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Volumn 13, Issue 3, 2004, Pages 269-284

Camptothecins in clinical development

Author keywords

Camptothecin; Clinical efficacy; DNA topoisomerase I

Indexed keywords

7 ETHYL 10 HYDROXYCAMPTOTHECIN; AFELETECAN; BAY 56 3722; BELOTECAN; BREAST CANCER RESISTANCE PROTEIN; CAMPTOTHECIN DERIVATIVE; CISPLATIN; CT 2106; CYTOTOXIC AGENT; DE 310; DIFLOMOTECAN; DNA TOPOISOMERASE; DNA TOPOISOMERASE (ATP HYDROLYSING); DNA TOPOISOMERASE INHIBITOR; DRF 1042; DX 8591F; EXATECAN; FLUOROURACIL; GIMATECAN; GLIMATECAN; GLYCOPROTEIN P; IRINOTECAN; KARENITECIN; LACTONE; LURTOTECAN; PACLITAXEL; PNU 166148; POLYMER; RUBITECAN; TOPOTECAN; UNCLASSIFIED DRUG; UNINDEXED DRUG; WATER;

EID: 1542603100     PISSN: 13543784     EISSN: None     Source Type: Journal    
DOI: 10.1517/13543784.13.3.269     Document Type: Review
Times cited : (102)

References (113)
  • 1
    • 0034040082 scopus 로고    scopus 로고
    • Topoisomerase I poisons and suppressors as anticancer drugs
    • BAILLY C: Topoisomerase I poisons and suppressors as anticancer drugs. Curr. Med. Chem. (2000) 7:39-58.
    • (2000) Curr. Med. Chem. , vol.7 , pp. 39-58
    • Bailly, C.1
  • 2
    • 0032189683 scopus 로고    scopus 로고
    • Mechanism of action of eukariotic DNA topoisomerase I and drugs targeted to the enzyme
    • POMMIER Y, POURQUIER P, FAN Y, STRUMBERG D: Mechanism of action of eukariotic DNA topoisomerase I and drugs targeted to the enzyme. Biochim. Biophys. Acta (1998) 1400:83-106.
    • (1998) Biochim. Biophys. Acta , vol.1400 , pp. 83-106
    • Pommier, Y.1    Pourquier, P.2    Fan, Y.3    Strumberg, D.4
  • 5
    • 0036085460 scopus 로고    scopus 로고
    • Cellular roles of DNA topoisomerases: A molecular perspective
    • WANG JC: Cellular roles of DNA tApoisomerases: a molecular perspective. Nat. Rev. Mol. Cell. Biol. (2002) 3:430-440.
    • (2002) Nat. Rev. Mol. Cell. Biol. , vol.3 , pp. 430-440
    • Wang, J.C.1
  • 6
    • 0346365373 scopus 로고    scopus 로고
    • Altered serine/arginine-rich protein phosphorylation and exonic enhancer-dependent splicing in mammalian cells lacking topoisomerase I
    • SORET J, GABUT M, DUPON C et al.: Altered serine/arginine-rich protein phosphorylation and exonic enhancer-dependent splicing in mammalian cells lacking topoisomerase I. Cancer Res. (2003) 63:8203-8211.
    • (2003) Cancer Res. , vol.63 , pp. 8203-8211
    • Soret, J.1    Gabut, M.2    Dupon, C.3
  • 7
    • 0032170499 scopus 로고    scopus 로고
    • Topotecan lactone selectively binds to double- and single-stranded DNA in the absence of topoisomerase I
    • YAO S, MURALI D, SEETHARAMULU P et al.: Topotecan lactone selectively binds to double- and single-stranded DNA in the absence of topoisomerase I. Cancer Res. (1998) 58:3782-3786.
    • (1998) Cancer Res. , vol.58 , pp. 3782-3786
    • Yao, S.1    Murali, D.2    Seetharamulu, P.3
  • 8
    • 0034509613 scopus 로고    scopus 로고
    • A spectrophotometric study of the pH-dependent and DNA binding properties of topotecan
    • MILLER SE, PILCH DS: A spectrophotometric study of the pH-dependent and DNA binding properties of topotecan. Ann. NY Acad. Sci. (2000) 922:309.
    • (2000) Ann. NY Acad. Sci. , vol.922 , pp. 309
    • Miller, S.E.1    Pilch, D.S.2
  • 10
    • 0028067913 scopus 로고
    • Topoisomerase I gene expression and cell sensitivity to camptothecin in human cell lines of different tumor types
    • PEREGO P, CAPRANICO G, SUPINO R, ZUNINO F: Topoisomerase I gene expression and cell sensitivity to camptothecin in human cell lines of different tumor types. Anticancer Drugs (1994) 5:645-649.
    • (1994) Anticancer Drugs , vol.5 , pp. 645-649
    • Perego, P.1    Capranico, G.2    Supino, R.3    Zunino, F.4
  • 14
    • 0036399299 scopus 로고    scopus 로고
    • Camptothecins. A review of their chemotherapeutic potential
    • ULUKAN H, SWAAN PW: Camptothecins. A review of their chemotherapeutic potential. Drugs (2002) 62:2039-2057.
    • (2002) Drugs , vol.62 , pp. 2039-2057
    • Ulukan, H.1    Swaan, P.W.2
  • 15
    • 0028012774 scopus 로고
    • The structural basis of camptothecin interactions with human serum albumin: Impact on drug stability
    • BURKE TG, MI Z: The structural basis of camptothecin interactions with human serum albumin: Impact on drug stability. J. Med. Chem. (1994) 37:40-46.
    • (1994) J. Med. Chem. , vol.37 , pp. 40-46
    • Burke, T.G.1    Mi, Z.2
  • 16
    • 0036304427 scopus 로고    scopus 로고
    • Current perspectives on the clinical experience, pharmacology, and continued development of the camptothecins
    • GARCIA-CARBONERO R, SOPKO JG: Current perspectives on the clinical experience, pharmacology, and continued development of the camptothecins. Clin. Cancer Res. (2002) 8:641-661.
    • (2002) Clin. Cancer Res. , vol.8 , pp. 641-661
    • Garcia-Carbonero, R.1    Sopko, J.G.2
  • 17
    • 0038167666 scopus 로고    scopus 로고
    • The camptothecins
    • PIZZOLATO JF, SALTZ LB: The camptothecins. Lancet (2003) 361:2235-2242.
    • (2003) Lancet , vol.361 , pp. 2235-2242
    • Pizzolato, J.F.1    Saltz, L.B.2
  • 18
    • 0035478878 scopus 로고    scopus 로고
    • Oral topotecan as single-agent second-line chemotherapy in patients with advanced ovarian cancer
    • CLARKE-PEARSON DL, VEN LE L, IVESON T et al.: Oral topotecan as single-agent second-line chemotherapy in patients with advanced ovarian cancer. J. Clin. Oncol. (2001) 19:3967-3975.
    • (2001) J. Clin. Oncol. , vol.19 , pp. 3967-3975
    • Clarke-pearson, D.L.1    Ven Le, L.2    Iveson, T.3
  • 19
    • 0036644903 scopus 로고    scopus 로고
    • Increased oral bioavailability of topotecan in combination with the breast cancer resistance protein and P-glycoprotein inhibitor GF120918
    • KRUIJTZER CMF, BEIJNEN JH, ROSING H et al.: Increased oral bioavailability of topotecan in combination with the breast cancer resistance protein and P-glycoprotein inhibitor GF120918. J. Clin. Oncol. (2002) 20:2943-2950.
