-
1
-
-
7144248725
-
Plant antitumour agents. I. The isolation and structure of camptothecin, a novel alkaloidal leukemia and tumor inhibitor from Camptotheca acuminata
-
Wall M, Wani M, Cook C et al. Plant antitumour agents. I. The isolation and structure of camptothecin, a novel alkaloidal leukemia and tumor inhibitor from Camptotheca acuminata. J Am Chem Soc 1966; 94: 3888-3890.
-
(1966)
J. Am. Chem. Soc.
, vol.94
, pp. 3888-3890
-
-
Wall, M.1
Wani, M.2
Cook, C.3
-
2
-
-
0015451631
-
Action of camptothecin on mammalian cells in culture
-
Li LH, Fraser TJ, Olin EJ et al. Action of camptothecin on mammalian cells in culture. Cancer Res 1972; 32: 2643-2650.
-
(1972)
Cancer Res.
, vol.32
, pp. 2643-2650
-
-
Li, L.H.1
Fraser, T.J.2
Olin, E.J.3
-
3
-
-
0016052023
-
Lethal activity of camptothecin sodium on human lymphoma cells
-
Drewinko B, Freireich EJ, Gottlieb JA. Lethal activity of camptothecin sodium on human lymphoma cells. Cancer Res 1974; 34: 747-750.
-
(1974)
Cancer Res.
, vol.34
, pp. 747-750
-
-
Drewinko, B.1
Freireich, E.J.2
Gottlieb, J.A.3
-
4
-
-
0015044313
-
Studies on the antitumor activity, mechanism of action, and cell cycle effects of camptothecin
-
Gallo RC, Whang-Peng J, Adamson RH. Studies on the antitumor activity, mechanism of action, and cell cycle effects of camptothecin. J Natl Cancer Inst 1971; 46: 789-795.
-
(1971)
J. Natl. Cancer Inst.
, vol.46
, pp. 789-795
-
-
Gallo, R.C.1
Whang-Peng, J.2
Adamson, R.H.3
-
5
-
-
0024229066
-
Evidence that DNA topoisomerase I is necessary for the cytotoxic effects of camptothecin
-
Eng WK, Faucette L, Johnson RK et al. Evidence that DNA topoisomerase I is necessary for the cytotoxic effects of camptothecin. Mol Pharmacol 1988; 34: 755-760.
-
(1988)
Mol. Pharmacol.
, vol.34
, pp. 755-760
-
-
Eng, W.K.1
Faucette, L.2
Johnson, R.K.3
-
6
-
-
0024560495
-
Structure-activity study of the actions of camptothecin derivatives on mammalian topoisomerase I: Evidence for a specific receptor site and a relation to antitumor activity
-
Jaxel C, Kohn KW, Wani MC et al. Structure-activity study of the actions of camptothecin derivatives on mammalian topoisomerase I: evidence for a specific receptor site and a relation to antitumor activity. Cancer Res 1989; 49: 1465-1469.
-
(1989)
Cancer Res.
, vol.49
, pp. 1465-1469
-
-
Jaxel, C.1
Kohn, K.W.2
Wani, M.C.3
-
7
-
-
0023924786
-
Identification of mammalian DNA topoisomerase I as an intracellular target of the anticancer drug camptothecin
-
Hsiang YH, Liu LF. Identification of mammalian DNA topoisomerase I as an intracellular target of the anticancer drug camptothecin. Cancer Res 1988; 48: 1722-1726.
-
(1988)
Cancer Res.
, vol.48
, pp. 1722-1726
-
-
Hsiang, Y.H.1
Liu, L.F.2
-
8
-
-
0030826929
-
Topoisomerase I inhibitors: Review and update
-
Rothenberg ML. Topoisomerase I inhibitors: review and update. Ann Oncol 1997; 8: 837-855.
-
(1997)
Ann. Oncol.
, vol.8
, pp. 837-855
-
-
Rothenberg, M.L.1
-
9
-
-
0015378084
-
Phase I clinical trial of weekly and daily treatment with camptothecin (NSC-100880): Correlation with preclinical studies
-
Muggia FM, Creaven PJ, Hansen HH et al. Phase I clinical trial of weekly and daily treatment with camptothecin (NSC-100880): correlation with preclinical studies. Cancer Chemother Rep 1972; 56: 515-521.
