Access the full text.
Sign up today, get DeepDyve free for 14 days.
E. Rowinsky, T. Johnson, C. Geyer, L. Hammond, S. Eckhardt, R. Drengler, L. Smetzer, J. Coyle, J. Rizzo, G. Schwartz, A. Tolcher, D. Hoff, R. Jager (2000)
DX-8951f, a hexacyclic camptothecin analog, on a daily-times-five schedule: a phase I and pharmacokinetic study in patients with advanced solid malignancies.Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 18 17
C. Verschraegen, E. Gupta, E. Loyer, J. Kavanagh, A. Kudelka, R. Freedman, C. Edwards, N. Harris, M. Steger, V. Steltz, B. Giovanella, J. Stehlin (1999)
A phase II clinical and pharmacological study of oral 9-nitrocamptothecin in patients with refractory epithelial ovarian, tubal or peritoneal cancer.Anti-cancer drugs, 10 4
J. Berek, K. Bertelsen, A. Bois, M. Brady, J. Carmichael, E. Eisenhauer, M. Gore, S. Grénman, T. Hamilton, S. Hansen, P. Harper, G. Horvath, S. Kaye, H. Lück, B. Lund, W. Mcguire, J. Neijt, R. Ozols, M. Parmar, M. Piccart-Gebhart, R. Rijswijk, P. Rosenberg, G. Rustin, C. Sessa, J. Thigpen, C. Tropé, M. Tuxen, I. Vergote, J. Vermorken, P. Willemse (1999)
Advanced epithelial ovarian cancerAnnals of Oncology, 10
(1993)
Antitumor activity of DX-8951, a new camptothecin derivative (abstract)
A. Gordon, M. Bookman, W. Huinink, M. Gore, H. Malmström, J. Krebs, S. Fields (1997)
Pooled analysis of patients (PTS) treated with topotecan (T) after progression or failure on platinum (PLAT) and paclitaxel (P)
S. Green, G. Weiss (1992)
Southwest Oncology Group standard response criteria, endpoint definitions and toxicity criteriaInvestigational New Drugs, 10
(1997)
ADAPT-II users manual
(2000)
A phase I pharmacokinetic (PK) study of the camptothecin (CPT) analog DX-8951f (exatecan mesylate): escalating infusion duration and dose
Y. Kawato, H. Terasawa (1997)
2 Recent Advances in the Medicinal Chemistry and Pharmacology of CamptothecinProgress in Medicinal Chemistry, 34
E. Kumazawa, T. Jimbo, Y. Ochi, A. Tohgo (1998)
Potent and broad antitumor effects of DX-8951f, a water-soluble camptothecin derivative, against various human tumors xenografted in nude miceCancer Chemotherapy and Pharmacology, 42
M. Ishii, M. Iwahana, I. Mitsui, M. Minami, S. Imagawa, A. Tohgo, A. Ejima (2000)
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-6Anti-Cancer Drugs, 11
C. Holschneider, J. Berek (2000)
Ovarian cancer: epidemiology, biology, and prognostic factors.Seminars in surgical oncology, 19 1
R. Lawrence, E. Izbicka, R. Jager, A. Tohgo, G. Clark, S. Weitman, E. Rowinsky, D. Hoff (1999)
Comparison of DX-8951f and topotecan effects on tumor colony formation from freshly explanted adult and pediatric human tumor cells.Anti-cancer drugs, 10 7
(2000)
DX8951f, a hexacyclic camptothecin analog, on a daily-times-five schedule: a phase I and pharmacokinetic study in patients with advanced solid malignancies
H. Minami, H. Fujii, T. Igarashi, K. Itoh, K. Tamanoi, T. Oguma, Y. Sasaki (2001)
Phase I and pharmacological study of a new camptothecin derivative, exatecan mesylate (DX-8951f), infused over 30 minutes every three weeks.Clinical cancer research : an official journal of the American Association for Cancer Research, 7 10
(1999)
Phase I and pharmacokinetic (PK) study of DX-8951f, a novel camptothecin analog, given as 30 minute infusion daily for 5 days
D. Marsden, M. Friedlander, N. Hacker (2000)
Current management of epithelial ovarian carcinoma: a review.Seminars in surgical oncology, 19 1
N. Joto, M. Ishii, M. Minami, H. Kuga, I. Mitsui, A. Tohgo (1997)
DX‐8951F, a water‐soluble camptothecin analog, exhibits potent antitumor activity against a human lung cancer cell line and its SN‐38‐resistant variantInternational Journal of Cancer, 72
(1982)
Multicompartment models. In: Swarbrick J (ed) Pharmacokinetics
T. Oguma, Y. Ohshima, M. Nakaoka (2000)
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.Journal of chromatography. B, Biomedical sciences and applications, 740 2
S. Takiguchi, E. Kumazawa, T. Shimazoe, A. Tohgo, A. Kono (1997)
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 MiceJapanese Journal of Cancer Research : Gann, 88