    • (2002) J. Clin. Oncol. , vol.20 , pp. 2943-2950
    • Kruijtzer, C.M.F.1    Beijnen, J.H.2    Rosing, H.3
  • 20
    • 0036645149 scopus 로고    scopus 로고
    • Boosting bioavailability of topotecan: What do we gain?
    • HUDES G: Boosting bioavailabilityWof topotecan: what do we gain? J. Clin. Oncol. (2002) 20:2918-2919.
    • (2002) J. Clin. Oncol. , vol.20 , pp. 2918-2919
    • Hudes, G.1
  • 21
    • 0035881280 scopus 로고    scopus 로고
    • A novel 7-modified camptothecin analog overcomes breast cancer resistance protein-associated resistance in a mitoxantrone-selected colon carcinoma cell line
    • PEREGO P, DE CESARE M, DE ISABELLA P et al.: A novel 7-modified camptothecin analog overcomes breast cancer resistance protein-associated resistance in a mitoxantrone-selected colon carcinoma cell line. Cancer Res. (2001) 61:6034-6037.
    • (2001) Cancer Res. , vol.61 , pp. 6034-6037
    • Perego, P.1    De Cesare, M.2    De Isabella, P.3
  • 22
  • 23
    • 0001744641 scopus 로고    scopus 로고
    • Multidrug resistance and pharmacological protection mediated by the breast cancer resistance protein (BCRP/ABCG2)
    • ALLEN JD, SCHINKEL AH: Multidrug resistance and pharmacological protection mediated by the breast cancer resistance protein (BCRP/ABCG2). Mol. Cancer Ther. (2002) 1:427-434.
    • (2002) Mol. Cancer Ther. , vol.1 , pp. 427-434
    • Allen, J.D.1    Schinkel, A.H.2
  • 24
    • 0242382628 scopus 로고    scopus 로고
    • Irinotecan (Campto) in the treatment of pancreatic cancer
    • PIZZOLATO JF, SALTZ LB: Irinotecan (Campto) in the treatment of pancreatic cancer. Expert Rev. Anticancer Ther. (2003) 3:587-593.
    • (2003) Expert Rev. Anticancer Ther. , vol.3 , pp. 587-593
    • Pizzolato, J.F.1    Saltz, L.B.2
  • 25
    • 0033118471 scopus 로고    scopus 로고
    • The anticancer prodrug CPT-11 is a potent inhibitor of acetylcholinesterase but is rapidly catalyzed to SN-38 by butyrylcholinesterase
    • MORTON CL, WADKINS RM, DANKS MK, POTTER PM: The anticancer prodrug CPT-11 is a potent inhibitor of acetylcholinesterase but is rapidly catalyzed to SN-38 by butyrylcholinesterase. Cancer Res. (1999) 59:1458-1463.
    • (1999) Cancer Res. , vol.59 , pp. 1458-1463
    • Morton, C.L.1    Wadkins, R.M.2    Danks, M.K.3    Potter, P.M.4
  • 26
    • 0028022585 scopus 로고
    • Metabolic fate or irinotecan in humans: Correlations of glucuronidation with diarrhea
    • GUPTA E, LESTINGI TM, MICK R, RAMIREZ J, VOKES EE, RATAIN MJ: Metabolic fate or irinotecan in humans: Correlations of glucuronidation with diarrhea. Cancer Res. (1994) 54:3723-3725.
    • (1994) Cancer Res. , vol.54 , pp. 3723-3725
    • Gupta, E.1    Lestingi, T.M.2    Mick, R.3    Ramirez, J.4    Vokes, E.E.5    Ratain, M.J.6
  • 28
    • 0035960061 scopus 로고    scopus 로고
    • Novel 7-oxyiminomethyl derivatives of camptothecin with potent in vitro and in vivo antitumor activity
    • DALLAVALLE S, FERRARI A, BIASOTTI B et al.: Novel 7-oxyiminomethyl derivatives of camptothecin with potent in vitro and in vivo antitumor activity. J. Med. Chem. (2001) 44:3264-3274.
    • (2001) J. Med. Chem. , vol.44 , pp. 3264-3274
    • Dallavalle, S.1    Ferrari, A.2    Biasotti, B.3
  • 30
    • 0037479850 scopus 로고    scopus 로고
    • Sequencing topotecan and etoposide plus cisplatin to overcome topoisomerase I and II resistance: A pharmacodynamically based Phase I trial
    • AISNER J, MUSANTI R, BEERS S, SMITH S, LOCSIN S, RUBIN EH: Sequencing topotecan and etoposide plus cisplatin to overcome topoisomerase I and II resistance: A pharmacodynamically based Phase I trial. Clin. Cancer Res. (2003) 9:2504-2509.
    • (2003) Clin. Cancer Res. , vol.9 , pp. 2504-2509
    • Aisner, J.1    Musanti, R.2    Beers, S.3    Smith, S.4    Locsin, S.5    Rubin, E.H.6
  • 31
    • 0038666413 scopus 로고    scopus 로고
    • Phase I evaluation of sequential topoisomerase targeting with irinotecan/cisplatin followed by etoposide in patients with advanced malignancy
    • LICITRA EJ, VYAS V, NELSON K et al.: Phase I evaluation of sequential topoisomerase targeting with irinotecan/ cisplatin followed by etoposide in patients with advanced malignancy. Clin. Cancer Res. (2003) 9:1673-1679.
    • (2003) Clin. Cancer Res. , vol.9 , pp. 1673-1679
    • Licitra, E.J.1    Vyas, V.2    Nelson, K.3
  • 32
    • 0032905667 scopus 로고    scopus 로고
    • Cellular pharmacology of the combination of the DNA topoisomerase I inhibitor SN-38 and the diaminocyclohexane platinum derivative oxaliplatin
    • ZEGHARI-SQUALLY N, RAYMOND E, CVITKOVIC E, GOLDWASSER F: Cellular pharmacology of the combination of the DNA topoisomerase I inhibitor SN-38 and the diaminocyclohexane platinum derivative oxaliplatin. Clin. Cancer Res. (1999) 5:1189-1196.
    • (1999) Clin. Cancer Res. , vol.5 , pp. 1189-1196
    • Zeghari-Squally, N.1    Raymond, E.2    Cvitkovic, E.3    Goldwasser, F.4
  • 33
    • 0034548798 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
    • 0035992308 scopus 로고    scopus 로고
    • Phase I and pharmacokinetic study of DX-8951f (exatecan mesylate), a hexacyclic camptothecin, on a daily-times-five schedule in patients with advanced leukemia
    • GILLES FJ, CORTES JE, THOMAS DA et al.: Phase I and pharmacokinetic study of DX-8951f (exatecan mesylate), a hexacyclic camptothecin, on a daily-times-five schedule in patients with advanced leukemia. Clin. Cancer Res. (2002) 8:2134-2141.
    • (2002) Clin. Cancer Res. , vol.8 , pp. 2134-2141
    • Gilles, F.J.1    Cortes, J.E.2    Thomas, D.A.3
  • 36
    • 12444261674 scopus 로고    scopus 로고
    • A Phase I and pharmacokinetic study of exatecan mesylate administered as a protracted 21-day infusion in patients with advanced solid malignancies
    • GARRISON MA, HAMMOND LA, GEYER CE et al.: A Phase I and pharmacokinetic study of exatecan mesylate administered as a protracted 21-day infusion in patients with advanced solid malignancies. Clin. Cancer Res. (2003) 9:2527-2537.