-
(1972)
Cancer Chemother. Rep.
, vol.56
, pp. 515-521
-
-
Muggia, F.M.1
Creaven, P.J.2
Hansen, H.H.3
-
11
-
-
0032585232
-
Randomised trial of irinotecan plus supportive care versus supportive care alone after fluorouracil failure for patients with metastatic colorectal cancer
-
Cunningham D, Pyrhonen S, James RD et al. Randomised trial of irinotecan plus supportive care versus supportive care alone after fluorouracil failure for patients with metastatic colorectal cancer. Lancet 1998; 352: 1413-1418.
-
(1998)
Lancet
, vol.352
, pp. 1413-1418
-
-
Cunningham, D.1
Pyrhonen, S.2
James, R.D.3
-
12
-
-
0032585197
-
Randomised trial of irinotecan versus fluorouracil by continuous infusion after fluorouracil failure in patients with metastatic colorectal cancer
-
Rougier P, Van Cutsem E, Bajetta E et al. Randomised trial of irinotecan versus fluorouracil by continuous infusion after fluorouracil failure in patients with metastatic colorectal cancer. Lancet 1998; 352: 1407-1412.
-
(1998)
Lancet
, vol.352
, pp. 1407-1412
-
-
Rougier, P.1
Van Cutsem, E.2
Bajetta, E.3
-
13
-
-
0034727063
-
Irinotecan plus fluorouracil and leucovorin for metastatic colorectal cancer
-
Irinotecan Study Group
-
Saltz LB, Cox JV, Blanke C et al. Irinotecan plus fluorouracil and leucovorin for metastatic colorectal cancer. Irinotecan Study Group. N Engl J Med 2000; 343: 905-914.
-
(2000)
N. Engl. J. Med.
, vol.343
, pp. 905-914
-
-
Saltz, L.B.1
Cox, J.V.2
Blanke, C.3
-
14
-
-
0034712536
-
Irinotecan combined with fluorouracil compared with fluorouracil alone as first-line treatment for metastatic colorectal cancer: A multicentre randomised trial
-
Douillard JY, Cunningham D, Roth AD et al. Irinotecan combined with fluorouracil compared with fluorouracil alone as first-line treatment for metastatic colorectal cancer: a multicentre randomised trial. Lancet 2000; 355: 1041-1047.
-
(2000)
Lancet
, vol.355
, pp. 1041-1047
-
-
Douillard, J.Y.1
Cunningham, D.2
Roth, A.D.3
-
15
-
-
10544229791
-
Topotecan, an active drug in the second-line treatment of epithelial ovarian cancer: Results of a large European phase II study
-
Creemers GJ, Bolis G, Gore M et al. Topotecan, an active drug in the second-line treatment of epithelial ovarian cancer: results of a large European phase II study. J Clin Oncol 1996; 14: 56-61.
-
(1996)
J. Clin. Oncol.
, vol.14
, pp. 56-61
-
-
Creemers, G.J.1
Bolis, G.2
Gore, M.3
-
16
-
-
0030900145
-
Topotecan versus paclitaxel for the treatment of recurrent epithelial ovarian cancer
-
Ten Bokkel Huinink W, Gore M, Carmichael J et al. Topotecan versus paclitaxel for the treatment of recurrent epithelial ovarian cancer. J Clin Oncol 1997: 15: 2183-2189.
-
(1997)
J. Clin. Oncol.
, vol.15
, pp. 2183-2189
-
-
Ten Bokkel Huinink, W.1
Gore, M.2
Carmichael, J.3
-
17
-
-
0031786482
-
Topotecan for the treatment of advanced epithelial ovarian cancer: An open-label phase II study in patients treated after prior chemotherapy that contained cisplatin or carboplatin and paclitaxel
-
Bookman MA, Malmstrom H, Bolis G et al. Topotecan for the treatment of advanced epithelial ovarian cancer: an open-label phase II study in patients treated after prior chemotherapy that contained cisplatin or carboplatin and paclitaxel. J Clin Oncol 1998; 16: 3345-3352.
