Phase I and pharmacokinetic study of continuous twice weekly intravenous administration of Cilengitide (EMD 121974), a novel inhibitor of the integrins αvβ3 and αvβ5 in patients with advanced solid tumours
A single-agent dose escalating phase I and pharmacokinetic study with Cilengitide, an inhibitor of the integrins αvβ3 and αvβ5, was performed to determine its safety and toxicity. Cilengitide was administered as a one-hour infusion twice weekly without interruption to patients with histologically- o...
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Published in: | European journal of cancer (1990) Vol. 39; no. 7; pp. 917 - 926 |
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Abstract | A single-agent dose escalating phase I and pharmacokinetic study with Cilengitide, an inhibitor of the integrins αvβ3 and αvβ5, was performed to determine its safety and toxicity. Cilengitide was administered as a one-hour infusion twice weekly without interruption to patients with histologically- or cytologically-confirmed metastatic solid tumours. Plasma pharmacokinetics were determined at days 1 and 15. 37 patients were enrolled into the study. Dose levels studied were 30, 60, 120, 180, 240, 400, 600, 850, 1200, and 1600 mg/m2/infusion. There was no dose-limiting toxicity (DLT). Pharmacokinetics were dose-independent and time-invariant. Apparent terminal half-life ranged from 3 to 5 h. At 120 mg/m2/infusion, peak plasma concentrations were attained that optimally inhibited tumour growth in preclinical models. Cilengitide can be safely administered using a continuous twice-weekly infusion regimen. As DLT was not reached, future trials should explore Cilengitide at different doses. |
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AbstractList | A single-agent dose escalating phase I and pharmacokinetic study with Cilengitide, an inhibitor of the integrins αvβ3 and αvβ5, was performed to determine its safety and toxicity. Cilengitide was administered as a one-hour infusion twice weekly without interruption to patients with histologically- or cytologically-confirmed metastatic solid tumours. Plasma pharmacokinetics were determined at days 1 and 15. 37 patients were enrolled into the study. Dose levels studied were 30, 60, 120, 180, 240, 400, 600, 850, 1200, and 1600 mg/m2/infusion. There was no dose-limiting toxicity (DLT). Pharmacokinetics were dose-independent and time-invariant. Apparent terminal half-life ranged from 3 to 5 h. At 120 mg/m2/infusion, peak plasma concentrations were attained that optimally inhibited tumour growth in preclinical models. Cilengitide can be safely administered using a continuous twice-weekly infusion regimen. As DLT was not reached, future trials should explore Cilengitide at different doses. |
Author | Brindley, C Böttcher, S Drevs, J Eskens, F.A.L.M Dumez, H Wynendaele, W Hoekstra, R van Oosterom, A.T Perschl, A Verweij, J |
Author_xml | – sequence: 1 givenname: F.A.L.M surname: Eskens fullname: Eskens, F.A.L.M email: f.eskens@erasmusmc.nl organization: Erasmus Medical Center, Department of Medical Oncology, PO Box 2040, 3000 CA Rotterdam, The Netherlands – sequence: 2 givenname: H surname: Dumez fullname: Dumez, H organization: University Hospital Gasthuisberg, 3000 Leuven, Belgium – sequence: 3 givenname: R surname: Hoekstra fullname: Hoekstra, R organization: Erasmus Medical Center, Department of Medical Oncology, PO Box 2040, 3000 CA Rotterdam, The Netherlands – sequence: 4 givenname: A surname: Perschl fullname: Perschl, A organization: Merck KGaA, D-64293 Darmstadt, Germany – sequence: 5 givenname: C surname: Brindley fullname: Brindley, C organization: Quintiles Scotland Limited, Edinburgh EH14 4AP, Scotland, UK – sequence: 6 givenname: S surname: Böttcher fullname: Böttcher, S organization: Merck KGaA, D-64293 Darmstadt, Germany – sequence: 7 givenname: W surname: Wynendaele fullname: Wynendaele, W organization: University Hospital Gasthuisberg, 3000 Leuven, Belgium – sequence: 8 givenname: J surname: Drevs fullname: Drevs, J organization: Tumour Biology Center, Freiburg, Germany – sequence: 9 givenname: J surname: Verweij fullname: Verweij, J organization: Erasmus Medical Center, Department of Medical Oncology, PO Box 2040, 3000 CA Rotterdam, The Netherlands – sequence: 10 givenname: A.T surname: van Oosterom fullname: van Oosterom, A.T organization: University Hospital Gasthuisberg, 3000 Leuven, Belgium |
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Keywords | Pharmacology Cilengitide (EMD 121974) Phase I clinical trial Angiogenesis inhibitor Integrins Antineoplastic agent Human Solid tumor Peptides Maximal dose Toxicity Inlegrins Treatment efficiency Chemotherapy Integrin Phase I trial Cilengitide Advanced stage Inhibitor Pharmacokinetics Therapeutic protocol |
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PublicationTitle | European journal of cancer (1990) |
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SubjectTerms | Angiogenesis inhibitor Antineoplastic agents Biological and medical sciences Chemotherapy Cilengitide (EMD 121974) Integrins Medical sciences Multiple tumors. Solid tumors. Tumors in childhood (general aspects) Pharmacology Pharmacology. Drug treatments Phase I clinical trial Tumors |
Title | Phase I and pharmacokinetic study of continuous twice weekly intravenous administration of Cilengitide (EMD 121974), a novel inhibitor of the integrins αvβ3 and αvβ5 in patients with advanced solid tumours |
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