    • (2003) Clin. Cancer Res. , vol.9 , pp. 2527-2537
    • Garrison, M.A.1    Hammond, L.A.2    Geyer, C.E.3
  • 37
    • 0042889292 scopus 로고    scopus 로고
    • A Phase II study of intravenous exatecan mesylate (DX-8951f) administered daily for 5 days every 3 weeks to patients with metastatic breast carcinoma
    • ESTEVA FJ, RIVERA E, CRISTOFANILLI M et al.: A Phase II study of intravenous exatecan mesylate (DX-8951f) administered daily for 5 days every 3 weeks to patients with metastatic breast carcinoma. Cancer (2003) 98:900-907.
    • (2003) Cancer , vol.98 , pp. 900-907
    • Esteva, F.J.1    Rivera, E.2    Cristofanilli, M.3
  • 38
    • 0033821727 scopus 로고    scopus 로고
    • Activity and toxicity of GI147211 in breast, colorectal and non-small-cell lung cancer patients: An EORTC-ECSG Phase II clinical study
    • GAMUCCI T, PARIDAENS R, HEINRICH B et al.: Activity and toxicity of GI147211 in breast, colorectal and non-small-cell lung cancer patients: An EORTC-ECSG Phase II clinical study. Ann. Oncol. (2000) 11:793-797.
    • (2000) Ann. Oncol. , vol.11 , pp. 793-797
    • Gamucci, T.1    Paridaens, R.2    Heinrich, B.3
  • 39
    • 0033984541 scopus 로고    scopus 로고
    • Liposomal lurtotecan (NX211): Determination of total drug levels in human plasma and urine by reversed-phase high-performance liquid chromatography
    • LOOS WJ, KEHRER D, BROUWER E et al.: Liposomal lurtotecan (NX211): Determination of total drug levels in human plasma and urine by reversed-phase high-performance liquid chromatography. J. Chromatogr. B. Biomed. Appl. (2000) 738:155-163.
    • (2000) J. Chromatogr. B. Biomed. Appl. , vol.738 , pp. 155-163
    • Loos, W.J.1    Kehrer, D.2    Brouwer, E.3
  • 40
    • 0036499054 scopus 로고    scopus 로고
    • Phase I and pharmacologic study of liposomal lurtotecan, NX211: Urinary excretion predicts hematologic toxicity
    • KEHRER DFS, BOS AM, VERWEIJ J et al.: Phase I and pharmacologic study of liposomal lurtotecan, NX211: Urinary excretion predicts hematologic toxicity. J. Clin. Oncol. (2002) 20:1222-1231.
    • (2002) J. Clin. Oncol. , vol.20 , pp. 1222-1231
    • Kehrer, D.F.S.1    Bos, A.M.2    Verweij, J.3
  • 41
    • 0005323414 scopus 로고    scopus 로고
    • Randomized Phase II trial of two intravenous schedules of the liposomal topoisomerase I inhibitor, NX211, in women with relapsed epithelial ovarian cancer (OVCA): An NCIC CTG study
    • (Abstract 830)
    • CALVERT AH, GRIMSHAW R, POOLE C et al.: Randomized Phase II trial of two intravenous schedules of the liposomal topoisomerase I inhibitor, NX211, in women with relapsed epithelial ovarian cancer (OVCA): An NCIC CTG study. Proc. Am. Soc. Clin. Oncol. (2002) 21(Abstract 830).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Calvert, A.H.1    Grimshaw, R.2    Poole, C.3
  • 42
    • 0034517554 scopus 로고    scopus 로고
    • Preclinical and Phase I clinical studies with CKD-602, a novel camptothecin derivative
    • LEE JH, LEE JM, LIM KH et al.: Preclinical and Phase I clinical studies with CKD-602, a novel camptothecin derivative. Ann. NY Acad. Sci. (2000) 922:324-325.
    • (2000) Ann. NY Acad. Sci. , vol.922 , pp. 324-325
    • Lee, J.H.1    Lee, J.M.2    Lim, K.H.3
  • 43
    • 1542546556 scopus 로고    scopus 로고
    • Phase II evaluation of ckd-602, a camptothecin analog, administered on a 5-day schedule in patients with recurrent or refractory ovarian cancer
    • (Abstract 1877)
    • SONG Y, SEO S-S, BANG Y-J et al.: Phase II evaluation of ckd-602, a camptothecin analog, administered on a 5-day schedule in patients with recurrent or refractory ovarian cancer. Proc. Am. Soc. Clin. Oncol. (2003) 22(Abstract 1877).
    • (2003) Proc. Am. Soc. Clin. Oncol. , vol.22
    • Song, Y.1    Seo, S.-S.2    Bang, Y.-J.3
  • 44
    • 0035935691 scopus 로고    scopus 로고
    • Design and optimization of 20-O-linked camptothecin glycocomjugates as anticancer agents
    • LERCHEN HG, BAUMGARTEN J, VON DEM BRUCH K et al.: Design and optimization of 20-O-linked camptothecin glycocomjugates as anticancer agents. J. Med. Chem. (2001) 44:4186-4195.
    • (2001) J. Med. Chem. , vol.44 , pp. 4186-4195
    • Lerchen, H.G.1    Baumgarten, J.2    Von Dem Bruch, K.3
  • 45
    • 85031149635 scopus 로고    scopus 로고
    • A Phase I dose scalation pharmacokinetic (PK) study of BAY 38-3441 administered as a short infusion once every three weeks
    • (Abstract 396)
    • MROSS K, SAUER U, HARING B et al.: A Phase I dose scalation pharmacokinetic (PK) study of BAY 38-3441 administered as a short infusion once every three weeks. Proc. Am. Soc. Clin. Oncol. (2002) 21(Abstract 396).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Mross, K.1    Sauer, U.2    Haring, B.3
  • 46
    • 0141653430 scopus 로고    scopus 로고
    • A Phase I study of BAY 38-3441 given as a short infusion daily for five days every 3 weeks: A National Cancer Institute of Canada Clinical Trials Group study
    • (Abstract 395)
    • SIU LL, BATIST G, BANGASH N et al.: A Phase I study of BAY 38-3441 given as a short infusion daily for five days every 3 weeks: A National Cancer Institute of Canada Clinical Trials Group study. Proc. Am. Soc. Clin. Oncol. (2002) 21(Abstract 395).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Siu, L.L.1    Batist, G.2    Bangash, N.3
  • 47
    • 1542441944 scopus 로고    scopus 로고
    • DRF-1042, a novel orally active camptothecin (CPT) analog: Safety, pharmacokinetic (PK) and pharmacodynamic evaluation in a Phase I dose escalation study
    • (Abstract 384)
    • CHATTERJEE A, DIGUMARTI R, MAMIDI RN et al.: DRF-1042, a novel orally active camptothecin (CPT) analog: Safety, pharmacokinetic (PK) and pharmacodynamic evaluation in a Phase I dose escalation study. Proc. Am. Soc. Clin. Oncol. (2002) 21(Abstract 384).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Chatterjee, A.1    Digumarti, R.2    Mamidi, R.N.3
  • 48
    • 0031909978 scopus 로고    scopus 로고
    • A Phase I clinical and pharmacological study of oral 9-nitrocamptothecin, a novel water-insoluble topoisomerase I inhibitor
    • VERSCHRAEGEN CF, NATELSON EA, GIOVANELLA BC et al.: A Phase I clinical and pharmacological study of oral 9-nitrocamptothecin, a novel water-insoluble topoisomerase I inhibitor. Anticancer Drugs (1998) 9:36-44.
