-
1
-
-
0027447420
-
The current status of camptothecin analogs as anticancer agents
-
Slichenmyer, W. J. Rowinsky, E. K., Donehower, R. C., and Kaufmann, S. H. The current status of camptothecin analogs as anticancer agents. J. Natl. Cancer Inst. (Bethesda), 85: 272-291, 1993.
-
(1993)
J. Natl. Cancer Inst. (Bethesda)
, vol.85
, pp. 272-291
-
-
Slichenmyer, W.J.1
Rowinsky, E.K.2
Donehower, R.C.3
Kaufmann, S.H.4
-
2
-
-
0031438522
-
Water-soluble campothecin derivatives
-
Bedeschi, A., Candiani, I., Geroni, C., and Capolongo, L. Water-soluble campothecin derivatives. Drugs of the Future, 22: 1259-1266, 1997.
-
(1997)
Drugs of the Future
, vol.22
, pp. 1259-1266
-
-
Bedeschi, A.1
Candiani, I.2
Geroni, C.3
Capolongo, L.4
-
3
-
-
0031311573
-
DNA topoisomerase I-inhibitors
-
Takimoto, C. H., Kieffer, L. V., and Arbuck, S. G. DNA topoisomerase I-inhibitors. Cancer Chemother. Bio. Resp. Mod., 17: 80-113, 1997.
-
(1997)
Cancer Chemother. Bio. Resp. Mod.
, vol.17
, pp. 80-113
-
-
Takimoto, C.H.1
Kieffer, L.V.2
Arbuck, S.G.3
-
4
-
-
0033865857
-
-
Verschraegen, C. F., Royce, M. Hammond, L., and Rowinsky, E. K. Exatecan. Curr. Opin. Oncol. End. Met. Invest. Drugs, 2: 312-313, 2000.
-
(2000)
Exatecan. Curr. Opin. Oncol. End. Met. Invest. Drugs
, vol.2
, pp. 312-313
-
-
Verschraegen, C.F.1
Royce, M.2
Hammond, L.3
Rowinsky, E.K.4
-
5
-
-
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., Aonuma, M., Sugimori, M., Ohsuki, S., Uoto, K., Ejima, A., Terasawa, H., and Sato, K. A new water-soluble camptothecin derivative, DX-8951f, exhibits potent antitumor activity against human tumors in vitro and in vivo. Jpn. J. Cancer Res., 86: 776-782, 1995.
-
(1995)
Jpn. J. Cancer Res.
, vol.86
, pp. 776-782
-
-
Mitsui, I.1
Kumazawa, E.2
Hirota, Y.3
Aonuma, M.4
Sugimori, M.5
Ohsuki, S.6
Uoto, K.7
Ejima, A.8
Terasawa, H.9
Sato, K.10
-
6
-
-
0032440216
-
Characterization of a human small-cell lung cancer cell line resistant to a new water-soluble camptothecin derivative, DX-8951f
-
Nomoto, T., Nishio, K., Ishidia, T., Mori, M., and Saijo, N. Characterization of a human small-cell lung cancer cell line resistant to a new water-soluble camptothecin derivative, DX-8951f. Jpn. J. Cancer Res., 89: 1179-1186, 1998.
-
(1998)
Jpn. J. Cancer Res.
, vol.89
, pp. 1179-1186
-
-
Nomoto, T.1
Nishio, K.2
Ishidia, T.3
Mori, M.4
Saijo, N.5
-
7
-
-
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., Tohgo, A., and Kono, A. 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., 88: 760-769, 1997.
-
(1997)
Jpn. J. Cancer Res.
, vol.88
, pp. 760-769
-
-
Takiguchi, S.1
Kumazawa, E.2
Shimazoe, T.3
Tohgo, A.4
Kono, A.5
-
8
-
-
0030785681
-
DX8951f, 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., Kuga, H., Mitsui, I., and Tohgo, A. DX8951f, 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, 72: 680-686, 1997.
-
(1997)
Int. J. Cancer
, vol.72
, pp. 680-686
-
-
Joto, N.1
Ishii, M.2
Minami, M.3
Kuga, H.4
Mitsui, I.5
Tohgo, A.6
-
9
-
-
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., and Tohgo, A. Potent and broad antitumor effects of DX-8951f, a water-soluble camptothecin derivative, against various human tumors xenografted in nude mice. Cancer Chemother. Pharmacol. 42: 210-220, 1998.
