaki, H.2
Okuda, K.3
-
132
-
-
38949101107
-
Expression signatures in lung cancer reveal a profile for EGFR-mutant tumours and identify selective PIK3CA overexpression by gene amplification
-
Angulo B, Suarez-Gauthier A, Lopez-Rios F, et al. Expression signatures in lung cancer reveal a profile for EGFR-mutant tumours and identify selective PIK3CA overexpression by gene amplification. J Pathol 2008;214:347-356.
-
(2008)
J Pathol
, vol.214
, pp. 347-356
-
-
Angulo, B.1
Suarez-Gauthier, A.2
Lopez-Rios, F.3
-
133
-
-
0036645101
-
Genomic copy number analysis of non-small cell lung cancer using array comparative genomic hybridization: Implications of the phosphatidylinositol 3-kinase pathway
-
Massion PP, Kuo WL, Stokoe D, et al. Genomic copy number analysis of non-small cell lung cancer using array comparative genomic hybridization: implications of the phosphatidylinositol 3-kinase pathway. Cancer Res 2002;62:3636-3640.
-
(2002)
Cancer Res
, vol.62
, pp. 3636-3640
-
-
Massion, P.P.1
Kuo, W.L.2
Stokoe, D.3
-
134
-
-
8444240824
-
Early involvement of the phosphatidylinositol 3-kinase/Akt pathway in lung cancer progression
-
Massion PP, Taflan PM, Shyr Y, et al. Early involvement of the phosphatidylinositol 3-kinase/Akt pathway in lung cancer progression. Am J Respir Crit Care Med 2004;170:1088-1094.
-
(2004)
Am J Respir Crit Care Med
, vol.170
, pp. 1088-1094
-
-
Massion, P.P.1
Taflan, P.M.2
Shyr, Y.3
-
135
-
-
0036645286
-
Inactivation of LKB1/STK11 is a common event in adenocarcinomas of the lung
-
Sanchez-Cespedes M, Parrella P, Esteller M, et al. Inactivation of LKB1/STK11 is a common event in adenocarcinomas of the lung. Cancer Res 2002;62:3659-3662.
-
(2002)
Cancer Res
, vol.62
, pp. 3659-3662
-
-
Sanchez-Cespedes, M.1
Parrella, P.2
Esteller, M.3
-
136
-
-
2542590883
-
Novel and natural knockout lung cancer cell lines for the LKB1/STK11 tumor suppressor gene
-
Carretero J, Medina PP, Pio R, Montuenga LM, Sanchez-Cespedes M. Novel and natural knockout lung cancer cell lines for the LKB1/STK11 tumor suppressor gene. Oncogene 2004;23:4037-4040.
-
(2004)
Oncogene
, vol.23
, pp. 4037-4040
-
-
Carretero, J.1
Medina, P.P.2
Pio, R.3
Montuenga, L.M.4
Sanchez-Cespedes, M.5
-
137
-
-
48249102662
-
Mutations in the LKB1 tumour suppressor are frequently detected in tumours from Caucasian but not Asian lung cancer patients
-
Koivunen JP, Kim J, Lee J, et al. Mutations in the LKB1 tumour suppressor are frequently detected in tumours from Caucasian but not Asian lung cancer patients. Br J Cancer 2008;99:245-252.
-
(2008)
Br J Cancer
, vol.99
, pp. 245-252
-
-
Koivunen, J.P.1
Kim, J.2
Lee, J.3
-
138
-
-
34748881277
-
LKB1 gene mutations in Japanese lung cancer patients
-
Onozato R, Kosaka T, Achiwa H, et al. LKB1 gene mutations in Japanese lung cancer patients. Cancer Sci 2007;98:1747-1751.