    • (1998) Anticancer Drugs , vol.9 , pp. 36-44
    • Verschraegen, C.F.1    Natelson, E.A.2    Giovanella, B.C.3
  • 49
    • 0033126463 scopus 로고    scopus 로고
    • A study of 9-nitrocamptothecin (RFS-2000) in patients with advanced pancreatic cancer
    • STEHLIN JS, GIOVANELLA BC, NATELSON EA et al.: A study of 9-nitrocamptothecin (RFS-2000) in patients with advanced pancreatic cancer. Int. J. Oncol. (1999) 14:821-831.
    • (1999) Int. J. Oncol. , vol.14 , pp. 821-831
    • Stehlin, J.S.1    Giovanella, B.C.2    Natelson, E.A.3
  • 50
    • 0037216220 scopus 로고    scopus 로고
    • A Phase I study of 9-nitrocamptothecin given concurrently with capecitabine in patients with refractory, metastatic solid tumors
    • MICHAELSON MD, RYAN DP, FUCHS CS et al.: A Phase I study of 9-nitrocamptothecin given concurrently with capecitabine in patients with refractory, metastatic solid tumors. Cancer (2003) 97:148-154.
    • (2003) Cancer , vol.97 , pp. 148-154
    • Michaelson, M.D.1    Ryan, D.P.2    Fuchs, C.S.3
  • 51
    • 0038069097 scopus 로고    scopus 로고
    • Differential effects of the breast cancer resistance protein on the cellular accumulation and cytotoxicity of 9-aminocamptothecin and 9-nitrocamptothecin
    • RAJENDRA R, GOUNDER MK, SALEEM A et al.: Differential effects of the breast cancer resistance protein on the cellular accumulation and cytotoxicity of 9-aminocamptothecin and 9-nitrocamptothecin. Cancer Res. (2003) 63:3228-3233.
    • (2003) Cancer Res. , vol.63 , pp. 3228-3233
    • Rajendra, R.1    Gounder, M.K.2    Saleem, A.3
  • 52
    • 0037501242 scopus 로고    scopus 로고
    • Phase I and pharmacological study of oral 9-aminocamptothecin colloidal dispersion (NSC 603071) in patients with advanced solid tumors
    • XIONG HQ, TRAN HT, MADDEN TL, NEWMAN RA, ABRUZZESE JL: Phase I and pharmacological study of oral 9-aminocamptothecin colloidal dispersion (NSC 603071) in patients with advanced solid tumors. Clin. Cancer Res. (2003) 9:2066-2071.
    • (2003) Clin. Cancer Res. , vol.9 , pp. 2066-2071
    • Xiong, H.Q.1    Tran, H.T.2    Madden, T.L.3    Newman, R.A.4    Abruzzese, J.L.5
  • 53
    • 0242298679 scopus 로고    scopus 로고
    • A Phase I study of 9-aminocamptothecin as a colloidal dispersion formulation given as a fortnightly 72-h infusion
    • LEGUIZAMO J, QUINN M, TAKIMOTO CH et al.: A Phase I study of 9-aminocamptothecin as a colloidal dispersion formulation given as a fortnightly 72-h infusion. Cancer Chemother. Pharmacol. (2003) 52:333-338.
    • (2003) Cancer Chemother. Pharmacol. , vol.52 , pp. 333-338
    • Leguizamo, J.1    Quinn, M.2    Takimoto, C.H.3
  • 54
    • 0034687233 scopus 로고    scopus 로고
    • The novel silatecan 7-tert-butyldimethylsilyl-10-hydroxycamptothecin displays high lipophilicity, improved human blood stability, and potent anticancer activity
    • BOM D, CURRAN DP, KRUSZEWSKI S, ZIMMER SG, STRODE JT, KOHLHAGEN G: The novel silatecan 7-tert-butyldimethylsilyl-10-hydroxycamptothecin displays high lipophilicity, improved human blood stability, and potent anticancer activity. J. Med. Chem. (2000) 43:3970-3980.
    • (2000) J. Med. Chem. , vol.43 , pp. 3970-3980
    • Bom, D.1    Curran, D.P.2    Kruszewski, S.3    Zimmer, S.G.4    Strode, J.T.5    Kohlhagen, G.6
  • 55
    • 0033213921 scopus 로고    scopus 로고
    • Potent topoisomerase I inhibition by novel silatecans eliminates glioma proliferation in vitro and in vivo
    • POLLACK IF, ERFF M, BOM D, BURKET G, STRODE JT, CURRAN DP: Potent topoisomerase I inhibition by novel silatecans eliminates glioma proliferation in vitro and in vivo. Cancer Res. (1999) 59:4898-4905.
    • (1999) Cancer Res. , vol.59 , pp. 4898-4905
    • Pollack, I.F.1    Erff, M.2    Bom, D.3    Burket, G.4    Strode, J.T.5    Curran, D.P.6
  • 56
    • 0033809224 scopus 로고    scopus 로고
    • New highly lipophilic camptothecin BNP1350 is an effective drug in experimental human cancer
    • VAN HATTUM AH, PINEDO HM, SCHLUPER HMM, HAUSHEER FH, BOVEN E: New highly lipophilic camptothecin BNP1350 is an effective drug in experimental human cancer. Int. J. Cancer (2000) 88:260-266.
    • (2000) Int. J. Cancer , vol.88 , pp. 260-266
    • Van Hattum, A.H.1    Pinedo, H.M.2    Schluper, H.M.M.3    Hausheer, F.H.4    Boven, E.5
  • 57
    • 0036643756 scopus 로고    scopus 로고
    • Novel camptothecin derivative BNP1350 in experimental human ovarian cancer: Determination of efficacy and possible mechanisms of resistance
    • VAN HATTUM AH, SCHLUPER HMM, HAUSHEER FH, PINEDO HM, BOVEN E: Novel camptothecin derivative BNP1350 in experimental human ovarian cancer: Determination of efficacy and possible mechanisms of resistance. Int. J. Cancer (2002) 100:22-29.
    • (2002) Int. J. Cancer , vol.100 , pp. 22-29
    • Van Hattum, A.H.1    Schluper, H.M.M.2    Hausheer, F.H.3    Pinedo, H.M.4    Boven, E.5
  • 59
    • 1542651513 scopus 로고    scopus 로고
    • Phase II trial of karenitecin, a novel topoisomerase I inhibitor in metastatic melanoma: Clinical and translational study
    • (Abstract 2871)
    • DAUD A, BALAR B, VALKOV N et al.: Phase II trial of karenitecin, a novel topoisomerase I inhibitor in metastatic melanoma: clinical and translational study. Proc. Am. Soc. Clin. Oncol. (2003) 22(Abstract 2871).
    • (2003) Proc. Am. Soc. Clin. Oncol. , vol.22
    • Daud, A.1    Balar, B.2    Valkov, N.3
  • 60
    • 1542756835 scopus 로고    scopus 로고
    • Phase II trial of karenitecin in patients with refractory non-small cell lung cancer (NSCLC): CALGB 30004
    • (Abstract 2706)
    • HERNDON JE, MILLER AA, ZHANG C et al.: Phase II trial of karenitecin in patients with refractory non-small cell lung cancer (NSCLC): CALGB 30004. Proc. Am. Soc. Clin. Oncol. (2003) 22(Abstract 2706).
    • (2003) Proc. Am. Soc. Clin. Oncol. , vol.22
    • Herndon, J.E.1    Miller, A.A.2    Zhang, C.3
  • 61
    • 0037212083 scopus 로고    scopus 로고
    • Homocamptothecins: Potent topoisomerase I inhibitors and promising anticancer drugs
    • BAILLY C: HomPcamptothecins: potent topoisomerase I inhibitors and promising anticancer drugs. Crit. Rev. in Oncol. Hematol. (2003) 45:91-108.