-
(1998)
Cancer Chemother. Pharmacol.
, vol.42
, pp. 210-220
-
-
Kumazawa, E.1
Jimbo, T.2
Ochi, Y.3
Tohgo, A.4
-
10
-
-
0026772298
-
Effect of P-glycoprotein expression on accumulation and cytotoxicity of topotecan (SK &F 104864), a new camptothecin analog
-
Hendricks, C. B., Rowinsky, E. K., Grochow, L. B., Donehower, R. C., and Kaufmann, S. H. Effect of P-glycoprotein expression on accumulation and cytotoxicity of topotecan (SK &F 104864), a new camptothecin analog. Cancer Res., 52: 2268-2278, 1992.
-
(1992)
Cancer Res.
, vol.52
, pp. 2268-2278
-
-
Hendricks, C.B.1
Rowinsky, E.K.2
Grochow, L.B.3
Donehower, R.C.4
Kaufmann, S.H.5
-
11
-
-
0026339352
-
Camptothecin overcomes mdr1-mediated resistance in human KB carcinoma cells
-
Chen, A. Y., Yu, C., Potmesil, M., Wall, M. E., Wani, M. C., and Liu, L. F. Camptothecin overcomes mdr1-mediated resistance in human KB carcinoma cells. Cancer Res., 51: 6039-6044, 1991.
-
(1991)
Cancer Res.
, vol.51
, pp. 6039-6044
-
-
Chen, A.Y.1
Yu, C.2
Potmesil, M.3
Wall, M.E.4
Wani, M.C.5
Liu, L.F.6
-
12
-
-
0023864510
-
Antitumor activity of CPT-11, a new derivative of camptothecin, against pleotropic drug resistant tumors in vitro and in vivo
-
Tsuruo, T., Matsuzaki, T., Matsushita, M., Saito, H., and Yokokura, T. Antitumor activity of CPT-11, a new derivative of camptothecin, against pleotropic drug resistant tumors in vitro and in vivo. Cancer Chemother. Pharmacol., 21: 71-74, 1988.
-
(1988)
Cancer Chemother. Pharmacol.
, vol.21
, pp. 71-74
-
-
Tsuruo, T.1
Matsuzaki, T.2
Matsushita, M.3
Saito, H.4
Yokokura, T.5
-
13
-
-
0027813132
-
In vitro and in vivo effects of clinically important camptothecin analogues in multi-drug resistant cells
-
Mattern, M. R., Hofmann, G. A., Polsky, R. M., Funk, L. R., McCabe, F. L., and Johnson, R. K. In vitro and in vivo effects of clinically important camptothecin analogues in multi-drug resistant cells. Oncol. Res., 5: 467-474, 1993.
-
(1993)
Oncol. Res.
, vol.5
, pp. 467-474
-
-
Mattern, M.R.1
Hofmann, G.A.2
Polsky, R.M.3
Funk, L.R.4
McCabe, F.L.5
Johnson, R.K.6
-
14
-
-
0034666736
-
BCRP/MXP/ABCP expression in topotecan resistant human breast carcinoma cells
-
Yang, C. H., Schneider, E., Kuo, M. L., Volk, E. L., Rocchi, E., and Chen, Y. C. BCRP/MXP/ABCP expression in topotecan resistant human breast carcinoma cells. Biochem. Pharmacol., 60: 831-837, 2000.
-
(2000)
Biochem. Pharmacol.
, vol.60
, pp. 831-837
-
-
Yang, C.H.1
Schneider, E.2
Kuo, M.L.3
Volk, E.L.4
Rocchi, E.5
Chen, Y.C.6
-
15
-
-
0033911659
-
Growth inhibitory effect of a new camptothecin analog, DX-8951f, on variant drug-resistant sublines including BCRP-mediated camptothecin derivative-resistant variants derived from the the human lung cancer cell line PC-6
-
Ishii, M., Iwana, M., Mitsui, I., Minami, M., and Imagawa, S. Growth inhibitory effect of a new camptothecin analog, DX-8951f, on variant drug-resistant sublines including BCRP-mediated camptothecin derivative-resistant variants derived from the the human lung cancer cell line PC-6. Anticancer Drugs, 11: 353-362, 2000.
