Literature DB >> 16133797

Phase I and pharmacokinetic study of Bay 38-3441, a camptothecin glycoconjugate, administered as a 30-minute infusion daily for five days every 3 weeks in patients with advanced solid malignancies.

Eric X Chen1, Gerald Batist, Lillian L Siu, Naeema Bangash, Martha Maclean, Lynn McIntosh, Wilson H Miller, Amit M Oza, Chetan Lathia, Oana Petrenciuc, Lesley Seymour.   

Abstract

Bay 38-3441 is a camptothecin glycoconjugate which stabilizes the active lactone form of camptothecin and allows selective uptake into tumor cells. We conducted a phase I study of Bay 38-3441 administered as a 30-minute infusion daily for five consecutive days every 21 days. Thirty-one patients were enrolled at 8 dose levels. Most common nonhematologic side effects were diarrhea (29%), vomiting (19%), nausea (19%), lethargy (13%), and abdominal pain (10%). The main hematologic toxicity was prolonged neutropenia. Nine patients had a best response of stable disease with a median duration of 2.7 months (range: 2.3-20.6 months). The study was closed without reaching the maximum tolerated dose (MTD) due to excessive toxicity in a companion trial resulting in termination of development of this agent. Bay 38-3441 was well tolerated in this study with granulocytopenia as the main hematologic toxicity. This study showed that glycoconjugation is a feasible delivery technique for camptothecin.

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Year:  2005        PMID: 16133797     DOI: 10.1007/s10637-005-2905-1

Source DB:  PubMed          Journal:  Invest New Drugs        ISSN: 0167-6997            Impact factor:   3.850


  25 in total

1.  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.

Authors:  P Therasse; S G Arbuck; E A Eisenhauer; J Wanders; R S Kaplan; L Rubinstein; J Verweij; M Van Glabbeke; A T van Oosterom; M C Christian; S G Gwyther
Journal:  J Natl Cancer Inst       Date:  2000-02-02       Impact factor: 13.506

2.  Mortality associated with irinotecan plus bolus fluorouracil/leucovorin: summary findings of an independent panel.

Authors:  M L Rothenberg; N J Meropol; E A Poplin; E Van Cutsem; S Wadler
Journal:  J Clin Oncol       Date:  2001-09-15       Impact factor: 44.544

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Journal:  J Pharm Sci       Date:  1995-04       Impact factor: 3.534

Review 4.  Clinical pharmacokinetics and metabolism of irinotecan (CPT-11).

Authors:  R H Mathijssen; R J van Alphen; J Verweij; W J Loos; K Nooter; G Stoter; A Sparreboom
Journal:  Clin Cancer Res       Date:  2001-08       Impact factor: 12.531

5.  Phase I clinical and pharmacological studies of 20-(S)-camptothecin and 20-(S)-9-nitrocamptothecin as anticancer agents.

Authors:  E A Natelson; B C Giovanella; C F Verschraegen; K M Fehir; P D De Ipolyi; N Harris; J S Stehlin
Journal:  Ann N Y Acad Sci       Date:  1996-12-13       Impact factor: 5.691

6.  Preliminary pharmacologic and clinical evaluation of camptothecin sodium (NSC-100880).

Authors:  J A Gottlieb; A M Guarino; J B Call; V T Oliverio; J B Block
Journal:  Cancer Chemother Rep       Date:  1970-12

7.  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.

Authors:  E K Rowinsky; L B Grochow; D S Ettinger; S E Sartorius; B G Lubejko; T L Chen; M K Rock; R C Donehower
Journal:  Cancer Res       Date:  1994-01-15       Impact factor: 12.701

8.  A phase I clinical and pharmacokinetic study of the camptothecin glycoconjugate, BAY 38-3441, as a daily infusion in patients with advanced solid tumors.

Authors:  K Mross; H Richly; N Schleucher; S Korfee; M Tewes; M E Scheulen; S Seeber; T Beinert; M Schweigert; U Sauer; C Unger; D Behringer; E Brendel; C G Haase; D Voliotis; D Strumberg
Journal:  Ann Oncol       Date:  2004-08       Impact factor: 32.976

9.  Phase I and pharmacokinetic study of DX-8951f (exatecan mesylate), a hexacyclic camptothecin, on a daily-times-five schedule in patients with advanced leukemia.

Authors:  Francis J Giles; Jorge E Cortes; Deborah A Thomas; Guillermo Garcia-Manero; Stephan Faderl; Sima Jeha; Robert L De Jager; Hagop M Kantarjian
Journal:  Clin Cancer Res       Date:  2002-07       Impact factor: 12.531

10.  Pharmacological correlation between total drug concentration and lactones of CPT-11 and SN-38 in patients treated with CPT-11.

Authors:  Y Sasaki; Y Yoshida; K Sudoh; H Hakusui; H Fujii; T Ohtsu; H Wakita; T Igarashi; K Itoh
Journal:  Jpn J Cancer Res       Date:  1995-01
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  2 in total

Review 1.  Camptothecin (CPT) and its derivatives are known to target topoisomerase I (Top1) as their mechanism of action: did we miss something in CPT analogue molecular targets for treating human disease such as cancer?

Authors:  Fengzhi Li; Tao Jiang; Qingyong Li; Xiang Ling
Journal:  Am J Cancer Res       Date:  2017-12-01       Impact factor: 6.166

2.  The fate of camptothecin glycoconjugate: report of a clinical hold during a phase II study of BAY 56-3722 (formerly BAY 38-3441), in patients with recurrent or metastatic colorectal cancer resistant/refractory to irinotecan.

Authors:  Marije Slingerland; Hans Gelderblom
Journal:  Invest New Drugs       Date:  2011-05-06       Impact factor: 3.850

  2 in total

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