    • (2003) Crit. Rev. in Oncol. Hematol. , vol.45 , pp. 91-108
    • Bailly, C.1
  • 62
    • 2442594110 scopus 로고    scopus 로고
    • A pharmacological comparison of Phase I studies of diflomotecan (BN80915) administered orally and intravenously daily for 5 days every 3 weeks in patients with solid tumors
    • (Abstract 534)
    • SCOTT LC, SOEPENBERG O, TWELVES C et al.: A pharmacological comparison of Phase I studies of diflomotecan (BN80915) administered orally and intravenously daily for 5 days every 3 weeks in patients with solid tumors. Proc. Am. Soc. Clin. Oncol. (2002) 21(Abstract 534).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Scott, L.C.1    Soepenberg, O.2    Twelves, C.3
  • 63
    • 0141455147 scopus 로고    scopus 로고
    • Phase I pharmacological and bioavailability study of oral diflomotecan (BN80915), a novel E-Ring-modified camptothecin analogue in adults with solid tumors
    • GELDERBLOM H, SALAZAR R, VERWEIJ J et al.: Phase I pharmacological and bioavailability study of oral diflomotecan (BN80915), a novel E-Ring-modified camptothecin analogue in adults with solid tumors. Clin. Cancer Res. (2003) 9:4101-4107.
    • (2003) Clin. Cancer Res. , vol.9 , pp. 4101-4107
    • Gelderblom, H.1    Salazar, R.2    Verweij, J.3
  • 64
    • 0034687256 scopus 로고    scopus 로고
    • Novel 7-substituted camptothecins with potent antitumor activity
    • DALLAVALLE S, DELSOLDATO T, FERRARI A et al.: Novel 7-substituted camptothecins with potent antitumor activity. J. Med. Chem. (2000) 43:3963-3969.
    • (2000) J. Med. Chem. , vol.43 , pp. 3963-3969
    • Dallavalle, S.1    Delsoldato, T.2    Ferrari, A.3
  • 65
    • 0035476245 scopus 로고    scopus 로고
    • Potent antitumor activity and improved pharmacological profile of ST1481, a novel 7-substituted camptothecin
    • DE CESARE M, PRATESI G, PEREGO P et al.: Potent antitumor activity and improved pharmacological profile of ST1481, a novel 7-substituted camptothecin. Cancer Res. (2001) 61:7189-7195.
    • (2001) Cancer Res. , vol.61 , pp. 7189-7195
    • De Cesare, M.1    Pratesi, G.2    Perego, P.3
  • 66
    • 0036898629 scopus 로고    scopus 로고
    • Pattern of antitumor activity of a novel camptothecin, ST1481, in a large panel of human tumor xenografts
    • PRATESI G, DE CESARE M, CARENINI N et al.: Pattern of antitumor activity of a novel camptothecin, ST1481, in a large panel of human tumor xenografts. Clin. Cancer Res. (2002) 8:3904-3909.
    • (2002) Clin. Cancer Res. , vol.8 , pp. 3904-3909
    • Pratesi, G.1    De Cesare, M.2    Carenini, N.3
  • 67
    • 3142700107 scopus 로고    scopus 로고
    • Clinical pharmacokinetic profile of gimatecan (ST1481), a new derivative
    • (Abstract 476)
    • ZUCCHETTI M, PACE S, FRAPOLLI R et al.: Clinical pharmacokinetic profile of gimatecan (ST1481), a new derivative. Proc. Am. Soc. Clin. Oncol. (2002) 21(Abstract 476).
    • (2002) Proc. Am. Soc. Clin. Oncol. , vol.21
    • Zucchetti, M.1    Pace, S.2    Frapolli, R.3
  • 68
    • 1542330612 scopus 로고    scopus 로고
    • Subcellular localization of the camptothecin analogues, topotecan and gimatecan
    • (In press)
    • CROCE A, BOTTIROLI G, SUPINO R et al.: Subcellular localization of the camptothecin analogues, topotecan and gimatecan. Biochem. Pharmacol. (2004) (In press).
    • (2004) Biochem. Pharmacol.
    • Croce, A.1    Bottiroli, G.2    Supino, R.3
  • 69
    • 12444297898 scopus 로고    scopus 로고
    • Antiangiogenic effects of the novel camptothecin ST1481 (gimatecan) in human tumor xenografts
    • PETRANGOLINI G, PRATESI G, DE CESARE M et al.: Antiangiogenic effects of the novel camptothecin ST1481 (gimatecan) in human tumor xenografts. Mol. Cancer Res. (2003) 1:863-870.
    • (2003) Mol. Cancer Res. , vol.1 , pp. 863-870
    • Petrangolini, G.1    Pratesi, G.2    De Cesare, M.3
  • 70
    • 3142761813 scopus 로고    scopus 로고
    • A Phase I study of the oral camptothecin gimatecan with a design of cencerted dose escalation in three schedules of different dosing-duration
    • (Abstract 554)
    • GIANNI L, HESS D, BASELGA J et al.: A Phase I study of the oral camptothecin gimatecan with a design of cencerted dose escalation in three schedules of different dosing-duration. Proc. Am. Soc. Clin. Oncol. (2003) 22(Abstract 554).
    • (2003) Proc. Am. Soc. Clin. Oncol. , vol.22
    • Gianni, L.1    Hess, D.2    Baselga, J.3
  • 71
    • 1542546557 scopus 로고    scopus 로고
    • Phase I/II trial of gimatecan in patients with recurrent malignant glioma
    • (Abstract 416)
    • ALDERSON L, SUPKO J, MAESTRI X et al. Phase I/II trial of gimatecan in patients with recurrent malignant glioma. Proc. Am. Soc. Clin. Oncol. (2003) 22:(Abstract 416).
    • (2003) Proc. Am. Soc. Clin. Oncol. , vol.22
    • Alderson, L.1    Supko, J.2    Maestri, X.3
  • 72
    • 2642540468 scopus 로고    scopus 로고
    • Phase I trial of gimatecan given orally once a week for 3 or 4 weeks in patients with advanced solid tumors
    • (Abstract 557)
    • ZHU AX, READY NE, CLARK JW et al.: Phase I trial of gimatecan given orally once a week for 3 or 4 weeks in patients with advanced solid tumors. Proc. Am. Soc. Clin. Oncol. (2003) 22(Abstract 557).
    • (2003) Proc. Am. Soc. Clin. Oncol. , vol.22
    • Zhu, A.X.1    Ready, N.E.2    Clark, J.W.3
  • 73
    • 0026694788 scopus 로고
    • Passive tumor targeting of soluble macromolecules drug conjugates
    • SEYMOUR LW: Passive tumor targeting of soluble macromolecules drug conjugates. Crit. Rev. Ther. Drug Carrier Sys. (1992) 9:135-187.
    • (1992) Crit. Rev. Ther. Drug Carrier Sys. , vol.9 , pp. 135-187
    • Seymour, L.W.1
  • 75
    • 0034725772 scopus 로고    scopus 로고
    • 20-O-acylcamptothecin derivatives: Evidence for lactone stabilization
    • ZHAO H, LEE C, SAI P et al.: 20-O-acylcamptothecin derivatives: Evidence for lactone stabilization. J. Org. Chem. (2000) 65:4601-4606.
    • (2000) J. Org. Chem. , vol.65 , pp. 4601-4606
    • Zhao, H.1    Lee, C.2    Sai, P.3
  • 76
    • 18744372716 scopus 로고    scopus 로고
    • A Phase I and pharmacokinetic study of pegylated camptothecin as a 1-hour infusion every 3 weeks in patients with advanced solid malignancies
    • ROWINSKY EK, RIZZO J, OCHOA L et al.: A Phase I and pharmacokinetic study of pegylated camptothecin as a 1-hour infusion every 3 weeks in patients with advanced solid malignancies. J. Clin. Oncol. (2003) 21:148-157.
