Search Results - "MCKEAGE, M. J"

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  1. 1

    Randomised phase II study of ASA404 combined with carboplatin and paclitaxel in previously untreated advanced non-small cell lung cancer by McKeage, M J, Von Pawel, J, Reck, M, Jameson, M B, Rosenthal, M A, Sullivan, R, Gibbs, D, Mainwaring, P N, Serke, M, Lafitte, J-J, Chouaid, C, Freitag, L, Quoix, E

    Published in British journal of cancer (16-12-2008)
    “…ASA404 (5,6-dimethylxanthenone-4-acetic acid or DMXAA) is a small-molecule tumour-vascular disrupting agent (Tumour-VDA). This randomised phase II study…”
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  2. 2

    Oxaliplatin causes selective atrophy of a subpopulation of dorsal root ganglion neurons without inducing cell loss by JAMIESON, S. M. F, LIU, J, CONNOR, B, MCKEAGE, M. J

    Published in Cancer chemotherapy and pharmacology (01-10-2005)
    “…Peripheral neuropathy is induced by multiple doses of oxaliplatin and interferes with the clinical utility of the drug in patients with colorectal cancer. In…”
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  3. 3

    Relationships between hydrophobicity, reactivity, accumulation and peripheral nerve toxicity of a series of platinum drugs by SCRENCI, D, MCKEAGE, M. J, GALETTIS, P, HAMBLEY, T. W, PALMER, B. D, BAGULEY, B. C

    Published in British journal of cancer (01-02-2000)
    “…Previous work has shown platinum drugs to differ in their effects on the peripheral nervous system. To test whether their differential toxicity was due to…”
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  4. 4

    Nucleolar damage correlates with neurotoxicity induced by different platinum drugs by MCKEAGE, M. J, HSU, T, SCRENCI, D, HADDAD, G, BAGULEY, B. C

    Published in British journal of cancer (19-10-2001)
    “…Platinum-based drugs are very useful in cancer therapy but are associated with neurotoxicity in the clinic. To investigate the mechanism of neurotoxicity,…”
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  5. 5

    Mass balance, excretion and metabolism of [14C] ASA404 in cancer patients in a phase I trial by McKeage, M. J., Fong, P. C., Hong, X., Flarakos, J., Mangold, J., Du, Y., Tanaka, C., Schran, H.

    Published in Cancer chemotherapy and pharmacology (01-05-2012)
    “…Purpose To determine the mass balance, excretion and metabolism of the small molecule flavonoid tumour vascular disrupting agent ASA404 in patients with…”
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  6. 6

    Lobaplatin: a new antitumour platinum drug by McKeage, M J

    Published in Expert opinion on investigational drugs (01-01-2001)
    “…Lobaplatin (D-19466) is a diastereometric mixture of platinum(II) complexes containing a 1,2-bis(aminomethyl)cyclobutane stable ligand and lactic acid as the…”
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  7. 7

    Nucleolar enlargement, nuclear eccentricity and altered cell body immunostaining characteristics of large-sized sensory neurons following treatment of rats with paclitaxel by Jamieson, S.M.F., Liu, J.J., Connor, B., Dragunow, M., McKeage, M.J.

    Published in Neurotoxicology (Park Forest South) (01-11-2007)
    “…Paclitaxel-induced sensory neuropathy is a problematic side-effect of cancer chemotherapy. Previous studies in rodents have shown paclitaxel treatment to have…”
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  8. 8

    Comparative adverse effect profiles of platinum drugs by MCKEAGE, M. J

    Published in Drug safety (01-10-1995)
    “…Since the discovery of the biologically active platinum complexes 30 years ago, 2 agents have become widely established in clinical oncology practice. Both…”
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  9. 9

    Phase I and pharmacokinetic study of an oral platinum complex given daily for 5 days in patients with cancer by McKeage, M J, Raynaud, F, Ward, J, Berry, C, O'Dell, D, Kelland, L R, Murrer, B, Santabárabara, P, Harrap, K R, Judson, I R

    Published in Journal of clinical oncology (01-07-1997)
    “…We aimed to determine the maximum-tolerated dose (MTD) clinical toxicities, pharmacokinetics, and pharmacodynamics of oral JM216 given once daily for 5 days to…”
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  10. 10

    Paclitaxel induces nucleolar enlargement in dorsal root ganglion neurons in vivo reducing oxaliplatin toxicity by JAMIESON, S. M. F, LIU, J, HSU, T, BAGULEY, B. C, MCKEAGE, M. J

    Published in British journal of cancer (16-06-2003)
    “…Paclitaxel and oxaliplatin are promising drugs for combination trials but both induce peripheral neurotoxicity. To investigate this toxicity, 10-week-old…”
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  11. 11

