-
1
-
-
84905579152
-
ALK-positive non-small cell lung cancer: mechanisms of resistance and emerging treatment options
-
[1] Steuer, C.E., Ramalingam, S.S., ALK-positive non-small cell lung cancer: mechanisms of resistance and emerging treatment options. Cancer 120 (2014), 2392–2402.
-
(2014)
Cancer
, vol.120
, pp. 2392-2402
-
-
Steuer, C.E.1
Ramalingam, S.S.2
-
2
-
-
84879071011
-
Crizotinib versus chemotherapy in advanced ALK-positive lung cancer
-
[2] Shaw, A.T., Kim, D.W., Nakagawa, K., Seto, T., Crino, L., Ahn, M.J., et al. Crizotinib versus chemotherapy in advanced ALK-positive lung cancer. N. Engl. J. Med. 368 (2013), 2385–2394.
-
(2013)
N. Engl. J. Med.
, vol.368
, pp. 2385-2394
-
-
Shaw, A.T.1
Kim, D.W.2
Nakagawa, K.3
Seto, T.4
Crino, L.5
Ahn, M.J.6
-
3
-
-
84896957081
-
Ceritinib in ALK-rearranged non-small-cell lung cancer
-
[3] Shaw, A.T., Kim, D.W., Mehra, R., Tan, D.S., Felip, E., Chow, L.Q., et al. Ceritinib in ALK-rearranged non-small-cell lung cancer. N. Engl. J. Med. 370 (2014), 1189–1197.
-
(2014)
N. Engl. J. Med.
, vol.370
, pp. 1189-1197
-
-
Shaw, A.T.1
Kim, D.W.2
Mehra, R.3
Tan, D.S.4
Felip, E.5
Chow, L.Q.6
-
4
-
-
54049149961
-
Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma
-
[4] Janoueix-Lerosey, I., Lequin, D., Brugieres, L., Ribeiro, A., de Pontual, L., Combaret, V., et al. Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma. Nature 455 (2008), 967–970.
-
(2008)
Nature
, vol.455
, pp. 967-970
-
-
Janoueix-Lerosey, I.1
Lequin, D.2
Brugieres, L.3
Ribeiro, A.4
de Pontual, L.5
Combaret, V.6
-
5
-
-
54049094708
-
Identification of ALK as a major familial neuroblastoma predisposition gene
-
[5] Mosse, Y.P., Laudenslager, M., Longo, L., Cole, K.A., Wood, A., Attiyeh, E.F., et al. Identification of ALK as a major familial neuroblastoma predisposition gene. Nature 455 (2008), 930–935.
-
(2008)
Nature
, vol.455
, pp. 930-935
-
-
Mosse, Y.P.1
Laudenslager, M.2
Longo, L.3
Cole, K.A.4
Wood, A.5
Attiyeh, E.F.6
-
6
-
-
84925687730
-
Identification of a novel HIP1-ALK fusion variant in Non-Small-Cell Lung Cancer (NSCLC) and discovery of ALK I1171 (I1171N/S) mutations in two ALK-rearranged NSCLC patients with resistance to alectinib
-
[6] Ou, S.H., Klempner, S.J., Greenbowe, J.R., Azada, M., Schrock, A.B., Ali, S.M., et al. Identification of a novel HIP1-ALK fusion variant in Non-Small-Cell Lung Cancer (NSCLC) and discovery of ALK I1171 (I1171N/S) mutations in two ALK-rearranged NSCLC patients with resistance to alectinib. J. Thorac. Oncol. 9 (2014), 1821–1825.
-
(2014)
J. Thorac. Oncol.
, vol.9
, pp. 1821-1825
-
-
Ou, S.H.1
Klempner, S.J.2
Greenbowe, J.R.3
Azada, M.4
Schrock, A.B.5
Ali, S.M.6
-
7
-
-
84926421984
-
Secondary mutations at I1171 in the ALK gene confer resistance to both crizotinib and alectinib
-
[7] Toyokawa, G., Hirai, F., Inamasu, E., Yoshida, T., Nosaki, K., Takenaka, T., et al. Secondary mutations at I1171 in the ALK gene confer resistance to both crizotinib and alectinib. J. Thorac. Oncol. 9 (2014), e86–7.