-
(1998)
J. Clin. Oncol.
, vol.16
, pp. 3345-3352
-
-
Bookman, M.A.1
Malmstrom, H.2
Bolis, G.3
-
18
-
-
0029150444
-
A new water-soluble camptothecin derivative, DX-8951f, exhibits potent antitumor activity against human tumors in vitro and in vivo
-
Mitsui I, Kumazawa E, Hirota Y et al. A new water-soluble camptothecin derivative, DX-8951f, exhibits potent antitumor activity against human tumors in vitro and in vivo. Jpn J Cancer Res 1995; 86: 776-782.
-
(1995)
Jpn. J. Cancer Res.
, vol.86
, pp. 776-782
-
-
Mitsui, I.1
Kumazawa, E.2
Hirota, Y.3
-
19
-
-
0030805173
-
Antitumor effect of DX-8951, a novel camptothecin analog, on human pancreatic tumor cells and their CPT-11-resistant variants cultured in vitro and xenografted into nude mice
-
Takiguchi S, Kumazawa E, Shimazoe T et al. Antitumor effect of DX-8951, a novel camptothecin analog, on human pancreatic tumor cells and their CPT-11-resistant variants cultured in vitro and xenografted into nude mice. Jpn J Cancer Res 1997; 88: 760-769.
-
(1997)
Jpn. J. Cancer Res.
, vol.88
, pp. 760-769
-
-
Takiguchi, S.1
Kumazawa, E.2
Shimazoe, T.3
-
20
-
-
0033911659
-
Growth inhibitory effect of a new camptothecin analog, DX-8951f, on various drug-resistant sublines including BCRP-mediated camptothecin derivative-resistant variants derived from the human lung cancer cell line PC-6
-
Ishii M, Iwahana M, Mitsui I et al. Growth inhibitory effect of a new camptothecin analog, DX-8951f, on various drug-resistant sublines including BCRP-mediated camptothecin derivative-resistant variants derived from the human lung cancer cell line PC-6. Anticancer Drugs 2000; 11: 353-356.
-
(2000)
Anticancer Drugs
, vol.11
, pp. 353-356
-
-
Ishii, M.1
Iwahana, M.2
Mitsui, I.3
-
21
-
-
0030785681
-
DX-8951f, a water-soluble camptothecin analog, exhibits potent antitumor activity against a human lung cancer cell line and its SN-38-resistant variant
-
Joto N, Ishii M, Minami M et al. DX-8951f, a water-soluble camptothecin analog, exhibits potent antitumor activity against a human lung cancer cell line and its SN-38-resistant variant. Int J Cancer 1997; 72: 80-86.
-
(1997)
Int. J. Cancer
, vol.72
, pp. 80-86
-
-
Joto, N.1
Ishii, M.2
Minami, M.3
-
22
-
-
0034906472
-
Circumvention of breast cancer resistance protein (BCRP)-mediated resistance to camptothecins in vitro using non-substrate drugs or the BCRP inhibitor GF120918
-
Maliepaard M, van Gastelen MA, Tohgo A et al. Circumvention of breast cancer resistance protein (BCRP)-mediated resistance to camptothecins in vitro using non-substrate drugs or the BCRP inhibitor GF120918. Clin Cancer Res 2001; 7: 935-941.
-
(2001)
Clin. Cancer Res.
, vol.7
, pp. 935-941
-
-
Maliepaard, M.1
van Gastelen, M.A.2
Tohgo, A.3
-
23
-
-
0031869877
-
Potent and broad antitumor effects of DX-8951f, a water-soluble camptothecin derivative, against various human tumors xenografted in nude mice
-
Kumazawa E, Jimbo T, Ochi Y et al. Potent and broad antitumor effects of DX-8951f, a water-soluble camptothecin derivative, against various human tumors xenografted in nude mice. Cancer Chemother Pharmacol 1998; 42: 210-220.
-
(1998)
Cancer Chemother. Pharmacol.
, vol.42
, pp. 210-220
-
-
Kumazawa, E.1
Jimbo, T.2
Ochi, Y.3
-
24
-
-
0033976287
-
The topoisomerase I inhibitor DX-8951f is active in a severe combined immunodeficient mouse model of human acute myelogenous leukemia
-
Vey N, Giles FJ, Kantarjian H et al. The topoisomerase I inhibitor DX-8951f is active in a severe combined immunodeficient mouse model of human acute myelogenous leukemia. Clin Cancer Res 2000; 6: 731-736.
-
(2000)
Clin. Cancer Res.