    • (2003) J. Clin. Oncol. , vol.21 , pp. 148-157
    • Rowinsky, E.K.1    Rizzo, J.2    Ochoa, L.3
  • 77
    • 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) 87:608-614.
    • (2002) Br. J. Cancer , vol.87 , pp. 608-614
    • Schoemaker, N.E.1    Van Kesteren, C.2    Rosing, H.3
  • 78
    • 0242360811 scopus 로고    scopus 로고
    • Assessment of normal and tumor tissue uptake of MAG-CPT, a polymer-bound prodrug of camptothecin, in patients undergoing elective surgery for colorectal carcinoma
    • SARAPA N, BRITTO MR, SPEED W et al.: Assessment of normal and tumor tissue uptake of MAG-CPT, a polymer-bound prodrug of camptothecin, in patients undergoing elective surgery for colorectal carcinoma. Cancer Chemother. Pharmacol. (2003) 52:424-430.
    • (2003) Cancer Chemother. Pharmacol. , vol.52 , pp. 424-430
    • Sarapa, N.1    Britto, M.R.2    Speed, W.3
  • 79
    • 0037619162 scopus 로고    scopus 로고
    • CM-dextran-polyalcohol-camptothecin conjugate: DE-310 with a novel carrier system and its preclinical data
    • INOUE K, KUMAZAWA E, KUGA H, SUSAKI H, MASUBUCHI N, KAJIMURA T: CM-dextran-polyalcohol-camptothecin conjugate: DE-310 with a novel carrier system and its preclinical data. Adv. Exp. Med. Biol. (2003) 519:145-153.
    • (2003) Adv. Exp. Med. Biol. , vol.519 , pp. 145-153
    • Inoue, K.1    Kumazawa, E.2    Kuga, H.3    Susaki, H.4    Masubuchi, N.5    Kajimura, T.6
  • 80
    • 1542441949 scopus 로고    scopus 로고
    • A Phase I and pharmacokinetic study of DE-310 administered as a 3 hour infusion every 4 weeks (wks) to patients (pts) with advanced solid tumors or lymphomas
    • (Abstract 522)
    • TAKIMOTO CHM, FORERO L, SCHWARTZ GH et al.: A Phase I and pharmacokinetic study of DE-310 administered as a 3 hour infusion every 4 weeks (wks) to patients (pts) with advanced solid tumors or lymphomas. Proc. Am. Soc. Clin. Oncol. (2003) 22(Abstract 522).
    • (2003) Proc. Am. Soc. Clin. Oncol. , vol.22
    • Takimoto, C.H.M.1    Forero, L.2    Schwartz, G.H.3
  • 81
    • 22144437831 scopus 로고    scopus 로고
    • Phase I and PK study of DE-310 (D) given once every 2 or 6 wks (w) in pts with solid tumors
    • (Abstract 523)
    • SOEPENBERG O, DE JONGE M, SPARREBOOM A et al.: Phase I and PK study of DE-310 (D) given once every 2 or 6 wks (w) in pts with solid tumors. Proc. Am. Soc. Clin. Oncol. (2003) 22(Abstract 523).
    • (2003) Proc. Am. Soc. Clin. Oncol. , vol.22
    • Soepenberg, O.1    De Jonge, M.2    Sparreboom, A.3
  • 82
    • 0037413560 scopus 로고    scopus 로고
    • Synthesis and in vivo antitumor activity of poly(L-glutamic acid) conjugates of 20S-camptothecin
    • BHATT R, DE VRIES P, TULINSKY J et al.: Synthesis and in vivo antitumor activity of poly(L-glutamic acid) conjugates of 20S-camptothecin. J. Med. Chem. (2003) 46:190-193.
    • (2003) J. Med. Chem. , vol.46 , pp. 190-193
    • Bhatt, R.1    De Vries, P.2    Tulinsky, J.3
  • 83
    • 0035816202 scopus 로고    scopus 로고
    • Water-soluble poly-(L-glutamic acid)-gly-camptothecin conjugates enhance camptothecin stability and efficacy in vivo
    • SINGER JW, BHATT R, TULINSKY J et al.: Water-soluble poly-(L-glutamic acid)-gly-camptothecin conjugates enhance camptothecin stability and efficacy in vivo. J. Control Release (2001) 74:243-247.
    • (2001) J. Control Release , vol.74 , pp. 243-247
    • Singer, J.W.1    Bhatt, R.2    Tulinsky, J.3
  • 84
    • 0034509559 scopus 로고    scopus 로고
    • Conjugation of camptothecins to poly-(L-glutamic acid)
    • SINGER JW, DE VRIES P, BHATT R et al.: Conjugation of camptothecins to poly-(L-glutamic acid). Ann. NY Acad. Sci. (2000) 922:136-150.
    • (2000) Ann. NY Acad. Sci. , vol.922 , pp. 136-150
    • Singer, J.W.1    De Vries, P.2    Bhatt, R.3
  • 85
    • 0026099599 scopus 로고
    • Synthesis of water-soluble (aminoalkyl) camptothecin analogues: Inhibition of topoisomerase I and antitumor activity
    • KINGSBURY WD, BOEHM JC, JAKAS DR et al.: Synthesis of water-soluble (aminoalkyl) camptothecin analogues: Inhibition of topoisomerase I and antitumor activity. J. Med. Chem. (1991) 34:98-107.
    • (1991) J. Med. Chem. , vol.34 , pp. 98-107
    • Kingsbury, W.D.1    Boehm, J.C.2    Jakas, D.R.3
  • 86
    • 0023552964 scopus 로고
    • Antitumor activity of 7-ethyl-10-[4-(1-piperidino)-1-piperidino]carbonyloxy-camptothecin, a novel water-soluble derivative of camptothecin, against murine tumors
    • KUNIMOTO T, NITTA K, TANAKA T et al.: Antitumor activity of 7-ethyl-10-[4-(1-piperidino)-1-piperidino]carbonyloxy-camptothecin, a novel water-soluble derivative of camptothecin, against murine tumors. Cancer Res. (1987) 47:5944-5947.
    • (1987) Cancer Res. , vol.47 , pp. 5944-5947
    • Kunimoto, T.1    Nitta, K.2    Tanaka, T.3
  • 87
    • 0025912553 scopus 로고
    • Complete growth inhibition of human cancer xenografts in nude mice by treatment with 20-(S)-camptothecin
    • GIOVANELLA BC, HINZ HR, KOZIELSIK AJ, STEHLIN JS Jr, SILBER R, POTMESIL M: Complete growth inhibition of human cancer xenografts in nude mice by treatment with 20-(S)-camptothecin. Cancer Res. (1991) 51:3052-3055.
    • (1991) Cancer Res. , vol.51 , pp. 3052-3055
    • Giovanella, B.C.1    Hinz, H.R.2    Kozielsik, A.J.3    Stehlin Jr., J.S.4    Silber, R.5    Potmesil, M.6
  • 88
    • 0029150444 scopus 로고
    • 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
  • 89
    • 0141590347 scopus 로고    scopus 로고
    • Quantitative determination of DRF-1042 in human plasma by HPLC: Validation and application in clinical pharmacokinetics
    • UPRETI VV, MAMIDI RNVS, KATNENI K, SRINIVAS NR: Quantitative determination of DRF-1042 in human plasma by HPLC: Validation and application in clinical pharmacokinetics. Biomed. Chromatog. (2003) 17:385-390.