M. Wall, M. Wani (1996)
Camptothecin. Discovery to clinic.Annals of the New York Academy of Sciences, 803
(1994)
High potency of a camptothecin derivative DX-8951 might be attributed to good membrane permeability (abstract)
(1997)
Recent advances in the medicinal chemistry and pharmacology of camptothecin. In: Ellis GP, Luscombe DK (eds) Progress in medicinal chemistry
(1984)
The calculation and interpretation of survival curves
M. Royce, P. Hoff, P. Dumas, Y. Lassere, J. Lee, J. Coyle, M. Ducharme, R. Jager, R. Pazdur (2001)
Phase I and pharmacokinetic study of exatecan mesylate (DX-8951f): a novel camptothecin analog.Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 19 5
(1995)
IT2S user s guide. State University of New York at Buffalo, Buffalo
M. Maliepaard, M. Gastelen, A. Tohgo, Frederick Hausheer, R. Waardenburg, L. Jong, D. Pluim, J. Beijnen, J. Schellens (2001)
Circumvention of breast cancer resistance protein (BCRP)-mediated resistance to camptothecins in vitro using non-substrate drugs or the BCRP inhibitor GF120918.Clinical cancer research : an official journal of the American Association for Cancer Research, 7 4
(1982)
Multicompartment models
I. Mitsui, E. Kumazawa, Y. Hirota, M. Aonuma, M. Sugimori, S. Ohsuki, K. Uoto, A. Ejima, H. Terasawa, Keiki Sato (1995)
A New Water‐soluble Camptothecin Derivative, DX‐8951f, Exhibits Potent Antitumor Activity against Human Tumors in vitro and in vivoJapanese Journal of Cancer Research : Gann, 86
S. Sharma, N. Kemeny, G. Schwartz, D. Kelsen, E. O’Reilly, D. Ilson, J. Coyle, R. Jager, M. Ducharme, S. Kleban, E. Hollywood, L. Saltz (2001)
Phase I study of topoisomerase I inhibitor exatecan mesylate (DX-8951f) given as weekly 24-hour infusions three of every four weeks.Clinical cancer research : an official journal of the American Association for Cancer Research, 7 12
(1995)
Antitumor effect of DX - 8951 , a new camptothecin derivative , in various murine models ( abstract )
G. Rustin, A. Nelstrop, P. McClean, M. Brady, W. McGuire, W Hoskins, H. Mitchell, H. Lambert (1996)
Defining response of ovarian carcinoma to initial chemotherapy according to serum CA 125.Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 14 5
R. Simon (1989)
Optimal two-stage designs for phase II clinical trials.Controlled clinical trials, 10 1
K. Yamaoka, T. Nakagawa, T. Uno (1978)
Application of Akaike's information criterion (AIC) in the evaluation of linear pharmacokinetic equationsJournal of Pharmacokinetics and Biopharmaceutics, 6
M. Wall, M. Wani (1996)
Discovery to Clinic aAnnals of the New York Academy of Sciences, 803
A. Hattum, H. Pinedo, H. Schlüper, C. Erkelens, A. Tohgo, E. Boven (2002)
The activity profile of the hexacyclic camptothecin derivative DX-8951f in experimental human colon cancer and ovarian cancer.Biochemical pharmacology, 64 8
J. Berek, K. Bertelsen, A. Bois, M. Brady, J. Carmichael, E. Eisenhauer, M. Gore, S. Grénman, T. Hamilton, S. Hansen, P. Harper, G. Horvath, S. Kaye, H. Lück, B. Lund, W. McGuire, J. Neijt, R. Ozols, M. Parmar, M. Piccart-Gebhart, R. Rijswijk, P. Rosenberg, G. Rustin, C. Sessa, J. Thigpen, C. Tropé, M. Tuxen, I. Vergote, J. Vermorken, P. Willemse (1999)
Advanced epithelial ovarian cancer: 1998 consensus statements.Annals of oncology : official journal of the European Society for Medical Oncology, 10 Suppl 1
DX-8951f administered parenterally as a single agent daily at a dose of either 0.5 or 0.3 mg/m 2 per day for 5 days is feasible in patients with advanced ovarian, tubal and peritoneal cancer resistant to platinum, taxane and topotecan. Although no responses were observed, a significant number of patients had stable disease with a decrease in CA-125 levels. In this heavily pretreated population, DX-8951f has clinically relevant hematologic and gastrointestinal toxicities in about 25% of patients. DX-8951 appeared to have linear pharmacokinetic characteristics on the basis of multiple administrations.
Cancer Chemotherapy and Pharmacology – Springer Journals
Published: Jan 1, 2004
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.