메뉴 건너뛰기




Volumn 14, Issue 22, 2008, Pages 7535-7544

Clinical and pharmacologic study of the novel prodrug delimotecan (MEN 4901/T-0128) in patients with solid tumors

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; CAMPTOTHECIN DERIVATIVE; DELIMOTECAN; DRUG METABOLITE; MEN 4901; T 0128; T 2513; UNCLASSIFIED DRUG; DEXTRAN; DRUG DERIVATIVE; PRODRUG; TOPOTECAN;

EID: 58149343899     PISSN: 10780432     EISSN: None     Source Type: Journal    
DOI: 10.1158/1078-0432.CCR-08-0438     Document Type: Article
Times cited : (39)

References (31)
  • 1
    • 0034712536 scopus 로고    scopus 로고
    • 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;355:1041-7.
    • (2000) Lancet , vol.355 , pp. 1041-1047
    • Douillard, J.Y.1    Cunningham, D.2    Roth, A.D.3
  • 2
    • 0032585232 scopus 로고    scopus 로고
    • 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;352:1413-8.
    • (1998) Lancet , vol.352 , pp. 1413-1418
    • Cunningham, D.1    Pyrhonen, S.2    James, R.D.3
  • 3
    • 33747475241 scopus 로고    scopus 로고
    • Synthesis and cytotoxic activity of polyamine analogues of camptothecin
    • Dallavalle S, Giannini G, Alloatti D, et al. Synthesis and cytotoxic activity of polyamine analogues of camptothecin. J Med Chem 2006;49:5177-86.
    • (2006) J Med Chem , vol.49 , pp. 5177-5186
    • Dallavalle, S.1    Giannini, G.2    Alloatti, D.3
  • 4
    • 0032189683 scopus 로고    scopus 로고
    • Mechanism of action of eukaryotic DNA topoisomerase I and drugs targeted to the enzyme
    • Pommier Y, Pourquier P, Fan Y, Strumberg D. Mechanism of action of eukaryotic DNA topoisomerase I and drugs targeted to the enzyme. Biochim Biophys Acta 1998;1400:83-105.
    • (1998) Biochim Biophys Acta , vol.1400 , pp. 83-105
    • Pommier, Y.1    Pourquier, P.2    Fan, Y.3    Strumberg, D.4
  • 5
    • 0024356003 scopus 로고
    • DNA topoisomerase I-mediated DNA cleavage and cytotoxicity of camptothecin analogues
    • Hsiang YH, Liu LF, Wall ME, et al. DNA topoisomerase I-mediated DNA cleavage and cytotoxicity of camptothecin analogues. Cancer Res 1989;49:4385-9.
    • (1989) Cancer Res , vol.49 , pp. 4385-4389
    • Hsiang, Y.H.1    Liu, L.F.2    Wall, M.E.3
  • 6
    • 0022340594 scopus 로고
    • Camptothecin induces protein-linked DNA breaks via mammalian DNA topoisomerase I
    • Hsiang YH, Hertzberg R, Hecht S, Liu LF. Camptothecin induces protein-linked DNA breaks via mammalian DNA topoisomerase I. J Biol Chem 1985;260:14873-8.
    • (1985) J Biol Chem , vol.260 , pp. 14873-14878
    • Hsiang, Y.H.1    Hertzberg, R.2    Hecht, S.3    Liu, L.F.4
  • 7
    • 0024420685 scopus 로고
    • Arrest of replication forks by drug-stabilized topoisomerase I-DNA cleavable complexes as a mechanism of cell killing by camptothecin
    • Hsiang YH, Lihou MG, Liu LF. Arrest of replication forks by drug-stabilized topoisomerase I-DNA cleavable complexes as a mechanism of cell killing by camptothecin. Cancer Res 1989;49:5077-82.
    • (1989) Cancer Res , vol.49 , pp. 5077-5082
    • Hsiang, Y.H.1    Lihou, M.G.2    Liu, L.F.3
  • 9
    • 0029116438 scopus 로고
    • Efficacy of topoisomerase I inhibitors, topotecan and irinotecan, administered at low dose levels in protracted schedules to mice bearing xenografts of human tumors
    • Houghton PJ, Cheshire PJ, Hallman JD, et al. Efficacy of topoisomerase I inhibitors, topotecan and irinotecan, administered at low dose levels in protracted schedules to mice bearing xenografts of human tumors. Cancer Chemother Pharmacol 1995;36:393-403.