    Preclinical antitumor evaluation of bis-acetato-ammine-dichloro-cyclohexylamine platinum(IV) : an orally active platinum drug by KELLAND, L. R, ABEL, G, MCKEAGE, M. J, JONES, M, GODDARD, P. M, VALENTI, M, MURRER, B. A, HARRAP, K. R

    Published in Cancer research (Chicago, Ill.) (01-06-1993)
    “…The cytotoxicity of a novel platinum(IV) complex, bis-acetato-amminedichloro-cyclohexylamine platinum(IV) (JM216), has been evaluated in vitro against a panel…”
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  12. 12

    Stereoselective peripheral sensory neurotoxicity of diaminocyclohexane platinum enantiomers related to ormaplatin and oxaliplatin by SCRENCI, D, ER, H. M, HAMBLEY, T. W, GALETTIS, P, BROUWER, W, MCKEAGE, M. J

    Published in British journal of cancer (01-01-1997)
    “…The diaminocyclohexane platinum (Pt(DACH)) derivatives ormaplatin and oxaliplatin have caused severe and dose-limiting peripheral sensory neurotoxicity in a…”
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  13. 13

    Preparation, DNA binding, and in vitro cytotoxicity of a pair of enantiomeric platinum(II) complexes, [(R)- and (S)-3-aminohexahydroazepine]dichloroplatinum(II). Crystal structure of the S enantiomer by FENTON, R. R, EASDALE, W. J, ER, H. M, O'MARA, S. M, MCKEAGE, M. J, RUSSELL, P. J, HAMBLEY, T. W

    Published in Journal of medicinal chemistry (28-03-1997)
    “…A pair of enantiomeric Pt(II) complexes, [Pt(R-ahaz)Cl2] and [Pt(S-ahaz)Cl2] (ahaz = 3-aminohexahydroazepine), has been investigated for their ability to bind…”
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  14. 14

    Lack of nephrotoxicity of oral ammine/amine platinum (IV) dicarboxylate complexes in rodents by MCKEAGE, M. J, MORGAN, S. E, BOXALL, F. E, MURRER, B. A, HARD, G. C, HARRAP, K. R

    Published in British journal of cancer (01-05-1993)
    “…The comparative nephrotoxicity of i.v. cisplatin, i.v. carboplatin and six p.o. ammine/amine Pt(IV) dicarboxylates was studied in rodents following single MTD…”
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  16. 16

    Phase I study of paclitaxel and oral etoposide in previously untreated non-small-cell and extensive small-cell lung cancer by Boyer, M. J., Zalcberg, J., Olver, I. N., Millward, M. J., Richardson, G., McKeage, M. J.

    Published in Annals of oncology (01-05-1997)
    “…Purpose: This phase I study of paclitaxel and oral etoposide was performed to determine the safety of the combination in patients with advanced lung cancer who…”
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  17. 17

    Platinum neurotoxicity: clinical profiles, experimental models and neuroprotective approaches by Screnci, Daniela, McKeage, Mark J

    Published in Journal of inorganic biochemistry (01-10-1999)
    “…This paper reviews the neurotoxic side-effects associated with platinum drugs, experimental approaches to studying this toxicity and attempts to use…”
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  18. 18

    Lack of neurotoxicity of oral bisacetatoamminedichlorocyclohexylamine-platinum(IV) in comparison to cisplatin and tetraplatin in the rat by MCKEAGE, M. J, BOXALL, F. E, JONES, M, HARRAP, K. R

    Published in Cancer research (Chicago, Ill.) (01-02-1994)
    “…This study compared the effect on sensory nerve conduction velocity in the hind limb of chronically treated age-matched rats of a novel lipophilic p.o…”
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  19. 19

    Overview of docetaxel (Taxotere)/cisplatin combination in non-small cell lung cancer by Le Chevalier, T, Bérille, J, Zalcberg, J R, Millward, M J, Monnier, A, Douillard, J Y, McKeage, M J, James, R, Soulas, F, Loret, C, Bougon, N, Bizzari, J P

    Published in Seminars in oncology (01-06-1999)
    “…Cisplatin-based chemotherapy is effective in non-small cell lung cancer (NSCLC), although it prolongs survival only modestly. Single-agent docetaxel (Taxotere;…”
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  20. 20

    Mechanism of action of an orally administered platinum complex [ammine bis butyrato cyclohexylamine dichloroplatinum (IV) (JM221)] in intrinsically cisplatin-resistant human ovarian carcinoma in vitro by MCKEAGE, M. J, ABEL, G, KELLAND, L. R, HARRAP, K. R

    Published in British journal of cancer (1994)
    “…Intrinsic resistance to existing clinical platinum drugs is a major cause of treatment failure; moreover, these agents have the drawbacks of cross-resistance…”
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