-
(2000)
Anticancer Drugs
, vol.11
, pp. 353-362
-
-
Ishii, M.1
Iwana, M.2
Mitsui, I.3
Minami, M.4
Imagawa, S.5
-
16
-
-
0033865075
-
DX-8951f (exatecan mesylate), a hexacyclic camptothecin analog on a daily x 5 schedule: A Phase I and pharmacokinetic study in advanced solid malignancies
-
Rowinsky, E. K., Johnson, T. R., Geyer, C. E., Hammond, L. A., Eckhardt, S. G., Drengler, R., Smetzer, L., Coyle, J., Rizzo, J., Schwartz, G., Tolcher, A., Von Hoff, D. D., and De Jager, R. L. DX-8951f (exatecan mesylate), a hexacyclic camptothecin analog on a daily x 5 schedule: a Phase I and pharmacokinetic study in 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
Hammond, L.A.4
Eckhardt, S.G.5
Drengler, R.6
Smetzer, L.7
Coyle, J.8
Rizzo, J.9
Schwartz, G.10
Tolcher, A.11
Von Hoff, D.D.12
De Jager, R.L.13
-
17
-
-
0034796438
-
Phase I pharmacological study of a new camptothecin derivative, exatecan mesylate (DX-8951f), infused over 30 minutes every three weeks
-
Minami, H., Fujii, H., Igarashi, T., Itoh, K., Tamanoi, K., Oguma, T., and Sasaki, Y. Phase I and pharmacological study of a new camptothecin derivative, exatecan mesylate (DX-8951f), infused over 30 minutes every three weeks. Clin. Cancer Res., 7: 3056-3064, 2001.
-
(2001)
Clin. Cancer Res.
, vol.7
, pp. 3056-3064
-
-
Minami, H.1
Fujii, H.2
Igarashi, T.3
Itoh, K.4
Tamanoi, K.5
Oguma, T.6
Sasaki, Y.7
-
18
-
-
0035281536
-
Phase I pharmacokinetic study of exatecan mesylate (DX-8951f): A novel camptothecin analog
-
Royce, M. E., Hoff, P. M., Dumas, P., Lassere, Y., Lee, J. J., Coyle, J., Ducharme, M. P., De Jager, R., and Pazdur, R. Phase I pharmacokinetic study of exatecan mesylate (DX-8951f): a novel camptothecin analog. J. Clin. Oncol., 19: 1493-1500, 2001.
-
(2001)
J. Clin. Oncol.
, vol.19
, pp. 1493-1500
-
-
Royce, M.E.1
Hoff, P.M.2
Dumas, P.3
Lassere, Y.4
Lee, J.J.5
Coyle, J.6
Ducharme, M.P.7
De Jager, R.8
Pazdur, R.9
-
19
-
-
0033976287
-
The topoisomerase I inhibitor DX-8951f is active in a severe combined immunodeficient mouse model of human acute myelogenous leukemia
-
Vey, N., Giles, F. J., Kantarjian, H., Smith, T. L., Beran, M., and Jeha, S. The topoisomerase I inhibitor DX-8951f is active in a severe combined immunodeficient mouse model of human acute myelogenous leukemia. Clin. Cancer Res., 6: 731-736, 2000.
-
(2000)
Clin. Cancer Res.
, vol.6
, pp. 731-736
-
-
Vey, N.1
Giles, F.J.2
Kantarjian, H.3
Smith, T.L.4
Beran, M.5
Jeha, S.6
-
20
-
-
0000202077
-
Final results of a Phase II study of DX-8951f (exatecan mesylate) in advanced pancreatic cancer
-
D'Adamo, D., Hammond, L., Donehower, R., Sharma, S., Aird, S., Kelsen, D., Ochoa, L., Rowinsky, E. K., De Jagger, R., and O'Reilly, E. M. Final results of a Phase II study of DX-8951f (exatecan mesylate) in advanced pancreatic cancer. Proc. Am. Soc. Clin. Oncol., 20: 134a, 2001.