-
(2014)
J. Thorac. Oncol.
, vol.9
, pp. e86-7
-
-
Toyokawa, G.1
Hirai, F.2
Inamasu, E.3
Yoshida, T.4
Nosaki, K.5
Takenaka, T.6
-
8
-
-
84926421697
-
I1171 missense mutation (particularly I1171N) is a common resistance mutation in ALK-positive NSCLC patients who have progressive disease while on alectinib and is sensitive to ceritinib
-
[8] Ou, S.H., Greenbowe, J., Khan, Z.U., Azada, M.C., Ross, J.S., Stevens, P.J., et al. I1171 missense mutation (particularly I1171N) is a common resistance mutation in ALK-positive NSCLC patients who have progressive disease while on alectinib and is sensitive to ceritinib. Lung Cancer 88 (2015), 231–234.
-
(2015)
Lung Cancer
, vol.88
, pp. 231-234
-
-
Ou, S.H.1
Greenbowe, J.2
Khan, Z.U.3
Azada, M.C.4
Ross, J.S.5
Stevens, P.J.6
-
9
-
-
84984918388
-
Detection of tumor ALK status in neuroblastoma patients using peripheral blood
-
[9] Combaret, V., Iacono, I., Bellini, A., Brejon, S., Bernard, V., Marabelle, A., et al. Detection of tumor ALK status in neuroblastoma patients using peripheral blood. Cancer Med. 4 (2015), 540–550.
-
(2015)
Cancer Med.
, vol.4
, pp. 540-550
-
-
Combaret, V.1
Iacono, I.2
Bellini, A.3
Brejon, S.4
Bernard, V.5
Marabelle, A.6
-
10
-
-
61549108338
-
EGFR T790M mutation: a double role in lung cancer cell survival?
-
[10] Suda, K., Onozato, R., Yatabe, Y., Mitsudomi, T., EGFR T790M mutation: a double role in lung cancer cell survival?. J. Thorac. Oncol. 4 (2009), 1–4.
-
(2009)
J. Thorac. Oncol.
, vol.4
, pp. 1-4
-
-
Suda, K.1
Onozato, R.2
Yatabe, Y.3
Mitsudomi, T.4
-
11
-
-
84960423132
-
Monitoring of treatment responses and clonal evolution of tumor cells by circulating tumor DNA of heterogeneous mutant EGFR genes in lung cancer
-
[11] Imamura, F., Uchida, J., Kukita, Y., Kumagai, T., Nishino, K., Inoue, T., et al. Monitoring of treatment responses and clonal evolution of tumor cells by circulating tumor DNA of heterogeneous mutant EGFR genes in lung cancer. Lung Cancer 94 (2016), 68–73.
-
(2016)
Lung Cancer
, vol.94
, pp. 68-73
-
-
Imamura, F.1
Uchida, J.2
Kukita, Y.3
Kumagai, T.4
Nishino, K.5
Inoue, T.6
-
12
-
-
84958569032
-
Plasma EGFR T790M ctDNA status is associated with clinical outcome in advanced NSCLC patients with acquired EGFR-TKI resistance
-
[12] Zheng, D., Ye, X., Zhang, M.Z., Sun, Y., Wang, J.Y., Ni, J., et al. Plasma EGFR T790M ctDNA status is associated with clinical outcome in advanced NSCLC patients with acquired EGFR-TKI resistance. Sci. Rep., 6, 2016, 20913.
-
(2016)
Sci. Rep.
, vol.6
, pp. 20913
-
-
Zheng, D.1
Ye, X.2
Zhang, M.Z.3
Sun, Y.4
Wang, J.Y.5
Ni, J.6
-
13
-
-
84872020299
-
Cancer genome scanning in plasma: detection of tumor-associated copy number aberrations, single-nucleotide variants, and tumoral heterogeneity by massively parallel sequencing
-
[13] Chan, K.C., Jiang, P., Zheng, Y.W., Liao, G.J., Sun, H., Wong, J., et al. Cancer genome scanning in plasma: detection of tumor-associated copy number aberrations, single-nucleotide variants, and tumoral heterogeneity by massively parallel sequencing. Clin. Chem. 59 (2013), 211–224.
-
(2013)
Clin. Chem.
, vol.59
, pp. 211-224
-
-
Chan, K.C.1
Jiang, P.2
Zheng, Y.W.3
Liao, G.J.4
Sun, H.5
Wong, J.6
|