Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/9880
Title: A randomized, double-blinded, placebo-controlled phase II trial of recombinant human leukemia inhibitory factor (rhuLIF, emfilermin, AM424) to prevent chemotherapy-induced peripheral neuropathy.
Authors: Davis, Ian D;Kiers, Lynette;MacGregor, Lachlan;Quinn, Michael;Arezzo, Joseph;Green, Michael;Rosenthal, Mark A;Chia, Michael;Michael, Michael;Bartley, Peter;Harrison, Leonie;Daly, Michael
Affiliation: Austin Health, Studley Road, Heidelberg, Victoria 3084, Australia. Ian.Davis@ludwig.edu.au
Issue Date: 1-Mar-2005
Citation: Clinical Cancer Research : An Official Journal of the American Association For Cancer Research; 11(5): 1890-8
Abstract: To determine whether recombinant human leukemia inhibitory factor (rhuLIF, AM424, emfilermin) can prevent or ameliorate the development of chemotherapy-induced peripheral neuropathy (CIPN) after treatment with carboplatin (AUC 6) and paclitaxel (175 mg/m(2) over 3 hours).Randomized double-blind placebo-controlled phase II clinical trial. Eligible patients had solid tumors for which treatment with carboplatin/paclitaxel was appropriate. The primary end point was a standardized composite peripheral nerve electrophysiology (CPNE) score, based on nerve velocities and amplitudes, measured at baseline and after four cycles of chemotherapy. Secondary efficacy end points included CPNE score at last cycle and at exit evaluation, vibration perception threshold, H-reflex latency, symptom scores, and quantitative assessment of neurologic signs. Study drug was given s.c. daily for 7 days starting the day before chemotherapy. Patients were randomized to receive low-dose rhuLIF (2 microg/kg), high-dose rhuLIF (4 microg/kg), or placebo.Patients (n = 117) were randomized across seven neurology test centers. Thirty-six patients received low dose rhuLIF (2 microg/kg), 39 received high dose rhuLIF (4 microg/kg) and 42 received placebo. rhuLIF was well tolerated with 95% compliance and no adverse effects on quality of life. No differences between groups in CPNE or any of the individual neurologic testing variables were observed between baseline and cycle 4 or by the secondary efficacy variables.rhuLIF is not effective in preventing CIPN caused by carboplatin and paclitaxel. CPNE is a reliable and valid tool that was sensitive to the onset and progression of CIPN.
Internal ID Number: 15756015
URI: http://ahro.austin.org.au/austinjspui/handle/1/9880
DOI: 10.1158/1078-0432.CCR-04-1655
URL: http://www.ncbi.nlm.nih.gov/pubmed/15756015
Type: Journal Article
Subjects: Adult
Aged
Antineoplastic Combined Chemotherapy Protocols.adverse effects.therapeutic use
Carboplatin.administration & dosage.adverse effects
Cytokines
Dose-Response Relationship, Drug
Double-Blind Method
Female
Humans
Interleukin-6
Leukemia Inhibitory Factor
Lipase
Male
Middle Aged
Neoplasms.drug therapy
Neural Conduction
Paclitaxel.administration & dosage.adverse effects
Peripheral Nervous System Diseases.chemically induced.prevention & control
Placebos
Prospective Studies
Proteins.administration & dosage.therapeutic use
Appears in Collections:Journal articles

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