-
(2001)
Proc. Am. Soc. Clin. Oncol.
, vol.20
-
-
D'Adamo, D.1
Hammond, L.2
Donehower, R.3
Sharma, S.4
Aird, S.5
Kelsen, D.6
Ochoa, L.7
Rowinsky, E.K.8
De Jagger, R.9
O'Reilly, E.M.10
-
21
-
-
33748790566
-
Phase II trial of DX-8951f (exatecan mesylate) in hepatocellular carcinoma; a final analysis
-
Patt, Y. Z., Rowinsky, E., O'Reilly, E., Eckardt, S. G., Duggal, A., Lubicz, P., Dumas, A., Lubicz, P., Dumas, P., Brown, T., and De Jagger, R. Phase II trial of DX-8951f (exatecan mesylate) in hepatocellular carcinoma; a final analysis. Proc. Am. Soc. Clin. Oncol., 21: 139a, 2002.
-
(2002)
Proc. Am. Soc. Clin. Oncol.
, vol.21
-
-
Patt, Y.Z.1
Rowinsky, E.2
O'Reilly, E.3
Eckardt, S.G.4
Duggal, A.5
Lubicz, P.6
Dumas, A.7
Lubicz, P.8
Dumas, P.9
Brown, T.10
De Jagger, R.11
-
22
-
-
0028357995
-
Phase I trial of low-dose continuous topotecan infusion in patients with cancer: An active and well-tolerated regimen
-
Hochster, H., Liebes, L., Speyer, J., Sorich, J., Taubes, B., Oratz, R., Wernz, J., Chachoua, A., Raphael, B., Vinci, R. Z., et al. Phase I trial of low-dose continuous topotecan infusion in patients with cancer: an active and well-tolerated regimen. J. Clin. Oncol., 12: 553-559, 1994.
-
(1994)
J. Clin. Oncol.
, vol.12
, pp. 553-559
-
-
Hochster, H.1
Liebes, L.2
Speyer, J.3
Sorich, J.4
Taubes, B.5
Oratz, R.6
Wernz, J.7
Chachoua, A.8
Raphael, B.9
Vinci, R.Z.10
-
23
-
-
0030855529
-
Effect of prolonged topotecan infusion on topoisomerase 1 levels: A Phase I and pharmacodynamic study
-
Hochster, H., Liebes, L., Speyer, J., Sorich, J., Taubes, B., Oratz, R., Wernz, J., Chachoua, A., Blum, R. H., Zeleniuch-Jacquotte, A., et al. Effect of prolonged topotecan infusion on topoisomerase 1 levels: a Phase I and pharmacodynamic study. Clin. Cancer Res., 3: 1245-1252, 1997.
-
(1997)
Clin. Cancer Res.
, vol.3
, pp. 1245-1252
-
-
Hochster, H.1
Liebes, L.2
Speyer, J.3
Sorich, J.4
Taubes, B.5
Oratz, R.6
Wernz, J.7
Chachoua, A.8
Blum, R.H.9
Zeleniuch-Jacquotte, A.10
-
24
-
-
15444349406
-
Pharamcodynamics of topoisomerase I inhibition: Western blot determination of topoisomerase I and cleavable complex in patients with upper gastrointestinal malignancies treated with topotecan
-
Liebes, L., Potmesil, M., Kim, T., Pease, D., Buckley, M., Fry, D., Cho, J., Adler, H., Dar, K., Zeleniuch-Jacquotte, A., and Hochster, H. Pharamcodynamics of topoisomerase I inhibition: Western blot determination of topoisomerase I and cleavable complex in patients with upper gastrointestinal malignancies treated with topotecan. Clin. Cancer Res., 4: 545-557, 1998.
-
(1998)
Clin. Cancer Res.