    • (2003) Biomed. Chromatog. , vol.17 , pp. 385-390
    • Upreti, V.V.1    Mamidi, R.N.V.S.2    Katneni, K.3    Srinivas, N.R.4
  • 90
    • 17444405966 scopus 로고    scopus 로고
    • Encapsulation of the topoisomerase I inhibitor GL147211C in pegylated (STEALTH) liposomes: Pharmacokinetics and antitumor activity in HT29 colon tumor xenografts
    • COLBERN GT, DYKES DJ, ENGBERS C et al.: Encapsulation of the topoisomerase I inhibitor GL147211C in pegylated (STEALTH) liposomes: pharmacokinetics and antitumor activity in HT29 colon tumor xenografts. Clin. Cancer Res. (1998) 4:3077-3082.
    • (1998) Clin. Cancer Res. , vol.4 , pp. 3077-3082
    • Colbern, G.T.1    Dykes, D.J.2    Engbers, C.3
  • 91
    • 0001207616 scopus 로고    scopus 로고
    • Karenitecins (part II): A novel class of orally active highly lipophilic topoisomerase I inhibitors
    • (Abstract 2862)
    • HAUSHEER F, HARIDAS K, ZHAO M et al.: Karenitecins (part II): a novel class of orally active highly lipophilic topoisomerase I inhibitors. Proc. Am. Ass. Cancer Res. (1998) 39:(Abstract 2862).
    • (1998) Proc. Am. Ass. Cancer Res. , vol.39
    • Hausheer, F.1    Haridas, K.2    Zhao, M.3
  • 92
    • 0032585548 scopus 로고    scopus 로고
    • Homocamptothecins: Synthesis and antitumor activity of novel E-ring-modified camptothecin analogues
    • LAVERGNE O, LESUEUR-GINOT L, PLA RODAS F et al.: Homocamptothecins: Synthesis and antitumor activity of novel E-ring-modified camptothecin analogues. J. Med. Chem. (1998) 41:5410-5419.
    • (1998) J. Med. Chem. , vol.41 , pp. 5410-5419
    • Lavergne, O.1    Lesueur-Ginot, L.2    Pla Rodas, F.3
  • 93
    • 1542546563 scopus 로고    scopus 로고
    • NCIC CTG Ind. 134: A Phase I study of a novel glycoconjugated camptothecin (BAY 38-3441) given as a short infusion daily for five days every 3 weeks
    • (Abstract 2896)
    • BATIST G, SIUAL, MACLEAN M et al.: NCIC CTG Ind. 134: a Phase I study of a novel glycoconjugated camptothecin (BAY 38-3441) given as a short infusion daily for five days every 3 weeks. Proc. Am. Ass. Cancer Res. (2001) 42:(Abstract 2896).
    • (2001) Proc. Am. Ass. Cancer Res. , vol.42
    • Batist, G.1    Siu, L.2    Maclean, M.3
  • 94
    • 0033997597 scopus 로고    scopus 로고
    • Polymer-bound camptothecin: Initial biodistribution and antitumor activity studies
    • CAIOLFA VR, ZAMAI M, FIORINO A et al.: Polymer-bound camptothecin: Initial biodistribution and antitumor activity studies. J. Control Release (2000) 65:105-119.
    • (2000) J. Control Release , vol.65 , pp. 105-119
    • Caiolfa, V.R.1    Zamai, M.2    Fiorino, A.3
  • 95
    • 0036354863 scopus 로고    scopus 로고
    • Enhancing the anticancer efficacy of camptothecin using biotinylated poly(ethyleneglycol) conjugates in sensitivie and multidrug-resistant human ovarian carcinoma cells
    • MINKO T, PARANJPE PV, LALLOO BQA et al.: Enhancing the anticancer efficacy of camptothecin using biotinylated poly(ethyleneglycol) conjugates in sensitivie and multidrug-resistant human ovarian carcinoma cells. Cancer Chemother. Pharmacol. (2002) 50:143-150.
    • (2002) Cancer Chemother. Pharmacol. , vol.50 , pp. 143-150
    • Minko, T.1    Paranjpe, P.V.2    Lalloo, B.Q.A.3
  • 96
    • 0003198535 scopus 로고    scopus 로고
    • Effective first line therapy of ovarian cancer (OC) with cisplatin and prolonged topotecan infusion-a NY-GOG/ECOG Study
    • (Abstract)
    • SPEYER J, HOCHSTER H, WADLER S et al.: Effective first line therapy of ovarian cancer (OC) with cisplatin and prolonged topotecan infusion-a NY-GOG/ECOG Study. Proc. Am. Soc. Clin. Oncol. (2000) 19:380a (Abstract).
    • (2000) Proc. Am. Soc. Clin. Oncol. , vol.19
    • Speyer, J.1    Hochster, H.2    Wadler, S.3
  • 97
    • 0001434179 scopus 로고    scopus 로고
    • A Phase II study of topotecan (T), carboplatin (C) and paclitaxel (P) as front line treatment in suboptimal advanced epithelial ovarian cancer (AEOC)
    • (Abstract)
    • BOLIS G, SCARFONE G, SCIATTA C, PARAZZIN F: A Phase II study of topotecan (T), carboplatin (C) and paclitaxel (P) as front line treatment in suboptimal advanced epithelial ovarian cancer (AEOC). Proc. Am. Soc. Clin. Oncol. (2000) 19:390a (Abstract).
    • (2000) Proc. Am. Soc. Clin. Oncol. , vol.19
    • Bolis, G.1    Scarfone, G.2    Sciatta, C.3    Parazzin, F.4
  • 98
    • 0003293064 scopus 로고    scopus 로고
    • Paclitaxel (P) + topotecan (T) + GCSF for previously untreated extensive small cell lung cancer (E-SCLC): Preliminary analysis of cancer and leukaemia group B (CALGB) 9430
    • (Abstract)
    • LYNCH T, HERNDON J, LYSS A et al.: Paclitaxel (P) + topotecan (T) + GCSF for previously untreated extensive small cell lung cancer (E-SCLC): Preliminary analysis of cancer and leukaemia group B (CALGB) 9430. Proc. Am. Soc. Clin. Oncol. (2000) 19:491a (Abstract).
    • (2000) Proc. Am. Soc. Clin. Oncol. , vol.19
    • Lynch, T.1    Herndon, J.2    Lyss, A.3
  • 99
    • 0001285863 scopus 로고    scopus 로고
    • Paclitaxel, carboplatin, and topotecan in the treatment of small cell lung cancer: A Phase II trial of the Minnie Pearl Cancer Research Network
    • (Abstract)
    • GRAY J, HAINSWORTH J, BURRIS H et al.: Paclitaxel, carboplatin, and topotecan in the treatment of small cell lung cancer: A Phase II trial of the Minnie Pearl Cancer Research Network. Proc. Am. Soc. Clin. Oncol. (2000) 19:494a (Abstract).
    • (2000) Proc. Am. Soc. Clin. Oncol. , vol.19
    • Gray, J.1    Hainsworth, J.2    Burris, H.3
  • 100
    • 12244253729 scopus 로고    scopus 로고
    • European organization for research and treatment of cancer (EORTC) 08957 Phase II study of topotecan in combination with cisplatin as second-line treatment of refractory and sensitive small cell lung cancer
    • ARDIZZONI A, MANEGOLD C, DEBRUYNE C et al.: European organization for research and treatment of cancer (EORTC) 08957 Phase II study of topotecan in combination with cisplatin as second-line treatment of refractory and sensitive small cell lung cancer. Clin. Cancer Res. (2003) 9:143-150.