, vol.6
, pp. 731-736
-
-
Vey, N.1
Giles, F.J.2
Kantarjian, H.3
-
25
-
-
0037694046
-
DX-8951f: Single intravenous dose toxicity study in dogs
-
Daiichi Pharmaceutical Co. Ltd. In house study report (8951J-TOXO19)
-
Kajimura T. DX-8951f: Single intravenous dose toxicity study in dogs. Daiichi Pharmaceutical Co. Ltd. In house study report (8951J-TOXO19), 1996.
-
(1996)
-
-
Kajimura, T.1
-
26
-
-
0037694055
-
-
ICH Harmonised Tripartite Guidelines for Good Clinical Practice: CPMP/ICH/135/95 which applies to all studies commencing after 17 January
-
ICH Harmonised Tripartite Guidelines for Good Clinical Practice: CPMP/ICH/135/95 which applies to all studies commencing after 17 January, 1997.
-
(1997)
-
-
-
27
-
-
0037694053
-
-
Declaration of Helsinki: Recommendations guiding physicians in biomedical research involving human subjects
-
Declaration of Helsinki: Recommendations guiding physicians in biomedical research involving human subjects, 1989.
-
(1989)
-
-
-
28
-
-
0038708535
-
-
National Cancer Institute: Guidelines for the Reporting of Adverse Drug Reactions. Bethesda, MD, Division of Cancer Treatment, National Cancer Institute
-
National Cancer Institute: Guidelines for the Reporting of Adverse Drug Reactions. Bethesda, MD, Division of Cancer Treatment, National Cancer Institute 1988.
-
(1988)
-
-
-
29
-
-
0027076295
-
Southwest Oncology Group standard response criteria, endpoint definitions and toxicity criteria
-
Green S, Weiss G. Southwest Oncology Group standard response criteria, endpoint definitions and toxicity criteria. Invest New Drugs 1992; 10: 239-253.
-
(1992)
Invest. New Drugs
, vol.10
, pp. 239-253
-
-
Green, S.1
Weiss, G.2
-
30
-
-
0034647066
-
Sensitive high-performance liquid chromatographic method for the determination of the lactone form and the lactone plus hydroxy-acid forms of the new camptothecin derivative DX-8951 in human plasma using fluorescence detection
-
Oguma T, Ohshima Y, Nakaoka M. Sensitive high-performance liquid chromatographic method for the determination of the lactone form and the lactone plus hydroxy-acid forms of the new camptothecin derivative DX-8951 in human plasma using fluorescence detection. J Chromatogr B Biomed Sci Appl 2000; 740: 237-245.
-
(2000)
J. Chromatogr. B Biomed. Sci. Appl.
, vol.740
, pp. 237-245
-
-
Oguma, T.1
Ohshima, Y.2
Nakaoka, M.3
-
31
-
-
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 2000; 18: 3151-3163.
-
(2000)
J. Clin. Oncol.
, vol.18
, pp. 3151-3163
-
-
Rowinsky, E.K.1
Johnson, T.R.2
Geyer C.E., Jr.3
-
32
-
-
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 2000; 18: 3986-3992.
-
(2000)
J. Clin. Oncol.
, vol.18
, pp. 3986-3992
-
-
Boige, V.1
Raymond, E.2
Faivre, S.3
-
34
-
-
0035281536
-
Phase I and pharmacokinetic study of exatecan mesylate (DX-8951f): A novel camptothecin analog
-
Royce ME, Hoff PM, Dumas P et al. Phase I and pharmacokinetic study of exatecan mesylate (DX-8951f): a novel camptothecin analog. J Clin Oncol 2001; 19: 1493-1500.
-
(2001)
J. Clin. Oncol.
, vol.19
, pp. 1493-1500
-
-
Royce, M.E.1
Hoff, P.M.2
Dumas, P.3
-
35
-
-
0029966916
-
Phase I and pharmacologic study of topotecan in patients with impaired renal function
-
O'Reilly S, Rowinsky EK, Slichenmyer W et al. Phase I and pharmacologic study of topotecan in patients with impaired renal function. J Clin Oncol 1996; 14: 3062-3073.
-
(1996)
J. Clin. Oncol.
, vol.14
, pp. 3062-3073
-
-
O'Reilly, S.1
Rowinsky, E.K.2
Slichenmyer, W.3
|