    • (1995) Cancer Chemother Pharmacol , vol.36 , pp. 393-403
    • Houghton, P.J.1    Cheshire, P.J.2    Hallman, J.D.3
  • 10
    • 0025366634 scopus 로고
    • Effect of administration schedules on the antitumor activity of CPT-11, a camptothecin derivative]
    • Furuta T, Yokokura T. [Effect of administration schedules on the antitumor activity of CPT-11, a camptothecin derivative]. GanTo Kagaku Ryoho 1990;17:121-30.
    • (1990) GanTo Kagaku Ryoho , vol.17 , pp. 121-130
    • Furuta, T.1    Yokokura, T.2
  • 11
    • 20044379959 scopus 로고    scopus 로고
    • MEN4901/T-0128, a new camptothecin derivative-carboxymethyldextran conjugate, has potent antitumor activities in a panel of human tumor xenografts in nude mice
    • Fujita F, Koike M, Fujita M, et al. MEN4901/T-0128, a new camptothecin derivative-carboxymethyldextran conjugate, has potent antitumor activities in a panel of human tumor xenografts in nude mice. Clin Cancer Res 2005;11:1650-7.
    • (2005) Clin Cancer Res , vol.11 , pp. 1650-1657
    • Fujita, F.1    Koike, M.2    Fujita, M.3
  • 12
    • 0034602605 scopus 로고    scopus 로고
    • Harada M, Imai J, Okuno S, Suzuki T. Macrophage-mediated activation of camptothecin analogue T-2513-carboxymethyl dextran conjugate T-0128, possible cellular mechanism for antitumor activity. J Control Release 2000;69:389-97
    • Harada M, Imai J, Okuno S, Suzuki T. Macrophage-mediated activation of camptothecin analogue T-2513-carboxymethyl dextran conjugate (T-0128): possible cellular mechanism for antitumor activity. J Control Release 2000;69:389-97.
  • 13
    • 33750564495 scopus 로고    scopus 로고
    • Human and murine macrophages mediate activation of MEN 4901/T-0128: A new promising camptothecin analogue-polysaccharide conjugate
    • Binaschi M, Parlani M, Bellarosa D, et al. Human and murine macrophages mediate activation of MEN 4901/T-0128: a new promising camptothecin analogue-polysaccharide conjugate. Anticancer Drugs 2006;17:1119-26.
    • (2006) Anticancer Drugs , vol.17 , pp. 1119-1126
    • Binaschi, M.1    Parlani, M.2    Bellarosa, D.3
  • 14
    • 0034212633 scopus 로고    scopus 로고
    • Complete regression of xenografted human carcinomas by camptothecin analogue-carboxymethyl dextran conjugate (T-0128)
    • Okuno S, Harada M, Yano T, et al. Complete regression of xenografted human carcinomas by camptothecin analogue-carboxymethyl dextran conjugate (T-0128). Cancer Res 2000;60:2988-95.
    • (2000) Cancer Res , vol.60 , pp. 2988-2995
    • Okuno, S.1    Harada, M.2    Yano, T.3
  • 15
    • 0034594628 scopus 로고    scopus 로고
    • New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada
    • Therasse P, Arbuck SG, Eisenhauer EA, et al. New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada. J Natl Cancer Inst 2000;92:205-16.
    • (2000) J Natl Cancer Inst , vol.92 , pp. 205-216
    • Therasse, P.1    Arbuck, S.G.2    Eisenhauer, E.A.3
  • 16
    • 0028833556 scopus 로고
    • Macromolecular drug carrier systems in cancer chemotherapy: Macromolecular prodrugs
    • Takakura Y, Hashida M. Macromolecular drug carrier systems in cancer chemotherapy: macromolecular prodrugs. Crit Rev Oncol Hematol 1995;18:207-31.