, vol.4
, pp. 545-557
-
-
Liebes, L.1
Potmesil, M.2
Kim, T.3
Pease, D.4
Buckley, M.5
Fry, D.6
Cho, J.7
Adler, H.8
Dar, K.9
Zeleniuch-Jacquotte, A.10
Hochster, H.11
-
25
-
-
0038297962
-
A Phase I study of DE-310 administered as a 3-hour infusion every 4 weeks to patients with advanced solid tumors or lymphoma
-
Takimoto, C. H., Forero, F., Schwartz, G. H., Tolcher, A. W., Hammond, L., Patnaik, A., Ducharme, M., Cooke, B., De Jagger, R., and Rowinsky, E. K. A Phase I study of DE-310 administered as a 3-hour infusion every 4 weeks to patients with advanced solid tumors or lymphoma. Eur. J. Cancer, 38 (Suppl. 7): S46, 2002.
-
(2002)
Eur. J. Cancer
, vol.38
, Issue.SUPPL. 7
-
-
Takimoto, C.H.1
Forero, F.2
Schwartz, G.H.3
Tolcher, A.W.4
Hammond, L.5
Patnaik, A.6
Ducharme, M.7
Cooke, B.8
De Jagger, R.9
Rowinsky, E.K.10
-
26
-
-
0029027770
-
Some practical improvements in the continual reassessment method in Phase I studies
-
Goodman, S. N., Zahurak, M. L., and Piantadosi, S. Some practical improvements in the continual reassessment method in Phase I studies. Stat. Med., 14: 1149-1161, 1995.
-
(1995)
Stat. Med.
, vol.14
, pp. 1149-1161
-
-
Goodman, S.N.1
Zahurak, M.L.2
Piantadosi, S.3
-
27
-
-
0003506753
-
-
Bethesda, MD: Division of Cancer Treatment, National Cancer Institute
-
Guidelines for the Reporting of Adverse Drug Reactions. Bethesda, MD: Division of Cancer Treatment, National Cancer Institute, 1988.
-
(1988)
Guidelines for the Reporting of Adverse Drug Reactions
-
-
-
29
-
-
0023369094
-
Extended least squares (ELS) for pharmacokinetic models
-
Metzler, C. M. Extended least squares (ELS) for pharmacokinetic models. J. Pharmacol. Sci., 76: 565-571, 1987.
-
(1987)
J. Pharmacol. Sci.
, vol.76
, pp. 565-571
-
-
Metzler, C.M.1
-
30
-
-
0002760710
-
Pharmacodynamics
-
W. E. Evans, J. J. Schentag, and W. J. Jusko (eds.). Vancouver, WA: Applied Therapeutics
-
Lalonde, R. L. Pharmacodynamics. In: W. E. Evans, J. J. Schentag, and W. J. Jusko (eds.), Applied Pharmacoknetics: Principles of Therapeutic Drug Monitoring, pp. 4-1-4-33. Vancouver, WA: Applied Therapeutics, 1992.
-
(1992)
Applied Pharmacoknetics: Principles of Therapeutic Drug Monitoring
, pp. 41-433
-
-
Lalonde, R.L.1
-
31
-
-
0004062826
-
-
Los Angeles, CA: Biomedical Simulation Resource, University of Southern California, Los Angeles
-
D'Argenio, D. Z., and Schumitzky, A. ADAPT-II Users Manual. Los Angeles, CA: Biomedical Simulation Resource, University of Southern California, Los Angeles, 1997.
-
(1997)
ADAPT-II Users Manual
-
-
D'Argenio, D.Z.1
Schumitzky, A.2
-
32
-
-
0018091195
-
Application of Akaike's information criterion (AIC) in the evaluation of linear pharmacokinetic equations
-
Yamaoka, K., Nakagawa, T., and Uno, T. Application of Akaike's information criterion (AIC) in the evaluation of linear pharmacokinetic equations. J. Pharmacokinet. Biopharm., 6: 165-175, 1978.
-
(1978)
J. Pharmacokinet. Biopharm.
, vol.6
, pp. 165-175
-
-
Yamaoka, K.1
Nakagawa, T.2
Uno, T.3
-
33
-
-
12444305114
-
DX-8951f for Injection
-
Fort Lee, NJ: Daiichi Pharmaceutical Corp
-
Daiichi Pharmaceutical Corp. DX-8951f for Injection. Investigators Brochure, 2nd ed. Fort Lee, NJ: Daiichi Pharmaceutical Corp., 1998.
-
(1998)
Investigators Brochure, 2nd Ed.