    • (2003) Clin. Cancer Res. , vol.9 , pp. 143-150
    • Ardizzoni, A.1    Manegold, C.2    Debruyne, C.3
  • 101
    • 0036784446 scopus 로고    scopus 로고
    • A Phase I-II study of sequential administration of topotecan and oral etoposide (topoisomerase I and II inhibitors) in the treatment of patients with small cell lung carcinoma
    • MOK TS, WONG H, ZEE B et al.: A Phase I-II study of sequential administration of topotecan and oral etoposide (topoisomerase I and II inhibitors) in the treatment of patients with small cell lung carcinoma. Cancer (2002) 95:1511-1519.
    • (2002) Cancer , vol.95 , pp. 1511-1519
    • Mok, T.S.1    Wong, H.2    Zee, B.3
  • 102
    • 0037105608 scopus 로고    scopus 로고
    • A Phase II trial of topotecan and gemcitabine in patients with previously treated, advanced nonsmall cell lung carcinoma
    • RINALDI DA, LORMAND NA, BRIERRE JE et al.: A Phase II trial of topotecan and gemcitabine in patients with previously treated, advanced nonsmall cell lung carcinoma. Cancer (2002) 95:1274-1278.
    • (2002) Cancer , vol.95 , pp. 1274-1278
    • Rinaldi, D.A.1    Lormand, N.A.2    Brierre, J.E.3
  • 103
    • 0032884937 scopus 로고    scopus 로고
    • Topotecan and cytarabine is an active combination regimen in myelodysplastic syndromes and chronic myelomonocytic leukaemia
    • BERAN M, ESTEY E, O'BRIEN S et al.: Topotecan and cytarabine is an active combination regimen in myelodysplastic syndromes and chronic myelomonocytic leukaemia. J. Clin. Oncol. (1999) 17:2819-2830.
    • (1999) J. Clin. Oncol. , vol.17 , pp. 2819-2830
    • Beran, M.1    Estey, E.2    O'brien, S.3
  • 104
    • 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 JT, 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.T.1    Cunningham, D.2    Roth, A.D.3
  • 105
    • 0034727063 scopus 로고    scopus 로고
    • Irinotecan plus fluorouracil and leucovorin for metastatic colorectal cancer
    • SALTZ LB, COX JV, BLANKE C et al.: Irinotecan plus fluorouracil and leucovorin for metastatic colorectal cancer. 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
  • 106
    • 0000437978 scopus 로고    scopus 로고
    • Randomized trial comparing cisplatin and irinotecan versus cisplatin and vindesine versus irinotecan alone in advanced non-small cell lung cancer, a multicenter Phase III study
    • (Abstract)
    • MASUDA N, FUKUOKA M, NEGORO S et al.: Randomized trial comparing cisplatin and irinotecan versus cisplatin and vindesine versus irinotecan alone in advanced non-small cell lung cancer, a multicenter Phase III study. Proc. Am. Soc. Clin. Oncol. (1999) 18:459a (Abstract).
    • (1999) Proc. Am. Soc. Clin. Oncol. , vol.18
    • Masuda, N.1    Fukuoka, M.2    Negoro, S.3
  • 107
    • 0000314976 scopus 로고    scopus 로고
    • Randomized multicenter Phase III trial of irinotecan (CPT-11) and cisplatin (CDDP) versus CDDP and vindesine (VDS) in patients with advanced non-small cell lung cancer (NSCLC)
    • (Abstract)
    • NIHO S, NAGAO K, NISHIWAKI Y et al.: Randomized multicenter Phase III trial of irinotecan (CPT-11) and cisplatin (CDDP) versus CDDP and vindesine (VDS) in patients with advanced non-small cell lung cancer (NSCLC). Proc. Am. Soc. Clin. Oncol. (1999) 18:1897 (Abstract).
    • (1999) Proc. Am. Soc. Clin. Oncol. , vol.18 , pp. 1897
    • Niho, S.1    Nagao, K.2    Nishiwaki, Y.3
  • 108
    • 0037050354 scopus 로고    scopus 로고
    • Irinotecan plus cisplatin compared with etoposide plus cisplatin for extensive small-cell lung cancer
    • NODA K, NISHIWAKA Y, KAWAHARA M. et al.: Irinotecan plus cisplatin compared with etoposide plus cisplatin for extensive small-cell lung cancer. N. Engl. J. Med. (2002) 346:85-91.
    • (2002) N. Engl. J. Med. , vol.346 , pp. 85-91
    • Noda, K.1    Nishiwaka, Y.2    Kawahara, M.3
  • 109
    • 0032919992 scopus 로고    scopus 로고
    • Phase II study of a combination of irinotecan and cisplatin against metastatic gastric cancer
    • BOKU N, OHTSU A, SHIMADA Y et al.: Phase II study of a combination of irinotecan and cisplatin against metastatic gastric cancer. J. Clin. Oncol. (1999) 17:319-323.
    • (1999) J. Clin. Oncol. , vol.17 , pp. 319-323
    • Boku, N.1    Ohtsu, A.2    Shimada, Y.3
  • 110
    • 0742271770 scopus 로고    scopus 로고
    • Phase II study of irinotecan and 5-fluorouracil/leucovorin in patients with primary refractory or relapsed advanced oesophageal and gastric carcinoma
    • ASSERSOHN L, BROWN G, CUNNINGHAM D et al.: Phase II study of irinotecan and 5-fluorouracil/leucovorin in patients with primary refractory or relapsed advanced oesophageal and gastric carcinoma. Ann. Oncol. (2004) 15:64-69.
    • (2004) Ann. Oncol. , vol.15 , pp. 64-69
    • Assersohn, L.1    Brown, G.2    Cunningham, D.3
  • 111
    • 0032887574 scopus 로고    scopus 로고
    • Phase II trial of weekly irinotecan plus cisplatin in advanced esophageal cancer
    • ILSON DH, SALTZ L, ENZINGER P et al.: Phase II trial of weekly irinotecan plus cisplatin in advanced esophageal cancer. J. Clin. Oncol. (1999) 17:3270-3275.
    • (1999) J. Clin. Oncol. , vol.17 , pp. 3270-3275
    • Ilson, D.H.1    Saltz, L.2    Enzinger, P.3
  • 112
    • 0036498787 scopus 로고    scopus 로고
    • Irinotecan plus gemcitabine induces both radiographic and CA 19-9 tumor marker responses in patients with previously untreated advanced pancreatic cancer
    • ROCHA LIMA CM, SAVARESE D, BRUCKNER H et al.: Irinotecan plus gemcitabine induces both radiographic and CA 19-9 tumor marker responses in patients with previously untreated advanced pancreatic cancer. J. Clin. Oncol. (2002) 20:1182-1191.
    • (2002) J. Clin. Oncol. , vol.20 , pp. 1182-1191
    • Rocha Lima, C.M.1    Savarese, D.2    Bruckner, H.3
  • 113
    • 12244297140 scopus 로고    scopus 로고
    • Treatment of pancreatic cancer with a combination of irinotecan (CPT-11) and gemcitabine: A multicenter Phase II study by the Greek Cooperative Groups for Pancreatic Cancer
    • STATHOPOULOS GP, RIGATOS SK, DIMOPOULOS MA et al.: Treatment of pancreatic cancer with a combination of irinotecan (CPT-11) and gemcitabine: A multicenter Phase II study by the Greek Cooperative Groups for Pancreatic Cancer. Ann. Oncol. (2003) 14:388-394.
    • (2003) Ann. Oncol. , vol.14 , pp. 388-394
    • Stathopoulos, G.P.1    Rigatos, S.K.2    Dimopoulos, M.A.3


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