    • (1995) Crit Rev Oncol Hematol , vol.18 , pp. 207-231
    • Takakura, Y.1    Hashida, M.2
  • 17
    • 24144457231 scopus 로고    scopus 로고
    • Macromolecular and nanotechnological modification of camptothecin and its analogs to improve the efficacy
    • Onishi H, Machida Y. Macromolecular and nanotechnological modification of camptothecin and its analogs to improve the efficacy. Curr Drug Discov Technol 2005;2:169-83.
    • (2005) Curr Drug Discov Technol , vol.2 , pp. 169-183
    • Onishi, H.1    Machida, Y.2
  • 18
    • 0032959549 scopus 로고    scopus 로고
    • Phase I clinical and pharmacokinetic study of PK1 [N-(2-hydroxypropyl) methacrylamide copolymer doxorubicin]: First member of a new class of chemotherapeutic agents-drug-polymer conjugates. Cancer Research Campaign Phase I/II Committee
    • Vasey PA., Kaye SB, Morrison R, et al. Phase I clinical and pharmacokinetic study of PK1 [N-(2-hydroxypropyl) methacrylamide copolymer doxorubicin]: first member of a new class of chemotherapeutic agents-drug-polymer conjugates. Cancer Research Campaign Phase I/II Committee. Clin Cancer Res 1999;5:83-94.
    • (1999) Clin Cancer Res , vol.5 , pp. 83-94
    • Vasey, P.A.1    Kaye, S.B.2    Morrison, R.3
  • 19
    • 0035012701 scopus 로고    scopus 로고
    • Phase I clinical and pharmacokinetic study of PNU166945, a novel water-soluble polymer-conjugated prodrug of paclitaxel
    • Meerum Terwogt JM, ten Bokkel Huinink WW, Schellens JHM, et al. Phase I clinical and pharmacokinetic study of PNU166945, a novel water-soluble polymer-conjugated prodrug of paclitaxel. Anticancer Drugs 2001;12:315-23.
    • (2001) Anticancer Drugs , vol.12 , pp. 315-323
    • Meerum Terwogt, J.M.1    ten Bokkel Huinink, W.W.2    Schellens, J.H.M.3
  • 20
    • 18544376660 scopus 로고    scopus 로고
    • A phase I and pharmacokinetic study of MAG-CPT, a water-soluble polymer conjugate of camptothecin
    • Schoemaker NE, van Kesteren C, Rosing H, et al. A phase I and pharmacokinetic study of MAG-CPT, a water-soluble polymer conjugate of camptothecin. Br J Cancer 2002;87:608-14.
    • (2002) Br J Cancer , vol.87 , pp. 608-614
    • Schoemaker, N.E.1    van Kesteren, C.2    Rosing, H.3
  • 21
    • 0030752757 scopus 로고    scopus 로고
    • Topoisomerase I inhibitors: The relevance of prolonged exposure for present clinical development
    • Gerrits CJ, de Jonge MJ, Schellens JHM, Stoter G, Verweij J. Topoisomerase I inhibitors: the relevance of prolonged exposure for present clinical development. Br J Cancer 1997;76:952-62.
    • (1997) Br J Cancer , vol.76 , pp. 952-962
    • Gerrits, C.J.1    de Jonge, M.J.2    Schellens, J.H.M.3    Stoter, G.4    Verweij, J.5
  • 22
    • 0032998172 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of irinotecan administered as a low-dose, continuous intravenous infusion over 14 days in patients with malignant solid tumors
    • Herben VM, Schellens JHM, Swart M, et al. Phase I and pharmacokinetic study of irinotecan administered as a low-dose, continuous intravenous infusion over 14 days in patients with malignant solid tumors. J Clin Oncol 1999;17:1897-905.
    • (1999) J Clin Oncol , vol.17 , pp. 1897-1905
    • Herben, V.M.1    Schellens, J.H.M.2    Swart, M.3
  • 23
    • 0022405120 scopus 로고
    • Premarketing observational studies of population pharmacokinetics of new drugs
    • Sheiner LB, Benet LZ. Premarketing observational studies of population pharmacokinetics of new drugs. Clin Pharmacol Ther 1985;38:481-7.