-
-
-
34
-
-
0033961915
-
The chemistry and biological activity of herbs used in Flor-Essence herbal tonic and Essiac
-
Tamayo, C., Richardson, M. A., Diamond, S., and Skoda, I. The chemistry and biological activity of herbs used in Flor-Essence herbal tonic and Essiac. Phytother. Res., 14: 1-14, 2000.
-
(2000)
Phytother. Res.
, vol.14
, pp. 1-14
-
-
Tamayo, C.1
Richardson, M.A.2
Diamond, S.3
Skoda, I.4
-
35
-
-
0032492669
-
Unconventional therapies for cancer: 1. Essiac
-
Kaegi, E. Unconventional therapies for cancer: 1. Essiac. Can. Med. Assoc. J., 158: 897-902, 1998.
-
(1998)
Can. Med. Assoc. J.
, vol.158
, pp. 897-902
-
-
Kaegi, E.1
-
37
-
-
0026646768
-
Pharmacokinetics and pharmacodynamics of topotecan in patients with advanced cancer
-
Grochow, L. B., Rowinsky, E. K., Johnson, R., Ludeman, S., Kaufmann, S. H., McCabe, F. L., Smith, B. R., Hurowitz, L., DeLisa, A., Donehower, R. C., et al. Pharmacokinetics and pharmacodynamics of topotecan in patients with advanced cancer. Drug Metab. Dispos., 20: 706-713, 1992.
-
(1992)
Drug Metab. Dispos.
, vol.20
, pp. 706-713
-
-
Grochow, L.B.1
Rowinsky, E.K.2
Johnson, R.3
Ludeman, S.4
Kaufmann, S.H.5
McCabe, F.L.6
Smith, B.R.7
Hurowitz, L.8
DeLisa, A.9
Donehower, R.C.10
-
38
-
-
0030580064
-
Conversion of irinotecan (CPT-11) to its active metabolite, 7-ethyl-10-hydroxycamptothecin (SN-38), by human liver carboxyesterase
-
Rivory, L. P., Bowles, M. R., Robert, J., and Pond, S. M. Conversion of irinotecan (CPT-11) to its active metabolite, 7-ethyl-10-hydroxycamptothecin (SN-38), by human liver carboxyesterase. Biochem. Pharmacol., 52: 1103-1111, 1996.
-
(1996)
Biochem. Pharmacol.
, vol.52
, pp. 1103-1111
-
-
Rivory, L.P.1
Bowles, M.R.2
Robert, J.3
Pond, S.M.4
-
39
-
-
0031055238
-
Modulation of glucuronidation of SN-38, the active metabolite of irinotecan, by valproic acid and phenobarbital
-
Gupta, E., Wang, X., Ramirez, J., and Ratain, M. J. Modulation of glucuronidation of SN-38, the active metabolite of irinotecan, by valproic acid and phenobarbital. Cancer Chemother. Pharmacol., 39: 440-444, 1997.
-
(1997)
Cancer Chemother. Pharmacol.
, vol.39
, pp. 440-444
-
-
Gupta, E.1
Wang, X.2
Ramirez, J.3
Ratain, M.J.4
-
40
-
-
0028158012
-
Phase I pharmacological study of the novel topoisomerase I inhibitor 7-ethyl-10-[4-(1-piperidino)-1-piperidino] carbonyloxycamptothecin (CPT-11) administered as a ninety-minute infusion every 3 weeks
-
Rowinsky, E. K., Grochow, L. B., Ettinger, D. S., Sartorius, S. E., Lubejko, B. G., Chen, T. L., Rock, M. K., and Donehower, R. C. Phase I and pharmacological study of the novel topoisomerase I inhibitor 7-ethyl-10-[4-(1-piperidino)-1-piperidino] carbonyloxycamptothecin (CPT-11) administered as a ninety-minute infusion every 3 weeks. Cancer Res., 54: 427-436, 1994.
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(1994)
Cancer Res.
, vol.54
, pp. 427-436
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Rowinsky, E.K.1
Grochow, L.B.2
Ettinger, D.S.3
Sartorius, S.E.4
Lubejko, B.G.5
Chen, T.L.6
Rock, M.K.7
Donehower, R.C.8
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