-
(2007)
Cancer Sci
, vol.98
, pp. 1747-1751
-
-
Onozato, R.1
Kosaka, T.2
Achiwa, H.3
-
139
-
-
68549083200
-
Detection of the transforming AKT1 mutation E17K in non-small cell lung cancer by high resolution melting
-
Do H, Solomon B, Mitchell PL, Fox SB, Dobrovic A. Detection of the transforming AKT1 mutation E17K in non-small cell lung cancer by high resolution melting. BMC Res Notes 2008;1:14.
-
(2008)
BMC Res Notes
, vol.1
, pp. 14
-
-
Do, H.1
Solomon, B.2
Mitchell, P.L.3
Fox, S.B.4
Dobrovic, A.5
-
141
-
-
80054748915
-
Phase i first-in-human study of the PI3 kinase inhibitor GSK2126458 (GSK458) in patients with advanced solid tumors (study P3K112826)
-
Munster PN, van der Noll R, Voest EE, et al. Phase I first-in-human study of the PI3 kinase inhibitor GSK2126458 (GSK458) in patients with advanced solid tumors (study P3K112826). ASCO Meet Abstr 2011;29:3018.
-
(2011)
ASCO Meet Abstr
, vol.29
, pp. 3018
-
-
Munster, P.N.1
Van Der Noll, R.2
Voest, E.E.3
-
142
-
-
43249131245
-
Dose- and schedule-dependent inhibition of the mammalian target of rapamycin pathway with everolimus: A phase i tumor pharmacodynamic study in patients with advanced solid tumors
-
Tabernero J, Rojo F, Calvo E, et al. Dose- and schedule-dependent inhibition of the mammalian target of rapamycin pathway with everolimus: a phase I tumor pharmacodynamic study in patients with advanced solid tumors. J Clin Oncol 2008;26:1603-1610.
-
(2008)
J Clin Oncol
, vol.26
, pp. 1603-1610
-
-
Tabernero, J.1
Rojo, F.2
Calvo, E.3
-
143
-
-
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 2004;22:2336-2347.
-
(2004)
J Clin Oncol
, vol.22
, pp. 2336-2347
-
-
Raymond, E.1
Alexandre, J.2
Faivre, S.3
-
144
-
-
77952236657
-
Phase I, pharmacokinetic study of temsirolimus administered orally to patients with advanced cancer
-
Buckner JC, Forouzesh B, Erlichman C, et al. Phase I, pharmacokinetic study of temsirolimus administered orally to patients with advanced cancer. Invest New Drugs 2010;28:334-342.
-
(2010)
Invest New Drugs
, vol.28
, pp. 334-342
-
-
Buckner, J.C.1
Forouzesh, B.2
Erlichman, C.3
-
145
-
-
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 2009;15:1428-1434.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 1428-1434
-
-
Hartford, C.M.1
Desai, A.A.2
Janisch, L.3
-
146
-
-
80054741601
-
First-in-human phase i study evaluating the safety, pharmacokinetics (PK), and intratumor pharmacodynamics (PD) of the novel, oral, ATP-competitive Akt inhibitor GDC-0068
-
Tabernero J, Saura C, Roda Perez D, et al. First-in-human phase I study evaluating the safety, pharmacokinetics (PK), and intratumor pharmacodynamics (PD) of the novel, oral, ATP-competitive Akt inhibitor GDC-0068. ASCO Meet Abstr 2011;29:3022.
-
(2011)
ASCO Meet Abstr
, vol.29
, pp. 3022
-
-
Tabernero, J.1
Saura, C.2
Roda Perez, D.3
-
147
-
-
9344270514
-
A phase i trial of perifosine (NSC 639966) on a loading dose/maintenance dose schedule in patients with advanced cancer
-
Van Ummersen L, Binger K, Volkman J, et al. A phase I trial of perifosine (NSC 639966) on a loading dose/maintenance dose schedule in patients with advanced cancer. Clin Cancer Res 2004;10:7450-7456.
-
(2004)
Clin Cancer Res
, vol.10
, pp. 7450-7456
-
-
Van Ummersen, L.1
Binger, K.2
Volkman, J.3
|