    • (1985) Clin Pharmacol Ther , vol.38 , pp. 481-487
    • Sheiner, L.B.1    Benet, L.Z.2
  • 25
    • 34447285021 scopus 로고    scopus 로고
    • UGT1A1 promoter genotype correlates with SN-38 pharmacokinetics, but not severe toxicity in patients receiving low-dose irinotecan
    • Stewart CF, Panetta JC, O'Shaughnessy MA, et al. UGT1A1 promoter genotype correlates with SN-38 pharmacokinetics, but not severe toxicity in patients receiving low-dose irinotecan. J Clin Oncol 2007;25:2594-600.
    • (2007) J Clin Oncol , vol.25 , pp. 2594-2600
    • Stewart, C.F.1    Panetta, J.C.2    O'Shaughnessy, M.A.3
  • 26
    • 33845759934 scopus 로고    scopus 로고
    • The role of SN-38 exposure, UGT1A1*28 polymorphism, and baseline bilirubin level in predicting severe irinotecan toxicity
    • Ramchandani RP, Wang Y, Booth BP, et al. The role of SN-38 exposure, UGT1A1*28 polymorphism, and baseline bilirubin level in predicting severe irinotecan toxicity. J Clin Pharmacol 2007;47:78-86.
    • (2007) J Clin Pharmacol , vol.47 , pp. 78-86
    • Ramchandani, R.P.1    Wang, Y.2    Booth, B.P.3
  • 27
    • 0033950287 scopus 로고    scopus 로고
    • Phase I and pharmacologic study of irinotecan administered as a 96-hour infusion weekly to adult cancer patients
    • Takimoto CH, Morrison G, Harold N, et al. Phase I and pharmacologic study of irinotecan administered as a 96-hour infusion weekly to adult cancer patients. J Clin Oncol 2000;18:659-67.
    • (2000) J Clin Oncol , vol.18 , pp. 659-667
    • Takimoto, C.H.1    Morrison, G.2    Harold, N.3
  • 28
    • 0027140524 scopus 로고
    • Phase I and pharmacokinetic trial of weekly CPT-11
    • Rothenberg ML, Kuhn JG, Burris HA, et al. Phase I and pharmacokinetic trial of weekly CPT-11. J Clin Oncol 1993;11:2194-204.
    • (1993) J Clin Oncol , vol.11 , pp. 2194-2204
    • Rothenberg, M.L.1    Kuhn, J.G.2    Burris, H.A.3
  • 29
    • 0010917253 scopus 로고    scopus 로고
    • Pharmacokinetics and pharmacodynamics of irinotecan during a phase II clinical trial in colorectal cancer. Pharmacology and Molecular Mechanisms Group of the European Organization for Research and Treatment of Cancer
    • Canal P, Gay C, Dezeuze A, et al. Pharmacokinetics and pharmacodynamics of irinotecan during a phase II clinical trial in colorectal cancer. Pharmacology and Molecular Mechanisms Group of the European Organization for Research and Treatment of Cancer. J Clin Oncol 1996;14:2688-95.
    • (1996) J Clin Oncol , vol.14 , pp. 2688-2695
    • Canal, P.1    Gay, C.2    Dezeuze, A.3
  • 30
    • 7944235231 scopus 로고    scopus 로고
    • A randomised phase II multicentre trial of irinotecan (CPT-11) using four different schedules in patients with metastatic colorectal cancer
    • Schoemaker NE, Kuppens IE, Moiseyenko V, et al. A randomised phase II multicentre trial of irinotecan (CPT-11) using four different schedules in patients with metastatic colorectal cancer. Br J Cancer 2004;91:1434-41.
    • (2004) Br J Cancer , vol.91 , pp. 1434-1441
    • Schoemaker, N.E.1    Kuppens, I.E.2    Moiseyenko, V.3
  • 31
    • 0028843263 scopus 로고
    • Pharmacologic correlation between total drug concentration and lactones of CPT-11 and SN-38 in patients treated with CPT-11
    • Sasaki Y, Yoshida Y, Sudoh K, et al. Pharmacologic correlation between total drug concentration and lactones of CPT-11 and SN-38 in patients treated with CPT-11. Jpn J Cancer Res 1995;86:111-6.
    • (1995) Jpn J Cancer Res , vol.86 , pp. 111-116
    • Sasaki, Y.1    Yoshida, Y.2    Sudoh, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.